chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13107486542107486544AC--4GENICheterozygous50566727
13107488687107488689CA--22GENICheterozygous50535447
13107495426107495427T-20GENICheterozygous49874481
13107496962107496967AGTAA-----12GENICheterozygous50535448
13107502915107502916G-7GENICheterozygous49874485
13107503439107503440CCTTTTTTTTTT4GENICheterozygous50535450
13107509953107509954C-18GENIChomozygous49874487
13107509962107509963AT27GENIChomozygous49874488
13107510030107510031C-33GENIChomozygous49874489
13107510045107510046A-25GENIChomozygous49874490
13107510046107510047GT25GENIChomozygous50498850
13107510048107510049GT23GENIChomozygous50498851
13107510055107510056GT23GENIChomozygous49874491
13107510067107510068AG20GENIChomozygous50498852
13107510068107510069GT20GENIChomozygous50498853
13107510074107510075AG19GENIChomozygous49874492
13107510080107510081TTGGGG16GENIChomozygous49874493
13107511680107511681CCTTA4GENIChomozygous49874494
13107515861107515863GT--18GENICheterozygous50554492
13107518230107518231T-2GENICheterozygous50535454
13107518254107518255GT9GENIChomozygous49874496
13107525270107525271T-20GENICheterozygous50498854
13107525441107525449GATAGATA--------12GENICheterozygous50620818
13107525445107525449GATA----12GENICheterozygous50554494
13107541465107541466GGA12GENICheterozygous50535456
13107545938107545939A-4GENICheterozygous49874500
13107546133107546134TC11GENIChomozygous49874504
13107546137107546138AG9GENIChomozygous50535458
13107546139107546140TA5GENIChomozygous50535460
13107546141107546142TTA3GENIChomozygous50535462
13107546144107546153GTTTAAGTG---------3GENIChomozygous50535464
13107552290107552291GC21GENIChomozygous49874509
13107553516107553520AAAC----12GENICheterozygous50371963
13107589651107589652AAG1GENIChomozygous49874516