| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:186806455-186806550 | Rare:31 | ||||
| chr3:188153767-188153931 | Common:1; Rare:33 | ||||
| chr3:188154058-188154224 | Rare:53 | ||||
| chr3:193593109-193593303 | Rare:58; Clinvar:1 | ||||
| chr3:195584103-195584399 | Common:12; Rare:60 | ||||
| chr3:196318191-196318340 | Common:1; Rare:61 | ||||
| chr3:196503664-196504045 | Common:7; Rare:124 | ||||
| chr3:196867758-196867927 | Rare:53 | ||||
| chr3:196942382-196942650 | Common:1; Rare:108 | ||||
| chr3:197029779-197029917 | Common:1; Rare:45 | ||||
| chr3:197949885-197950298 | Common:4; Rare:122; Clinvar (benign):2 | ||||
| chr3:197950836-197950978 | Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959979-197960242 | Common:1; Rare:92 | ||||
| chr4:337532-337837 | Common:1; Rare:73 | ||||
| chr4:499124-499284 | Common:3; Rare:59 |