chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81297409712974098CT10GENIChomozygous126680770
81297482412974825T51GENIChomozygous131041321
81297755412977555GA55GENIChomozygous117090122
81297582212975823GC50GENIChomozygous117090119
81297613812976139AG38GENIChomozygous117090120
81297618512976186CT37GENIChomozygous117090121
81297786612977867CT53GENIChomozygous117090123
81297829312978294AG42GENIChomozygous117090124
81297962212979623AG32GENIChomozygous117090125
81297999812979999CT42GENIChomozygous117090126
81298068712980688GA50GENIChomozygous117090127
81298226712982268CT52GENIChomozygous117090129
81298366712983668A48GENICpossibly homozygous131041322
81298394312983943C61GENIChomozygous131041323
81298417212984173GA46GENIChomozygous117090130
81298433312984333A36GENICpossibly homozygous131041324
81298732912987339GGTGAGGTGA14GENIChomozygous131041325
81298745112987452GA1GENIChomozygous117090133
81298745412987455AC2GENIChomozygous117090134
81298928112989282C55GENIChomozygous131041326
81298990212989906ATGT37GENIChomozygous131041327
81299018512990186T29GENICpossibly homozygous131041328
81299199612991997T39GENIChomozygous131041329
81299244212992443CT55GENIChomozygous117090142
81299286012992861GT50GENIChomozygous117090143
81299316312993164AG32GENIChomozygous117090144
81299318112993182GA31GENIChomozygous117090145