| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75710567-75711133 | Common:4; Rare:204 | ||||
| chr2:84458752-84458919 | Common:1; Rare:33 | ||||
| chr2:84459198-84459666 | Common:4; Rare:119; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84881049-84881215 | Common:1; Rare:50 | ||||
| chr2:84894922-84895030 | Rare:26 | ||||
| chr2:84905239-84905345 | Rare:21 | ||||
| chr2:84905435-84905924 | Common:2; Rare:147 | ||||
| chr2:84906117-84906334 | Common:2; Rare:49 | ||||
| chr2:84907123-84907237 | Rare:30 | ||||
| chr2:84970563-84970756 | Common:1; Rare:51 | ||||
| chr2:84970887-84971293 | Common:3; Rare:123 | ||||
| chr2:84971638-84971793 | Rare:30 | ||||
| chr2:84971916-84972164 | Common:1; Rare:71 | ||||
| chr2:84972350-84972592 | Common:1; Rare:53 | ||||
| chr2:85327856-85328167 | Common:5; Rare:127 |