| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3518791-3519391 | Common:4; Rare:186 | ||||
| chr2:3519443-3519753 | Common:3; Rare:89 | ||||
| chr2:3558035-3558112 | Common:1; Rare:21 | ||||
| chr2:3558144-3558761 | Common:6; Rare:216 | ||||
| chr2:3558969-3559271 | Common:4; Rare:57 | ||||
| chr2:3575049-3575396 | Common:3; Rare:102; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:3576003-3576140 | Common:2; Rare:37 | ||||
| chr2:6865888-6865915 | Rare:9 | ||||
| chr2:6917861-6917917 | Rare:11 | ||||
| chr2:8678014-8678470 | Common:2; Rare:156 | ||||
| chr2:8678724-8679111 | Common:5; Rare:158 | ||||
| chr2:8679187-8679360 | Rare:67 | ||||
| chr2:8681290-8681550 | Common:1; Rare:66 | ||||
| chr2:8681849-8682208 | Common:2; Rare:165 | ||||
| chr2:8837367-8837428 | Common:1; Rare:8 |