| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24971897-24972213 | Common:2; Rare:131 | ||||
| chr2:25041880-25042210 | Common:8; Rare:149 | ||||
| chr2:25341897-25342054 | Common:1; Rare:31 | ||||
| chr2:25342481-25342858 | Common:1; Rare:76 | ||||
| chr2:25673379-25673750 | Common:2; Rare:209 | ||||
| chr2:25878226-25878796 | Common:10; Rare:265 | ||||
| chr2:26033725-26034213 | Common:7; Rare:329 | ||||
| chr2:26034460-26034720 | Common:4; Rare:119 | ||||
| chr2:26244561-26244989 | Common:4; Rare:309; Clinvar:12; Clinvar (benign):18 | ||||
| chr2:26345718-26346229 | Common:4; Rare:292 | ||||
| chr2:26764161-26764357 | Common:4; Rare:151 | ||||
| chr2:26785717-26786146 | Rare:205 | ||||
| chr2:27032812-27033050 | Rare:172 | ||||
| chr2:27051535-27051721 | Rare:108 | ||||
| chr2:27071413-27071874 | Common:3; Rare:244 |