| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:106077326-106077706 | Common:2; Rare:113 | ||||
| chr11:107457753-107457934 | Common:2; Rare:61 | ||||
| chr11:108008734-108008989 | Rare:72 | ||||
| chr11:108009273-108009363 | Rare:42 | ||||
| chr11:108222580-108223128 | Common:1; Rare:174; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108223282-108223424 | Rare:38 | ||||
| chr11:108467506-108467610 | Common:1; Rare:36 | ||||
| chr11:111299649-111299899 | Common:5; Rare:64 | ||||
| chr11:111766332-111766433 | Common:1; Rare:63 | ||||
| chr11:111879152-111879471 | Rare:92 | ||||
| chr11:111912673-111912826 | Common:1; Rare:32 | ||||
| chr11:111913117-111913289 | Rare:46 | ||||
| chr11:112025297-112025464 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:112073995-112074351 | Common:1; Rare:73 | ||||
| chr11:112086719-112086921 | Rare:85; Clinvar:3; Clinvar (pathogenic):2 |