| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42494896-42495211 | Common:1; Rare:70 | ||||
| chr2:42567821-42568582 | Common:4; Rare:249 | ||||
| chr2:42568597-42568776 | Common:2; Rare:58 | ||||
| chr2:42569338-42569547 | Rare:63 | ||||
| chr2:42569951-42570469 | Common:1; Rare:124 | ||||
| chr2:43225850-43226200 | Common:4; Rare:241 | ||||
| chr2:43226260-43226933 | Common:13; Rare:598 | ||||
| chr2:43226958-43227560 | Common:4; Rare:319 | ||||
| chr2:43463087-43463614 | Rare:255 | ||||
| chr2:43595834-43596249 | Common:3; Rare:331 | ||||
| chr2:43637057-43637349 | Common:6; Rare:251 | ||||
| chr2:43676323-43676480 | Common:3; Rare:46 | ||||
| chr2:43773601-43774421 | Common:9; Rare:310; Clinvar (pathogenic):2 | ||||
| chr2:43995799-43996510 | Common:17; Rare:721; Clinvar:17; Clinvar (benign):17; Clinvar (pathogenic):3 | ||||
| chr2:44167737-44168148 | Common:8; Rare:260 |