| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39153539-39153745 | Common:3; Rare:64 | ||||
| chr3:39383075-39383437 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:40309470-40309937 | Common:9; Rare:157 | ||||
| chr3:40524815-40525013 | Common:1; Rare:58 | ||||
| chr3:41199839-41200158 | Common:2; Rare:88 | ||||
| chr3:41224382-41224659 | Rare:59; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr3:42581913-42582139 | Common:3; Rare:69 | ||||
| chr3:42582255-42582444 | Common:1; Rare:45 | ||||
| chr3:42600276-42600485 | Common:2; Rare:77 | ||||
| chr3:42600522-42600777 | Common:1; Rare:96 | ||||
| chr3:42600888-42601010 | Rare:48 | ||||
| chr3:42630793-42631249 | Common:1; Rare:82 | ||||
| chr3:42633485-42633612 | Rare:31 | ||||
| chr3:42773206-42773357 | Common:1; Rare:44 | ||||
| chr3:42804266-42804667 | Common:2; Rare:110 |