| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:83193194-83193403 | Common:3; Rare:70 | ||||
| chr6:85449889-85450118 | Common:1; Rare:65 | ||||
| chr6:85593776-85593919 | Common:1; Rare:50 | ||||
| chr6:85643801-85643949 | Common:3; Rare:45 | ||||
| chr6:87155268-87155631 | Rare:106 | ||||
| chr6:87472900-87473004 | Common:1; Rare:40; Clinvar (benign):4 | ||||
| chr6:87589946-87590169 | Common:3; Rare:104; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:88963569-88963822 | Common:2; Rare:85 | ||||
| chr6:89145848-89146100 | Rare:61 | ||||
| chr6:89352644-89353007 | Common:1; Rare:82 | ||||
| chr6:89412061-89412356 | Common:3; Rare:69 | ||||
| chr6:89638434-89638538 | Common:1; Rare:23 | ||||
| chr6:89638712-89638824 | Common:3; Rare:42 | ||||
| chr6:89829595-89829914 | Rare:77 | ||||
| chr6:90587017-90587334 | Common:2; Rare:86 |