Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:35290183-35290384 | Common:2; Rare:72 | ||||
chr18:35972462-35972713 | Common:3; Rare:78 | ||||
chr18:36129209-36129498 | Common:4; Rare:88 | ||||
chr18:36129772-36129936 | Common:1; Rare:66 | ||||
chr18:36187428-36187669 | Common:5; Rare:77 | ||||
chr18:36828748-36829182 | Common:3; Rare:173 | ||||
chr18:45967261-45967465 | Rare:74 | ||||
chr18:46098248-46098571 | Common:11; Rare:89; Clinvar (benign):5 | ||||
chr18:46104135-46104396 | Common:3; Rare:74; Clinvar (benign):1 | ||||
chr18:47150461-47150558 | Common:3; Rare:35 | ||||
chr18:49561879-49562086 | Rare:53 | ||||
chr18:49813826-49814312 | Common:2; Rare:194 | ||||
chr18:50281445-50281840 | Common:3; Rare:125 | ||||
chr18:50878870-50879235 | Common:4; Rare:121 | ||||
chr18:51030064-51030222 | Rare:51 |