| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10319337-10319477 | Rare:25 | ||||
| chr3:11572795-11573161 | Common:7; Rare:67 | ||||
| chr3:14403715-14403877 | Common:1; Rare:33 | ||||
| chr3:14810556-14810761 | Common:1; Rare:69 | ||||
| chr3:15052631-15052914 | Common:2; Rare:71 | ||||
| chr3:15059368-15059548 | Rare:63 | ||||
| chr3:15260240-15260496 | Common:2; Rare:40 | ||||
| chr3:16279147-16279294 | Rare:29 | ||||
| chr3:16306935-16307257 | Common:2; Rare:64 | ||||
| chr3:16320548-16320670 | Common:1; Rare:24 | ||||
| chr3:27632775-27633183 | Common:9; Rare:158 | ||||
| chr3:37055128-37055260 | Rare:36 | ||||
| chr3:37244200-37244461 | Common:3; Rare:81 | ||||
| chr3:38011437-38011558 | Rare:38; Clinvar (pathogenic):1 | ||||
| chr3:40453172-40453435 | Common:5; Rare:58 |