ERS18008196 SAMEA115165807 9606 Homo sapiens Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). ENA first public 2024-01-01 External Id SAMEA115165807 INSDC center name Center of Clinical Research, Shanghai Children's Medical Center, Shanghai, 200127, PR China INSDC last update 2024-01-30T22:15:00Z INSDC status public Submitter Id E-MTAB-13750:SS 11 broker name ArrayExpress collection date not collected common name human disease short stature geographic location (country and/or sea) not collected isolate not applicable organism part blood sample name E-MTAB-13750:SS 11 scientific_name Homo sapiens ERS18008180 SAMEA115165791 9606 Homo sapiens Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). ENA first public 2024-01-01 External Id SAMEA115165791 INSDC center name Center of Clinical Research, Shanghai Children's Medical Center, Shanghai, 200127, PR China INSDC last update 2024-01-30T22:15:00Z INSDC status public Submitter Id E-MTAB-13750:Normal 10 broker name ArrayExpress collection date not collected common name human disease normal geographic location (country and/or sea) not collected isolate not applicable organism part blood sample name E-MTAB-13750:Normal 10 scientific_name Homo sapiens ERS18008181 SAMEA115165792 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease normal organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008206 SAMEA115165817 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008187 SAMEA115165798 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease normal organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008195 SAMEA115165806 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008184 SAMEA115165795 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease normal organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008202 SAMEA115165813 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008190 SAMEA115165801 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease normal organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008197 SAMEA115165808 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008182 SAMEA115165793 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease normal organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008186 SAMEA115165797 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease normal organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008191 SAMEA115165802 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease normal organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008198 SAMEA115165809 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008193 SAMEA115165804 9606 Homo sapiens Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). ENA first public 2024-01-01 External Id SAMEA115165804 INSDC center name Center of Clinical Research, Shanghai Children's Medical Center, Shanghai, 200127, PR China INSDC last update 2024-01-30T22:15:00Z INSDC status public Submitter Id E-MTAB-13750:Normal 9 broker name ArrayExpress collection date not collected common name human disease normal geographic location (country and/or sea) not collected isolate not applicable organism part blood sample name E-MTAB-13750:Normal 9 scientific_name Homo sapiens ERS18008192 SAMEA115165803 9606 Homo sapiens Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). ENA first public 2024-01-01 External Id SAMEA115165803 INSDC center name Center of Clinical Research, Shanghai Children's Medical Center, Shanghai, 200127, PR China INSDC last update 2024-01-30T22:15:00Z INSDC status public Submitter Id E-MTAB-13750:Normal 8 broker name ArrayExpress collection date not collected common name human disease normal geographic location (country and/or sea) not collected isolate not applicable organism part blood sample name E-MTAB-13750:Normal 8 scientific_name Homo sapiens ERS18008179 SAMEA115165790 9606 Homo sapiens Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). ENA first public 2024-01-01 External Id SAMEA115165790 INSDC center name Center of Clinical Research, Shanghai Children's Medical Center, Shanghai, 200127, PR China INSDC last update 2024-01-30T22:15:00Z INSDC status public Submitter Id E-MTAB-13750:Normal 1 broker name ArrayExpress collection date not collected common name human disease normal geographic location (country and/or sea) not collected isolate not applicable organism part blood sample name E-MTAB-13750:Normal 1 scientific_name Homo sapiens ERS18008205 SAMEA115165816 9606 Homo sapiens Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). ENA first public 2024-01-01 External Id SAMEA115165816 INSDC center name Center of Clinical Research, Shanghai Children's Medical Center, Shanghai, 200127, PR China INSDC last update 2024-01-30T22:15:00Z INSDC status public Submitter Id E-MTAB-13750:SS 6 broker name ArrayExpress collection date not collected common name human disease short stature geographic location (country and/or sea) not collected isolate not applicable organism part blood sample name E-MTAB-13750:SS 6 scientific_name Homo sapiens ERS18008189 SAMEA115165800 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease normal organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008201 SAMEA115165812 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008203 SAMEA115165814 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008194 SAMEA115165805 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008185 SAMEA115165796 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease normal organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008208 SAMEA115165819 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008199 SAMEA115165810 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008204 SAMEA115165815 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008207 SAMEA115165818 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008188 SAMEA115165799 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease normal organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008183 SAMEA115165794 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease normal organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30 ERS18008200 SAMEA115165811 9606 Homo sapiens human Protocols: Genomic DNA was extracted from the whole blood of children using a Blood DNA Extraction Kit (Tiangen Biotech, China), then treated with EpiTect Fast DNA Bisulfite Kit (QIAGEN, Germany) for bisulfite conversion. The converted DNA was PCR amplified with primer sequences designed to cover the CpGs in two promoter regions: each region included near 1,000 bp centering around the transcription start sites (TSSs) of SLC22A18. The PCR products were purified and used for DNA library preparation. According to the manufacturer's protocol, the library was prepared with the KAPA HTP Library Preparation Kit (KAPA Biosystems, USA). isolate not applicable disease short stature organism Homo sapiens organism Homo sapiens collection date not collected scientific_name Homo sapiens common name human organism part blood geographic location (country and/or sea) not collected ENA-LAST-UPDATE 2024-01-30