| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24049601-24049760 | Rare:44 | ||||
| chr2:24076197-24076913 | Common:3; Rare:150 | ||||
| chr2:24123391-24123520 | Common:1; Rare:39 | ||||
| chr2:24123723-24123761 | Rare:8 | ||||
| chr2:24793093-24793175 | Rare:43 | ||||
| chr2:24971902-24972168 | Common:1; Rare:84 | ||||
| chr2:25247710-25247963 | Rare:53 | ||||
| chr2:25878449-25878671 | Common:1; Rare:66 | ||||
| chr2:26033771-26034221 | Common:4; Rare:166 | ||||
| chr2:26034259-26034710 | Common:4; Rare:111 | ||||
| chr2:26244573-26244993 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345783-26346189 | Common:1; Rare:122 | ||||
| chr2:26764194-26764424 | Common:3; Rare:75 | ||||
| chr2:27032814-27033026 | Rare:80 | ||||
| chr2:27035615-27035974 | Common:2; Rare:90 |