chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119557168119557169T19GENIChomozygous128511514
7119557171119557171GGG19GENIChomozygous128511515
7119557179119557180G19GENIChomozygous128511516
7119557185119557186GT21GENIChomozygous115852521
7119557187119557188G21GENIChomozygous128511517
7119557230119557230G20GENIChomozygous128511518
7119557236119557238GT19GENIChomozygous128511519
7119557247119557247A19GENIChomozygous128511520
7119557341119557342C20GENIChomozygous128511521
7119557344119557344T21GENIChomozygous128511522
7119557395119557396A20GENIChomozygous128511523
7119557469119557469AG12GENIChomozygous128511524
7119557471119557474AGG14GENIChomozygous128511525
7119557565119557565A13GENIChomozygous128511526
7119557617119557618C14GENIChomozygous128511527
7119557632119557633A16GENIChomozygous128511528
7119557677119557678AT17GENIChomozygous116081165
7119557678119557679TG17GENIChomozygous115852529
7119557749119557749A16GENIChomozygous128511529
7119557774119557774T16GENIChomozygous128511530
7119557815119557816GT14GENIChomozygous116081166
7119557816119557817CG13GENIChomozygous116081167
7119557847119557848C14GENIChomozygous128511531
7119557858119557858T19GENIChomozygous128511532
7119557897119557898T21GENIChomozygous128511533
7119557967119557967T24GENIChomozygous128511534
7119558013119558015GC21GENIChomozygous128511535
7119558069119558069T15GENIChomozygous128511536
7119558073119558074A16GENIChomozygous128511537
7119558104119558105C14GENIChomozygous128511538
7119557826119557827GA12GENIChomozygous118395890
7119557706119557707T14GENIChomozygous130346199
7119557825119557826AT12GENIChomozygous118395889