| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:142877511-142877694 | Common:1; Rare:28 | ||||
| chr2:143129047-143129437 | Common:2; Rare:85 | ||||
| chr2:143435332-143435482 | Common:1; Rare:28 | ||||
| chr2:144513791-144513955 | Rare:44 | ||||
| chr2:144514493-144514860 | Common:1; Rare:60 | ||||
| chr2:144514908-144514924 | Rare:4 | ||||
| chr2:144517276-144517826 | Common:7; Rare:149; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:144518134-144518245 | Common:1; Rare:26 | ||||
| chr2:144518367-144518506 | Rare:31 | ||||
| chr2:144520136-144520561 | Common:4; Rare:73; Clinvar (benign):1 | ||||
| chr2:148020656-148021147 | Common:2; Rare:118; Clinvar (benign):2 | ||||
| chr2:148021345-148021541 | Rare:59 | ||||
| chr2:148021560-148021679 | Rare:24; Clinvar (benign):1 | ||||
| chr2:149038064-149038132 | Rare:9 | ||||
| chr2:149330394-149330672 | Common:2; Rare:110 |