chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108631858886318589GA5GENIChomozygous887239402
108631921086319211GA9GENICheterozygous887239403
108632007386320074GT20GENIChomozygous887239404
108632117686321177AG22GENIChomozygous887239405
108632166286321663GA16GENIChomozygous887239406
108632223486322235CT18GENIChomozygous887239407
108632227186322272GA27GENIChomozygous887239408
108632232886322329CT7GENIChomozygous887239409
108632233386322334AG5GENIChomozygous887239410
108632329686323297GA13GENIChomozygous887239411
108632330386323304AG14GENIChomozygous887239412
108632353486323535AT15GENIChomozygous887239413
108632359286323593CT9GENIChomozygous887239414
108632453686324537CT25GENIChomozygous887239415
108632529086325291CT19GENIChomozygous887239416
108632572886325729AG20GENIChomozygous887239417
108632634986326350TG5GENIChomozygous887239418
108632636786326368TC5GENIChomozygous887239419
108632745486327455AG23GENIChomozygous887239420
108632769686327697TG10GENIChomozygous887239421
108632795486327955AG19GENIChomozygous887239422
108633008786330088CA17GENIChomozygous887239423
108633092486330925GA24GENIChomozygous887239424
108633483286334833CT18GENIChomozygous887239425
108633483586334836TC20GENIChomozygous887239426
108633488086334881AG18GENIChomozygous887239427
108633534886335349CT15GENIChomozygous887239428