| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:24014470-24014830 | Common:4; Rare:92 | ||||
| chr18:24426410-24427516 | Common:35; Rare:947 | ||||
| chr18:25230869-25231285 | Rare:92 | ||||
| chr18:25352010-25352680 | Common:14; Rare:848 | ||||
| chr18:26089332-26089949 | Common:6; Rare:229 | ||||
| chr18:26089870-26090344 | Common:3; Rare:371 | ||||
| chr18:26090253-26091101 | Common:33; Rare:1392 | ||||
| chr18:26091080-26091397 | Common:8; Rare:221 | ||||
| chr18:26226010-26226730 | Common:22; Rare:583 | ||||
| chr18:26227020-26227520 | Common:2; Rare:181 | ||||
| chr18:31101250-31102258 | Common:43; Rare:599; Clinvar:17; Clinvar (benign):14; Clinvar (pathogenic):3 | ||||
| chr18:31102300-31102518 | Rare:98; Clinvar:5 | ||||
| chr18:31102491-31102891 | Common:1; Rare:71 | ||||
| chr18:31446776-31447941 | Common:13; Rare:267 | ||||
| chr18:31497182-31497591 | Common:2; Rare:109 |