chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144612760144612761CG10GENICpossibly homozygous56068235
5144612816144612817AC16GENICpossibly homozygous56068236
5144612923144612924TC10GENICpossibly homozygous55763269
5144613178144613179AG10GENICheterozygous56068237
5144613887144613888AG10GENICpossibly homozygous56068238
5144615056144615057AG23GENICpossibly homozygous56068241
5144615105144615106TC24GENICpossibly homozygous55914923
5144615244144615245TC24GENICpossibly homozygous56068242
5144615402144615403CT9GENICpossibly homozygous56068243
5144616587144616588AG10GENIChomozygous56068245
5144616693144616694TC37GENIChomozygous55914930
5144617364144617365GC12GENIChomozygous56068246
5144617495144617496TC10GENICheterozygous56068248
5144617752144617753CT5GENIChomozygous56068249
5144617854144617855TTGA12GENIChomozygous56068250
5144617863144617864AC13GENIChomozygous56068251
5144618062144618063AAGGG1GENIChomozygous56068252
5144618219144618220GA10GENIChomozygous55763282
5144618570144618571TC3GENIChomozygous55914936
5144620593144620594GA2GENIChomozygous56068253
5144621924144621925TTA5GENIChomozygous56068254
5144622443144622444GA21GENICpossibly homozygous56068255
5144622902144622903CT11GENICpossibly homozygous55763290
5144623071144623072TC21GENIChomozygous55763292
5144623265144623266TC20GENIChomozygous55763294
5144624112144624113G-1GENIChomozygous56458707
5144624176144624177TC17GENIChomozygous56068257
5144624197144624198TC13GENIChomozygous56068258
5144625216144625217GA8GENICpossibly homozygous56068259
5144625373144625374AT9GENIChomozygous55763299