| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178478495-178478668 | Common:1; Rare:54 | ||||
| chr2:178480642-178480904 | Common:2; Rare:71 | ||||
| chr2:180007082-180007129 | Rare:9 | ||||
| chr2:180980281-180980545 | Common:1; Rare:86 | ||||
| chr2:180980868-180980960 | Rare:19 | ||||
| chr2:183078689-183078799 | Rare:21 | ||||
| chr2:183124218-183124459 | Common:4; Rare:80 | ||||
| chr2:186485978-186486427 | Common:3; Rare:130 | ||||
| chr2:186589923-186590372 | Rare:139 | ||||
| chr2:188291619-188292060 | Common:5; Rare:122 | ||||
| chr2:188292128-188292190 | Rare:13 | ||||
| chr2:188292760-188292869 | Common:1; Rare:29 | ||||
| chr2:188293005-188293071 | Rare:8 | ||||
| chr2:188974352-188974560 | Rare:59; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189441050-189441527 | Common:3; Rare:159 |