| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102452619-102452905 | Common:1; Rare:90 | ||||
| chr11:103092072-103092259 | Common:1; Rare:63 | ||||
| chr11:106077326-106077711 | Common:2; Rare:115 | ||||
| chr11:107457812-107457934 | Common:1; Rare:36 | ||||
| chr11:108222587-108222779 | Rare:62 | ||||
| chr11:111766363-111766425 | Rare:28 | ||||
| chr11:111878856-111878946 | Common:2; Rare:23 | ||||
| chr11:111879147-111879252 | Rare:41 | ||||
| chr11:112073996-112074358 | Common:1; Rare:75 | ||||
| chr11:112086719-112086930 | Rare:91; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr11:112226259-112226459 | Rare:80 | ||||
| chr11:113314414-113314596 | Rare:64 | ||||
| chr11:113875497-113875781 | Common:4; Rare:106 | ||||
| chr11:114296310-114296533 | Rare:41 | ||||
| chr11:114400444-114400723 | Common:2; Rare:116 |