chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13107486542107486544AC--3GENICheterozygous50566727
13107496962107496967AGTAA-----13GENICheterozygous50535448
13107502915107502916G-3GENICheterozygous49874485
13107503439107503440CCTTTTTTTTTT4GENICheterozygous50535450
13107509953107509954C-20GENIChomozygous49874487
13107509962107509963AT19GENIChomozygous49874488
13107510030107510031C-13GENIChomozygous49874489
13107510045107510046A-7GENIChomozygous49874490
13107510046107510047GT5GENIChomozygous50498850
13107510048107510049GT5GENIChomozygous50498851
13107510055107510056GT8GENIChomozygous49874491
13107510067107510068AG9GENIChomozygous50498852
13107510068107510069GT9GENIChomozygous50498853
13107510074107510075AG12GENIChomozygous49874492
13107510080107510081TTGGGG11GENIChomozygous49874493
13107511680107511681CCTTA2GENIChomozygous49874494
13107518254107518255GT9GENIChomozygous49874496
13107541465107541466GGA2GENIChomozygous50535456
13107545938107545939A-2GENIChomozygous49874500
13107546133107546134TC14GENIChomozygous49874504
13107546137107546138AG13GENIChomozygous50535458
13107546139107546140TA6GENIChomozygous50535460
13107546141107546142TTA6GENIChomozygous50535462
13107546144107546153GTTTAAGTG---------12GENIChomozygous50535464
13107552290107552291GC27GENIChomozygous49874509
13107559444107559446GT--5GENICheterozygous50535466
13107589651107589652AAG9GENIChomozygous49874516
13107589147107589149CA--8GENICheterozygous50554496