| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:24397784-24398078 | Common:2; Rare:109 | ||||
| chr18:24426620-24426765 | Common:3; Rare:61 | ||||
| chr18:25352003-25352410 | Common:2; Rare:155 | ||||
| chr18:26090071-26090228 | Common:1; Rare:61 | ||||
| chr18:26657374-26657545 | Rare:40 | ||||
| chr18:26865107-26865337 | Rare:50 | ||||
| chr18:26865681-26865865 | Common:1; Rare:53 | ||||
| chr18:28176968-28177169 | Common:3; Rare:104 | ||||
| chr18:31101948-31102095 | Rare:35; Clinvar:2; Clinvar (benign):2 | ||||
| chr18:31685814-31686007 | Rare:55 | ||||
| chr18:31943098-31943400 | Common:7; Rare:101 | ||||
| chr18:32018443-32018860 | Common:3; Rare:122 | ||||
| chr18:32091809-32091969 | Common:3; Rare:54 | ||||
| chr18:32092378-32092732 | Common:5; Rare:160 | ||||
| chr18:33578256-33578547 | Common:4; Rare:81 |