chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121598584515985846CT8GENICpossibly homozygous781758380
121598598015985981GA48GENICheterozygous781758381
121599507015995071CT54GENIChomozygous781758382
121599507315995074AG52GENIChomozygous781758383
121599589115995892GT50GENIChomozygous781758384
121599867415998675AG23GENICheterozygous781758385
121599868515998686AC33GENICheterozygous781758386
121599874115998742CA91GENICheterozygous781758387
121600590716005908TC41GENIChomozygous781758388
121600768616007687AC57GENIChomozygous781758389
121600811316008114CT41GENIChomozygous781758390
121600870616008707GC37GENICpossibly homozygous781758391
121600879516008796AG42GENIChomozygous781758392
121600901716009018TC50GENICpossibly homozygous781758393
121601035116010352AC59GENIChomozygous781758394
121601044516010446CT51GENIChomozygous781758395
121601066516010666TC72GENICpossibly homozygous781758396