| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32239648-32239921 | Rare:55 | ||||
| chr3:36765067-36765366 | Rare:44 | ||||
| chr3:37017010-37017055 | Common:1; Rare:12 | ||||
| chr3:37860460-37860665 | Common:2; Rare:66 | ||||
| chr3:38455351-38455571 | Common:1; Rare:57 | ||||
| chr3:39411646-39411960 | Common:1; Rare:83; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:39435040-39435216 | Common:2; Rare:19 | ||||
| chr3:40453162-40453426 | Common:6; Rare:58 | ||||
| chr3:43086788-43087092 | Common:4; Rare:54 | ||||
| chr3:43153956-43154016 | Rare:12 | ||||
| chr3:43203089-43203413 | Common:1; Rare:64 | ||||
| chr3:43999111-43999403 | Rare:92 | ||||
| chr3:44685620-44685668 | Rare:16 | ||||
| chr3:46845867-46846200 | Common:3; Rare:77 | ||||
| chr3:48232786-48232915 | Common:3; Rare:23 |