| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79234556-79234772 | Common:2; Rare:55 | ||||
| chr6:79537351-79537650 | Common:2; Rare:90; Clinvar:4 | ||||
| chr6:80004407-80004702 | Common:6; Rare:73 | ||||
| chr6:82247704-82247978 | Common:1; Rare:91 | ||||
| chr6:82364194-82364281 | Common:2; Rare:21 | ||||
| chr6:83193203-83193397 | Common:3; Rare:68 | ||||
| chr6:84764588-84764755 | Rare:49 | ||||
| chr6:85593692-85594064 | Common:2; Rare:123 | ||||
| chr6:85642795-85643006 | Common:1; Rare:83 | ||||
| chr6:85643763-85643941 | Common:3; Rare:56 | ||||
| chr6:87155240-87155601 | Rare:95 | ||||
| chr6:87472876-87472997 | Common:1; Rare:45; Clinvar (benign):4 | ||||
| chr6:87589955-87590169 | Common:3; Rare:97; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87702199-87702481 | Common:1; Rare:92 | ||||
| chr6:88963555-88963830 | Common:2; Rare:93 |