| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23135117-23135161 | Rare:6 | ||||
| chr18:23135295-23135511 | Common:2; Rare:47 | ||||
| chr18:23135519-23135562 | Common:1; Rare:11 | ||||
| chr18:23135724-23135806 | Rare:18 | ||||
| chr18:23135811-23136128 | Common:4; Rare:103 | ||||
| chr18:23136324-23136436 | Common:1; Rare:32 | ||||
| chr18:23136509-23136545 | Rare:11 | ||||
| chr18:23437325-23437519 | Common:1; Rare:35 | ||||
| chr18:23437639-23437695 | Rare:5 | ||||
| chr18:23453107-23453454 | Rare:109 | ||||
| chr18:23503026-23503138 | Common:1; Rare:20 | ||||
| chr18:23503199-23503613 | Common:4; Rare:165 | ||||
| chr18:23586372-23586665 | Common:4; Rare:124; Clinvar:6; Clinvar (benign):3 | ||||
| chr18:23586677-23587133 | Common:3; Rare:127 | ||||
| chr18:23689402-23689481 | Rare:21 |