chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104888044548880446GC35GENIChomozygous116588646
104888044848880449C35GENIChomozygous128815377
104888046448880464C41GENIChomozygous128815378
104888049048880490G42GENIChomozygous128815379
104888049848880499G46GENIChomozygous128815380
104888050648880506C47GENIChomozygous128815381
104888051248880512G48GENIChomozygous128815382
104888054448880544C50GENIChomozygous128815383
104888055048880551A51GENIChomozygous128815384
104888055548880556C51GENIChomozygous128815385
104888055848880559T49GENIChomozygous128815386
104888056148880561GGGGGAAG49GENIChomozygous128815387
104888056548880566GA49GENIChomozygous118074756
104888057548880575C50GENIChomozygous128815388
104888059348880593TTA52GENIChomozygous128815389
104888060048880600ATCTTT47GENIChomozygous128815390
104888060748880608CG46GENIChomozygous123355719
104888061048880610TC46GENIChomozygous128815391
104888062048880621A40GENIChomozygous128815392
104888062948880629T39GENIChomozygous128815393
104888074048880740T13GENIChomozygous128815399
104888075848880759TG23GENIChomozygous116977675
104888057248880573TG49GENIChomozygous118036948
104888076748880767AG25GENIChomozygous128815400
104888076948880769G27GENIChomozygous128815401
104888077048880770GG27GENIChomozygous128815402
104888078248880782C30GENIChomozygous128815403
104888078748880787AT30GENIChomozygous128815404
104888080348880803C31GENIChomozygous128815405
104888083248880832G32GENIChomozygous128815406
104888079248880793AT30GENIChomozygous117218399
104888086448880865GC2GENIChomozygous116977677
104888145948881460CT77GENICheterozygous117993760
104888147448881475GA92GENIChomozygous117993761