| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:73695699-73696098 | Common:4; Rare:77 | ||||
| chr6:73696110-73696303 | Rare:65 | ||||
| chr6:75243442-75243503 | Rare:12 | ||||
| chr6:75243522-75243628 | Rare:25 | ||||
| chr6:75243693-75243985 | Common:1; Rare:129 | ||||
| chr6:75284679-75285070 | Common:1; Rare:122 | ||||
| chr6:75601764-75601924 | Rare:60 | ||||
| chr6:75602327-75602555 | Common:1; Rare:71 | ||||
| chr6:75749080-75749308 | Common:3; Rare:74; Clinvar:3 | ||||
| chr6:78867471-78867600 | Rare:59 | ||||
| chr6:79078178-79078623 | Common:1; Rare:188 | ||||
| chr6:79234574-79234977 | Common:4; Rare:89 | ||||
| chr6:79537340-79537672 | Common:2; Rare:106; Clinvar:4 | ||||
| chr6:79947544-79947716 | Common:1; Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:80004482-80004697 | Common:4; Rare:54 |