| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166365911-166366311 | Common:2; Rare:81; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr6:166626087-166626505 | Common:2; Rare:118 | ||||
| chr6:166687930-166688170 | Rare:45 | ||||
| chr6:166904385-166905188 | Common:3; Rare:227 | ||||
| chr6:167140720-167141480 | Common:8; Rare:131 | ||||
| chr6:167241437-167242051 | Common:11; Rare:162 | ||||
| chr6:167350920-167351410 | Common:7; Rare:99 | ||||
| chr6:167441590-167442180 | Common:6; Rare:93 | ||||
| chr6:167442471-167442602 | Common:1; Rare:22 | ||||
| chr6:167443160-167443540 | Common:3; Rare:72 | ||||
| chr6:167493701-167494237 | Common:4; Rare:285 | ||||
| chr6:167533798-167534198 | Common:1; Rare:57 | ||||
| chr6:167668181-167668581 | Common:3; Rare:153 | ||||
| chr6:167677133-167677285 | Common:2; Rare:31 | ||||
| chr6:167678101-167678233 | Common:2; Rare:29 |