| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36876657-36876900 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:39074381-39074486 | Common:1; Rare:43 | ||||
| chr5:40798152-40798353 | Common:1; Rare:79 | ||||
| chr5:40835167-40835460 | Common:3; Rare:114 | ||||
| chr5:41925161-41925329 | Common:1; Rare:65 | ||||
| chr5:43067422-43067552 | Rare:23 | ||||
| chr5:43121389-43121655 | Common:1; Rare:100 | ||||
| chr5:43483837-43483935 | Common:1; Rare:38 | ||||
| chr5:43602874-43603266 | Rare:95 | ||||
| chr5:44808730-44808959 | Common:2; Rare:76 | ||||
| chr5:50441365-50441444 | Common:2; Rare:24 | ||||
| chr5:50667768-50667915 | Common:1; Rare:46 | ||||
| chr5:52989203-52989367 | Common:4; Rare:45; Clinvar (benign):1 | ||||
| chr5:53109725-53109890 | Common:1; Rare:83; Clinvar:2 | ||||
| chr5:55307631-55308023 | Common:4; Rare:133 |