| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201183002-201183148 | Common:1; Rare:19; Clinvar (benign):2 | ||||
| chr2:201233347-201233554 | Common:1; Rare:39 | ||||
| chr2:201257971-201258269 | Common:2; Rare:62; Clinvar (benign):1 | ||||
| chr2:201258271-201258348 | Rare:24 | ||||
| chr2:201357316-201357531 | Rare:40 | ||||
| chr2:201451435-201451874 | Common:3; Rare:109 | ||||
| chr2:201619140-201619281 | Rare:61 | ||||
| chr2:201642623-201642780 | Common:1; Rare:72; Clinvar (benign):1 | ||||
| chr2:201643422-201643577 | Rare:46; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:201780890-201781227 | Common:2; Rare:105; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238498-202238625 | Rare:42 | ||||
| chr2:202265623-202265819 | Rare:71 | ||||
| chr2:202634862-202635015 | Common:4; Rare:53 | ||||
| chr2:202911886-202912554 | Common:4; Rare:182 | ||||
| chr2:203014547-203014944 | Common:1; Rare:128 |