chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123934247139342473AG--19GENIChomozygous50451899
123934316839343169GA32GENIChomozygous50946323
123934350839343509AG30GENIChomozygous50198384
123934371039343711AG15GENIChomozygous50198386
123934398139343982GGA14GENIChomozygous50599102
123934399239343993GA18GENIChomozygous50198390
123934432639344327CT35GENIChomozygous50198392
123934468539344686GGAAA9GENICheterozygous50198394
123934468539344686GGAA9GENICheterozygous50542862
123934468539344686GGAAAA9GENICheterozygous50599104
123934469739344698AAATTT10GENIChomozygous50599106
123934470539344708CCC---20GENIChomozygous50542864
123934491839344919GGAACCAAAAAAAAAA4GENICheterozygous50563408
123934494039344941AAAAAAAAAAAAAAAAAACAAAAC3GENICheterozygous50542866
123934500939345010AT9GENIChomozygous50198400
123934501939345020GGT8GENIChomozygous50198402
123934534539345346CCACTG4GENIChomozygous50198404
123934542239345423TC10GENIChomozygous50198406
123934542539345426CG11GENIChomozygous50198408
123934611139346112CT23GENIChomozygous50198410
123934612639346127GC24GENIChomozygous50198412
123934628739346288AG32GENIChomozygous50198414
123934657139346572TC21GENIChomozygous50198416
123934680039346801CCT29GENIChomozygous50198418
123934691839346919TC21GENIChomozygous50198420
123934718139347182CT15GENIChomozygous50198424
123934723039347231TG22GENIChomozygous50198426
123934758539347586GA5GENIChomozygous50198427
123934760739347608AG10GENIChomozygous50198429
123934771939347720AG16GENIChomozygous50198431
123934815039348151AG20GENIChomozygous50198435
123934847739348478CA40GENIChomozygous50198439
123934888439348885GC28GENIChomozygous50198441
123934893139348932GA35GENIChomozygous50946326
123934894039348941CG33GENIChomozygous50198443
123934925439349255CG28GENIChomozygous50198444
123934937039349371AG43GENIChomozygous50946329
123934944739349448GGC29GENICpossibly homozygous50198446
123934946839349469AG19GENIChomozygous50198448
123935017939350180CCTT12GENIChomozygous50451902
123935084239350843AAC2GENIChomozygous50198452