| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:86194899-86195246 | Common:2; Rare:92 | ||||
| chr2:86195333-86195772 | Common:9; Rare:125 | ||||
| chr2:86199339-86199532 | Common:1; Rare:67 | ||||
| chr2:86337618-86337846 | Rare:61 | ||||
| chr2:86441149-86441492 | Common:2; Rare:134 | ||||
| chr2:86442219-86442331 | Rare:35 | ||||
| chr2:86562882-86563296 | Rare:157 | ||||
| chr2:86563299-86563586 | Common:2; Rare:105 | ||||
| chr2:86622987-86623061 | Rare:20 | ||||
| chr2:86623208-86623657 | Common:1; Rare:105 | ||||
| chr2:86720168-86720307 | Rare:69 | ||||
| chr2:86721281-86721479 | Common:3; Rare:49 | ||||
| chr2:88055496-88056022 | Common:1; Rare:153 | ||||
| chr2:88170257-88170404 | Common:3; Rare:37 | ||||
| chr2:88627340-88627996 | Common:3; Rare:180; Clinvar:4; Clinvar (benign):1 |