chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X120625392120625393GA21GENIChomozygous108421285
X120625488120625489TA27GENIChomozygous108320557
X120625906120625907GT26GENIChomozygous108421287
X120626025120626026AC26GENICpossibly homozygous108421290
X120626300120626301TC28GENIChomozygous108421292
X120627353120627354CG21GENIChomozygous108421294
X120628572120628573AT27GENIChomozygous108421296
X120629261120629262TG12GENIChomozygous108421298
X120629267120629268TG12GENIChomozygous108421300
X120630143120630144CT21GENIChomozygous108421302
X120630284120630285CA27GENIChomozygous108421304
X120630745120630746AC26GENIChomozygous108421306
X120630844120630845AG27GENIChomozygous108421308
X120632615120632616AG16GENIChomozygous108421314
X120631462120631463GA23GENIChomozygous108421310
X120631530120631531TC23GENIChomozygous108421312
X120632899120632900GC12GENIChomozygous133462548
X120632895120632896GC13GENIChomozygous133462546
X120632897120632898GC13GENIChomozygous133462547
X120632901120632902GC12GENIChomozygous133462549
X120632905120632906GC13GENIChomozygous133462550
X120632907120632908GC12GENIChomozygous133462551
X120633059120633060AG21GENIChomozygous108421316
X120633301120633302CT17GENIChomozygous108421318
X120634237120634238CA27GENIChomozygous108421320
X120634333120634334CT32GENIChomozygous108421322
X120636291120636292GA27GENIChomozygous108421324
X120636323120636324TA23GENIChomozygous108421326
X120636899120636900CA27GENIChomozygous108421328
X120637018120637019GC22GENIChomozygous108421330
X120637794120637795GA27GENIChomozygous108421332
X120637959120637960TC29GENIChomozygous108421334
X120644576120644577AT27GENIChomozygous108454368
X120638350120638351AC25GENIChomozygous108421336
X120638623120638624TC29GENIChomozygous108421338
X120640193120640194AC15GENIChomozygous108421340
X120640919120640920AG26GENIChomozygous108421342
X120647403120647404CA22GENIChomozygous108421344
X120638729120638731AA20GENIChomozygous131243522
X120639633120639633AAG26GENIChomozygous131243523
X120642747120642747A17GENIChomozygous131243524