chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144033382144033383AG2GENIChomozygous119064566
5144033944144033945GA7GENIChomozygous114036380
5144034457144034458CA3GENIChomozygous114036381
5144034850144034851AG6GENIChomozygous114036382
5144035010144035011TC8GENIChomozygous114036385
5144035765144035766GC7GENIChomozygous114036386
5144035788144035789GA5GENIChomozygous114036387
5144035907144035908TG4GENIChomozygous114036388
5144035924144035925TC3GENIChomozygous114036389
5144037281144037282AG5GENIChomozygous114036390
5144039221144039222TC4GENIChomozygous114036391
5144040538144040539CT6GENIChomozygous114036392
5144040906144040907AT11GENIChomozygous114036394
5144042372144042373GT8GENIChomozygous114036395
5144042774144042775CT7GENIChomozygous114036396
5144043642144043643CT2GENIChomozygous114036397
5144043890144043891TC4GENIChomozygous114036398
5144044088144044089AG4GENIChomozygous114036399
5144044149144044150CA3GENIChomozygous114036400
5144044212144044213AG6GENIChomozygous114036401
5144044646144044647TC8GENIChomozygous118846216
5144046585144046586GC7GENIChomozygous114036403
5144047310144047311TC4GENIChomozygous114036404
5144050006144050007AG2GENIChomozygous114036405
5144050189144050190AG3GENIChomozygous114036406
5144050617144050618CT9GENIChomozygous114036407