| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:59125446-59125759 | Common:1; Rare:54 | ||||
| chr5:59169191-59169383 | Common:1; Rare:34 | ||||
| chr5:59174115-59174448 | Common:4; Rare:45 | ||||
| chr5:59187375-59187639 | Common:2; Rare:48 | ||||
| chr5:59189359-59189380 | Rare:2 | ||||
| chr5:59193500-59193740 | Common:1; Rare:37; Clinvar (pathogenic):1 | ||||
| chr5:59193901-59194260 | Common:1; Rare:72 | ||||
| chr5:59276926-59277073 | Rare:21 | ||||
| chr5:59304390-59304519 | Common:1; Rare:25 | ||||
| chr5:59305039-59305343 | Rare:54 | ||||
| chr5:59305473-59305582 | Common:1; Rare:17 | ||||
| chr5:59305598-59305673 | Rare:10 | ||||
| chr5:59337320-59337545 | Common:4; Rare:65 | ||||
| chr5:59348660-59348693 | Rare:2 | ||||
| chr5:59382099-59382380 | Common:2; Rare:44 |