chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161818523718185237CCTTAGGGG56GENIChomozygous139824490
161818570118185705TTCC46GENICpossibly homozygous139824491
161818577818185779CG58GENIChomozygous139888425
161818754118187543AA44GENIChomozygous139824492
161818826618188267CT47GENIChomozygous139888426
161818830818188309CT50GENIChomozygous139888427
161818837518188376GA75GENIChomozygous139888428
161818897318188985GGCCTCTGCACA46GENIChomozygous139824493
161818927318189273AAG50GENIChomozygous139824494
161818948518189486CT70GENIChomozygous139888433
161818886418188865CT56GENIChomozygous139888429
161818889318188894TC52GENIChomozygous139888430
161818902418189025GA55GENIChomozygous139888431
161818930418189305GA58GENIChomozygous139888432
161819018918190189A64GENIChomozygous139824495
161819034518190346GA67GENIChomozygous139888434
161819064118190649GTGCGCGC29GENICpossibly homozygous139824496
161819115418191155TC54GENIChomozygous139888435
161819446218194462ATAGAGTGCTTGTAGCTCAGTTA51GENIChomozygous139824497
161819609818196099CT45GENIChomozygous139888440
161819118818191189TC48GENIChomozygous139888436
161819300518193006TC52GENIChomozygous139888437
161819547518195476GA72GENIChomozygous139888438
161819567218195673CT25GENIChomozygous139888439
161819266618192667A15GENICheterozygous140920538
161819683518196836TG13GENIChomozygous139888441
161819689818196899GA40GENIChomozygous139888442
161819064818190649CT34GENICheterozygous403745794
161819064818190649C34GENICpossibly homozygous403745793