| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33798985-33799029 | Rare:13 | ||||
| chr3:36993077-36993549 | Common:2; Rare:158; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr3:37243036-37243381 | Common:5; Rare:92 | ||||
| chr3:39051912-39052028 | Common:1; Rare:38 | ||||
| chr3:39107562-39107656 | Common:1; Rare:36 | ||||
| chr3:39153524-39153742 | Common:3; Rare:72 | ||||
| chr3:39383306-39383432 | Common:1; Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39383494-39383682 | Common:1; Rare:44; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:39406922-39407003 | Common:2; Rare:30 | ||||
| chr3:40309496-40309808 | Common:9; Rare:108 | ||||
| chr3:40457207-40457402 | Common:3; Rare:99 | ||||
| chr3:40505934-40506137 | Rare:45 | ||||
| chr3:40524821-40524911 | Common:1; Rare:22 | ||||
| chr3:41962045-41962365 | Common:4; Rare:79 | ||||
| chr3:42581900-42582083 | Common:2; Rare:62 |