| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74206513-74206634 | Common:1; Rare:30 | ||||
| chr2:74290568-74290796 | Common:1; Rare:41 | ||||
| chr2:74391781-74392158 | Common:2; Rare:174 | ||||
| chr2:74421271-74421391 | Common:1; Rare:11 | ||||
| chr2:74421451-74421815 | Rare:103 | ||||
| chr2:74422139-74422275 | Rare:56 | ||||
| chr2:74440389-74440710 | Rare:79 | ||||
| chr2:74441675-74442089 | Common:2; Rare:115 | ||||
| chr2:74442328-74442466 | Common:1; Rare:25 | ||||
| chr2:74454654-74455162 | Rare:118 | ||||
| chr2:74457841-74457935 | Rare:38 | ||||
| chr2:74457956-74458509 | Common:1; Rare:166 | ||||
| chr2:74465286-74465747 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:74472195-74472308 | Rare:41 | ||||
| chr2:74472334-74472861 | Common:4; Rare:246 |