chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2149332609149332610TC28GENIChomozygous110051489
2149338542149338543CT23GENIChomozygous110051490
2149338971149338972CA32GENIChomozygous110051491
2149341859149341860GA21GENIChomozygous110051492
2149344145149344146CT24GENIChomozygous110051493
2149346224149346225TC16GENIChomozygous110051494
2149351267149351268CT24GENIChomozygous110051495
2149351293149351294TC24GENIChomozygous110051496
2149351682149351683CG27GENICpossibly homozygous110051497
2149352036149352037TC18GENIChomozygous110051498
2149352503149352504CA30GENIChomozygous110051499
2149352777149352778CT14GENIChomozygous110051500
2149353451149353452GA34GENIChomozygous110051502
2149353980149353981GA22GENIChomozygous110051503
2149355806149355807GC27GENIChomozygous110051505
2149355860149355861CT29GENIChomozygous110051506
2149357319149357320AG18GENIChomozygous110051507
2149357652149357653CG27GENIChomozygous110051508
2149358124149358125CT16GENIChomozygous110051510
2149358862149358863TC32GENIChomozygous110051511
2149359365149359366GA34GENIChomozygous110051512
2149360268149360269AG24GENIChomozygous110051513
2149360529149360530CT25GENIChomozygous110051514
2149360777149360778AG30GENIChomozygous110051515
2149361979149361980GA24GENIChomozygous110051516
2149362956149362957TA14GENIChomozygous110051517
2149363569149363570AC25GENIChomozygous110051518
2149363746149363747TG18GENIChomozygous110051519
2149364149149364150TC35GENIChomozygous110051520
2149366830149366831GA35GENIChomozygous110051521
2149366900149366901TC28GENIChomozygous110051522
2149370985149370986CT25GENIChomozygous110051523
2149372335149372336TC16GENIChomozygous110051524
2149375263149375264AG21GENIChomozygous110051525
2149376365149376366CT19GENIChomozygous110051526
2149377859149377860AC25GENIChomozygous110051527