chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45758576757585768CT30GENIChomozygous57321890
45758589257585893CA20GENIChomozygous57321892
45758610057586101TC31GENIChomozygous57321894
45758618357586184AG27GENIChomozygous57321896
45758667757586678C-23GENIChomozygous56908605
45758667857586679CA23GENIChomozygous58279356
45758669357586694AC24GENIChomozygous57321898
45758673257586733TTA15GENICpossibly homozygous57321904
45758713457587135TG24GENIChomozygous57321906
45758746457587465TTA9GENIChomozygous57321908
45758822257588223AT28GENIChomozygous57321910
45758829057588291TC31GENIChomozygous56908607
45758842957588430TC33GENIChomozygous57321912
45758885057588851GA33GENIChomozygous57730467
45758700957587010TTCC5GENIChomozygous57730463
45758729557587296CG32GENIChomozygous57730465
45758948557589486AG29GENIChomozygous57730469
45758956757589568CT26GENIChomozygous57321918
45759038057590381CCTT22GENICheterozygous57321922
45759038057590381CCT22GENICheterozygous57834916
45759038057590381CCTTT22GENICheterozygous58335374
45759040957590410T-11GENIChomozygous57321926
45759079257590793TC27GENIChomozygous57321930
45759120657591207GA30GENIChomozygous57321932
45759140957591410AG19GENIChomozygous57730473
45759143757591438A-7GENIChomozygous56908609
45759175257591753GA26GENIChomozygous57730475
45759239757592398GGCTT47GENIChomozygous57730477
45759250357592504CCTTGT46GENIChomozygous57730479
45759342657593427GT43GENIChomozygous57730481
45759377757593778AT32GENIChomozygous57730483
45759397057593971TA32GENIChomozygous56908610
45759405257594053CT38GENIChomozygous57730485
45759492457594925CT40GENIChomozygous57730487
45759516257595163TC42GENIChomozygous56908612
45759537757595379TG--13GENIChomozygous58335375
45759538057595497TCTTTTTTTTTTTTTTTTTTTTTTTGGGTCTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGTCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCCATAT---------------------------------------------------------------------------------------------------------------------16GENIChomozygous58335376