| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39406574-39406761 | Common:2; Rare:79 | ||||
| chr3:40309479-40309880 | Common:9; Rare:135 | ||||
| chr3:40457201-40457379 | Common:3; Rare:86 | ||||
| chr3:40477083-40477228 | Common:2; Rare:40 | ||||
| chr3:40505948-40506165 | Rare:44 | ||||
| chr3:40524815-40525019 | Common:1; Rare:60 | ||||
| chr3:41224687-41225184 | Common:1; Rare:96; Clinvar (pathogenic):2 | ||||
| chr3:42160056-42160466 | Common:3; Rare:115 | ||||
| chr3:42581889-42582171 | Common:3; Rare:86 | ||||
| chr3:42582229-42582453 | Common:1; Rare:55 | ||||
| chr3:42600409-42600778 | Common:2; Rare:134 | ||||
| chr3:42600870-42601009 | Rare:52 | ||||
| chr3:42630950-42631321 | Common:1; Rare:62 | ||||
| chr3:42633465-42633736 | Common:1; Rare:71 | ||||
| chr3:42633977-42634313 | Rare:65 |