chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141561395141561396AG42GENIChomozygous60873576
1141561823141561824CG32GENIChomozygous61529865
1141562053141562054GGGTGT28GENIChomozygous61673045
1141562071141562072TTG31GENICpossibly homozygous61673046
1141562072141562073TG35GENICheterozygous61529866
1141562072141562073TTGTG31GENICpossibly homozygous61765357
1141562433141562434GT39GENIChomozygous60873578
1141563525141563526CT28GENIChomozygous61529867
1141564268141564269GA16GENIChomozygous61765359
1141564713141564714TTC32GENIChomozygous61529868
1141566309141566310CT18GENIChomozygous61529869
1141566648141566649CT9GENICheterozygous60873585
1141567259141567260AG27GENIChomozygous60873586
1141569707141569708CT15INTERGENIChomozygous61765363
1141569801141569803TT--2INTERGENICheterozygous61765365
1141569885141569886AACTGAGCTAAATCCCCAACCCCC6INTERGENIChomozygous60873587
1141571266141571267TC22INTERGENIChomozygous60873590
1141571895141571896CT10INTERGENIChomozygous61765367
1141572752141572753GA36INTERGENIChomozygous61765369
1141572959141572960AG39INTERGENIChomozygous60873592
1141573633141573634CT44INTERGENIChomozygous61765371
1141574158141574159G-21INTERGENIChomozygous60873593
1141579513141579514CT35GENIChomozygous61765373
1141580031141580035GGGT----23GENICheterozygous61765375
1141580034141580035TTTTTTG12GENIChomozygous60873596
1141580074141580075GA17GENIChomozygous61765377
1141582437141582438GGC36GENIChomozygous61765379
1141583119141583120TC20INTERGENIChomozygous61529892
1141583255141583256CCA4INTERGENICheterozygous61529894
1141583255141583256CCAA4INTERGENICheterozygous61765381
1141584941141584942AG34INTERGENIChomozygous60873602
1141585722141585723GA25INTERGENICheterozygous60873605
1141585842141585843AAG22INTERGENICheterozygous60873606
1141585878141585879GT18INTERGENIChomozygous61765383
1141586154141586155AC53INTERGENICheterozygous60873607
1141601139141601140TC13INTERGENIChomozygous60873615
1141603416141603417CCT29INTERGENIChomozygous60873631
1141603495141603496CT27INTERGENIChomozygous60873632