| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108009304-108009361 | Rare:27 | ||||
| chr11:108121404-108121637 | Common:5; Rare:80; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:108222538-108223014 | Rare:159; Clinvar:6 | ||||
| chr11:108223022-108223142 | Common:1; Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:108223282-108223455 | Rare:45 | ||||
| chr11:108467388-108467638 | Common:4; Rare:97 | ||||
| chr11:108664789-108665120 | Common:5; Rare:126 | ||||
| chr11:109421871-109422194 | Common:1; Rare:76 | ||||
| chr11:110130730-110131028 | Rare:61 | ||||
| chr11:110296498-110296789 | Common:1; Rare:135; Clinvar:8 | ||||
| chr11:110429993-110430212 | Common:4; Rare:55 | ||||
| chr11:110712297-110712553 | Common:2; Rare:97 | ||||
| chr11:111601807-111601959 | Common:3; Rare:24 | ||||
| chr11:111602265-111602641 | Common:1; Rare:121 | ||||
| chr11:111766345-111766420 | Rare:40 |