| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127030482-127030764 | Common:3; Rare:69 | ||||
| chr5:127073466-127073523 | Common:1; Rare:13 | ||||
| chr5:127517507-127517722 | Common:5; Rare:97 | ||||
| chr5:128083592-128083783 | Common:2; Rare:85 | ||||
| chr5:131252995-131253088 | Common:1; Rare:14 | ||||
| chr5:131635177-131635424 | Common:1; Rare:94 | ||||
| chr5:131796862-131797215 | Rare:101 | ||||
| chr5:132227793-132227923 | Common:2; Rare:32 | ||||
| chr5:132257391-132257709 | Common:7; Rare:72 | ||||
| chr5:132294092-132294450 | Common:1; Rare:84 | ||||
| chr5:132295328-132295436 | Rare:23 | ||||
| chr5:132369553-132369849 | Common:6; Rare:90; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:132410760-132411003 | Rare:48 | ||||
| chr5:132490774-132491020 | Rare:64 | ||||
| chr5:132556895-132557018 | Rare:50; Clinvar:1 |