chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135406133135406136CAT---29GENIChomozygous57336952
4135406266135406267TTATACCAGA25GENIChomozygous57336954
4135406268135406269TG23GENIChomozygous58282858
4135406388135406389TA23GENIChomozygous57336956
4135406556135406561GTGTC-----22GENICheterozygous58338576
4135406563135406581TGTCTTTATTCAAGTTGC------------------28GENICheterozygous58338577
4135406586135406587CCAA24GENICheterozygous58338578
4135406596135406597CT26GENIChomozygous56937470
4135406870135406872TG--34GENICheterozygous58338579
4135406876135406877GGAC33GENICheterozygous58338580
4135406882135406883GGA35GENICheterozygous58338581
4135406921135406922AG39GENICheterozygous57336969
4135406926135406928AC--42GENICheterozygous58338582
4135406929135406930TTGTA40GENICheterozygous58338583
4135407001135407002TTC50GENICheterozygous58282860
4135407019135407020CCTGGGTTCTAAACCA43GENICheterozygous58338584
4135407028135407029AG43GENICheterozygous57336971
4135407029135407030AAC42GENICheterozygous58338585
4135407032135407034AG--40GENICheterozygous58338586
4135407037135407042TTTCA-----36GENICheterozygous58338587
4135407046135407052GTATGG------34GENICheterozygous58338588
4135407150135407151CT19GENIChomozygous57336973
4135407191135407193AG--22GENIChomozygous56937478
4135407390135407391CA35GENIChomozygous56937486
4135407460135407461AAT46GENICheterozygous58338589
4135407464135407465T-45GENICheterozygous58338590
4135407489135407490AC44GENIChomozygous56937490
4135407589135407590CA43GENIChomozygous56937496
4135407736135407737TTG33GENIChomozygous56937499
4135407742135407743T-31GENIChomozygous56937500
4135407747135407748AC31GENIChomozygous56937501
4135407748135407749AC31GENIChomozygous56937502
4135408544135408545GA20GENIChomozygous57336985