| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:93741154-93741711 | Common:8; Rare:204 | ||||
| chr11:93784170-93784388 | Common:3; Rare:68 | ||||
| chr11:93784826-93784855 | Rare:9 | ||||
| chr11:94128782-94129151 | Common:3; Rare:125 | ||||
| chr11:94493719-94494062 | Common:7; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94973531-94973751 | Rare:64 | ||||
| chr11:95067434-95067573 | Rare:48 | ||||
| chr11:95089725-95089919 | Common:3; Rare:85 | ||||
| chr11:95231402-95231624 | Common:2; Rare:62 | ||||
| chr11:95789430-95789994 | Common:5; Rare:243 | ||||
| chr11:95790319-95790690 | Common:3; Rare:146 | ||||
| chr11:95923764-95924170 | Common:2; Rare:169; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389803-96390065 | Common:1; Rare:107 | ||||
| chr11:101583468-101583541 | Common:1; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:101583893-101584078 | Rare:51; Clinvar:1 |