SRX2170016 AB1 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697704 AB1 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170017 AB12 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697705 AB12 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170018 AE16 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697706 AE16 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170019 AE17 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697707 AE17 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170020 AE19 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697708 AE19 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170021 BM109 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697709 BM109 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170022 BM163 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697710 BM163 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170023 BALB SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697711 BALB WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170024 CBA SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697712 CBA WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170025 C57BL/6 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697713 C57BL/6 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170026 AB13 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697715 AB13 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170027 AB22 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697716 AB22 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170028 AC16 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697717 AC16 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170029 AC24 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697718 AC24 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170030 AC28 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697719 AC28 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170031 AC29 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697720 AC29 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170032 AC31 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697721 AC31 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton SRX2170033 AE3 SRP089985 DNA was extracted using standard isopropanol purification. Genomic DNA was fragmented using an S2 sonicator (Covaris, USA). Whole genome libraries were constructed using a NEBNext Ultra DNA Library kit (New England Biosciences, Ipswich, MA) with local modifications (specifically Ion Torrent sequencing adaptors were added) and the exome was enriched using a SureSelectXT Mouse All Exon kit (Agilent, Mulgrave, Vic, Australia) that targets 49.6 Mb of the murine genome (221,784 exons across 24,306 coding genes). Sequencing was performed using a Proton sequencer (Ion Torrent, Thermofisher Scientific) system according to manufacturer’s instructions. Two samples were pooled and sequenced on a P1 chip for 520 flows to an average depth of 42x. SRS1697722 AE3 WXS GENOMIC Hybrid Selection 0 0 Technical Read Adapter 1 1 Application Read Forward 5 Ion Torrent Proton