| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33289186-33289333 | Common:1; Rare:42 | ||||
| chr6:33298915-33299064 | Rare:39 | ||||
| chr6:33299417-33299501 | Common:1; Rare:18 | ||||
| chr6:33322900-33323185 | Common:5; Rare:86 | ||||
| chr6:33391606-33391885 | Common:1; Rare:66 | ||||
| chr6:33410878-33411042 | Rare:37 | ||||
| chr6:33417869-33417948 | Rare:35 | ||||
| chr6:33418030-33418480 | Common:3; Rare:108 | ||||
| chr6:33454420-33454607 | Rare:49 | ||||
| chr6:33746806-33747106 | Common:5; Rare:56 | ||||
| chr6:34236755-34236906 | Common:2; Rare:62 | ||||
| chr6:34392265-34392471 | Rare:84 | ||||
| chr6:34424667-34425195 | Common:3; Rare:143; Clinvar:1; Clinvar (benign):6 | ||||
| chr6:34426000-34426182 | Common:5; Rare:76; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696550-34696981 | Common:1; Rare:111 |