chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4104374181104374182AG12GENIChomozygous137186326
4104376155104376156CT20GENIChomozygous137186328
4104378518104378518TTTG20GENIChomozygous136909078
4104379313104379314CA19GENIChomozygous137186330
4104381520104381521AG22GENIChomozygous144681629
4104380988104380989AG15GENIChomozygous144681628
4104381604104381605GA23GENIChomozygous144681630
4104381833104381834TC21GENIChomozygous144681631
4104382015104382016CG32GENIChomozygous144681632
4104382209104382213GAAG12GENIChomozygous136909080
4104382438104382439AG17GENIChomozygous137186334
4104384092104384093GA22GENIChomozygous137186339
4104385068104385069GC17GENIChomozygous137186340
4104386415104386415A20GENIChomozygous143058033
4104386451104386452CG21GENIChomozygous143136123
4104387845104387846TC16GENIChomozygous137186343
4104392051104392052GT23GENIChomozygous144681633
4104392442104392443GA19GENIChomozygous137186345
4104392470104392471CT16GENIChomozygous137186346
4104393162104393163CT16GENIChomozygous144681634
4104393946104393947CA17GENIChomozygous144681635
4104394238104394239GA21GENIChomozygous144681636
4104394262104394263AG22GENIChomozygous137186351
4104399039104399040TG27GENIChomozygous137186352
4104402054104402055CT23GENIChomozygous137186357
4104406132104406133AG16GENIChomozygous137186360
4104381928104381929TC26GENIChomozygous149554280
4104393440104393441AG20GENICheterozygous154233260
4104404314104404315CT25GENIChomozygous149554281
4104393440104393441A20GENICpossibly homozygous403116801
4104394262104394263A22GENICheterozygous403116802
4104394306104394307G18GENIChomozygous403116803
4104394306104394307GA18GENICheterozygous403116804
4104394288104394290AG21GENIChomozygous149552239
4104394294104394296AA20GENIChomozygous149552240
4104394298104394308AAAGAAAGGA18GENIChomozygous149552241