chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1151919155151919156AG14GENIChomozygous109148337
1151919808151919809CT4GENIChomozygous120506120
1151920107151920108AG10GENIChomozygous108306970
1151920841151920842TC23GENIChomozygous120506121
1151922388151922389CT15GENIChomozygous120506122
1151923213151923214GA21GENIChomozygous108306972
1151923722151923723TC6GENICheterozygous108306974
1151923723151923724TC6GENIChomozygous108306976
1151925451151925452TC23GENIChomozygous108306980
1151925837151925838TC24GENIChomozygous108306982
1151925973151925974GA19GENIChomozygous120506123
1151927009151927010TC15GENIChomozygous120506124
1151927504151927505TC10GENIChomozygous120506125
1151929221151929222GA31GENIChomozygous120506126
1151929317151929318AG22GENIChomozygous108306998
1151929438151929439GT17GENIChomozygous108307000
1151929470151929471GA20GENIChomozygous125402311
1151930170151930171TC21GENIChomozygous108307006
1151930821151930822AT20GENIChomozygous108307015
1151931294151931295GC17GENIChomozygous108307017
1151933337151933338TA8GENIChomozygous120474106
1151933548151933549AC11GENIChomozygous108307037
1151933742151933743AT27GENIChomozygous109148350
1151946112151946113AG19GENIChomozygous108307047
1151946736151946737CT26GENIChomozygous108307048
1151946895151946896GT20GENIChomozygous108307050
1151947078151947079TG24GENIChomozygous120506127
1151948708151948709AT6GENICheterozygous125402315