| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179580583-179580646 | Rare:15 | ||||
| chr3:179583144-179583423 | Common:4; Rare:47 | ||||
| chr3:182859050-182859306 | Common:1; Rare:52 | ||||
| chr3:183905366-183905424 | Rare:12 | ||||
| chr3:183909285-183909420 | Common:1; Rare:35 | ||||
| chr3:183910481-183910756 | Common:4; Rare:41 | ||||
| chr3:183913120-183913611 | Common:4; Rare:93 | ||||
| chr3:183935840-183936169 | Common:3; Rare:49 | ||||
| chr3:184015611-184015832 | Rare:27 | ||||
| chr3:184322700-184322827 | Rare:43 | ||||
| chr3:184711177-184711478 | Common:2; Rare:105; Clinvar (benign):1 | ||||
| chr3:185418816-185419056 | Common:1; Rare:31 | ||||
| chr3:185465640-185465831 | Common:2; Rare:49 | ||||
| chr3:185519217-185519468 | Rare:62; Clinvar (pathogenic):3 | ||||
| chr3:187741410-187741502 | Rare:18 |