| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7309760-7310320 | Common:9; Rare:219 | ||||
| chr6:7542806-7543309 | Common:12; Rare:282 | ||||
| chr6:7548330-7548720 | Common:3; Rare:121 | ||||
| chr6:7548761-7549064 | Common:4; Rare:59 | ||||
| chr6:7555490-7555960 | Common:4; Rare:174; Clinvar:16; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr6:7904420-7904930 | Rare:206 | ||||
| chr6:10721412-10721602 | Common:19; Rare:135 | ||||
| chr6:11012263-11012796 | Common:3; Rare:169 | ||||
| chr6:11043276-11043720 | Common:27; Rare:198 | ||||
| chr6:11233300-11233660 | Common:6; Rare:155 | ||||
| chr6:11299072-11299404 | Common:3; Rare:62 | ||||
| chr6:11367480-11368100 | Common:10; Rare:211 | ||||
| chr6:11392980-11393400 | Common:4; Rare:61 | ||||
| chr6:11399040-11399260 | Rare:38 | ||||
| chr6:13710737-13710957 | Rare:133 |