| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:33599222-33599445 | Common:1; Rare:83 | ||||
| chr2:37084275-37084569 | Common:3; Rare:112 | ||||
| chr2:37231487-37231703 | Common:5; Rare:113; Clinvar (benign):3 | ||||
| chr2:37324724-37324911 | Common:1; Rare:75 | ||||
| chr2:37671632-37671745 | Common:1; Rare:53 | ||||
| chr2:38076143-38076260 | Rare:27 | ||||
| chr2:38602895-38603183 | Common:4; Rare:113 | ||||
| chr2:38751348-38751645 | Common:4; Rare:137 | ||||
| chr2:38875886-38876064 | Common:1; Rare:65 | ||||
| chr2:39437078-39437453 | Common:4; Rare:134 | ||||
| chr2:39779177-39779397 | Common:4; Rare:78 | ||||
| chr2:42169160-42169476 | Common:1; Rare:152 | ||||
| chr2:43226188-43226416 | Rare:104 | ||||
| chr2:43226597-43226815 | Common:1; Rare:78 | ||||
| chr2:43595931-43596207 | Common:1; Rare:98 |