| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:41225708-41226214 | Common:1; Rare:114; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:41226218-41226658 | Common:1; Rare:76 | ||||
| chr3:41229971-41230324 | Rare:54 | ||||
| chr3:41231655-41232138 | Rare:69 | ||||
| chr3:41232877-41233096 | Common:2; Rare:42 | ||||
| chr3:41237722-41238159 | Common:1; Rare:116; Clinvar (pathogenic):1 | ||||
| chr3:41241688-41241789 | Rare:24 | ||||
| chr3:41469835-41470011 | Common:2; Rare:22 | ||||
| chr3:41721290-41721321 | Rare:2 | ||||
| chr3:41881151-41881277 | Rare:19 | ||||
| chr3:42019522-42019610 | Rare:15 | ||||
| chr3:42025604-42025878 | Rare:60 | ||||
| chr3:42043327-42043630 | Common:3; Rare:77 | ||||
| chr3:42044249-42044350 | Common:2; Rare:12 | ||||
| chr3:42053225-42053391 | Common:5; Rare:34 |