| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102317254-102317495 | Rare:47 | ||||
| chr11:102347113-102347342 | Common:2; Rare:78 | ||||
| chr11:102452613-102452943 | Common:2; Rare:102 | ||||
| chr11:103092078-103092278 | Common:2; Rare:72 | ||||
| chr11:106077335-106077690 | Common:2; Rare:103 | ||||
| chr11:108009234-108009361 | Rare:58 | ||||
| chr11:108222609-108223050 | Rare:140; Clinvar:7 | ||||
| chr11:110296504-110296772 | Common:1; Rare:128; Clinvar:8 | ||||
| chr11:111766364-111766425 | Rare:27 | ||||
| chr11:111879152-111879482 | Rare:97 | ||||
| chr11:111911996-111912158 | Common:2; Rare:31 | ||||
| chr11:111913131-111913511 | Common:1; Rare:99 | ||||
| chr11:112074171-112074363 | Common:1; Rare:45 | ||||
| chr11:112086729-112086932 | Rare:87; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr11:113314454-113314602 | Rare:51 |