| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141580133-141580460 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr3:141592127-141592392 | Rare:39 | ||||
| chr3:141594680-141595016 | Common:2; Rare:61 | ||||
| chr3:141595294-141595588 | Rare:46 | ||||
| chr3:141597930-141598174 | Rare:46 | ||||
| chr3:141599264-141599472 | Common:1; Rare:35 | ||||
| chr3:141599480-141599752 | Rare:61 | ||||
| chr3:141600697-141600702 | |||||
| chr3:141717913-141718217 | Rare:53 | ||||
| chr3:141739560-141739644 | Common:1; Rare:18 | ||||
| chr3:141908855-141908948 | Rare:15 | ||||
| chr3:141913706-141914130 | Common:4; Rare:70 | ||||
| chr3:141920595-141920885 | Common:2; Rare:37 | ||||
| chr3:141925274-141925634 | Common:4; Rare:69 | ||||
| chr3:142327140-142327417 | Common:1; Rare:59 |