chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144612760144612761CG11GENIChomozygous56068235
5144612816144612817AC20GENIChomozygous56068236
5144612923144612924TC19GENIChomozygous55763269
5144613178144613179AG12GENIChomozygous56068237
5144613887144613888AG24GENIChomozygous56068238
5144615056144615057AG19GENIChomozygous56068241
5144615105144615106TC13GENIChomozygous55914923
5144615244144615245TC24GENIChomozygous56068242
5144615402144615403CT23GENIChomozygous56068243
5144615663144615664TC17GENIChomozygous56068244
5144616587144616588AG22GENIChomozygous56068245
5144616693144616694TC22GENIChomozygous55914930
5144617364144617365GC26GENIChomozygous56068246
5144617465144617469CTAA----20GENIChomozygous56068247
5144617495144617496TC21GENIChomozygous56068248
5144617752144617753CT10GENIChomozygous56068249
5144617854144617855TTGA20GENIChomozygous56068250
5144617863144617864AC19GENIChomozygous56068251
5144618062144618063AAGGG18GENIChomozygous56068252
5144618219144618220GA25GENIChomozygous55763282
5144618529144618530CCAAA5GENICheterozygous56589344
5144618570144618571TC10GENIChomozygous55914936
5144620593144620594GA13GENICpossibly homozygous56068253
5144621924144621925TTA15GENIChomozygous56068254
5144622443144622444GA25GENIChomozygous56068255
5144622902144622903CT26GENIChomozygous55763290
5144623071144623072TC30GENIChomozygous55763292
5144623265144623266TC21GENIChomozygous55763294
5144624101144624102TG8GENIChomozygous56068256
5144624176144624177TC9GENIChomozygous56068257
5144624197144624198TC18GENIChomozygous56068258
5144625216144625217GA15GENIChomozygous56068259
5144625373144625374AT16GENIChomozygous55763299
5144625464144625465TC3GENIChomozygous56068260
5144624112144624113G-6GENIChomozygous56458707
5144624092144624093TG8GENIChomozygous56458705