| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40453165-40453422 | Common:6; Rare:56 | ||||
| chr3:41221122-41221440 | Common:2; Rare:60 | ||||
| chr3:42632303-42632638 | Common:2; Rare:71 | ||||
| chr3:42645751-42645926 | Common:1; Rare:40 | ||||
| chr3:44392714-44392922 | Common:1; Rare:45 | ||||
| chr3:45595734-45595870 | Common:2; Rare:45 | ||||
| chr3:45894215-45894223 | |||||
| chr3:46111160-46111396 | Common:3; Rare:53 | ||||
| chr3:46130567-46131013 | Common:2; Rare:64 | ||||
| chr3:46206520-46206861 | Common:1; Rare:63 | ||||
| chr3:46987774-46988044 | Common:1; Rare:83 | ||||
| chr3:46998556-46998846 | Rare:80; Clinvar:2 | ||||
| chr3:47005794-47005883 | Common:1; Rare:25; Clinvar (benign):1 | ||||
| chr3:47164775-47164923 | Common:2; Rare:31 | ||||
| chr3:48333639-48333756 | Rare:15 |