| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79631156-79631329 | Common:2; Rare:46 | ||||
| chr6:83193194-83193414 | Common:3; Rare:75 | ||||
| chr6:85449939-85450169 | Common:1; Rare:71 | ||||
| chr6:85593714-85593955 | Common:1; Rare:84 | ||||
| chr6:85643801-85643923 | Common:3; Rare:38 | ||||
| chr6:87155270-87155588 | Rare:85 | ||||
| chr6:87589946-87590169 | Common:3; Rare:104; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:89081049-89081343 | Common:1; Rare:117 | ||||
| chr6:89352619-89353008 | Common:2; Rare:90 | ||||
| chr6:89638443-89638532 | Common:1; Rare:16 | ||||
| chr6:89638712-89638837 | Common:3; Rare:46 | ||||
| chr6:89819703-89819881 | Rare:60 | ||||
| chr6:89829595-89829919 | Rare:78 | ||||
| chr6:95577434-95577591 | Common:5; Rare:43 | ||||
| chr6:96521674-96521871 | Common:8; Rare:95 |