chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104888044548880446GC27GENIChomozygous116588646
104888044848880449C26GENIChomozygous128815377
104888046448880464C25GENIChomozygous128815378
104888049048880490G25GENIChomozygous128815379
104888049848880499G28GENIChomozygous128815380
104888050648880506C28GENIChomozygous128815381
104888051248880512G30GENIChomozygous128815382
104888054448880544C25GENIChomozygous128815383
104888055048880551A26GENIChomozygous128815384
104888055548880556C27GENIChomozygous128815385
104888055848880559T26GENIChomozygous128815386
104888056148880561GGGGGAAG26GENIChomozygous128815387
104888056548880566GA25GENIChomozygous118074756
104888057248880573TG29GENIChomozygous118036948
104888057548880575C31GENIChomozygous128815388
104888059348880593TTA33GENIChomozygous128815389
104888060048880600ATCTTT33GENIChomozygous128815390
104888060748880608CG37GENIChomozygous123355719
104888064348880644G32GENIChomozygous128815394
104888061048880610TC38GENIChomozygous128815391
104888062048880621A35GENIChomozygous128815392
104888062948880629T36GENIChomozygous128815393
104888065748880657A31GENIChomozygous128815395
104888066848880669C32GENIChomozygous128815396
104888068448880684TG34GENIChomozygous128815397
104888068748880687G33GENIChomozygous128815398
104888069748880698GT33GENIChomozygous116977671
104888069848880699AG33GENIChomozygous116977673
104888074048880740T9GENIChomozygous128815399
104888075848880759TG12GENIChomozygous116977675
104888076748880767AG14GENIChomozygous128815400
104888076948880769G16GENIChomozygous128815401
104888077048880770GG16GENIChomozygous128815402
104888078248880782C22GENIChomozygous128815403
104888078748880787AT22GENIChomozygous128815404
104888080348880803C24GENIChomozygous128815405
104888083248880832G24GENIChomozygous128815406
104888086448880865GC16GENIChomozygous116977677
104888089048880890A13GENIChomozygous128815407
104888089148880893CC12GENIChomozygous128815408
104888147448881475GA62GENICheterozygous117993761
104888079248880793AT22GENIChomozygous117218399