chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242322324232233TC19GENIChomozygous602222420
1242327264232727AG15GENIChomozygous602222421
1242328904232891TTCCCTCC13GENIChomozygous729852258
1242336624233668GTGTGT------21GENIChomozygous729852259
1242338354233836GC35GENIChomozygous602222422
1242338884233889GA29GENIChomozygous602222423
1242340884234089TC26GENIChomozygous602222424
1242343054234306TC27GENIChomozygous602222425
1242344524234453TC33GENIChomozygous602222426
1242346594234660A-7GENICpossibly homozygous729852261
1242346614234664ACA---7GENICheterozygous729852264
1242348524234867AAAAAAAGAAAGAAA---------------15GENIChomozygous729852265
1242350874235088TG28GENIChomozygous602222427
1242355454235546GC46GENIChomozygous602222428
1242358524235853CA37GENIChomozygous602222429
1242359274235928TC33GENIChomozygous602222430
1242359854235986TC36GENIChomozygous602222431
1242373164237317GT31GENIChomozygous602222432
1242374124237413TTGGTTATTCAACTCGACCTTTGAA30GENIChomozygous729852266
1242374454237446AAT33GENIChomozygous729852267
1242374524237453GA34GENIChomozygous602222433
1242396454239646TA29GENIChomozygous602222434
1242401504240151CCT19GENIChomozygous729852268
1242415714241573GT--9GENIChomozygous729852270
1242420704242071T-27GENIChomozygous729852271
1242440344244035TTTC4GENICheterozygous729852272
1242440824244083AAGTGT7GENIChomozygous729852278
1242445504244551CCTTTTTT6GENICheterozygous729852281
1242445504244551CCTTTTTTT6GENICheterozygous729852282
1242455704245571TTAC16GENIChomozygous729852283
1242484574248458CCT3GENICheterozygous729852284
1242484834248484CA11GENIChomozygous602222435
1242491904249191G-16GENICheterozygous729852285
1242492094249211AC--9GENIChomozygous729852287
1242519794251980AG19GENIChomozygous602222436
1242547054254709TACA----23GENIChomozygous729852289
1242555614255562CT30GENIChomozygous602222437
1242570074257008GA29GENIChomozygous602222438
1242590844259085GA23GENIChomozygous602222439