chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14114128031114128032TA44GENIChomozygous113558457
14114130099114130100AG53GENIChomozygous113558459
14114135111114135111TATT67GENIChomozygous129198926
14114139803114139804GA48GENIChomozygous113558461
14114141618114141619CG68GENIChomozygous113558463
14114141680114141681CT59GENIChomozygous113558465
14114143926114143926A65GENICheterozygous129198928
14114143954114143955AG65GENICheterozygous113558467
14114143988114143989AT67GENICheterozygous113558469
14114143995114143996TG69GENICheterozygous113558471
14114144024114144025AG74GENICheterozygous113558473
14114147140114147141G17GENICheterozygous129198929
14114148216114148217TC61GENIChomozygous113558475
14114149745114149746TG50GENIChomozygous113558477
14114149795114149796CA42GENIChomozygous113558479
14114143872114143873TC60GENICheterozygous113699777
14114148982114148983GC65GENIChomozygous113699779
14114148349114148350CT31GENIChomozygous118727286
14114154793114154793AGAGTGATGGG29GENIChomozygous129198930
14114157086114157087AG40GENIChomozygous113558481
14114157363114157364CA45GENIChomozygous113558483
14114159356114159357AT55GENIChomozygous113558485
14114159488114159489CT45GENIChomozygous113558487
14114160023114160024TC31GENIChomozygous113558489
14114160324114160445CTTATTACTAGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCC45GENIChomozygous129198931
14114160918114160918T40GENIChomozygous129198932
14114163015114163016GT48GENIChomozygous113558491
14114163563114163563A43GENIChomozygous129198933
14114163564114163564AAACA44GENIChomozygous129198934
14114163566114163567TA47GENIChomozygous113558493
14114164034114164035GA27GENIChomozygous113831531
14114164276114164277AG50GENIChomozygous113558495
14114172727114172728TC75GENIChomozygous113558497
14114172907114172933TAGGTATGATGCTCACTCTTAGACGG50GENICpossibly homozygous129198935
14114156790114156791AT24GENIChomozygous114094312