| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24793047-24793171 | Rare:57 | ||||
| chr2:24971597-24971821 | Common:2; Rare:78 | ||||
| chr2:24971902-24972227 | Common:1; Rare:103 | ||||
| chr2:25041925-25042259 | Common:4; Rare:91 | ||||
| chr2:25247701-25247973 | Rare:63; Clinvar (pathogenic):1 | ||||
| chr2:25252201-25252508 | Rare:69 | ||||
| chr2:25673340-25673747 | Common:1; Rare:138 | ||||
| chr2:25878462-25878773 | Common:4; Rare:98 | ||||
| chr2:25982200-25982287 | Rare:17 | ||||
| chr2:25982365-25982629 | Common:2; Rare:67 | ||||
| chr2:26033705-26034234 | Common:4; Rare:197 | ||||
| chr2:26034275-26034677 | Common:3; Rare:104 | ||||
| chr2:26244581-26244965 | Common:2; Rare:140; Clinvar:5; Clinvar (benign):9 | ||||
| chr2:26345766-26346217 | Common:1; Rare:141 | ||||
| chr2:26401829-26401987 | Common:3; Rare:46 |