Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:35290193-35290377 | Common:2; Rare:67 | ||||
chr18:35972491-35972713 | Common:3; Rare:69 | ||||
chr18:36067355-36067723 | Common:2; Rare:127 | ||||
chr18:36129290-36129523 | Common:1; Rare:72 | ||||
chr18:36129808-36129936 | Rare:56 | ||||
chr18:36187441-36187536 | Common:3; Rare:40 | ||||
chr18:36828736-36829158 | Common:3; Rare:166 | ||||
chr18:45967261-45967465 | Rare:74 | ||||
chr18:46098239-46098592 | Common:11; Rare:96; Clinvar (benign):5 | ||||
chr18:46104135-46104412 | Common:4; Rare:80; Clinvar (benign):1 | ||||
chr18:46917355-46917611 | Common:1; Rare:108 | ||||
chr18:47150452-47150554 | Common:3; Rare:37 | ||||
chr18:49487167-49487328 | Common:2; Rare:62 | ||||
chr18:49813503-49813606 | Rare:23 | ||||
chr18:49813826-49814312 | Common:2; Rare:194 |