| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37196428-37196520 | Rare:30 | ||||
| chr2:37231509-37231726 | Common:5; Rare:123; Clinvar (benign):4 | ||||
| chr2:37344601-37344761 | Common:1; Rare:64 | ||||
| chr2:37925208-37925301 | Rare:35 | ||||
| chr2:38076147-38076260 | Rare:27 | ||||
| chr2:38377206-38377481 | Common:3; Rare:122 | ||||
| chr2:38602895-38603149 | Common:4; Rare:95 | ||||
| chr2:38751296-38751645 | Common:6; Rare:177 | ||||
| chr2:38875857-38876059 | Common:2; Rare:72 | ||||
| chr2:39023787-39023982 | Rare:42 | ||||
| chr2:39437297-39437464 | Common:2; Rare:59 | ||||
| chr2:39665119-39665483 | Common:3; Rare:87 | ||||
| chr2:40451875-40452265 | Common:5; Rare:121 | ||||
| chr2:42169141-42169444 | Common:1; Rare:145 | ||||
| chr2:42169563-42169595 | Common:2; Rare:18 |