chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104861158148611582AC19GENIChomozygous116588620
104861327948613280A53GENIChomozygous128815259
104861328248613283G53GENIChomozygous128815260
104861329948613300G49GENIChomozygous128815261
104861330848613309G52GENIChomozygous128815262
104861337648613377G55GENIChomozygous128815263
104861338148613382G56GENIChomozygous128815264
104861339948613400G55GENIChomozygous128815265
104861342548613426G56GENIChomozygous128815266
104861343248613433T60GENIChomozygous128815267
104861344748613448T58GENIChomozygous128815268
104861346648613467A58GENIChomozygous128815269
104861347148613472A59GENIChomozygous128815270
104861350348613504GA52GENIChomozygous116977667
104861350448613505AT52GENIChomozygous116588622
104861350948613509A54GENIChomozygous128815271
104861351748613517G58GENIChomozygous128815272
104861352748613527TTTTTCTGAATATT53GENIChomozygous128815273
104861355948613559A52GENIChomozygous128815274
104861332848613329CG52GENIChomozygous116774465