| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:74767042-74767362 | Common:3; Rare:102 | ||||
| chr5:74866819-74866997 | Common:2; Rare:40 | ||||
| chr5:75336880-75337292 | Common:4; Rare:139 | ||||
| chr5:75511610-75511913 | Common:1; Rare:112 | ||||
| chr5:75717358-75717653 | Common:5; Rare:73 | ||||
| chr5:76083206-76083492 | Common:3; Rare:69 | ||||
| chr5:77030300-77030416 | Rare:38 | ||||
| chr5:77086603-77086736 | Common:1; Rare:30 | ||||
| chr5:77087193-77087271 | Rare:20 | ||||
| chr5:77776232-77776494 | Common:1; Rare:103 | ||||
| chr5:78360355-78360707 | Common:5; Rare:135 | ||||
| chr5:78648524-78648538 | Rare:3 | ||||
| chr5:79069627-79069775 | Rare:51; Clinvar (benign):2 | ||||
| chr5:79235962-79236128 | Common:1; Rare:69 | ||||
| chr5:79689720-79689860 | Common:1; Rare:32 |