| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:207332-207737 | Common:8; Rare:138 | ||||
| chr11:208625-208865 | Rare:88 | ||||
| chr11:236324-236525 | Common:6; Rare:66 | ||||
| chr11:236906-237059 | Common:1; Rare:60 | ||||
| chr11:307579-307792 | Common:6; Rare:61 | ||||
| chr11:307993-308437 | Common:17; Rare:137 | ||||
| chr11:320558-320932 | Common:5; Rare:146; Clinvar:1 | ||||
| chr11:504426-504697 | Common:3; Rare:75 | ||||
| chr11:506658-506981 | Common:3; Rare:99 | ||||
| chr11:560703-561003 | Common:6; Rare:140 | ||||
| chr11:576427-576531 | Rare:40 | ||||
| chr11:615940-616099 | Common:1; Rare:47 | ||||
| chr11:695614-695825 | Rare:53 | ||||
| chr11:706517-706666 | Rare:29 | ||||
| chr11:747323-747514 | Rare:79; Clinvar:2; Clinvar (benign):1 |