| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:157480783-157480940 | Common:2; Rare:19 | ||||
| chr2:159892502-159892639 | Rare:28 | ||||
| chr2:159893199-159893394 | Common:1; Rare:30 | ||||
| chr2:159895646-159895671 | Rare:3 | ||||
| chr2:159903723-159903921 | Common:2; Rare:31 | ||||
| chr2:159921921-159922082 | Common:1; Rare:42 | ||||
| chr2:160406922-160407090 | Common:1; Rare:54 | ||||
| chr2:161078209-161078241 | Rare:3 | ||||
| chr2:161103561-161103649 | Rare:17 | ||||
| chr2:161238032-161238158 | Rare:29 | ||||
| chr2:161243330-161243595 | Rare:43 | ||||
| chr2:161244011-161244021 | Rare:2 | ||||
| chr2:161244499-161244549 | Rare:10 | ||||
| chr2:161244575-161244754 | Common:1; Rare:44 | ||||
| chr2:162317938-162318053 | Rare:47; Clinvar:1; Clinvar (benign):1 |