chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1288092118809212TC8GENIChomozygous50036222
1288097078809708GA13GENIChomozygous50462681
1288097178809718CA17GENICpossibly homozygous50462683
1288101158810116CA16GENIChomozygous50462684
1288101478810148CT15GENIChomozygous50462686
1288105778810578AG13GENIChomozygous50361570
1288107608810767AAAACAA-------14GENIChomozygous50361574
1288108928810894AG--13GENIChomozygous50361578
1288109968810997TC22GENIChomozygous50361580
1288110388811039GGA24GENIChomozygous50361582
1288110398811040GA24GENIChomozygous50361584
1288111918811192GA14GENIChomozygous50361586
1288115128811517TTAAA-----28GENIChomozygous50462688
1288115488811549TC29GENIChomozygous50361588
1288121628812163CT16GENIChomozygous50462690
1288121848812185AG23GENIChomozygous50462692
1288133348813335TC12GENICpossibly homozygous50462694
1288140198814025TATATA------1GENIChomozygous50036233
1288148498814850GA20GENIChomozygous50462698
1288151268815127CT15GENIChomozygous50462700
1288151908815191CT22GENIChomozygous50462702
1288154088815409GA18GENIChomozygous50462704
1288155298815530TC21GENIChomozygous50361652
1288156598815660TC25GENIChomozygous50361654
1288158168815817CT9GENIChomozygous50462706
1288158698815870TC14GENIChomozygous50036237
1288159328815933GA22GENIChomozygous50036239
1288162898816290AG22GENIChomozygous50361656
1288165318816532AT18GENIChomozygous50361658
1288169368816937TTAC17GENIChomozygous50361662
1288170518817052GGATTTATTT1GENIChomozygous50560160
1288174498817451TG--1GENIChomozygous50529121
1288180368818042ACACAC------7GENIChomozygous50529125
1288184918818492GA16GENIChomozygous50462708
1288187178818718GGTGTCTCTC10GENIChomozygous50036270
1288195798819580CT22GENIChomozygous50462710
1288204958820496TA16GENIChomozygous50462712
1288213408821341CG9GENIChomozygous50036276
1288214998821500CCTCCTCTCCTCTCCTCTCCTCTCCT1GENIChomozygous50529131
1288134498813450AAC9GENICheterozygous50794540