| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42843692-42844029 | Common:2; Rare:44 | ||||
| chr3:43621919-43622298 | Common:2; Rare:113; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690734-43691023 | Common:6; Rare:151; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:43691545-43691656 | Common:1; Rare:19 | ||||
| chr3:44338316-44338518 | Common:3; Rare:73 | ||||
| chr3:44338714-44338811 | Common:3; Rare:33 | ||||
| chr3:44477646-44477752 | Common:1; Rare:19 | ||||
| chr3:44510611-44510661 | Common:1; Rare:9 | ||||
| chr3:44584727-44584990 | Rare:49 | ||||
| chr3:44624932-44625095 | Common:2; Rare:45 | ||||
| chr3:44648544-44648810 | Rare:60 | ||||
| chr3:44761529-44761813 | Common:3; Rare:120 | ||||
| chr3:44861811-44861925 | Common:2; Rare:55 | ||||
| chr3:44976041-44976280 | Common:3; Rare:92 | ||||
| chr3:45146375-45146504 | Common:1; Rare:43 |