| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184174624-184174951 | Common:3; Rare:92 | ||||
| chr3:184248906-184249032 | Common:1; Rare:59; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:184249518-184249689 | Rare:44 | ||||
| chr3:184299331-184299395 | Rare:17 | ||||
| chr3:184325320-184325627 | Common:1; Rare:85 | ||||
| chr3:193593067-193593292 | Rare:69; Clinvar:1 | ||||
| chr3:195543191-195543475 | Common:3; Rare:102 | ||||
| chr3:196287646-196287814 | Common:1; Rare:53 | ||||
| chr3:196942375-196942676 | Common:1; Rare:126 | ||||
| chr3:197736912-197737133 | Common:2; Rare:64 | ||||
| chr3:197949896-197950231 | Common:4; Rare:98; Clinvar (benign):1 | ||||
| chr4:499149-499280 | Common:2; Rare:40 | ||||
| chr4:673888-673982 | Rare:41 | ||||
| chr4:674211-674596 | Common:4; Rare:179 | ||||
| chr4:932279-932492 | Common:2; Rare:84 |