chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144033944144033945GA15GENIChomozygous114036380
5144034457144034458CA17GENIChomozygous114036381
5144034937144034938AC20GENIChomozygous114036383
5144034975144034976TC12GENIChomozygous114036384
5144035010144035011TC16GENIChomozygous114036385
5144035765144035766GC11GENIChomozygous114036386
5144035788144035789GA17GENIChomozygous114036387
5144035907144035908TG8GENIChomozygous114036388
5144035924144035925TC10GENIChomozygous114036389
5144037281144037282AG19GENIChomozygous114036390
5144039221144039222TC7GENIChomozygous114036391
5144040538144040539CT17GENIChomozygous114036392
5144042372144042373GT17GENIChomozygous114036395
5144042774144042775CT7GENIChomozygous114036396
5144043642144043643CT17GENIChomozygous114036397
5144043890144043891TC11GENIChomozygous114036398
5144044088144044089AG26GENIChomozygous114036399
5144044149144044150CA21GENIChomozygous114036400
5144044212144044213AG26GENIChomozygous114036401
5144044646144044647TC8GENIChomozygous118846216
5144046585144046586GC13GENIChomozygous114036403
5144047310144047311TC15GENIChomozygous114036404
5144050006144050007AG13GENIChomozygous114036405
5144050189144050190AG15GENIChomozygous114036406
5144050617144050618CT9GENIChomozygous114036407