| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:56671779-56671939 | Rare:29 | ||||
| chr6:57961316-57961669 | Common:2; Rare:113 | ||||
| chr6:63527631-63527986 | Common:1; Rare:66 | ||||
| chr6:71420109-71420216 | Rare:36 | ||||
| chr6:71420827-71421029 | Common:1; Rare:61 | ||||
| chr6:73517768-73518266 | Common:2; Rare:134 | ||||
| chr6:79233647-79233716 | Common:1; Rare:19 | ||||
| chr6:79233941-79233987 | Rare:13 | ||||
| chr6:81753276-81753509 | Common:1; Rare:86 | ||||
| chr6:85678712-85678962 | Rare:84 | ||||
| chr6:87520192-87520428 | Common:1; Rare:63; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:89083486-89083859 | Common:2; Rare:104 | ||||
| chr6:110700866-110700925 | Rare:6 | ||||
| chr6:116277818-116277943 | Common:1; Rare:13 | ||||
| chr6:117999195-117999316 | Common:3; Rare:32 |