| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6493746-6494140 | Common:2; Rare:116 | ||||
| chr12:6568241-6568388 | Rare:58 | ||||
| chr12:6663091-6663292 | Rare:61 | ||||
| chr12:6753063-6753223 | Common:4; Rare:58 | ||||
| chr12:6851238-6851405 | Rare:39 | ||||
| chr12:6851902-6852175 | Rare:71 | ||||
| chr12:6873281-6873541 | Common:2; Rare:74 | ||||
| chr12:6943946-6944165 | Common:4; Rare:218; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970611-6970983 | Common:4; Rare:121; Clinvar (benign):1 | ||||
| chr12:8697802-8698014 | Rare:87 | ||||
| chr12:8914399-8914721 | Common:6; Rare:98 | ||||
| chr12:10212819-10212926 | Common:2; Rare:28 | ||||
| chr12:10613508-10613694 | Common:1; Rare:73 | ||||
| chr12:11170962-11171249 | Common:2; Rare:81 | ||||
| chr12:11171545-11171687 | Common:2; Rare:44 |