| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:147421246-147421384 | Common:2; Rare:41 | ||||
| chr3:147421536-147421665 | Rare:37 | ||||
| chr3:148991377-148991626 | Common:2; Rare:113; Clinvar (benign):1 | ||||
| chr3:149086478-149086720 | Rare:70 | ||||
| chr3:149129549-149129711 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377640-149377812 | Common:1; Rare:43 | ||||
| chr3:149657982-149658273 | Rare:71 | ||||
| chr3:149752406-149752622 | Common:2; Rare:72 | ||||
| chr3:149812979-149813308 | Common:2; Rare:108 | ||||
| chr3:150408090-150408302 | Common:1; Rare:73 | ||||
| chr3:150603139-150603409 | Common:2; Rare:109 | ||||
| chr3:150703726-150704033 | Common:3; Rare:156 | ||||
| chr3:151086423-151086634 | Common:5; Rare:56 | ||||
| chr3:151249078-151249231 | Rare:36 | ||||
| chr3:151329542-151329648 | Rare:19 |