chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77037876170378762AT59GENIChomozygous115708893
77037880970378810CT63GENIChomozygous115708894
77037886870378869CA55GENIChomozygous115708895
77037900470379005TG56GENICpossibly homozygous115708896
77037952070379521CT61GENIChomozygous115708897
77038029070380291CT42GENIChomozygous115708899
77038041770380418GT36GENIChomozygous115708900
77038042270380423AC40GENIChomozygous115708901
77038105770381058AG49GENICpossibly homozygous115708902
77038183470381835AG46GENIChomozygous115708903
77038296670382967CT54GENIChomozygous115708904
77038376170383762GA39GENIChomozygous115708905
77038434570384346CT40GENIChomozygous115708906
77038476670384767CT46GENIChomozygous115708907
77038596370385964CT36GENIChomozygous115708908
77038891170388912GA32GENIChomozygous115708909
77038981070389811GA42GENIChomozygous115708911
77038988370389884AT35GENIChomozygous115708912
77039177370391774TC28GENIChomozygous115708914
77039222870392229TC48GENIChomozygous115708915
77039247570392476AT46GENIChomozygous115708916
77039652070396521CT53GENIChomozygous115708918
77039673570396736TC54GENIChomozygous115708919
77039728070397281TC52GENIChomozygous115708920
77039909170399092CT49GENICpossibly homozygous115708921
77039995470399955CT50GENIChomozygous115708923
77040112070401121TC47GENIChomozygous115708924
77040115270401153AC44GENIChomozygous115708925
77038363970383639A23GENICpossibly homozygous128477816
77038364170383641CACCCA26GENICpossibly homozygous128477817
77038600470386097AATGTACTCTTCTGGTGTGTCTGAAGAGAGTGACAGTGTGCTCATAGATAATAAATAAATAAATAAATAAATAAATAGATGTATCTTTAAAAA32GENIChomozygous128477818
77039719270397193T32GENICheterozygous128477820
77038932070389320CG16GENICheterozygous132109297
77039049670390497G16GENICpossibly homozygous132109298
77040407570404076T54GENICpossibly homozygous132109299
77040587070405882CTGTCTGTCTGT36GENIChomozygous132109300
77039380970393810TC63GENICpossibly homozygous116190255
77040468970404690AG70GENIChomozygous116190257
77040476770404768TG59GENIChomozygous116190259