chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141561395141561396AG60GENIChomozygous60873576
1141561823141561824CG38GENIChomozygous61529865
1141562071141562072TTG19GENIChomozygous61673046
1141562433141562434GT28GENIChomozygous60873578
1141563525141563526CT37GENIChomozygous61529867
1141564268141564269GA23GENIChomozygous61765359
1141564713141564714TTC33GENIChomozygous61529868
1141566309141566310CT27GENIChomozygous61529869
1141567259141567260AG33GENIChomozygous60873586
1141569802141569804TT--4INTERGENIChomozygous62161469
1141566557141566558AATTTATTTAT2GENIChomozygous62161463
1141566575141566576TTA2GENIChomozygous62161465
1141569885141569886AACTGAGCTAAATCCCCAACCCCC11INTERGENIChomozygous60873587
1141571207141571208GT45INTERGENIChomozygous62161471
1141571266141571267TC41INTERGENIChomozygous60873590
1141571895141571896CT29INTERGENIChomozygous61765367
1141572575141572576A-22INTERGENICpossibly homozygous61304280
1141572752141572753GA57INTERGENIChomozygous61765369
1141572959141572960AG34INTERGENIChomozygous60873592
1141573633141573634CT31INTERGENIChomozygous61765371
1141574158141574159G-14INTERGENIChomozygous60873593
1141579513141579514CT30GENIChomozygous61765373
1141580034141580035TTTTTTGTTTTGTTTTG8GENIChomozygous62161473
1141580074141580075GA21GENIChomozygous61765377
1141582437141582438GGC39GENIChomozygous61765379
1141583119141583120TC26INTERGENIChomozygous61529892
1141583255141583256CCA6INTERGENIChomozygous61529894
1141584941141584942AG35INTERGENIChomozygous60873602
1141585878141585879GT27INTERGENIChomozygous61765383
1141601139141601140TC51INTERGENIChomozygous60873615
1141603416141603417CCT21INTERGENIChomozygous60873631
1141603495141603496CT38INTERGENIChomozygous60873632