| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95923799-95924120 | Common:2; Rare:133; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389862-96390065 | Common:1; Rare:84 | ||||
| chr11:101914869-101915033 | Common:2; Rare:42 | ||||
| chr11:101915106-101915298 | Common:3; Rare:54 | ||||
| chr11:102317201-102317518 | Rare:57 | ||||
| chr11:102347111-102347298 | Common:2; Rare:62 | ||||
| chr11:102452663-102452858 | Rare:63 | ||||
| chr11:106077326-106077705 | Common:2; Rare:112 | ||||
| chr11:108009291-108009345 | Rare:30 | ||||
| chr11:108121404-108121603 | Common:4; Rare:65; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:108222594-108222947 | Rare:118; Clinvar:3 | ||||
| chr11:111540577-111540749 | Rare:45 | ||||
| chr11:111766348-111766459 | Common:1; Rare:68 | ||||
| chr11:111878903-111878950 | Common:1; Rare:13 | ||||
| chr11:111879158-111879539 | Rare:112 |