| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:122399351-122399752 | Common:6; Rare:151 | ||||
| chr6:122471703-122471937 | Common:3; Rare:81 | ||||
| chr6:122779623-122779752 | Rare:23 | ||||
| chr6:122788965-122789410 | Common:2; Rare:108 | ||||
| chr6:122789491-122789826 | Common:1; Rare:85 | ||||
| chr6:123636902-123637082 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:124962866-124962989 | Rare:42 | ||||
| chr6:124962991-124963220 | Common:1; Rare:85 | ||||
| chr6:124963229-124963327 | Common:1; Rare:31 | ||||
| chr6:124963391-124963428 | Rare:10 | ||||
| chr6:124963461-124963558 | Rare:23 | ||||
| chr6:125154197-125154502 | Common:3; Rare:79 | ||||
| chr6:125749393-125749760 | Common:5; Rare:146 | ||||
| chr6:125781059-125781228 | Rare:31 | ||||
| chr6:125790872-125791124 | Common:2; Rare:63 |