chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1138550521138550522TG56GENICpossibly homozygous135679483
1138551048138551049TC52GENIChomozygous135679484
1138552095138552096AC48GENICpossibly homozygous147645033
1138552584138552585TG57GENIChomozygous135679485
1138554187138554188AG68GENIChomozygous135679486
1138557103138557104CA69GENIChomozygous135679487
1138558090138558091AG64GENIChomozygous135679488
1138561079138561080AG56GENIChomozygous135679489
1138561562138561563AG48GENIChomozygous135679490
1138561605138561606TC56GENIChomozygous135679491
1138561709138561710TG61GENIChomozygous135679492
1138562543138562544GA56GENIChomozygous135679493
1138562636138562637TC62GENIChomozygous135679494
1138562658138562659CT62GENIChomozygous135679495
1138562704138562705AG64GENIChomozygous135679496
1138563945138563946AC44GENIChomozygous135679497
1138564778138564779GA60GENIChomozygous135679498
1138566498138566499GA58GENIChomozygous135679499
1138566558138566559TC57GENIChomozygous135679500
1138566586138566587TC53GENIChomozygous135679501
1138566813138566814TC48GENIChomozygous135679502
1138567129138567130GA65GENIChomozygous135679503
1138567735138567736TC48GENIChomozygous135679504
1138568297138568298GA54GENIChomozygous135679505
1138569141138569142CT54GENIChomozygous135679506
1138569244138569245AG52GENIChomozygous135679507
1138569797138569798TC54GENIChomozygous135679508
1138570949138570950GA68GENIChomozygous135679509
1138571521138571522CT60GENIChomozygous135679510
1138563240138563249TGAGGAAGG11GENICheterozygous140850537
1138563647138563649AA39GENIChomozygous135431943
1138564580138564586AGTAAT51GENIChomozygous135431944
1138565197138565197A52GENICpossibly homozygous135431945
1138568340138568344AATG47GENIChomozygous135431946
1138570860138570863TGA55GENIChomozygous135431947
1138563293138563294GA13GENIChomozygous402965275
1138563293138563294G13GENICheterozygous402965276