chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141561395141561396AG10GENIChomozygous60873576
1141561823141561824CG14GENIChomozygous61529865
1141562071141562072TTG20GENIChomozygous61673046
1141562433141562434GT33GENIChomozygous60873578
1141563525141563526CT22GENIChomozygous61529867
1141564268141564269GA25GENIChomozygous61765359
1141564713141564714TTC21GENIChomozygous61529868
1141566309141566310CT6GENIChomozygous61529869
1141566557141566558AATTTATTTATTTAT7GENIChomozygous62351857
1141566575141566576TTA9GENIChomozygous62161465
1141567259141567260AG20GENIChomozygous60873586
1141569801141569804TTT---9INTERGENICheterozygous62161467
1141569802141569804TT--9INTERGENICheterozygous62161469
1141569885141569886AACTGAGCTAAATCCCCAACCCCC5INTERGENIChomozygous60873587
1141571207141571208GT18INTERGENIChomozygous62161471
1141571266141571267TC29INTERGENIChomozygous60873590
1141571895141571896CT28INTERGENIChomozygous61765367
1141572575141572576A-21INTERGENIChomozygous61304280
1141572752141572753GA17INTERGENIChomozygous61765369
1141572959141572960AG14INTERGENIChomozygous60873592
1141573633141573634CT19INTERGENIChomozygous61765371
1141574158141574159G-8INTERGENIChomozygous60873593
1141579513141579514CT21GENIChomozygous61765373
1141580034141580035TTTTTTGTTTTGTTTTG15GENIChomozygous62161473
1141580074141580075GA26GENIChomozygous61765377
1141582437141582438GGC14GENIChomozygous61765379
1141583119141583120TC13INTERGENIChomozygous61529892
1141601139141601140TC13INTERGENIChomozygous60873615
1141583255141583256CCA7INTERGENIChomozygous61529894
1141584941141584942AG22INTERGENIChomozygous60873602
1141585878141585879GT13INTERGENIChomozygous61765383
1141603416141603417CCT19INTERGENIChomozygous60873631
1141603495141603496CT18INTERGENIChomozygous60873632