| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:11539521-11539742 | Rare:33 | ||||
| chr2:11539763-11540067 | Common:5; Rare:42 | ||||
| chr2:11540304-11540660 | Common:2; Rare:53 | ||||
| chr2:11724162-11724397 | Rare:45 | ||||
| chr2:11746351-11746655 | Common:1; Rare:82; Clinvar:2 | ||||
| chr2:12716643-12717062 | Common:3; Rare:128 | ||||
| chr2:12717866-12718513 | Common:4; Rare:176 | ||||
| chr2:15561260-15561395 | Rare:65 | ||||
| chr2:17518107-17518706 | Common:5; Rare:197 | ||||
| chr2:17753003-17753353 | Common:1; Rare:74 | ||||
| chr2:17753370-17753425 | Common:5; Rare:10 | ||||
| chr2:17753608-17754174 | Common:5; Rare:177; Clinvar (benign):1 | ||||
| chr2:17754510-17754808 | Common:4; Rare:80 | ||||
| chr2:17800127-17800290 | Common:1; Rare:25 | ||||
| chr2:17879262-17879374 | Rare:29 |