| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33746902-33747099 | Common:2; Rare:34 | ||||
| chr6:34236752-34236974 | Common:2; Rare:87 | ||||
| chr6:34237128-34237315 | Rare:54 | ||||
| chr6:34248974-34249293 | Common:1; Rare:77 | ||||
| chr6:34392246-34392880 | Common:1; Rare:228 | ||||
| chr6:34425964-34426246 | Common:5; Rare:113; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696738-34696995 | Common:1; Rare:62 | ||||
| chr6:34757289-34757615 | Common:2; Rare:94 | ||||
| chr6:34757765-34757955 | Common:3; Rare:49 | ||||
| chr6:34791903-34792117 | Common:3; Rare:65 | ||||
| chr6:34887962-34888122 | Common:1; Rare:38 | ||||
| chr6:34889100-34889399 | Common:4; Rare:68 | ||||
| chr6:35259396-35259812 | Common:3; Rare:128 | ||||
| chr6:35292270-35292590 | Common:1; Rare:69 | ||||
| chr6:35342362-35342645 | Common:2; Rare:74 |