| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24971584-24972285 | Common:11; Rare:637 | ||||
| chr2:25041816-25042337 | Common:13; Rare:322 | ||||
| chr2:25042807-25043210 | Rare:105 | ||||
| chr2:25252077-25252820 | Rare:258 | ||||
| chr2:25341828-25342118 | Common:2; Rare:92 | ||||
| chr2:25342438-25342638 | Common:2; Rare:84 | ||||
| chr2:25672784-25673140 | Common:3; Rare:145 | ||||
| chr2:25673379-25673860 | Common:3; Rare:391 | ||||
| chr2:25878246-25878848 | Common:13; Rare:394 | ||||
| chr2:25982436-25982890 | Common:2; Rare:286 | ||||
| chr2:26033655-26034466 | Common:10; Rare:460 | ||||
| chr2:26244520-26245018 | Common:6; Rare:484; Clinvar:20; Clinvar (benign):27; Clinvar (pathogenic):1 | ||||
| chr2:26345647-26346243 | Common:5; Rare:437 | ||||
| chr2:26346700-26347620 | Common:4; Rare:277 | ||||
| chr2:26692440-26692950 | Common:4; Rare:186; Clinvar:1 |