chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2238255881238255882GA8GENIChomozygous110326326
2238255938238255939GA8GENIChomozygous110326328
2238255951238255952GA12GENIChomozygous110326330
2238256431238256432GC26GENIChomozygous110840916
2238256902238256903TA28GENIChomozygous110840917
2238257328238257329TA27GENIChomozygous110840918
2238258223238258224AG13GENIChomozygous110326332
2238258474238258475CA26GENIChomozygous110326336
2238258535238258536CA18GENIChomozygous110840919
2238259119238259120TC13GENIChomozygous110326338
2238260019238260020GA14GENIChomozygous110631557
2238260212238260213GA15GENIChomozygous110840920
2238260630238260631CG22GENIChomozygous110326346
2238260765238260766GA23GENIChomozygous110326348
2238260766238260767TC22GENIChomozygous110326350
2238261830238261831TC21GENIChomozygous110326366
2238261896238261897AC17GENIChomozygous110326368
2238261968238261969CT30GENIChomozygous110840921
2238262260238262261AG23GENIChomozygous110326370
2238262341238262342CA24GENIChomozygous110326374
2238262875238262876TC26GENIChomozygous110326376
2238262985238262986GA24GENIChomozygous110326378
2238263617238263618AG10GENIChomozygous110326380
2238264592238264593GT13GENICpossibly homozygous110840922
2238264754238264755CT8GENIChomozygous110326387
2238265960238265961GA20GENIChomozygous110326391
2238266589238266590CT29GENIChomozygous110326393
2238266726238266727AG21GENIChomozygous110326395
2238266990238266991AG24GENIChomozygous110326399
2238267010238267011GT22GENIChomozygous110840923
2238267070238267071GT17GENIChomozygous110840924
2238267071238267072AT17GENIChomozygous110840925
2238267783238267784GA17GENIChomozygous110326401
2238268795238268796GA17GENIChomozygous110840926
2238269034238269035TC11GENIChomozygous110840927
2238269345238269346TC25GENIChomozygous110840928
2238269883238269884GA21GENIChomozygous110840929
2238270166238270167TC18GENIChomozygous110326405