chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144612760144612761CG14GENICheterozygous56068235
5144612816144612817AC18GENIChomozygous56068236
5144612923144612924TC6GENIChomozygous55763269
5144613178144613179AG10GENIChomozygous56068237
5144613887144613888AG15GENIChomozygous56068238
5144615056144615057AG11GENIChomozygous56068241
5144615105144615106TC11GENICpossibly homozygous55914923
5144615244144615245TC17GENIChomozygous56068242
5144615402144615403CT13GENICheterozygous56068243
5144615663144615664TC1GENIChomozygous56068244
5144616587144616588AG14GENIChomozygous56068245
5144616693144616694TC22GENICpossibly homozygous55914930
5144617364144617365GC25GENIChomozygous56068246
5144617465144617469CTAA----2GENIChomozygous56068247
5144617495144617496TC18GENIChomozygous56068248
5144617752144617753CT4GENIChomozygous56068249
5144617854144617855TTGA13GENICpossibly homozygous56068250
5144617863144617864AC12GENICpossibly homozygous56068251
5144618062144618063AAGGG4GENICheterozygous56068252
5144618219144618220GA18GENIChomozygous55763282
5144618570144618571TC4GENIChomozygous55914936
5144620593144620594GA6GENIChomozygous56068253
5144621924144621925TTA8GENICheterozygous56068254
5144622443144622444GA10GENIChomozygous56068255
5144622902144622903CT18GENICpossibly homozygous55763290
5144623071144623072TC20GENIChomozygous55763292
5144623265144623266TC11GENIChomozygous55763294
5144624092144624093TG4GENICheterozygous56458705
5144624101144624102TG2GENIChomozygous56068256
5144624112144624113G-2GENIChomozygous56458707
5144624176144624177TC16GENIChomozygous56068257
5144624197144624198TC13GENIChomozygous56068258
5144625216144625217GA14GENICpossibly homozygous56068259
5144625373144625374AT11GENIChomozygous55763299