chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135406133135406136CAT---24GENIChomozygous57336952
4135406266135406267TTATACCAGA22GENIChomozygous57336954
4135406268135406269TG22GENIChomozygous58282858
4135406388135406389TA24GENIChomozygous57336956
4135406556135406561GTGTC-----25GENICheterozygous58338576
4135406563135406581TGTCTTTATTCAAGTTGC------------------27GENICheterozygous58338577
4135406586135406587CCAA22GENICheterozygous58338578
4135406596135406597CT24GENIChomozygous56937470
4135406870135406872TG--44GENICheterozygous58338579
4135406876135406877GGAC44GENICheterozygous58338580
4135406882135406883GGA44GENICheterozygous58338581
4135406921135406922AG61GENICheterozygous57336969
4135406926135406928AC--63GENICheterozygous58338582
4135406929135406930TTGTA64GENICheterozygous58338583
4135407001135407002TTC46GENICheterozygous58282860
4135407019135407020CCTGGGTTCTAAACCA36GENICheterozygous58338584
4135407028135407029AG33GENICheterozygous57336971
4135407029135407030AAC33GENICheterozygous58338585
4135407032135407034AG--34GENICheterozygous58338586
4135407037135407042TTTCA-----35GENICheterozygous58338587
4135407046135407052GTATGG------32GENICheterozygous58338588
4135407150135407151CT19GENIChomozygous57336973
4135407191135407193AG--28GENIChomozygous56937478
4135407390135407391CA36GENIChomozygous56937486
4135407460135407461AAT53GENICheterozygous58338589
4135407464135407465T-54GENICheterozygous58338590
4135407489135407490AC50GENIChomozygous56937490
4135407589135407590CA51GENIChomozygous56937496
4135407736135407737TTG36GENIChomozygous56937499
4135407742135407743T-34GENIChomozygous56937500
4135407747135407748AC35GENIChomozygous56937501
4135407748135407749AC34GENIChomozygous56937502
4135408544135408545GA28GENIChomozygous57336985