| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21612204-21612460 | Common:1; Rare:75 | ||||
| chr18:21704674-21704991 | Common:3; Rare:100 | ||||
| chr18:22933305-22933476 | Common:3; Rare:65; Clinvar:4; Clinvar (benign):3 | ||||
| chr18:22933807-22933916 | Common:1; Rare:43 | ||||
| chr18:23134392-23134570 | Common:3; Rare:27 | ||||
| chr18:23437887-23438047 | Common:2; Rare:71 | ||||
| chr18:23453057-23453389 | Rare:113 | ||||
| chr18:23503287-23503576 | Common:2; Rare:106 | ||||
| chr18:23586421-23586547 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24138942-24139064 | Common:2; Rare:43 | ||||
| chr18:24397733-24398102 | Common:2; Rare:124 | ||||
| chr18:24426551-24426788 | Common:5; Rare:94 | ||||
| chr18:25352092-25352435 | Common:2; Rare:141 | ||||
| chr18:26090067-26090221 | Rare:61 | ||||
| chr18:26090526-26090876 | Common:4; Rare:138 |