| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184248875-184249008 | Rare:73; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249489-184249771 | Common:1; Rare:87 | ||||
| chr3:184298981-184299354 | Common:4; Rare:111 | ||||
| chr3:184314368-184314673 | Common:3; Rare:90 | ||||
| chr3:184335825-184335937 | Common:1; Rare:36 | ||||
| chr3:184711940-184712260 | Common:1; Rare:108 | ||||
| chr3:185282855-185283013 | Common:1; Rare:40 | ||||
| chr3:185498911-185499140 | Rare:84 | ||||
| chr3:185586044-185586358 | Common:1; Rare:69 | ||||
| chr3:185821122-185821321 | Rare:35 | ||||
| chr3:185824825-185824922 | Rare:23 | ||||
| chr3:185937869-185938292 | Common:2; Rare:168 | ||||
| chr3:186567291-186567431 | Common:3; Rare:37 | ||||
| chr3:186783228-186783639 | Common:2; Rare:182 | ||||
| chr3:186806396-186806616 | Rare:74 |