| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196867748-196867946 | Rare:67 | ||||
| chr3:196942399-196942682 | Common:1; Rare:115 | ||||
| chr3:197029779-197029938 | Common:1; Rare:51 | ||||
| chr3:197298577-197298731 | Rare:48 | ||||
| chr3:197555858-197556066 | Rare:59 | ||||
| chr3:197749568-197749978 | Common:1; Rare:137 | ||||
| chr3:197791089-197791274 | Common:2; Rare:62 | ||||
| chr3:197949890-197950309 | Common:4; Rare:127; Clinvar (benign):2 | ||||
| chr3:197959979-197960245 | Common:1; Rare:92 | ||||
| chr4:124316-124589 | Common:7; Rare:77 | ||||
| chr4:337504-337857 | Common:1; Rare:94 | ||||
| chr4:499124-499284 | Common:3; Rare:59 | ||||
| chr4:674234-674500 | Rare:125 | ||||
| chr4:932239-932464 | Common:2; Rare:87 | ||||
| chr4:1289650-1289943 | Common:1; Rare:105 |