chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17897762678977627TC14GENIChomozygous894740173
17897778178977782CT13GENIChomozygous894740174
17897801978978020AG24GENIChomozygous894740175
17897814678978147TC20GENICheterozygous894740176
17897870878978709CT15GENIChomozygous894740177
17897917778979178CT14GENIChomozygous894740178
17897927378979274CT27GENIChomozygous894740179
17897938978979390CT20GENIChomozygous894740180
17898242278982423TA11GENIChomozygous894740181
17898330978983310AT8GENIChomozygous894740182
17898379178983792CT13GENIChomozygous894740183
17898381078983811TC11GENIChomozygous894740184
17898403978984040TG14GENICheterozygous894740185
17898535578985356TC21GENIChomozygous894740186
17898771378987714TC26GENIChomozygous894740187
17898848778988488GA16GENIChomozygous894740188
17898918278989183TC34GENIChomozygous894740189
17898947678989477GA27GENIChomozygous894740190
17898995778989958TC21GENIChomozygous894740191
17899010278990103AG18GENIChomozygous894740192
17899097878990979TC10GENIChomozygous894740193
17899191478991915GC6GENICheterozygous894740194
17899258778992588AG16GENIChomozygous894740195
17899274978992750TC20GENIChomozygous894740196
17899300878993009TC6GENIChomozygous894740197
17899385278993853CT10GENIChomozygous894740198
17899447178994472GA16GENIChomozygous894740199
17899475078994751CT24GENIChomozygous894740200
17899562578995626CT4GENIChomozygous894740201
17899567078995671AT14GENIChomozygous894740202
17899644878996449TG12GENIChomozygous894740203