| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:93741474-93741702 | Common:5; Rare:83 | ||||
| chr11:94128804-94129125 | Common:3; Rare:105 | ||||
| chr11:94493781-94494025 | Common:4; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94973531-94973711 | Rare:56 | ||||
| chr11:95066789-95066919 | Rare:24 | ||||
| chr11:95067452-95067590 | Rare:57 | ||||
| chr11:95089697-95089930 | Common:3; Rare:104 | ||||
| chr11:95789478-95789893 | Common:4; Rare:191 | ||||
| chr11:95790346-95790598 | Common:1; Rare:101 | ||||
| chr11:95923829-95924157 | Common:2; Rare:145; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389854-96390043 | Common:1; Rare:77 | ||||
| chr11:101127534-101127721 | Rare:84 | ||||
| chr11:101129790-101129849 | Rare:17 | ||||
| chr11:101914869-101915321 | Common:8; Rare:129 | ||||
| chr11:102110224-102110467 | Common:1; Rare:94 |