| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203535155-203535549 | Common:3; Rare:151 | ||||
| chr2:205682351-205682514 | Rare:29 | ||||
| chr2:206085772-206085965 | Common:1; Rare:55 | ||||
| chr2:206086145-206086254 | Rare:14 | ||||
| chr2:206159205-206160058 | Common:4; Rare:248; Clinvar (benign):2 | ||||
| chr2:206765276-206765670 | Common:3; Rare:108; Clinvar:5; Clinvar (benign):5 | ||||
| chr2:207165925-207166134 | Rare:42 | ||||
| chr2:207166184-207166387 | Common:3; Rare:89 | ||||
| chr2:207529876-207530116 | Rare:67 | ||||
| chr2:207624565-207624737 | Rare:43 | ||||
| chr2:207625193-207625410 | Common:1; Rare:63 | ||||
| chr2:208025480-208025618 | Common:1; Rare:37 | ||||
| chr2:208189982-208190139 | Rare:46 | ||||
| chr2:208255019-208255238 | Common:2; Rare:58 | ||||
| chr2:208266103-208266376 | Common:6; Rare:90; Clinvar:1; Clinvar (benign):2 |