chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2186685119186685120TC21GENIChomozygous110166394
2186685455186685456GA11GENIChomozygous110166395
2186685716186685717AT23GENIChomozygous110166396
2186686338186686339CT30GENIChomozygous110166397
2186688134186688135CT10GENICheterozygous110166398
2186688309186688310CT19GENIChomozygous110166399
2186688334186688335TC17GENIChomozygous110166400
2186689174186689175GT19GENIChomozygous110166401
2186688059186688060GA3GENICheterozygous125700133
2186690143186690144CT13GENIChomozygous110166402
2186690169186690170TG14GENIChomozygous110166403
2186690329186690330TC17GENIChomozygous110166404
2186690354186690355TG17GENIChomozygous110166405
2186690369186690370CT28GENIChomozygous110166406
2186690446186690447CT5GENIChomozygous110166408
2186690517186690518GA18GENIChomozygous110166409
2186690591186690592AC20GENIChomozygous110166410
2186690618186690619AG19GENIChomozygous110166411
2186691163186691164AG25GENIChomozygous110166412
2186691263186691264CT14GENIChomozygous110166413
2186691398186691399CA18GENIChomozygous110166414
2186691713186691714AG17GENIChomozygous110166415
2186692771186692772TC13GENIChomozygous110166416
2186693089186693090CA12GENIChomozygous110166417
2186693906186693907TG4GENIChomozygous110166419
2186694445186694446TG10GENIChomozygous110166420
2186694448186694449CG9GENIChomozygous110166421
2186695866186695867AG19GENIChomozygous110166422
2186690151186690152TC8GENIChomozygous110614103
2186690155186690156CT9GENIChomozygous110614104