| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3247477-3247912 | Common:1; Rare:171 | ||||
| chr18:3261743-3262224 | Common:13; Rare:297 | ||||
| chr18:3447280-3447660 | Rare:100 | ||||
| chr18:3448111-3448496 | Common:2; Rare:191 | ||||
| chr18:3449283-3449771 | Common:8; Rare:234 | ||||
| chr18:3450022-3450356 | Common:2; Rare:171 | ||||
| chr18:3451423-3451696 | Common:4; Rare:172 | ||||
| chr18:5295090-5295510 | Common:6; Rare:305 | ||||
| chr18:5295991-5296360 | Common:2; Rare:380 | ||||
| chr18:5296860-5297180 | Common:4; Rare:134 | ||||
| chr18:6729072-6729857 | Common:42; Rare:350 | ||||
| chr18:7567039-7567447 | Common:8; Rare:191 | ||||
| chr18:8704760-8705400 | Common:4; Rare:285 | ||||
| chr18:9102441-9102781 | Common:2; Rare:142; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136428-9136886 | Rare:302 |