| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128650774-128650997 | Common:1; Rare:87 | ||||
| chr3:128680663-128680960 | Common:3; Rare:92 | ||||
| chr3:128681000-128681400 | Common:1; Rare:111 | ||||
| chr3:128725976-128726232 | Common:1; Rare:77; Clinvar:3 | ||||
| chr3:128726680-128727080 | Common:2; Rare:122 | ||||
| chr3:128879353-128879708 | Common:5; Rare:165; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:128994045-128994290 | Common:1; Rare:65 | ||||
| chr3:129000970-129001370 | Common:3; Rare:94 | ||||
| chr3:129001390-129001700 | Common:3; Rare:90 | ||||
| chr3:129161013-129161119 | Rare:41 | ||||
| chr3:129161320-129161518 | Common:3; Rare:63 | ||||
| chr3:129183829-129184167 | Common:2; Rare:126 | ||||
| chr3:129249478-129249641 | Common:2; Rare:48 | ||||
| chr3:129278669-129279094 | Common:4; Rare:109 | ||||
| chr3:129279360-129279760 | Common:1; Rare:104 |