| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95923960-95924158 | Rare:83; Clinvar (benign):1 | ||||
| chr11:96389862-96390050 | Common:1; Rare:77 | ||||
| chr11:101914869-101915025 | Common:1; Rare:40 | ||||
| chr11:101915124-101915261 | Common:1; Rare:37 | ||||
| chr11:102317241-102317507 | Rare:51 | ||||
| chr11:102347111-102347328 | Common:2; Rare:72 | ||||
| chr11:102452596-102452900 | Common:1; Rare:99 | ||||
| chr11:103092044-103092278 | Common:2; Rare:78 | ||||
| chr11:103109286-103109577 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:106077326-106077711 | Common:2; Rare:115 | ||||
| chr11:107457805-107457940 | Common:1; Rare:42 | ||||
| chr11:108009291-108009349 | Rare:32 | ||||
| chr11:108222597-108223115 | Common:1; Rare:165; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:110296553-110296808 | Common:1; Rare:127; Clinvar:6 | ||||
| chr11:111540585-111540805 | Rare:58 |