chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2186685119186685120TC17GENIChomozygous110166394
2186685455186685456GA18GENIChomozygous110166395
2186685716186685717AT20GENIChomozygous110166396
2186686338186686339CT20GENIChomozygous110166397
2186688134186688135CT10GENIChomozygous110166398
2186688309186688310CT14GENIChomozygous110166399
2186688334186688335TC19GENIChomozygous110166400
2186689174186689175GT23GENIChomozygous110166401
2186690143186690144CT19GENIChomozygous110166402
2186690151186690152TC21GENIChomozygous110614103
2186690155186690156CT20GENIChomozygous110614104
2186690169186690170TG23GENIChomozygous110166403
2186690329186690330TC28GENIChomozygous110166404
2186690354186690355TG20GENIChomozygous110166405
2186690369186690370CT19GENIChomozygous110166406
2186690438186690439CA15GENIChomozygous110166407
2186690446186690447CT13GENIChomozygous110166408
2186690517186690518GA19GENIChomozygous110166409
2186690591186690592AC26GENIChomozygous110166410
2186690618186690619AG22GENIChomozygous110166411
2186691163186691164AG23GENIChomozygous110166412
2186691263186691264CT18GENIChomozygous110166413
2186691398186691399CA18GENIChomozygous110166414
2186691713186691714AG12GENIChomozygous110166415
2186692771186692772TC23GENIChomozygous110166416
2186693089186693090CA16GENIChomozygous110166417
2186693904186693905TC12GENIChomozygous110166418
2186693906186693907TG12GENIChomozygous110166419
2186694445186694446TG14GENIChomozygous110166420
2186694448186694449CG14GENIChomozygous110166421
2186695866186695867AG21GENIChomozygous110166422