| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36288856-36289229 | Common:2; Rare:106; Clinvar:3; Clinvar (benign):4 | ||||
| chr22:39521555-39521834 | Common:1; Rare:132 | ||||
| chr22:46069855-46070056 | Rare:43 | ||||
| chr3:4831316-4831665 | Common:4; Rare:68 | ||||
| chr3:15738459-15738513 | Rare:15 | ||||
| chr3:40453159-40453466 | Common:6; Rare:68 | ||||
| chr3:42654324-42654609 | Rare:85 | ||||
| chr3:52694952-52695162 | Common:1; Rare:59 | ||||
| chr3:75435013-75435378 | Common:4; Rare:126 | ||||
| chr3:75641095-75641276 | Rare:29 | ||||
| chr3:75672517-75672720 | Rare:1 | ||||
| chr3:80770346-80770726 | Common:9; Rare:103 | ||||
| chr3:81761493-81761532 | Rare:15; Clinvar:1 | ||||
| chr3:101576954-101576992 | Common:1; Rare:9 | ||||
| chr3:107240630-107240769 | Rare:56 |