| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166342498-166342679 | Common:3; Rare:73 | ||||
| chr6:166382874-166383246 | Common:5; Rare:131 | ||||
| chr6:166626429-166627146 | Common:8; Rare:232 | ||||
| chr6:166627052-166627821 | Common:8; Rare:314 | ||||
| chr6:166627922-166628037 | Rare:23 | ||||
| chr6:166862326-166862816 | Common:7; Rare:115 | ||||
| chr6:166956531-166956737 | Common:4; Rare:75; Clinvar:3 | ||||
| chr6:166999028-166999465 | Common:2; Rare:153 | ||||
| chr6:167826695-167826956 | Common:1; Rare:162 | ||||
| chr6:167827224-167827416 | Common:3; Rare:44 | ||||
| chr6:169701955-169702200 | Common:3; Rare:121 | ||||
| chr6:169724455-169724815 | Rare:96 | ||||
| chr6:169725397-169725506 | Common:1; Rare:26 | ||||
| chr6:169751476-169751851 | Common:2; Rare:145; Clinvar (benign):5 | ||||
| chr6:170290923-170291221 | Common:1; Rare:59 |