| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:148644581-148644903 | Rare:200 | ||||
| chr2:148644850-148645060 | Common:1; Rare:53 | ||||
| chr2:148645108-148645483 | Rare:161 | ||||
| chr2:148874983-148875288 | Common:9; Rare:180 | ||||
| chr2:149037850-149038129 | Common:3; Rare:32 | ||||
| chr2:149038519-149038864 | Common:9; Rare:248 | ||||
| chr2:149329770-149330226 | Common:5; Rare:200 | ||||
| chr2:149330297-149330725 | Common:8; Rare:428 | ||||
| chr2:149330863-149331594 | Common:9; Rare:277 | ||||
| chr2:149587070-149587610 | Common:5; Rare:170; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:149587663-149587978 | Common:2; Rare:139; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:150485151-150485613 | Common:5; Rare:222 | ||||
| chr2:150486076-150486461 | Common:1; Rare:87 | ||||
| chr2:150486504-150487207 | Common:8; Rare:240 | ||||
| chr2:151261734-151261928 | Common:7; Rare:114 |