chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1252920587252920588CT24GENIChomozygous109020297
1252920757252920758AC20GENIChomozygous108612904
1252929515252929516TA17GENIChomozygous108612905
1252936295252936296CT32GENICheterozygous109057773
1252936333252936334GA30GENICheterozygous109020301
1252937395252937396AG70GENICheterozygous108612907
1252937482252937483AG65GENICheterozygous108612908
1252937590252937591CT54GENICheterozygous108612909
1252939092252939093CA19GENICheterozygous109020303
1252939098252939099CA21GENICheterozygous108612911
1252939116252939117CA17GENICpossibly homozygous109020304
1252941474252941475CT20GENIChomozygous109020305
1252944488252944489AG29GENIChomozygous108612914
1252946572252946573GA20GENIChomozygous109020306
1252946716252946717CG15GENICheterozygous109057774
1252947964252947965GA19GENIChomozygous109020307
1252948020252948021AT22GENIChomozygous109020308
1252948262252948263AG21GENIChomozygous109020309
1252948584252948585TC45GENIChomozygous109020310
1252948698252948699AG21GENIChomozygous109020311
1252949314252949315GA8GENIChomozygous109020312
1252949549252949550AG15GENIChomozygous109020313
1252949776252949777CT24GENIChomozygous109020314
1252950461252950462TC22GENIChomozygous109020315
1252951059252951060TG25GENIChomozygous109020316
1252951063252951064GT30GENIChomozygous109020317
1252951733252951734AG9GENICheterozygous109020318
1252951864252951865CT50GENICheterozygous108612917
1252953013252953014AT25GENIChomozygous109020319
1252953158252953159GA25GENIChomozygous109020320
1252954536252954537CT16GENIChomozygous109020321
1252955164252955165TC24GENIChomozygous109020322
1252955441252955442TC29GENIChomozygous109020323
1252955542252955543AG25GENIChomozygous109020324
1252956523252956524AC12GENIChomozygous109020325
1252956786252956787CT18GENIChomozygous109020326
1252958013252958014AG23GENIChomozygous108612919
1252958113252958114AG37GENIChomozygous109020327