| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:2920419-2920688 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:2923775-2923969 | Common:1; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:3452605-3452733 | Rare:46 | ||||
| chr18:3593938-3594123 | Common:3; Rare:30 | ||||
| chr18:3594168-3594492 | Rare:63 | ||||
| chr18:5237984-5238135 | Common:1; Rare:58 | ||||
| chr18:5238502-5238551 | Common:1; Rare:16 | ||||
| chr18:8623890-8624041 | Common:2; Rare:24 | ||||
| chr18:9838532-9838727 | Common:1; Rare:44 | ||||
| chr18:9915143-9915147 | Rare:1 | ||||
| chr18:12059775-12060045 | Common:2; Rare:57 | ||||
| chr18:12329730-12329994 | Common:1; Rare:57; Clinvar:1 | ||||
| chr18:13502673-13502743 | Rare:14 | ||||
| chr18:23235679-23235968 | Common:2; Rare:57 | ||||
| chr18:23252843-23253052 | Rare:59 |