| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:223602346-223602652 | Common:5; Rare:67 | ||||
| chr2:223944665-223945299 | Common:3; Rare:254 | ||||
| chr2:223957232-223957504 | Common:4; Rare:105; Clinvar (benign):1 | ||||
| chr2:224039278-224039488 | Rare:67 | ||||
| chr2:224585331-224585492 | Common:3; Rare:65 | ||||
| chr2:224585523-224585975 | Common:2; Rare:104 | ||||
| chr2:225042400-225042690 | Common:3; Rare:84 | ||||
| chr2:225400306-225400455 | Rare:26 | ||||
| chr2:226794820-226795003 | Common:1; Rare:30 | ||||
| chr2:226795011-226795291 | Rare:102 | ||||
| chr2:226799203-226799337 | Rare:30 | ||||
| chr2:226799680-226800150 | Common:1; Rare:129 | ||||
| chr2:226835935-226836166 | Common:1; Rare:91 | ||||
| chr2:227325125-227325298 | Common:4; Rare:72 | ||||
| chr2:229922402-229922552 | Rare:58 |