chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118014741118014742TC11GENIChomozygous116673005
8118026909118026910GA6GENIChomozygous126689647
8118027958118027959AC9GENICheterozygous126689648
8118031927118031928GC10GENIChomozygous116673033
8118034686118034687CT17GENIChomozygous117969091
8118037692118037693GT6GENICheterozygous126689649
8118037756118037757AG17GENIChomozygous126675070
8118037813118037814AG13GENIChomozygous126675071
8118044270118044271TC18GENIChomozygous116887521
8118044619118044620GT19GENIChomozygous116887523
8118050865118050866CA13GENIChomozygous126675072
8118050906118050907GC13GENIChomozygous126675073
8118050944118050945TC21GENIChomozygous126675074
8118051062118051063AC12GENIChomozygous126675075
8118051157118051158CT20GENIChomozygous126675076
8118065050118065051AG16GENIChomozygous117969092
8118066820118066821CT14GENIChomozygous117969093
8118073164118073165CA19GENIChomozygous116673077
8118077004118077005GT17GENIChomozygous126675077
8118078277118078278CA4GENIChomozygous116673083
8118080926118080927GA15GENIChomozygous116673089
8118094204118094205GA20GENIChomozygous116673131
8118097458118097459CT16GENIChomozygous126675078
8118099197118099198CT14GENIChomozygous116673139
8118099459118099460TA7GENIChomozygous126675079
8118103727118103728AC22GENIChomozygous116673149
8118108357118108358CT13GENIChomozygous117969101
8118109866118109867TC17GENIChomozygous116673153
8118110607118110608TA12GENIChomozygous116887799
8118113428118113429AT27GENIChomozygous116673157
8118115240118115241CA3GENICheterozygous126689650
8118126115118126116GT12GENIChomozygous117969105
8118130761118130762AC11GENIChomozygous117969106
8118131209118131210GC20GENIChomozygous116673169
8118132293118132294AC10GENIChomozygous126675080
8118134738118134739AT10GENIChomozygous123050356
8118134808118134809GA3GENICheterozygous126689651
8118150532118150533CG27GENIChomozygous116673185
8118154830118154831GT5GENIChomozygous126689652