| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:136132750-136132936 | Common:1; Rare:55 | ||||
| chr5:137889306-137889457 | Common:1; Rare:53 | ||||
| chr5:138032673-138032780 | Common:1; Rare:24 | ||||
| chr5:138033062-138033180 | Common:1; Rare:40 | ||||
| chr5:138543095-138543518 | Common:2; Rare:129 | ||||
| chr5:138753236-138753488 | Common:2; Rare:86 | ||||
| chr5:138875209-138875513 | Rare:61; Clinvar (benign):1 | ||||
| chr5:139198289-139198531 | Rare:81; Clinvar (benign):1 | ||||
| chr5:139341552-139341943 | Common:1; Rare:99 | ||||
| chr5:139439453-139439592 | Common:1; Rare:39 | ||||
| chr5:139561100-139561363 | Common:1; Rare:103 | ||||
| chr5:139561721-139561794 | Rare:34 | ||||
| chr5:140303065-140303165 | Common:1; Rare:29 | ||||
| chr5:140401439-140401660 | Common:2; Rare:39 | ||||
| chr5:140557437-140557515 | Rare:43 |