| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:90223039-90223120 | Rare:31 | ||||
| chr11:93741493-93741684 | Common:4; Rare:68 | ||||
| chr11:93784189-93784330 | Common:2; Rare:50 | ||||
| chr11:94493789-94494003 | Common:3; Rare:60; Clinvar (benign):1 | ||||
| chr11:94973542-94973705 | Rare:48 | ||||
| chr11:95790350-95790571 | Rare:88 | ||||
| chr11:96389860-96390033 | Common:1; Rare:64 | ||||
| chr11:102317234-102317495 | Rare:47 | ||||
| chr11:102452619-102452897 | Common:1; Rare:88 | ||||
| chr11:106077332-106077682 | Common:2; Rare:96 | ||||
| chr11:107457812-107457934 | Common:1; Rare:36 | ||||
| chr11:108009290-108009336 | Rare:27 | ||||
| chr11:108121404-108121598 | Common:3; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:108222597-108222808 | Rare:77 | ||||
| chr11:111879154-111879234 | Rare:25 |