| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95789708-95790014 | Common:8; Rare:250 | ||||
| chr11:95790333-95790612 | Common:2; Rare:295 | ||||
| chr11:95790998-95791130 | Rare:85 | ||||
| chr11:95923630-95923830 | Common:1; Rare:51 | ||||
| chr11:95924050-95924189 | Rare:56; Clinvar:1 | ||||
| chr11:95924093-95924206 | Rare:42; Clinvar:1 | ||||
| chr11:96389777-96390110 | Common:4; Rare:276 | ||||
| chr11:99020550-99021090 | Rare:152 | ||||
| chr11:100687222-100687501 | Common:2; Rare:115 | ||||
| chr11:100687822-100688045 | Common:2; Rare:67 | ||||
| chr11:101063642-101064042 | Common:2; Rare:115 | ||||
| chr11:101126262-101127574 | Common:8; Rare:511 | ||||
| chr11:101128798-101129292 | Common:11; Rare:208 | ||||
| chr11:101129618-101129847 | Common:2; Rare:84 | ||||
| chr11:101583814-101584075 | Common:1; Rare:77; Clinvar:3; Clinvar (benign):3 |