| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:40841086-40841476 | Common:1; Rare:98 | ||||
| chr5:40972262-40972620 | Common:2; Rare:105; Clinvar (pathogenic):1 | ||||
| chr5:41510523-41510816 | Common:1; Rare:74 | ||||
| chr5:41870360-41870483 | Rare:52; Clinvar:2 | ||||
| chr5:43043176-43043327 | Common:1; Rare:29 | ||||
| chr5:43064781-43065144 | Common:1; Rare:82 | ||||
| chr5:43067438-43067509 | Rare:11 | ||||
| chr5:43121420-43121696 | Common:1; Rare:100 | ||||
| chr5:43191972-43192225 | Common:1; Rare:58 | ||||
| chr5:43313374-43313651 | Common:3; Rare:72 | ||||
| chr5:43483807-43483970 | Common:3; Rare:53 | ||||
| chr5:43515133-43515186 | Common:2; Rare:13 | ||||
| chr5:43603045-43603280 | Rare:58 | ||||
| chr5:44808727-44808982 | Common:2; Rare:91 | ||||
| chr5:50441140-50441421 | Common:2; Rare:79 |