| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:185552421-185552663 | Common:1; Rare:48 | ||||
| chr3:185586000-185586358 | Common:1; Rare:81 | ||||
| chr3:185824811-185825137 | Rare:93 | ||||
| chr3:185937918-185938304 | Common:2; Rare:146 | ||||
| chr3:186567266-186567469 | Common:3; Rare:56 | ||||
| chr3:186783215-186783673 | Common:2; Rare:210 | ||||
| chr3:186784142-186784456 | Common:1; Rare:128 | ||||
| chr3:186806447-186806550 | Rare:32 | ||||
| chr3:187291690-187291864 | Common:1; Rare:63 | ||||
| chr3:188152908-188153241 | Common:1; Rare:60 | ||||
| chr3:188153761-188154021 | Common:1; Rare:46 | ||||
| chr3:188154034-188154232 | Rare:67 | ||||
| chr3:190120388-190120561 | Rare:69; Clinvar (pathogenic):1 | ||||
| chr3:190120815-190120999 | Rare:54 | ||||
| chr3:191329325-191329707 | Common:3; Rare:113 |