chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1138550521138550522TG54GENIChomozygous135679483
1138551048138551049TC48GENIChomozygous135679484
1138552584138552585TG52GENIChomozygous135679485
1138554187138554188AG63GENIChomozygous135679486
1138557103138557104CA48GENIChomozygous135679487
1138558090138558091AG63GENIChomozygous135679488
1138561079138561080AG40GENIChomozygous135679489
1138561562138561563AG64GENIChomozygous135679490
1138561605138561606TC52GENIChomozygous135679491
1138561709138561710TG57GENIChomozygous135679492
1138562543138562544GA45GENIChomozygous135679493
1138562636138562637TC44GENIChomozygous135679494
1138562658138562659CT51GENIChomozygous135679495
1138562704138562705AG52GENIChomozygous135679496
1138563240138563249TGAGGAAGG16GENIChomozygous140850537
1138563647138563649AA37GENIChomozygous135431943
1138563945138563946AC53GENIChomozygous135679497
1138564580138564586AGTAAT66GENIChomozygous135431944
1138564778138564779GA62GENIChomozygous135679498
1138565197138565197A56GENICpossibly homozygous135431945
1138566498138566499GA62GENIChomozygous135679499
1138566558138566559TC53GENIChomozygous135679500
1138566586138566587TC62GENIChomozygous135679501
1138566813138566814TC67GENIChomozygous135679502
1138567129138567130GA58GENIChomozygous135679503
1138567735138567736TC59GENIChomozygous135679504
1138568297138568298GA76GENIChomozygous135679505
1138568340138568344AATG73GENIChomozygous135431946
1138569141138569142CT63GENIChomozygous135679506
1138569244138569245AG62GENIChomozygous135679507
1138569797138569798TC51GENIChomozygous135679508
1138570860138570863TGA69GENIChomozygous135431947
1138570949138570950GA57GENIChomozygous135679509
1138571521138571522CT57GENIChomozygous135679510
1138563293138563294GA7GENIChomozygous402965275
1138563293138563294G7GENICheterozygous402965276