chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3125504316125504317GA7GENIChomozygous112298169
3125505655125505656AC15GENIChomozygous111696516
3125506849125506850AG9GENIChomozygous111696520
3125506879125506880GA11GENIChomozygous111696522
3125507227125507228CT11GENIChomozygous112298173
3125507406125507407AG8GENIChomozygous111696525
3125508089125508090CT8GENIChomozygous111696529
3125508570125508571GA8GENIChomozygous111696530
3125508990125508991AC20GENIChomozygous111696534
3125509022125509023GA15GENIChomozygous111696536
3125509309125509310TG9GENIChomozygous111696538
3125509749125509750CT9GENIChomozygous112298175
3125510039125510040TC7GENIChomozygous111696539
3125510114125510115AG10GENIChomozygous111696541
3125510119125510120TG11GENIChomozygous111696543
3125510249125510250TC12GENIChomozygous111696545
3125511372125511373GA10GENIChomozygous111696548
3125511396125511397AT12GENIChomozygous111696550
3125511406125511407GA11GENIChomozygous111696552
3125511429125511430CT12GENIChomozygous111696554
3125511730125511731TG7GENIChomozygous111696556
3125512008125512009AT13GENIChomozygous111696558
3125512166125512167TC10GENIChomozygous111696560
3125512204125512205TA13GENIChomozygous111696562
3125512249125512250TA19GENIChomozygous112298179
3125512524125512525TC7GENIChomozygous111696564
3125512630125512631GA10GENIChomozygous111696568
3125512730125512731GA14GENIChomozygous111696572
3125512841125512842AT6GENICheterozygous111696574
3125512854125512855AG5GENIChomozygous111696576
3125513326125513327CA8GENIChomozygous111696578
3125513328125513329TA9GENIChomozygous111696580
3125513363125513364CT13GENIChomozygous111696582
3125513761125513762GT13GENIChomozygous111696584
3125514008125514009CT15GENIChomozygous112298181
3125513816125513817CT15GENIChomozygous119685370