| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138575670-138575804 | Rare:34 | ||||
| chr5:138753113-138753457 | Common:2; Rare:108 | ||||
| chr5:139198280-139198531 | Rare:83; Clinvar (benign):1 | ||||
| chr5:139273971-139274142 | Rare:80 | ||||
| chr5:139293532-139293793 | Rare:86 | ||||
| chr5:139293935-139293987 | Rare:14 | ||||
| chr5:139341671-139341960 | Common:1; Rare:79 | ||||
| chr5:139389723-139390030 | Rare:74 | ||||
| chr5:139404072-139404302 | Rare:62 | ||||
| chr5:139561091-139561359 | Common:1; Rare:106 | ||||
| chr5:139561731-139561800 | Rare:30 | ||||
| chr5:140175017-140175231 | Rare:57 | ||||
| chr5:140303059-140303170 | Common:1; Rare:35 | ||||
| chr5:140401393-140401836 | Common:3; Rare:89 | ||||
| chr5:140557454-140557555 | Common:2; Rare:57 |