| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33711666-33711752 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr6:33789108-33789247 | Common:1; Rare:70 | ||||
| chr6:34236629-34236906 | Common:3; Rare:127 | ||||
| chr6:34248977-34249379 | Common:1; Rare:99 | ||||
| chr6:34392348-34392383 | Rare:22 | ||||
| chr6:34424761-34425180 | Common:3; Rare:108; Clinvar (benign):5 | ||||
| chr6:34555975-34556037 | Rare:11 | ||||
| chr6:34696613-34697029 | Common:1; Rare:102 | ||||
| chr6:34757220-34757554 | Common:2; Rare:81 | ||||
| chr6:35141239-35141403 | Common:6; Rare:43 | ||||
| chr6:35259373-35259778 | Common:3; Rare:129 | ||||
| chr6:35497525-35497637 | Rare:26 | ||||
| chr6:35921057-35921187 | Rare:66 | ||||
| chr6:36442891-36443070 | Common:2; Rare:75 | ||||
| chr6:36594193-36594468 | Common:5; Rare:99 |