| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138542925-138543020 | Rare:28 | ||||
| chr5:138543129-138543512 | Common:2; Rare:122 | ||||
| chr5:138753277-138753503 | Common:2; Rare:77 | ||||
| chr5:139198289-139198555 | Rare:90; Clinvar (benign):1 | ||||
| chr5:139293532-139293793 | Rare:86 | ||||
| chr5:139341701-139341972 | Common:1; Rare:73 | ||||
| chr5:139404072-139404185 | Rare:35 | ||||
| chr5:139561137-139561397 | Common:1; Rare:107 | ||||
| chr5:139561650-139561794 | Rare:54 | ||||
| chr5:140107696-140107811 | Rare:32 | ||||
| chr5:140175017-140175242 | Rare:60 | ||||
| chr5:140303065-140303161 | Common:1; Rare:29 | ||||
| chr5:140557426-140557487 | Rare:37 | ||||
| chr5:140564326-140564462 | Common:1; Rare:41 | ||||
| chr5:140564556-140564834 | Rare:73 |