chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3109816430109816431GC19GENIChomozygous141529363
3109818826109818827CT22GENIChomozygous141529364
3109820292109820293CT24GENIChomozygous141529365
3109820884109820885CT22GENIChomozygous141529366
3109823494109823495AG18GENIChomozygous154110720
3109823498109823499AG18GENIChomozygous141529367
3109823502109823503AG18GENIChomozygous141529368
3109823645109823646TC8GENIChomozygous141529369
3109824137109824138GA10GENICheterozygous154110722
3109824586109824587TC22GENIChomozygous141529370
3109824979109824980AG14GENIChomozygous141529371
3109823494109823495A18GENICheterozygous403073989
3109824137109824138G10GENICpossibly homozygous403073990
3109818972109818974TG20GENIChomozygous136583637
3109824084109824094TCTCTGTCTC18GENIChomozygous141479408