| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22417828-22418023 | Rare:59 | ||||
| chr18:22933249-22933440 | Common:2; Rare:74; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933756-22933916 | Common:1; Rare:68 | ||||
| chr18:23452714-23452985 | Common:2; Rare:45 | ||||
| chr18:23453057-23453353 | Rare:102 | ||||
| chr18:23503282-23503603 | Common:4; Rare:130 | ||||
| chr18:23586388-23586538 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:23619634-23619815 | Rare:37 | ||||
| chr18:24138935-24139330 | Common:3; Rare:102 | ||||
| chr18:24155540-24155861 | Common:3; Rare:64 | ||||
| chr18:24397742-24398078 | Common:2; Rare:119 | ||||
| chr18:24426560-24426828 | Common:4; Rare:100 | ||||
| chr18:25351020-25351149 | Rare:44 | ||||
| chr18:25352070-25352453 | Common:2; Rare:153 | ||||
| chr18:26090061-26090216 | Rare:62 |