chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104888044548880446GC21GENIChomozygous116588646
104888044848880449C21GENIChomozygous128815377
104888046448880464C21GENIChomozygous128815378
104888049048880490G16GENIChomozygous128815379
104888049848880499G17GENIChomozygous128815380
104888050648880506C16GENIChomozygous128815381
104888051248880512G20GENIChomozygous128815382
104888054448880544C23GENIChomozygous128815383
104888055048880551A23GENIChomozygous128815384
104888055548880556C24GENIChomozygous128815385
104888056548880566GA23GENIChomozygous118074756
104888057248880573TG23GENIChomozygous118036948
104888059348880593TTA23GENIChomozygous128815389
104888055848880559T24GENIChomozygous128815386
104888056148880561GGGGGAAG24GENIChomozygous128815387
104888057548880575C22GENIChomozygous128815388
104888060048880600ATCTTT23GENIChomozygous128815390
104888060748880608CG23GENIChomozygous123355719
104888061048880610TC22GENIChomozygous128815391
104888062048880621A21GENIChomozygous128815392
104888062948880629T19GENIChomozygous128815393
104888064348880644G18GENIChomozygous128815394
104888074048880740T9GENIChomozygous128815399
104888076748880767AG11GENIChomozygous128815400
104888076948880769G11GENIChomozygous128815401
104888077048880770GG11GENIChomozygous128815402
104888078248880782C13GENIChomozygous128815403
104888078748880787AT13GENIChomozygous128815404
104888079248880793AT13GENIChomozygous117218399
104888080348880803C13GENIChomozygous128815405
104888083248880832G13GENIChomozygous128815406
104888075848880759TG10GENIChomozygous116977675
104888172048881721GT38GENICheterozygous118036951
104888147448881475GA26GENIChomozygous117993761