| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37243166-37243481 | Common:1; Rare:76 | ||||
| chr3:38024510-38024667 | Common:1; Rare:59 | ||||
| chr3:38029612-38029864 | Common:1; Rare:51 | ||||
| chr3:39051942-39052056 | Common:1; Rare:43 | ||||
| chr3:39107531-39107684 | Common:2; Rare:48 | ||||
| chr3:39153539-39153745 | Common:3; Rare:64 | ||||
| chr3:39383582-39383686 | Rare:24; Clinvar:1 | ||||
| chr3:40309491-40309815 | Common:9; Rare:112 | ||||
| chr3:40387154-40387198 | Rare:11 | ||||
| chr3:40457201-40457456 | Common:6; Rare:116 | ||||
| chr3:40505945-40506115 | Rare:38 | ||||
| chr3:40524832-40525013 | Common:1; Rare:50 | ||||
| chr3:41224717-41224991 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
| chr3:42581898-42582137 | Common:3; Rare:75 | ||||
| chr3:42582256-42582577 | Common:3; Rare:67 |