chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1181135654181135655AC55GENICpossibly homozygous135762700
1181135781181135781A12GENIChomozygous135448847
1181135838181135839AT17GENIChomozygous135762701
1181136680181136681GA54GENIChomozygous135762702
1181136891181136892T40GENIChomozygous135448848
1181139965181139966GT45GENIChomozygous135762703
1181140233181140233A18GENICpossibly homozygous135448849
1181140519181140520CT51GENIChomozygous135762704
1181141093181141095CA57GENIChomozygous135448850
1181141450181141451AG56GENIChomozygous135762705
1181141649181141650GA52GENIChomozygous135762706
1181142089181142090CT46GENIChomozygous135762707
1181142519181142520AG51GENIChomozygous135762708
1181142520181142521AG50GENIChomozygous135762709
1181142522181142523TG49GENIChomozygous135762710
1181143014181143015CT30GENIChomozygous135762711
1181143124181143124AAAC38GENIChomozygous135448851
1181143200181143203CTT64GENIChomozygous135448852
1181144625181144626GT53GENIChomozygous135762712
1181145427181145428TC55GENIChomozygous135762713
1181146584181146585GA57GENIChomozygous135762714
1181146792181146792AC30GENIChomozygous135448853
1181146814181146815AC29GENIChomozygous135762715
1181146826181146826AAAC28GENIChomozygous135448854
1181147127181147128TC62GENIChomozygous135762716
1181147204181147205CT32GENIChomozygous135762717
1181147281181147282CT28GENIChomozygous135762718
1181147884181147885TC60GENIChomozygous135762719
1181148963181148964GA47GENIChomozygous135762720
1181149147181149148AT52GENICpossibly homozygous135762721
1181149824181149825AC67GENICpossibly homozygous135762722
1181151668181151669GA68GENICheterozygous135762723
1181151739181151740CT228GENICheterozygous135762724
1181151746181151747GT238GENICheterozygous135762725
1181151759181151760CT244GENICheterozygous135762726
1181151763181151764AG246GENICheterozygous135762727
1181151779181151780CG251GENICheterozygous135762728
1181151790181151790GA248GENICheterozygous135448855