| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160449710-160450033 | Common:2; Rare:109 | ||||
| chr3:160565400-160565842 | Common:2; Rare:155 | ||||
| chr3:160755448-160755615 | Common:1; Rare:60 | ||||
| chr3:161221209-161221360 | Common:2; Rare:50 | ||||
| chr3:167734825-167735254 | Common:5; Rare:136; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735551-167735752 | Rare:49 | ||||
| chr3:169773313-169773424 | Rare:37 | ||||
| chr3:169812538-169812586 | Common:1; Rare:9 | ||||
| chr3:169966181-169966234 | Rare:10 | ||||
| chr3:169966697-169967092 | Common:5; Rare:133 | ||||
| chr3:170037866-170038204 | Common:7; Rare:94 | ||||
| chr3:170222362-170222545 | Common:1; Rare:62 | ||||
| chr3:170870032-170870315 | Common:1; Rare:109 | ||||
| chr3:170908583-170908861 | Common:1; Rare:80 | ||||
| chr3:172523428-172523545 | Common:1; Rare:26 |