| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74958431-74958697 | Common:4; Rare:86 | ||||
| chr2:74958866-74959011 | Rare:58 | ||||
| chr2:75646659-75646836 | Rare:55 | ||||
| chr2:75646962-75647119 | Common:2; Rare:38 | ||||
| chr2:75710658-75710779 | Common:2; Rare:47 | ||||
| chr2:75710872-75711148 | Common:2; Rare:80 | ||||
| chr2:77522183-77522411 | Rare:30 | ||||
| chr2:77593194-77593365 | Common:5; Rare:56 | ||||
| chr2:80304426-80304466 | Rare:8 | ||||
| chr2:84458578-84458865 | Common:1; Rare:74 | ||||
| chr2:84459202-84459581 | Common:3; Rare:98; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:85327916-85328084 | Common:2; Rare:76 | ||||
| chr2:85354517-85354807 | Common:1; Rare:98 | ||||
| chr2:85418427-85418729 | Common:4; Rare:80 | ||||
| chr2:85539068-85539194 | Common:2; Rare:55 |