| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:88337714-88337888 | Common:3; Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:90222973-90223164 | Common:2; Rare:72 | ||||
| chr11:93741480-93741695 | Common:5; Rare:80 | ||||
| chr11:93784189-93784369 | Common:3; Rare:55 | ||||
| chr11:94128810-94129177 | Common:3; Rare:122 | ||||
| chr11:94493792-94494053 | Common:4; Rare:76; Clinvar (benign):1 | ||||
| chr11:94973531-94973728 | Rare:59 | ||||
| chr11:95789478-95789872 | Common:4; Rare:182 | ||||
| chr11:95790359-95790674 | Common:3; Rare:118 | ||||
| chr11:96389831-96390042 | Common:1; Rare:87 | ||||
| chr11:101914858-101915033 | Common:2; Rare:48 | ||||
| chr11:101915108-101915329 | Common:3; Rare:65 | ||||
| chr11:102317254-102317550 | Rare:62 | ||||
| chr11:102347158-102347336 | Common:2; Rare:70 | ||||
| chr11:102452605-102452887 | Common:1; Rare:90 |