| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139198270-139198532 | Rare:85; Clinvar (benign):1 | ||||
| chr5:139273971-139274158 | Rare:89 | ||||
| chr5:139294434-139294586 | Rare:60 | ||||
| chr5:139404018-139404309 | Rare:84 | ||||
| chr5:139439452-139439630 | Common:2; Rare:48 | ||||
| chr5:139561091-139561386 | Common:1; Rare:118 | ||||
| chr5:139561733-139561809 | Rare:29 | ||||
| chr5:140043119-140043380 | Rare:72 | ||||
| chr5:140107608-140107797 | Rare:63 | ||||
| chr5:140175011-140175285 | Common:2; Rare:66 | ||||
| chr5:140303050-140303171 | Common:1; Rare:40 | ||||
| chr5:140346601-140346715 | Common:1; Rare:32 | ||||
| chr5:140401433-140401632 | Common:2; Rare:32 | ||||
| chr5:140547454-140547719 | Common:2; Rare:56 | ||||
| chr5:140557404-140557548 | Common:2; Rare:92 |