| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43313371-43313657 | Common:3; Rare:75 | ||||
| chr5:43483805-43483986 | Common:3; Rare:57 | ||||
| chr5:43484315-43484420 | Rare:26 | ||||
| chr5:43515030-43515264 | Common:3; Rare:79 | ||||
| chr5:43556997-43557206 | Common:1; Rare:57 | ||||
| chr5:43602540-43602729 | Common:2; Rare:33 | ||||
| chr5:43602852-43603277 | Rare:103 | ||||
| chr5:44808710-44809023 | Common:2; Rare:115 | ||||
| chr5:50441167-50441451 | Common:3; Rare:84 | ||||
| chr5:52989188-52989365 | Common:4; Rare:52; Clinvar (benign):1 | ||||
| chr5:53109705-53109939 | Common:1; Rare:113; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310501-54310714 | Rare:69 | ||||
| chr5:55160090-55160212 | Rare:34 | ||||
| chr5:55233603-55233889 | Common:4; Rare:104 | ||||
| chr5:55307594-55307834 | Common:3; Rare:89 |