chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141561395141561396AG22GENIChomozygous60873576
1141561823141561824CG14GENIChomozygous61529865
1141562071141562072TTG22GENICpossibly homozygous61673046
1141562433141562434GT20GENIChomozygous60873578
1141563525141563526CT22GENIChomozygous61529867
1141564268141564269GA21GENIChomozygous61765359
1141564713141564714TTC23GENIChomozygous61529868
1141566309141566310CT3GENIChomozygous61529869
1141566557141566558AATTTATTTATTTAT1GENIChomozygous62351857
1141567259141567260AG36GENIChomozygous60873586
1141569802141569804TT--12INTERGENICheterozygous62161469
1141566575141566576TTA2GENIChomozygous62161465
1141569801141569804TTT---12INTERGENICheterozygous62161467
1141569885141569886AACTGAGCTAAATCCCCAACCCCC10INTERGENIChomozygous60873587
1141571207141571208GT27INTERGENIChomozygous62161471
1141571266141571267TC16INTERGENIChomozygous60873590
1141571895141571896CT36INTERGENIChomozygous61765367
1141572575141572576A-14INTERGENICheterozygous61304280
1141572752141572753GA28INTERGENIChomozygous61765369
1141572959141572960AG25INTERGENIChomozygous60873592
1141573633141573634CT15INTERGENIChomozygous61765371
1141574158141574159G-9INTERGENIChomozygous60873593
1141579513141579514CT21GENIChomozygous61765373
1141580034141580035TTTTTTGTTTTGTTTTG11GENIChomozygous62161473
1141580074141580075GA27GENIChomozygous61765377
1141582437141582438GGC8GENIChomozygous61765379
1141583119141583120TC26INTERGENIChomozygous61529892
1141583217141583218T-10INTERGENICheterozygous61529893
1141583255141583256CCA6INTERGENIChomozygous61529894
1141584941141584942AG25INTERGENIChomozygous60873602
1141585878141585879GT19INTERGENIChomozygous61765383
1141601139141601140TC13INTERGENIChomozygous60873615
1141603416141603417CCT38INTERGENIChomozygous60873631
1141603495141603496CT13INTERGENIChomozygous60873632