| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:148079620-148079766 | Common:5; Rare:37 | ||||
| chr3:148082733-148082746 | Rare:1 | ||||
| chr3:148084003-148084101 | Rare:17 | ||||
| chr3:148093167-148093272 | Rare:17 | ||||
| chr3:150408860-150409153 | Rare:77 | ||||
| chr3:155744068-155744290 | Rare:49 | ||||
| chr3:157174866-157175253 | Common:3; Rare:172 | ||||
| chr3:168249535-168249691 | Common:1; Rare:41 | ||||
| chr3:169661459-169661590 | Rare:25 | ||||
| chr3:169765038-169765203 | Rare:73; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:181699511-181699630 | Rare:17 | ||||
| chr3:181699692-181699788 | Common:1; Rare:18 | ||||
| chr3:181711040-181711123 | Rare:13 | ||||
| chr3:181713021-181713396 | Common:1; Rare:109; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:181726768-181727059 | Rare:42 |