| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6752911-6753329 | Common:18; Rare:306 | ||||
| chr12:6753404-6753747 | Common:7; Rare:94 | ||||
| chr12:6764937-6765186 | Rare:42 | ||||
| chr12:6765770-6766593 | Common:7; Rare:449 | ||||
| chr12:6766830-6767320 | Common:7; Rare:159 | ||||
| chr12:6821600-6821920 | Common:3; Rare:84 | ||||
| chr12:6851224-6851796 | Common:3; Rare:253 | ||||
| chr12:6851838-6852237 | Common:2; Rare:256 | ||||
| chr12:6852200-6852650 | Common:3; Rare:214 | ||||
| chr12:6856045-6857101 | Common:9; Rare:367 | ||||
| chr12:6867338-6867687 | Common:6; Rare:439; Clinvar:6; Clinvar (benign):6 | ||||
| chr12:6867865-6868320 | Common:22; Rare:334 | ||||
| chr12:6868641-6869160 | Common:3; Rare:174; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:6869164-6869793 | Common:3; Rare:305; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr12:6873203-6873659 | Common:10; Rare:257 |