| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106629486-106629588 | Common:1; Rare:19 | ||||
| chr6:107459535-107459732 | Common:2; Rare:48 | ||||
| chr6:107958102-107958383 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:108294776-108295071 | Common:1; Rare:78 | ||||
| chr6:109009440-109009669 | Common:2; Rare:73 | ||||
| chr6:109382369-109382517 | Common:3; Rare:77; Clinvar (benign):1 | ||||
| chr6:109440571-109440870 | Common:2; Rare:107 | ||||
| chr6:109455726-109455842 | Rare:26 | ||||
| chr6:109691204-109691318 | Common:3; Rare:26; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179937-110180154 | Common:2; Rare:63 | ||||
| chr6:110958603-110958764 | Common:3; Rare:54 | ||||
| chr6:110981959-110982113 | Common:2; Rare:78 | ||||
| chr6:112087463-112087684 | Rare:63 | ||||
| chr6:113971110-113971495 | Common:3; Rare:121 | ||||
| chr6:116100695-116100911 | Common:1; Rare:82 |