| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:149587192-149587291 | Rare:21 | ||||
| chr2:149587298-149587466 | Common:1; Rare:37 | ||||
| chr2:149587662-149587838 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:150485382-150485503 | Rare:30 | ||||
| chr2:151289611-151289672 | Rare:19 | ||||
| chr2:151828439-151828793 | Common:2; Rare:100 | ||||
| chr2:152175882-152176142 | Common:1; Rare:64 | ||||
| chr2:152659092-152659353 | Common:1; Rare:72 | ||||
| chr2:152717829-152717964 | Rare:56 | ||||
| chr2:152717991-152718296 | Common:1; Rare:98 | ||||
| chr2:152718485-152718641 | Rare:59 | ||||
| chr2:153478775-153479129 | Common:1; Rare:76 | ||||
| chr2:156332673-156332904 | Rare:73; Clinvar:3 | ||||
| chr2:156341619-156341869 | Rare:75 | ||||
| chr2:156435636-156435769 | Rare:30 |