| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44976028-44976309 | Common:5; Rare:110 | ||||
| chr3:45030018-45030213 | Common:1; Rare:31 | ||||
| chr3:45388454-45388653 | Common:1; Rare:53 | ||||
| chr3:45689161-45689474 | Common:2; Rare:105 | ||||
| chr3:45842021-45842237 | Common:2; Rare:60 | ||||
| chr3:45995794-45995850 | Rare:17; Clinvar:1 | ||||
| chr3:46407059-46407150 | Rare:15 | ||||
| chr3:46693642-46693781 | Common:1; Rare:36 | ||||
| chr3:46736411-46736524 | Common:1; Rare:22 | ||||
| chr3:46882154-46882352 | Common:1; Rare:64 | ||||
| chr3:46979525-46979827 | Common:2; Rare:71; Clinvar:1 | ||||
| chr3:47163328-47163382 | Common:1; Rare:11 | ||||
| chr3:47163544-47163785 | Common:1; Rare:68 | ||||
| chr3:47163893-47164483 | Common:2; Rare:159; Clinvar (pathogenic):1 | ||||
| chr3:47380794-47381123 | Rare:111 |