| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:87037793-87038040 | Common:2; Rare:117 | ||||
| chr11:88175262-88175563 | Common:3; Rare:125 | ||||
| chr11:88337560-88337898 | Common:4; Rare:157; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:90222998-90223133 | Common:1; Rare:53 | ||||
| chr11:93741381-93741702 | Common:7; Rare:131 | ||||
| chr11:93784165-93784380 | Common:3; Rare:67 | ||||
| chr11:94128819-94129181 | Common:3; Rare:120 | ||||
| chr11:94129405-94129518 | Rare:36 | ||||
| chr11:94493789-94494062 | Common:5; Rare:80; Clinvar (benign):1 | ||||
| chr11:94768084-94768433 | Common:2; Rare:97 | ||||
| chr11:94973535-94973749 | Rare:61 | ||||
| chr11:95067452-95067567 | Rare:41 | ||||
| chr11:95089715-95089930 | Common:3; Rare:93 | ||||
| chr11:95789478-95789886 | Common:4; Rare:189 | ||||
| chr11:95790359-95790704 | Common:3; Rare:131 |