| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36151874-36152120 | Rare:68 | ||||
| chr5:36606564-36606653 | Rare:17 | ||||
| chr5:36876650-36876913 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877102-36877133 | Rare:13 | ||||
| chr5:37371075-37371208 | Rare:43 | ||||
| chr5:38556420-38556801 | Common:3; Rare:132 | ||||
| chr5:38557246-38557260 | Rare:3 | ||||
| chr5:38845717-38846073 | Common:2; Rare:93 | ||||
| chr5:39074327-39074539 | Common:1; Rare:105 | ||||
| chr5:40679698-40679960 | Common:1; Rare:59 | ||||
| chr5:40798152-40798343 | Rare:74 | ||||
| chr5:41870358-41870591 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:41870593-41870652 | Rare:11 | ||||
| chr5:41925068-41925312 | Common:1; Rare:89 | ||||
| chr5:43067438-43067495 | Rare:10 |