chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13104630935104630936CT75GENIChomozygous139368395
13104632207104632208CT60GENIChomozygous139368396
13104632644104632644GCCCCT58GENIChomozygous139191371
13104633038104633039GA74GENIChomozygous139368397
13104633235104633236CA70GENICpossibly homozygous139368398
13104633263104633264TG65GENIChomozygous139368399
13104633474104633475CA49GENIChomozygous139368400
13104634012104634013CT67GENIChomozygous139368401
13104634076104634077AG59GENIChomozygous139368402
13104635901104635901A55GENIChomozygous139191372
13104636483104636484AG57GENIChomozygous139368403
13104639331104639332GT67GENICpossibly homozygous139368404
13104639556104639557TC69GENIChomozygous139368405
13104642258104642259TC70GENIChomozygous139368406
13104643262104643263AG57GENIChomozygous139368407
13104643306104643307TC57GENIChomozygous139368408
13104644153104644154TA63GENIChomozygous139368409
13104645765104645766TC73GENIChomozygous139368410
13104646018104646019AT56GENIChomozygous139368411
13104646365104646366AG51GENIChomozygous139368412
13104646387104646388GA55GENIChomozygous139368413
13104646389104646390TC57GENIChomozygous139368414
13104646459104646460CT57GENIChomozygous139368415
13104646548104646549AC51GENIChomozygous139368416
13104646611104646612TC55GENIChomozygous139368417
13104646665104646666AG61GENIChomozygous139368418
13104646704104646705AG53GENIChomozygous139368419
13104646736104646737TC55GENIChomozygous139368420
13104646974104646974T68GENIChomozygous139191373
13104647939104647939AATG59GENICpossibly homozygous139191374
13104649186104649187CG52GENIChomozygous139368421
13104649409104649410AG67GENIChomozygous139368422
13104649862104649862TCC41GENIChomozygous139191375
13104651041104651045AATA66GENIChomozygous139191376