| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36151816-36152205 | Rare:111 | ||||
| chr5:36241112-36241384 | Common:2; Rare:67 | ||||
| chr5:36241851-36242351 | Common:5; Rare:153; Clinvar (benign):2 | ||||
| chr5:36876598-36876788 | Rare:50 | ||||
| chr5:36877091-36877181 | Rare:33; Clinvar:1 | ||||
| chr5:37249015-37249118 | Common:1; Rare:26 | ||||
| chr5:37249240-37249540 | Common:1; Rare:102; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37370861-37371537 | Common:4; Rare:199 | ||||
| chr5:37379209-37379403 | Rare:61 | ||||
| chr5:39073937-39074158 | Common:4; Rare:65 | ||||
| chr5:39074288-39074752 | Common:2; Rare:176 | ||||
| chr5:40679291-40679460 | Common:1; Rare:35 | ||||
| chr5:40679645-40679980 | Common:2; Rare:84 | ||||
| chr5:40681496-40681593 | Rare:26 | ||||
| chr5:40755155-40755490 | Common:2; Rare:49 |