SRX5493482 9454 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463340 SAMN11080363 9454 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493483 9451 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463341 SAMN11080362 9451 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493484 9671 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463342 SAMN11080365 9671 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493485 9474 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463343 SAMN11080364 9474 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493486 9439 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463344 SAMN11080359 9439 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493487 9434 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463345 SAMN11080358 9434 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493488 9445 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463346 SAMN11080361 9445 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493489 9670 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463347 SAMN11080360 9670 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493490 9484 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463348 SAMN11080366 9484 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493491 9320 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463349 SAMN11080307 9320 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493492 9309 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463350 SAMN11080306 9309 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493493 8824 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463351 SAMN11080301 8824 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493494 9483 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463352 SAMN11080300 9483 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493495 9481 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463353 SAMN11080299 9481 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493496 9473 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463354 SAMN11080298 9473 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493497 9304 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463355 SAMN11080305 9304 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493498 9411 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463356 SAMN11080304 9411 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493499 9042 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463357 SAMN11080303 9042 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493500 8356 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463358 SAMN11080302 8356 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493501 9408 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463359 SAMN11080354 9408 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493502 9414 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463360 SAMN11080355 9414 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493503 9399 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463361 SAMN11080352 9399 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493504 9402 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463362 SAMN11080353 9402 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493505 9392 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463363 SAMN11080350 9392 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493506 9438 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463364 SAMN11080326 9438 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493507 9343 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463365 SAMN11080310 9343 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493508 9348 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463366 SAMN11080311 9348 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493509 9323 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463367 SAMN11080308 9323 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493510 9340 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463368 SAMN11080309 9340 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493511 9366 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463369 SAMN11080314 9366 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493512 9380 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463370 SAMN11080315 9380 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493513 9354 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463371 SAMN11080312 9354 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493514 9359 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463372 SAMN11080313 9359 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493515 9389 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463373 SAMN11080316 9389 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493516 9393 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463374 SAMN11080317 9393 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493517 9342 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463375 SAMN11080277 9342 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493518 9339 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463376 SAMN11080276 9339 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493519 9308 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463377 SAMN11080273 9308 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493520 9303 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463378 SAMN11080272 9303 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493521 9322 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463379 SAMN11080275 9322 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493522 9319 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463380 SAMN11080274 9319 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493523 8355 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463381 SAMN11080269 8355 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493524 6322 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463382 SAMN11080268 6322 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493525 9409 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463383 SAMN11080271 9409 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493526 9041 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463384 SAMN11080270 9041 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493527 9367 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463385 SAMN11080347 9367 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493528 9360 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463386 SAMN11080346 9360 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493529 9353 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463387 SAMN11080345 9353 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493530 9349 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463388 SAMN11080344 9349 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493531 9344 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463389 SAMN11080343 9344 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493532 9341 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463390 SAMN11080342 9341 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493533 9324 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463391 SAMN11080341 9324 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493534 9321 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463392 SAMN11080340 9321 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493535 9310 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463393 SAMN11080339 9310 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493536 9305 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463394 SAMN11080338 9305 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493537 9400 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463395 SAMN11080287 9400 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493538 9397 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463396 SAMN11080286 9397 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493539 9388 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463397 SAMN11080283 9388 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493540 9378 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463398 SAMN11080282 9378 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493541 9394 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463399 SAMN11080285 9394 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493542 9391 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463400 SAMN11080284 9391 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493543 9352 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463401 SAMN11080279 9352 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493544 9347 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463402 SAMN11080278 9347 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493545 9365 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463403 SAMN11080281 9365 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493546 9358 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463404 SAMN11080280 9358 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493547 9040 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463405 SAMN11080336 9040 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493548 9410 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463406 SAMN11080337 9410 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493549 9446 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463407 SAMN11080328 9446 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493550 9452 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463408 SAMN11080329 9452 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493551 9455 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463409 SAMN11080330 9455 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493552 9475 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463410 SAMN11080331 9475 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493553 9482 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463411 SAMN11080332 9482 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493554 9485 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463412 SAMN11080333 9485 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493555 8823 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463413 SAMN11080334 8823 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493556 8357 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463414 SAMN11080335 8357 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493557 9395 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463415 SAMN11080351 9395 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493558 9379 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463416 SAMN11080348 9379 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493559 9390 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463417 SAMN11080349 9390 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493560 9333 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463418 SAMN11080356 9333 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493561 9428 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463419 SAMN11080357 9428 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493562 9432 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463420 SAMN11080292 9432 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493563 9437 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463421 SAMN11080293 9437 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493564 9440 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463422 SAMN11080294 9440 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493565 9444 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463423 SAMN11080295 9444 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493566 9406 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463424 SAMN11080288 9406 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493567 9412 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463425 SAMN11080289 9412 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493568 9420 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463426 SAMN11080290 9420 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493569 9427 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463427 SAMN11080291 9427 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493570 9450 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463428 SAMN11080296 9450 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493571 9453 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463429 SAMN11080297 9453 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493572 9398 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463430 SAMN11080319 9398 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493573 9396 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463431 SAMN11080318 9396 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493574 9407 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463432 SAMN11080321 9407 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493575 9401 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463433 SAMN11080320 9401 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493576 9334 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463434 SAMN11080323 9334 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493577 9413 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463435 SAMN11080322 9413 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493578 9433 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463436 SAMN11080325 9433 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493579 9672 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463437 SAMN11080324 9672 WXS GENOMIC size fractionation Illumina HiSeq 2500 SRX5493580 9441 SRP187882 PRJNA525890 Exome was captured and enriched from genomic DNA using the SureSelectXT Reagent Kit (Agilent Technologies Inc, Santa Clara, California,USA), representing 72 Mbp of the human genome (hg19 build). Sequencing wasperformed using the system HiSeq 2500 (Illumina). Fragments are aligned around the hg19 reference genome using Burrows-Wheeler alignment (BWA), and variant calling is performed with GATK (Genome Analysis Toolkit) SRS4463438 SAMN11080327 9441 WXS GENOMIC size fractionation Illumina HiSeq 2500