chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151512638151512639CT26GENIChomozygous112310751
3151515994151515995G14GENIChomozygous130913971
3151517534151517535AG21GENIChomozygous111777672
3151519994151519995GC26GENIChomozygous111777676
3151522448151522449CA19GENIChomozygous112310753
3151522593151522594A17GENIChomozygous127943658
3151523454151523455AG20GENIChomozygous111777684
3151526739151526740TC21GENIChomozygous111777688
3151527834151527836CC13GENIChomozygous127943659
3151528785151528786AG14GENIChomozygous111777692
3151529623151529623TGAT25GENIChomozygous130913972
3151530256151530257CT29GENIChomozygous111777694
3151531761151531762TC27GENIChomozygous111777696
3151535190151535191AG16GENIChomozygous111777698
3151535237151535238CT18GENIChomozygous112310757
3151539359151539360AG21GENIChomozygous112310759
3151540068151540069CT16GENIChomozygous112310761
3151541015151541016AG20GENIChomozygous111777700
3151542729151542730CT19GENIChomozygous112310763
3151543171151543172AG20GENIChomozygous111777702
3151534446151534447TC14GENIChomozygous130923396