chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7107186524107186528AAAG13GENIChomozygous128503329
7107186529107186529TTC13GENIChomozygous128503330
7107186530107186531AT14GENIChomozygous118258153
7107186530107186530T15GENIChomozygous128503331
7107205964107205970GAGGCA3GENIChomozygous129938771
7107206179107206180G7GENIChomozygous129938772
7107206195107206196T6GENIChomozygous128503332
7107206218107206219G5GENIChomozygous128503333
7107206232107206233T5GENIChomozygous128503334
7107206252107206253C7GENIChomozygous128503335
7107206342107206343TG13GENICpossibly homozygous115807345
7107215478107215479CT23GENIChomozygous115807367
7107216392107216392C12GENIChomozygous128503337
7107216401107216403TT11GENIChomozygous128503338
7107216447107216448T24GENIChomozygous128503339
7107216486107216487A25GENIChomozygous128503340
7107216498107216498AT22GENIChomozygous128503341
7107216502107216503A22GENIChomozygous128503342
7107216506107216507A21GENIChomozygous128503343
7107216549107216550CA18GENIChomozygous118258155
7107216550107216551AC18GENIChomozygous118320210
7107216584107216585GA25GENIChomozygous115807369
7107216630107216631G16GENIChomozygous128503344
7107216653107216654T14GENIChomozygous128503345
7107216681107216681A12GENIChomozygous128503346