chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144282433144282434CT53GENIChomozygous114036903
5144282912144282913AG37GENIChomozygous114254031
5144283764144283765TC54GENIChomozygous114254033
5144286519144286520AG52GENIChomozygous114036906
5144287271144287272AG41GENIChomozygous114036907
5144287753144287754CT9GENIChomozygous114254043
5144284384144284384GCTCCT35GENIChomozygous128249917
5144285454144285455GA40GENIChomozygous114254035
5144285681144285682GA51GENIChomozygous114254037
5144285831144285832GC54GENIChomozygous114254039
5144287752144287753GA9GENIChomozygous114254041
5144287759144287760TC7GENIChomozygous114036908
5144288066144288067CA38GENICpossibly homozygous114254045
5144288542144288543GA51GENIChomozygous114254047
5144289021144289022AT49GENIChomozygous114036910
5144289180144289181AG51GENIChomozygous114254049
5144289691144289692T46GENICpossibly homozygous128249918
5144287711144287712G21GENICpossibly homozygous132079403
5144287720144287720TT21GENIChomozygous132079404
5144286082144286083T57GENIChomozygous131651331
5144289781144289782GT48GENIChomozygous114254051
5144290212144290212TTT11GENICheterozygous131651332
5144291141144291142TC54GENIChomozygous114036912
5144291627144291628CT21GENIChomozygous114254053
5144292664144292665AG2GENIChomozygous114254055
5144295068144295069AG40GENIChomozygous114036916