| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33425621-33425946 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:33426567-33426665 | Common:1; Rare:11 | ||||
| chr6:33428464-33428500 | Rare:13 | ||||
| chr6:33432403-33432558 | Common:1; Rare:35 | ||||
| chr6:33571126-33571447 | Common:1; Rare:62 | ||||
| chr6:33571796-33572118 | Rare:45 | ||||
| chr6:33696483-33696756 | Rare:54 | ||||
| chr6:33697210-33697326 | Common:2; Rare:11 | ||||
| chr6:33702504-33702648 | Common:3; Rare:17 | ||||
| chr6:33710912-33711049 | Rare:28 | ||||
| chr6:33768584-33768878 | Common:3; Rare:49 | ||||
| chr6:33771096-33771837 | Common:5; Rare:160 | ||||
| chr6:33788159-33788320 | Common:1; Rare:46 | ||||
| chr6:33840130-33840380 | Common:2; Rare:44 | ||||
| chr6:33843812-33844021 | Common:2; Rare:31 |