| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206274906-206275036 | Rare:47 | ||||
| chr2:206765288-206765654 | Common:3; Rare:100; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165937-207166088 | Rare:26 | ||||
| chr2:207529818-207529993 | Common:1; Rare:58 | ||||
| chr2:207625195-207625587 | Common:1; Rare:110 | ||||
| chr2:208255047-208255238 | Common:2; Rare:51 | ||||
| chr2:208266074-208266302 | Common:7; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002471-210002659 | Common:5; Rare:60 | ||||
| chr2:213284238-213284486 | Rare:80 | ||||
| chr2:216081761-216081925 | Common:1; Rare:58 | ||||
| chr2:216498754-216498894 | Common:4; Rare:61 | ||||
| chr2:218217058-218217246 | Common:1; Rare:67 | ||||
| chr2:218270104-218270534 | Common:5; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218568290-218568612 | Common:2; Rare:87 | ||||
| chr2:218659606-218659742 | Rare:32 |