chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13107486542107486544AC--3GENIChomozygous50566727
13107488687107488689CA--8GENICheterozygous50535447
13107496962107496967AGTAA-----14GENICheterozygous50535448
13107502914107502916GG--1GENIChomozygous50152407
13107504162107504163GGA12GENICheterozygous50152409
13107510045107510046A-10GENIChomozygous49874490
13107509953107509954C-17GENIChomozygous49874487
13107509962107509963AT16GENIChomozygous49874488
13107510030107510031C-11GENIChomozygous49874489
13107499226107499227AAGTGT1GENIChomozygous50894240
13107510046107510047GT7GENIChomozygous50498850
13107510048107510049GT8GENIChomozygous50498851
13107510055107510056GT7GENIChomozygous49874491
13107510067107510068AG13GENIChomozygous50498852
13107510068107510069GT13GENIChomozygous50498853
13107510074107510075AG13GENIChomozygous49874492
13107510080107510081TTGGGG13GENIChomozygous49874493
13107511680107511681CCTTA1GENIChomozygous49874494
13107518229107518230CCTT2GENICheterozygous50535452
13107518254107518255GT8GENIChomozygous49874496
13107521432107521433GGT11GENICheterozygous50152439
13107541465107541466GGA5GENICheterozygous50535456
13107546133107546134TC8GENIChomozygous49874504
13107546137107546138AG7GENIChomozygous50535458
13107546139107546140TA5GENIChomozygous50535460
13107546141107546142TTA6GENIChomozygous50535462
13107546144107546153GTTTAAGTG---------8GENIChomozygous50535464
13107552290107552291GC25GENIChomozygous49874509
13107589177107589207CACACACGCACACACACACACACACGCACG------------------------------14GENICheterozygous50498855
13107589651107589652AAG4GENIChomozygous49874516
13107553515107553516TTAAAC13GENIChomozygous51156640