| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:226125652-226125862 | Rare:51 | ||||
| chr2:226137370-226137760 | Common:3; Rare:80 | ||||
| chr2:226151070-226151518 | Common:6; Rare:154 | ||||
| chr2:226154560-226155003 | Common:19; Rare:190 | ||||
| chr2:226478020-226478420 | Common:4; Rare:68 | ||||
| chr2:226790733-226791177 | Common:4; Rare:103 | ||||
| chr2:226791500-226791994 | Common:3; Rare:531 | ||||
| chr2:226794035-226794689 | Common:2; Rare:142 | ||||
| chr2:226795928-226796316 | Common:3; Rare:136; Clinvar (benign):1 | ||||
| chr2:226796616-226797093 | Common:1; Rare:219; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:226797160-226798024 | Common:3; Rare:473; Clinvar (benign):1 | ||||
| chr2:226798147-226799004 | Common:4; Rare:571 | ||||
| chr2:226801024-226801727 | Common:1; Rare:408 | ||||
| chr2:227462668-227462914 | Rare:42 | ||||
| chr2:227466180-227466730 | Common:11; Rare:185 |