chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144282433144282434CT38GENIChomozygous114036903
5144282912144282913AG34GENIChomozygous114254031
5144283764144283765TC28GENIChomozygous114254033
5144285454144285455GA41GENIChomozygous114254035
5144285681144285682GA38GENIChomozygous114254037
5144285831144285832GC48GENIChomozygous114254039
5144286519144286520AG47GENIChomozygous114036906
5144287271144287272AG43GENIChomozygous114036907
5144287711144287712G12GENIChomozygous132079403
5144287720144287720TT9GENIChomozygous132079404
5144287752144287753GA5GENIChomozygous114254041
5144287753144287754CT5GENIChomozygous114254043
5144287759144287760TC5GENIChomozygous114036908
5144288066144288067CA23GENIChomozygous114254045
5144288542144288543GA39GENIChomozygous114254047
5144289021144289022AT35GENIChomozygous114036910
5144289180144289181AG44GENIChomozygous114254049
5144289781144289782GT36GENICpossibly homozygous114254051
5144291141144291142TC45GENIChomozygous114036912
5144291627144291628CT31GENIChomozygous114254053
5144292664144292665AG5GENIChomozygous114254055
5144295068144295069AG33GENIChomozygous114036916
5144284384144284384GCTCCT37GENIChomozygous128249917
5144289691144289692T36GENICpossibly homozygous128249918
5144286082144286083T29GENIChomozygous131651331
5144290212144290212TTT7GENICpossibly homozygous131651332
5144292662144292663TG5GENICheterozygous132090102