| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:85628340-85628610 | Common:6; Rare:81 | ||||
| chr11:88337661-88337851 | Common:4; Rare:98; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:90223035-90223231 | Common:2; Rare:75 | ||||
| chr11:93741535-93741683 | Common:2; Rare:43 | ||||
| chr11:94493789-94494011 | Common:3; Rare:64; Clinvar (benign):1 | ||||
| chr11:94973542-94973711 | Rare:50 | ||||
| chr11:95790373-95790547 | Rare:68 | ||||
| chr11:96389866-96390024 | Common:1; Rare:58 | ||||
| chr11:102452683-102452949 | Common:1; Rare:81 | ||||
| chr11:106077335-106077682 | Common:2; Rare:96 | ||||
| chr11:108009284-108009333 | Rare:26 | ||||
| chr11:112074005-112074349 | Common:1; Rare:71 | ||||
| chr11:112086729-112086932 | Rare:87; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr11:114400456-114400713 | Common:2; Rare:109 | ||||
| chr11:116772975-116773107 | Common:1; Rare:41 |