chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104861158148611582AC15GENIChomozygous116588620
104861327948613280A26GENIChomozygous128815259
104861328248613283G26GENIChomozygous128815260
104861329948613300G22GENIChomozygous128815261
104861330848613309G22GENIChomozygous128815262
104861337648613377G16GENIChomozygous128815263
104861338148613382G17GENIChomozygous128815264
104861339948613400G18GENIChomozygous128815265
104861347148613472A18GENIChomozygous128815270
104861342548613426G16GENIChomozygous128815266
104861343248613433T15GENIChomozygous128815267
104861344748613448T16GENIChomozygous128815268
104861346648613467A17GENIChomozygous128815269
104861332848613329CG22GENIChomozygous116774465
104861350348613504GA18GENIChomozygous116977667
104861350448613505AT19GENIChomozygous116588622
104861350948613509A21GENIChomozygous128815271
104861351748613517G22GENIChomozygous128815272
104861352748613527TTTTTCTGAATATT23GENIChomozygous128815273
104861355948613559A22GENIChomozygous128815274