| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102110112-102110454 | Rare:122 | ||||
| chr11:102347111-102347312 | Common:2; Rare:67 | ||||
| chr11:102452546-102452899 | Common:1; Rare:117 | ||||
| chr11:106077326-106077711 | Common:2; Rare:115 | ||||
| chr11:108009069-108009237 | Rare:38 | ||||
| chr11:108009273-108009368 | Rare:43 | ||||
| chr11:108121384-108121672 | Common:5; Rare:101; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108146071-108146250 | Rare:58; Clinvar:1; Clinvar (pathogenic):4 | ||||
| chr11:108222609-108223108 | Common:1; Rare:156; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:111871275-111871342 | Rare:20 | ||||
| chr11:111879158-111879548 | Common:1; Rare:117 | ||||
| chr11:111912712-111913108 | Common:3; Rare:83 | ||||
| chr11:111913111-111913575 | Common:1; Rare:127 | ||||
| chr11:111923724-111923796 | Common:1; Rare:8 | ||||
| chr11:111937120-111937209 | Common:5; Rare:35 |