chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119557168119557169T47GENIChomozygous128511514
7119557171119557171GGG47GENIChomozygous128511515
7119557179119557180G45GENIChomozygous128511516
7119557185119557186GT46GENIChomozygous115852521
7119557187119557188G45GENIChomozygous128511517
7119557230119557230G44GENIChomozygous128511518
7119557236119557238GT45GENIChomozygous128511519
7119557247119557247A46GENIChomozygous128511520
7119557341119557342C39GENIChomozygous128511521
7119557344119557344T38GENIChomozygous128511522
7119557395119557396A37GENIChomozygous128511523
7119557469119557469AG41GENIChomozygous128511524
7119557471119557474AGG43GENIChomozygous128511525
7119557565119557565A49GENIChomozygous128511526
7119557617119557618C40GENIChomozygous128511527
7119557632119557633A40GENIChomozygous128511528
7119557677119557678AT35GENIChomozygous116081165
7119557678119557679TG37GENIChomozygous115852529
7119557749119557749A39GENIChomozygous128511529
7119557774119557774T41GENIChomozygous128511530
7119557815119557816GT42GENIChomozygous116081166
7119557816119557817CG41GENIChomozygous116081167
7119557847119557848C46GENIChomozygous128511531
7119557858119557858T46GENIChomozygous128511532
7119557897119557898T45GENIChomozygous128511533
7119557967119557967T41GENIChomozygous128511534
7119558013119558015GC30GENIChomozygous128511535
7119558069119558069T27GENIChomozygous128511536
7119558073119558074A27GENIChomozygous128511537
7119558104119558105C28GENIChomozygous128511538
7119557826119557827GA39GENIChomozygous118395890
7119557706119557707T34GENIChomozygous130346199
7119557825119557826AT40GENIChomozygous118395889