| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:88337510-88337927 | Common:5; Rare:176; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:90134411-90134752 | Common:1; Rare:89 | ||||
| chr11:90209231-90209545 | Common:4; Rare:65 | ||||
| chr11:90223015-90223125 | Common:1; Rare:42 | ||||
| chr11:93197835-93198152 | Common:3; Rare:96 | ||||
| chr11:93543279-93543528 | Common:3; Rare:65 | ||||
| chr11:93741221-93741711 | Common:8; Rare:185 | ||||
| chr11:93784183-93784423 | Common:3; Rare:63 | ||||
| chr11:94128751-94129253 | Common:4; Rare:171 | ||||
| chr11:94129420-94129540 | Common:1; Rare:46 | ||||
| chr11:94493490-94493623 | Rare:32 | ||||
| chr11:94493736-94494072 | Common:7; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94544297-94544437 | Common:1; Rare:75 | ||||
| chr11:94973509-94973757 | Rare:76 | ||||
| chr11:95089723-95089871 | Common:3; Rare:59 |