| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:103092056-103092229 | Common:1; Rare:56 | ||||
| chr11:106077335-106077711 | Common:2; Rare:114 | ||||
| chr11:108009273-108009345 | Rare:36 | ||||
| chr11:108121404-108121603 | Common:4; Rare:65; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:108222594-108222834 | Rare:90 | ||||
| chr11:108223012-108223120 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:108664789-108665120 | Common:5; Rare:126 | ||||
| chr11:108929338-108929573 | Common:1; Rare:47 | ||||
| chr11:111766363-111766433 | Common:1; Rare:39 | ||||
| chr11:111879147-111879471 | Rare:96 | ||||
| chr11:111912724-111912774 | Rare:4 | ||||
| chr11:111913121-111913269 | Rare:40 | ||||
| chr11:112025344-112025456 | Rare:21; Clinvar:1 | ||||
| chr11:112074011-112074363 | Common:1; Rare:73 | ||||
| chr11:112086725-112086905 | Rare:74; Clinvar:1 |