| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95067429-95067590 | Rare:63 | ||||
| chr11:95790359-95790598 | Common:1; Rare:91 | ||||
| chr11:95924078-95924127 | Rare:16 | ||||
| chr11:96389857-96390042 | Common:1; Rare:74 | ||||
| chr11:101915121-101915329 | Common:3; Rare:62 | ||||
| chr11:102347115-102347279 | Common:2; Rare:49 | ||||
| chr11:102452586-102452943 | Common:2; Rare:114 | ||||
| chr11:104164014-104164155 | Common:1; Rare:32 | ||||
| chr11:106077326-106077705 | Common:2; Rare:112 | ||||
| chr11:108009116-108009133 | Rare:1 | ||||
| chr11:108009291-108009349 | Rare:32 | ||||
| chr11:108222585-108223128 | Common:1; Rare:172; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:110296551-110296741 | Rare:100; Clinvar:6 | ||||
| chr11:111766338-111766426 | Rare:48 | ||||
| chr11:111878903-111878991 | Common:1; Rare:37 |