chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1273260827273260828CT18GENIChomozygous61224089
1273261605273261606AG22GENIChomozygous61224091
1273262075273262076AAC13GENIChomozygous61224093
1273262370273262371CCTTT6GENIChomozygous61224094
1273262799273262800CT9GENIChomozygous61646274
1273262993273262994TA23GENIChomozygous61224096
1273262994273262995CG23GENIChomozygous61224097
1273263179273263180TC24GENIChomozygous61646275
1273264227273264228TA13GENIChomozygous61224099
1273265255273265256GGTTTTT7GENIChomozygous61646276
1273265276273265277TC18GENICheterozygous61646277
1273265661273265662CG27GENIChomozygous61646278
1273265874273265875AC15GENIChomozygous61646279
1273267271273267272AG17GENIChomozygous61646280
1273267329273267330GT20GENIChomozygous61646281
1273267833273267834AG28GENIChomozygous61224104
1273267954273267955GA20GENIChomozygous61646282
1273268317273268318GA37GENIChomozygous61646283
1273268464273268465TTGAG34GENIChomozygous61646284
1273269106273269107GA29GENIChomozygous61646285
1273270345273270348CAT---22GENIChomozygous61646286
1273270637273270638G-18GENIChomozygous61224105
1273270852273270853GA17GENIChomozygous61646287
1273270904273270905CT21GENIChomozygous61646288