| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:33891982-33892233 | Rare:51 | ||||
| chr5:34656061-34656467 | Common:4; Rare:113 | ||||
| chr5:34915461-34915741 | Common:1; Rare:68 | ||||
| chr5:35617687-35617989 | Common:1; Rare:73 | ||||
| chr5:35938569-35938823 | Common:1; Rare:49 | ||||
| chr5:36151885-36152174 | Rare:91 | ||||
| chr5:36876657-36876885 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:38556618-38556809 | Common:2; Rare:75 | ||||
| chr5:38557236-38557480 | Rare:63 | ||||
| chr5:38845746-38846053 | Common:2; Rare:80 | ||||
| chr5:39074381-39074486 | Common:1; Rare:43 | ||||
| chr5:40679714-40679929 | Common:1; Rare:45 | ||||
| chr5:40798161-40798316 | Rare:61 | ||||
| chr5:40835181-40835385 | Common:2; Rare:81 | ||||
| chr5:43067438-43067494 | Rare:10 |