| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:11296762-11297005 | Common:2; Rare:48 | ||||
| chr6:11300976-11301027 | Common:1; Rare:7 | ||||
| chr6:11305520-11305546 | Rare:4 | ||||
| chr6:11434738-11434984 | Common:2; Rare:40 | ||||
| chr6:11723466-11723752 | Common:2; Rare:51 | ||||
| chr6:12287850-12288038 | Common:1; Rare:23 | ||||
| chr6:12293883-12293963 | Common:1; Rare:25; Clinvar (pathogenic):1 | ||||
| chr6:12314230-12314430 | Common:1; Rare:29 | ||||
| chr6:13486774-13486860 | Common:1; Rare:24 | ||||
| chr6:13710814-13710917 | Rare:41 | ||||
| chr6:13813702-13813848 | Rare:33 | ||||
| chr6:14300248-14300269 | Common:1; Rare:5 | ||||
| chr6:15524648-15524783 | Rare:41; Clinvar:2 | ||||
| chr6:16436761-16436786 | Rare:3 | ||||
| chr6:16760084-16760203 | Rare:40 |