| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94128600-94129345 | Common:6; Rare:244 | ||||
| chr11:94493735-94494072 | Common:7; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94973509-94973759 | Rare:77 | ||||
| chr11:95067434-95067597 | Rare:69 | ||||
| chr11:95231090-95231150 | Rare:17 | ||||
| chr11:95231155-95231390 | Common:1; Rare:88 | ||||
| chr11:95778920-95779062 | Rare:35 | ||||
| chr11:95789459-95789568 | Common:1; Rare:54 | ||||
| chr11:95789757-95789856 | Common:1; Rare:38 | ||||
| chr11:95790365-95790723 | Common:3; Rare:136; Clinvar:1 | ||||
| chr11:95923780-95924157 | Common:2; Rare:157; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96342707-96342863 | Rare:26 | ||||
| chr11:96389730-96390104 | Common:2; Rare:142 | ||||
| chr11:96390249-96390332 | Rare:17 | ||||
| chr11:101915150-101915272 | Common:1; Rare:36 |