| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3377811-3378028 | Common:2; Rare:61 | ||||
| chr2:3379608-3379779 | Common:2; Rare:72 | ||||
| chr2:3519477-3519651 | Common:2; Rare:56 | ||||
| chr2:3558204-3558708 | Common:6; Rare:189 | ||||
| chr2:3575098-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:3594947-3595123 | Rare:60 | ||||
| chr2:8678797-8679130 | Common:4; Rare:135 | ||||
| chr2:8837563-8837734 | Common:1; Rare:65 | ||||
| chr2:9003957-9004115 | Rare:65 | ||||
| chr2:9423163-9423771 | Common:1; Rare:171 | ||||
| chr2:9474498-9474642 | Common:6; Rare:70 | ||||
| chr2:9555621-9555992 | Common:2; Rare:122 | ||||
| chr2:9630909-9631316 | Common:3; Rare:131 | ||||
| chr2:9843250-9843541 | Common:6; Rare:88 | ||||
| chr2:10043326-10043637 | Common:3; Rare:127; Clinvar:2 |