chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106850673668506737GC25GENIChomozygous116622249
106850673968506740AT26GENIChomozygous116622251
106850674068506741AG27GENIChomozygous116622253
106850675268506753TG28GENIChomozygous116622255
106850675768506758CG27GENIChomozygous116622257
106850676368506764TC28GENIChomozygous116622259
106850676768506768TG26GENIChomozygous116622261
106850677668506777CA23GENIChomozygous116622263
106853705868537059GA34GENIChomozygous116622344
106853706368537064AT35GENIChomozygous116622346
106853708668537087GT35GENIChomozygous116622348
106853712568537126GT28GENIChomozygous116622350
106853718068537181TG21GENIChomozygous116622352
106854754868547549GA25GENIChomozygous116622376
106854754968547550GA25GENIChomozygous116622378
106854765768547658AG23GENIChomozygous116622380
106863429868634299AT17GENIChomozygous116622738
106863450568634506GT16GENIChomozygous116622746
106876114268761143GA24GENIChomozygous117130963
106885585468855855GA27GENIChomozygous117142738
106891517268915173AT28GENIChomozygous116623906
106897390168973902GT12GENIChomozygous116624094
106897390668973907CG11GENIChomozygous116624096
106897390868973909CT12GENIChomozygous116624098
106914957969149580GT7GENIChomozygous116798374
106914958069149581CG6GENIChomozygous116893353
106914959069149591CT4GENIChomozygous116978880
106915797669157977AG15GENICheterozygous117142740