| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:106077326-106077700 | Common:2; Rare:110 | ||||
| chr11:108008692-108008864 | Rare:40 | ||||
| chr11:108008882-108009174 | Common:1; Rare:75 | ||||
| chr11:108009291-108009361 | Rare:36 | ||||
| chr11:108222585-108223115 | Common:1; Rare:169; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:110429927-110430206 | Common:4; Rare:78 | ||||
| chr11:111299674-111299724 | Common:2; Rare:11 | ||||
| chr11:111602226-111602593 | Common:1; Rare:121 | ||||
| chr11:111766354-111766417 | Rare:33 | ||||
| chr11:111878677-111878973 | Common:2; Rare:82 | ||||
| chr11:111879158-111879537 | Rare:112 | ||||
| chr11:111913138-111913260 | Rare:39 | ||||
| chr11:112025068-112025486 | Common:2; Rare:110; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:112074195-112074392 | Rare:46 | ||||
| chr11:112086725-112086921 | Rare:82; Clinvar:3; Clinvar (pathogenic):2 |