| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:11465848-11466305 | Common:11; Rare:197 | ||||
| chr2:11482367-11482941 | Common:11; Rare:274 | ||||
| chr2:11539335-11539752 | Common:2; Rare:104 | ||||
| chr2:11539959-11540166 | Common:2; Rare:66 | ||||
| chr2:11542509-11542712 | Common:6; Rare:55 | ||||
| chr2:11746377-11746674 | Common:4; Rare:141; Clinvar:8 | ||||
| chr2:12716612-12716987 | Common:4; Rare:154 | ||||
| chr2:15561245-15561427 | Rare:129 | ||||
| chr2:15591390-15592110 | Common:5; Rare:194 | ||||
| chr2:17518338-17518738 | Common:13; Rare:339 | ||||
| chr2:17538855-17539165 | Common:7; Rare:173 | ||||
| chr2:17539717-17540036 | Common:4; Rare:115 | ||||
| chr2:17540304-17540806 | Common:5; Rare:216 | ||||
| chr2:17753697-17753955 | Common:4; Rare:161 | ||||
| chr2:17754061-17754195 | Common:5; Rare:69; Clinvar (benign):2 |