| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9749761-9750105 | Common:2; Rare:181 | ||||
| chr3:9750142-9750352 | Common:2; Rare:150 | ||||
| chr3:9769886-9770057 | Common:2; Rare:77 | ||||
| chr3:9792376-9792586 | Rare:116 | ||||
| chr3:9792627-9793136 | Common:7; Rare:328 | ||||
| chr3:9843954-9844161 | Common:4; Rare:149 | ||||
| chr3:9878792-9878951 | Rare:28 | ||||
| chr3:9890508-9890743 | Common:2; Rare:93; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:9902554-9902901 | Common:2; Rare:190 | ||||
| chr3:9916896-9917202 | Common:7; Rare:112 | ||||
| chr3:9933503-9933913 | Common:5; Rare:251; Clinvar:3 | ||||
| chr3:9933920-9934200 | Common:1; Rare:82 | ||||
| chr3:9986740-9987172 | Common:7; Rare:213 | ||||
| chr3:10026283-10026489 | Common:1; Rare:111 | ||||
| chr3:10115510-10115762 | Common:8; Rare:169 |