| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21741236-21741371 | Common:1; Rare:36 | ||||
| chr18:22933174-22933624 | Common:6; Rare:137; Clinvar:8; Clinvar (benign):3 | ||||
| chr18:22933708-22933963 | Common:2; Rare:96 | ||||
| chr18:23134326-23134609 | Common:3; Rare:48 | ||||
| chr18:23135414-23135826 | Common:3; Rare:119 | ||||
| chr18:23136006-23136054 | Rare:16 | ||||
| chr18:23437866-23438051 | Common:4; Rare:81 | ||||
| chr18:23453057-23453396 | Rare:113 | ||||
| chr18:23503017-23503070 | Common:1; Rare:10 | ||||
| chr18:23503205-23503620 | Common:4; Rare:171 | ||||
| chr18:23586370-23586647 | Common:4; Rare:120; Clinvar:7; Clinvar (benign):3 | ||||
| chr18:23586870-23587103 | Common:2; Rare:75 | ||||
| chr18:23619209-23619428 | Common:1; Rare:48 | ||||
| chr18:23619441-23619570 | Rare:49 | ||||
| chr18:23689411-23689499 | Rare:22 |