| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68074544-68074572 | Rare:1 | ||||
| chr10:68074612-68075149 | Common:4; Rare:122 | ||||
| chr10:68075171-68075531 | Common:4; Rare:144 | ||||
| chr10:68231420-68231676 | Common:1; Rare:97; Clinvar (pathogenic):2 | ||||
| chr10:68331438-68332207 | Common:3; Rare:237 | ||||
| chr10:68332443-68332547 | Common:1; Rare:28 | ||||
| chr10:68332688-68332768 | Common:1; Rare:26 | ||||
| chr10:68332851-68332977 | Common:1; Rare:36 | ||||
| chr10:68406474-68406507 | Rare:6 | ||||
| chr10:68406517-68406652 | Rare:35 | ||||
| chr10:68406843-68407083 | Common:1; Rare:73 | ||||
| chr10:68407161-68407569 | Common:5; Rare:116 | ||||
| chr10:68471659-68472102 | Common:2; Rare:182; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:68527367-68527747 | Common:3; Rare:117 | ||||
| chr10:68720918-68721317 | Common:3; Rare:125 |