| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109009423-109009689 | Common:2; Rare:82 | ||||
| chr6:109095372-109095551 | Common:1; Rare:37 | ||||
| chr6:109382377-109382860 | Common:7; Rare:159; Clinvar (benign):1 | ||||
| chr6:109455553-109455842 | Common:3; Rare:72 | ||||
| chr6:109691157-109691335 | Common:3; Rare:40; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110180031-110180163 | Common:1; Rare:36 | ||||
| chr6:110815843-110816106 | Common:2; Rare:64 | ||||
| chr6:110874624-110874913 | Common:4; Rare:90 | ||||
| chr6:110958386-110958527 | Common:2; Rare:32 | ||||
| chr6:110958582-110958806 | Common:5; Rare:89 | ||||
| chr6:110981959-110982109 | Common:2; Rare:76 | ||||
| chr6:111483216-111483544 | Common:1; Rare:116 | ||||
| chr6:111483748-111483899 | Rare:67 | ||||
| chr6:111565969-111566164 | Common:1; Rare:36 | ||||
| chr6:112087409-112087667 | Rare:85 |