| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22933203-22933617 | Common:6; Rare:129; Clinvar:8; Clinvar (benign):3 | ||||
| chr18:22933631-22934063 | Common:2; Rare:133 | ||||
| chr18:23134320-23134605 | Common:3; Rare:50 | ||||
| chr18:23135105-23135846 | Common:6; Rare:191 | ||||
| chr18:23136019-23136109 | Common:4; Rare:29 | ||||
| chr18:23136497-23136872 | Common:3; Rare:99 | ||||
| chr18:23136983-23137017 | Common:1; Rare:9 | ||||
| chr18:23437672-23437707 | Rare:3 | ||||
| chr18:23437847-23438023 | Common:4; Rare:80 | ||||
| chr18:23453002-23453377 | Rare:119 | ||||
| chr18:23453770-23453831 | Rare:6 | ||||
| chr18:23503010-23503130 | Common:1; Rare:25 | ||||
| chr18:23503191-23503612 | Common:4; Rare:166 | ||||
| chr18:23586311-23586608 | Common:5; Rare:132; Clinvar:7; Clinvar (benign):4 | ||||
| chr18:23586866-23587102 | Common:2; Rare:77 |