chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8110604182110604183CA13GENICheterozygous52802111
8110604482110604483CG2GENIChomozygous52802113
8110604804110604805AG17GENIChomozygous52802115
8110604922110604923AC25GENIChomozygous52802117
8110605180110605181CT12GENIChomozygous52802121
8110605702110605703TC17GENIChomozygous52802123
8110606000110606001CT17GENICpossibly homozygous52802125
8110607345110607346GA3GENIChomozygous52802129
8110607598110607700AATCTACTCTCTTTTTTTTTTTTCCTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC------------------------------------------------------------------------------------------------------23GENICheterozygous53367571
8110608349110608350GGGTGT3GENICheterozygous52802132
8110608352110608354GT--3GENICheterozygous52802136
8110612611110612612GA38GENIChomozygous52802142
8110613628110613629TTC7GENIChomozygous52802144
8110614033110614034GA21GENIChomozygous53164394
8110614289110614290AG5GENIChomozygous52802146
8110614667110614668AG16GENICpossibly homozygous52802148
8110614837110614838CT36GENICpossibly homozygous52802150
8110614881110614882CG14GENIChomozygous52802152
8110614884110614885AG15GENIChomozygous52802154
8110615410110615411GGC10GENIChomozygous52802156
8110615905110615906GC19GENICpossibly homozygous52802158
8110616387110616388TC23GENICpossibly homozygous52802160