| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95789766-95790014 | Common:3; Rare:86 | ||||
| chr11:95790394-95790587 | Common:1; Rare:69 | ||||
| chr11:96389851-96390035 | Common:1; Rare:72 | ||||
| chr11:102317241-102317613 | Common:1; Rare:82 | ||||
| chr11:102347115-102347285 | Common:2; Rare:52 | ||||
| chr11:102452525-102452586 | Rare:23 | ||||
| chr11:102452683-102452903 | Rare:68 | ||||
| chr11:106077319-106077684 | Common:2; Rare:100 | ||||
| chr11:108009240-108009354 | Rare:54 | ||||
| chr11:108222728-108223109 | Common:1; Rare:118; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:112074008-112074383 | Common:1; Rare:79 | ||||
| chr11:112086716-112086910 | Rare:82; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:112228537-112228672 | Rare:50; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr11:113875508-113875762 | Common:4; Rare:93 | ||||
| chr11:114400444-114400755 | Common:2; Rare:124 |