| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85464852-85465196 | Common:3; Rare:62 | ||||
| chr6:85547096-85547342 | Rare:69; Clinvar (pathogenic):1 | ||||
| chr6:85677103-85677177 | Common:1; Rare:13 | ||||
| chr6:85677770-85677980 | Rare:53 | ||||
| chr6:85678676-85678918 | Rare:94 | ||||
| chr6:99544177-99544436 | Rare:34 | ||||
| chr6:99564321-99564571 | Common:2; Rare:32 | ||||
| chr6:100530219-100530266 | Rare:14 | ||||
| chr6:105992536-105992724 | Common:1; Rare:64 | ||||
| chr6:106510780-106510794 | Rare:4 | ||||
| chr6:106530065-106530323 | Common:2; Rare:67 | ||||
| chr6:108987471-108987755 | Common:1; Rare:59 | ||||
| chr6:109376064-109376181 | Rare:35 | ||||
| chr6:111008094-111008371 | Common:2; Rare:57 | ||||
| chr6:111301544-111301640 | Common:1; Rare:17 |