| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143511243-143511313 | Rare:14 | ||||
| chr6:143677798-143678140 | Common:2; Rare:85 | ||||
| chr6:143842665-143842959 | Common:2; Rare:63 | ||||
| chr6:143843186-143843402 | Common:2; Rare:70 | ||||
| chr6:144095494-144095741 | Common:4; Rare:87 | ||||
| chr6:144150325-144150521 | Common:5; Rare:55 | ||||
| chr6:144285230-144285378 | Common:2; Rare:37 | ||||
| chr6:144286116-144286546 | Common:6; Rare:81 | ||||
| chr6:145686902-145687016 | Rare:25 | ||||
| chr6:145734844-145734882 | Common:1; Rare:12 | ||||
| chr6:145735243-145735525 | Common:6; Rare:83; Clinvar:16; Clinvar (benign):11 | ||||
| chr6:145814669-145814950 | Common:1; Rare:129 | ||||
| chr6:145964028-145964132 | Common:4; Rare:25 | ||||
| chr6:145964217-145964561 | Common:1; Rare:107 | ||||
| chr6:146598853-146599016 | Common:1; Rare:46 |