chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2186778336186778337AC15GENIChomozygous110166553
2186782012186782013TC29GENIChomozygous110166555
2186783052186783053AG26GENIChomozygous110166561
2186785712186785713TC40GENIChomozygous110803549
2186791550186791551AG15GENIChomozygous110166567
2186791598186791599TC14GENIChomozygous110166568
2186791870186791871CT20GENIChomozygous110803551
2186792691186792692CT39GENIChomozygous110803552
2186792855186792856TC39GENIChomozygous110166570
2186793015186793016TC24GENIChomozygous110166571
2186793051186793052TC25GENIChomozygous110803554
2186793118186793119AT23GENIChomozygous110803555
2186793145186793146AT15GENIChomozygous110803556
2186793256186793257AG16GENIChomozygous110166572
2186793376186793377GA12GENIChomozygous110803557
2186793386186793387AC13GENIChomozygous110803558
2186793452186793453GA19GENIChomozygous110803559
2186793690186793691GA33GENIChomozygous110803560
2186793947186793948CT32GENIChomozygous110803561
2186794632186794633GA31GENIChomozygous110803562
2186796296186796297CT33GENIChomozygous110166590
2186796872186796873TC12GENIChomozygous110803566
2186796970186796971TC9GENIChomozygous110803567
2186797621186797622CA24GENIChomozygous110803568
2186797722186797723AT20GENIChomozygous120129795
2186797723186797724TG21GENIChomozygous120129796
2186797785186797786CA14GENICpossibly homozygous110166592