chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X120625392120625393GA14GENIChomozygous108421285
X120625488120625489TA12GENIChomozygous108320557
X120626025120626026AC15GENIChomozygous108421290
X120626300120626301TC8GENIChomozygous108421292
X120627353120627354CG13GENIChomozygous108421294
X120628572120628573AT13GENIChomozygous108421296
X120630143120630144CT8GENIChomozygous108421302
X120630745120630746AC7GENIChomozygous108421306
X120630844120630845AG8GENIChomozygous108421308
X120631462120631463GA15GENIChomozygous108421310
X120631530120631531TC17GENIChomozygous108421312
X120632615120632616AG10GENIChomozygous108421314
X120633059120633060AG14GENICheterozygous108421316
X120633301120633302CT9GENIChomozygous108421318
X120634237120634238CA10GENIChomozygous108421320
X120634333120634334CT11GENIChomozygous108421322
X120636323120636324TA4GENIChomozygous108421326
X120637018120637019GC5GENIChomozygous108421330
X120637794120637795GA7GENIChomozygous108421332
X120637959120637960TC7GENIChomozygous108421334
X120638350120638351AC14GENIChomozygous108421336
X120638623120638624TC16GENIChomozygous108421338
X120640193120640194AC11GENIChomozygous108421340
X120640919120640920AG13GENIChomozygous108421342
X120647403120647404CA22GENIChomozygous108421344