| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:107565692-107565767 | Rare:23 | ||||
| chr11:108009176-108009363 | Rare:77 | ||||
| chr11:108222595-108223129 | Common:1; Rare:169; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108498258-108498564 | Common:5; Rare:95 | ||||
| chr11:110296473-110296661 | Common:1; Rare:75; Clinvar:6 | ||||
| chr11:110430111-110430295 | Common:4; Rare:41 | ||||
| chr11:111540558-111540778 | Rare:55 | ||||
| chr11:111541180-111541568 | Common:3; Rare:86 | ||||
| chr11:111541688-111541753 | Rare:12 | ||||
| chr11:111766305-111766425 | Rare:71 | ||||
| chr11:111814670-111814911 | Common:1; Rare:37 | ||||
| chr11:111871235-111871337 | Common:1; Rare:29 | ||||
| chr11:111878845-111878950 | Common:2; Rare:28 | ||||
| chr11:111879147-111879520 | Rare:113 | ||||
| chr11:111911942-111912180 | Common:3; Rare:48 |