| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39120995-39121141 | Rare:54 | ||||
| chr2:39437060-39437469 | Common:4; Rare:147 | ||||
| chr2:40451945-40452330 | Common:7; Rare:130 | ||||
| chr2:40511982-40512031 | Rare:9 | ||||
| chr2:40512401-40512437 | Rare:9 | ||||
| chr2:40512474-40512546 | Rare:17 | ||||
| chr2:42169185-42169492 | Common:1; Rare:148 | ||||
| chr2:42792742-42792960 | Common:1; Rare:56 | ||||
| chr2:43226178-43226416 | Rare:106 | ||||
| chr2:43226577-43226815 | Common:2; Rare:89 | ||||
| chr2:43595935-43596228 | Common:1; Rare:104 | ||||
| chr2:43995960-43996304 | Common:4; Rare:147; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:44361483-44362010 | Common:4; Rare:166 | ||||
| chr2:45009652-45009703 | Common:1; Rare:12 | ||||
| chr2:45675389-45675433 | Common:1; Rare:7 |