chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144612760144612761CG29GENIChomozygous56068235
5144612816144612817AC25GENIChomozygous56068236
5144612923144612924TC28GENIChomozygous55763269
5144613178144613179AG23GENIChomozygous56068237
5144613887144613888AG22GENIChomozygous56068238
5144615056144615057AG27GENIChomozygous56068241
5144615105144615106TC30GENIChomozygous55914923
5144615244144615245TC26GENIChomozygous56068242
5144615402144615403CT28GENIChomozygous56068243
5144615663144615664TC34GENIChomozygous56068244
5144616587144616588AG26GENIChomozygous56068245
5144616693144616694TC21GENIChomozygous55914930
5144617364144617365GC31GENIChomozygous56068246
5144617465144617469CTAA----21GENIChomozygous56068247
5144617495144617496TC19GENIChomozygous56068248
5144617752144617753CT20GENIChomozygous56068249
5144617854144617855TTGA20GENIChomozygous56068250
5144617863144617864AC21GENIChomozygous56068251
5144618062144618063AAGGG18GENIChomozygous56068252
5144618219144618220GA20GENIChomozygous55763282
5144618529144618530CCAAA6GENICheterozygous56589344
5144618570144618571TC22GENIChomozygous55914936
5144620593144620594GA28GENIChomozygous56068253
5144621924144621925TTA14GENIChomozygous56068254
5144622443144622444GA18GENIChomozygous56068255
5144622902144622903CT15GENIChomozygous55763290
5144623071144623072TC21GENIChomozygous55763292
5144623265144623266TC28GENICpossibly homozygous55763294
5144624092144624093TG7GENIChomozygous56458705
5144624101144624102TG7GENIChomozygous56068256
5144624112144624113G-11GENICpossibly homozygous56458707
5144624176144624177TC19GENIChomozygous56068257
5144624197144624198TC19GENIChomozygous56068258
5144625216144625217GA18GENIChomozygous56068259
5144625373144625374AT21GENIChomozygous55763299
5144625464144625465TC32GENIChomozygous56068260