| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9917033-9917195 | Common:2; Rare:30 | ||||
| chr3:9933507-9933870 | Common:2; Rare:146; Clinvar:3 | ||||
| chr3:9952373-9952606 | Common:1; Rare:38 | ||||
| chr3:10026286-10026434 | Common:1; Rare:51 | ||||
| chr3:11154346-11154538 | Common:3; Rare:51 | ||||
| chr3:11719419-11719605 | Rare:64 | ||||
| chr3:12158806-12158995 | Rare:67 | ||||
| chr3:12663974-12664330 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):7 | ||||
| chr3:13480040-13480339 | Common:2; Rare:70 | ||||
| chr3:14124728-14125184 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178537-14178879 | Common:2; Rare:176; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402437-14402736 | Common:1; Rare:67 | ||||
| chr3:14651486-14651818 | Rare:98 | ||||
| chr3:14947236-14947583 | Common:4; Rare:158 | ||||
| chr3:14948011-14948193 | Rare:85 |