| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108121356-108121700 | Common:5; Rare:116; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108222495-108223191 | Common:1; Rare:221; Clinvar:10; Clinvar (benign):2 | ||||
| chr11:108223199-108223366 | Rare:45 | ||||
| chr11:108223688-108223804 | Rare:29 | ||||
| chr11:108223896-108224172 | Common:1; Rare:48 | ||||
| chr11:108224560-108224606 | Rare:6 | ||||
| chr11:108467154-108467702 | Common:5; Rare:172 | ||||
| chr11:108498246-108498708 | Common:5; Rare:126 | ||||
| chr11:108664813-108665165 | Common:6; Rare:142 | ||||
| chr11:110092649-110092865 | Common:1; Rare:49 | ||||
| chr11:110092981-110093226 | Common:2; Rare:84 | ||||
| chr11:110093728-110093838 | Common:3; Rare:38 | ||||
| chr11:110296472-110296969 | Common:3; Rare:190; Clinvar:9 | ||||
| chr11:110429808-110430210 | Common:6; Rare:111 | ||||
| chr11:110711954-110712159 | Common:3; Rare:91 |