| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138543110-138543506 | Common:2; Rare:120 | ||||
| chr5:138753283-138753498 | Common:2; Rare:71 | ||||
| chr5:138875204-138875496 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr5:139198289-139198513 | Rare:73; Clinvar (benign):1 | ||||
| chr5:139273551-139273817 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr5:139294442-139294535 | Rare:45 | ||||
| chr5:139341658-139341978 | Common:1; Rare:90 | ||||
| chr5:139404002-139404187 | Rare:64 | ||||
| chr5:139439446-139439634 | Common:2; Rare:51 | ||||
| chr5:139561714-139561794 | Rare:38 | ||||
| chr5:139651195-139651461 | Common:1; Rare:56 | ||||
| chr5:140303065-140303162 | Common:1; Rare:29 | ||||
| chr5:140401499-140401838 | Common:3; Rare:68 | ||||
| chr5:140557374-140557548 | Common:3; Rare:114 | ||||
| chr5:140564273-140564462 | Common:2; Rare:58 |