chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118554844118554846CA--15GENIChomozygous694274132
8118555175118555176AG16GENICpossibly homozygous530226160
8118555184118555185AG19GENICpossibly homozygous530226161
8118555604118555608AAAA----7GENICpossibly homozygous694274133
8118555605118555608AAA---7GENICheterozygous694274134
8118556845118556846AG27GENIChomozygous530226162
8118557229118557230GGA4GENICheterozygous694274135
8118557231118557232AAACTGAATATCAGGGAT5GENIChomozygous694274136
8118557615118557617AC--19GENICheterozygous694274137
8118557617118557618A-18GENICheterozygous694274138
8118557618118557620CC--9GENICheterozygous694274139
8118557707118557708AG19GENIChomozygous532610324
8118557709118557710TC18GENIChomozygous532610325
8118557936118557937AATT28GENIChomozygous694274140
8118557998118557999CT17GENIChomozygous532610326
8118558034118558035GGA18GENICpossibly homozygous694274142
8118558064118558065AG19GENIChomozygous532610327
8118558125118558126GA15GENIChomozygous532610328
8118558134118558135TG13GENIChomozygous530226163
8118558258118558259C-28GENIChomozygous694274143
8118558663118558664CT18GENIChomozygous532610329
8118558832118558834AA--10GENICheterozygous694274145
8118558833118558834A-10GENICheterozygous694274146
8118560021118560022CT25GENIChomozygous530226164