chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135406133135406136CAT---23GENIChomozygous57336952
4135406266135406267TTATACCAGA24GENIChomozygous57336954
4135406268135406269TG24GENIChomozygous58282858
4135406388135406389TA22GENIChomozygous57336956
4135406556135406561GTGTC-----35GENICheterozygous58338576
4135406563135406581TGTCTTTATTCAAGTTGC------------------39GENICheterozygous58338577
4135406586135406587CCAA35GENICheterozygous58338578
4135406596135406597CT37GENIChomozygous56937470
4135406870135406872TG--59GENICheterozygous58338579
4135406876135406877GGAC55GENICheterozygous58338580
4135406882135406883GGA54GENICheterozygous58338581
4135406921135406922AG45GENICheterozygous57336969
4135406926135406928AC--49GENICheterozygous58338582
4135406929135406930TTGTA47GENICheterozygous58338583
4135407001135407002TTC40GENICheterozygous58282860
4135407019135407020CCTGGGTTCTAAACCA40GENICheterozygous58338584
4135407028135407029AG36GENICheterozygous57336971
4135407029135407030AAC36GENICheterozygous58338585
4135407032135407034AG--37GENICheterozygous58338586
4135407037135407042TTTCA-----35GENICheterozygous58338587
4135407046135407052GTATGG------33GENICheterozygous58338588
4135407150135407151CT26GENIChomozygous57336973
4135407191135407193AG--31GENIChomozygous56937478
4135407390135407391CA33GENIChomozygous56937486
4135407460135407461AAT43GENICheterozygous58338589
4135407464135407465T-44GENICheterozygous58338590
4135407489135407490AC51GENIChomozygous56937490
4135407589135407590CA45GENIChomozygous56937496
4135407736135407737TTG49GENIChomozygous56937499
4135407742135407743T-45GENIChomozygous56937500
4135407747135407748AC48GENIChomozygous56937501
4135407748135407749AC49GENIChomozygous56937502
4135408544135408545GA53GENICpossibly homozygous57336985