| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108009273-108009368 | Rare:43 | ||||
| chr11:108121356-108121685 | Common:5; Rare:111; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108222585-108223128 | Common:1; Rare:172; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108467512-108467644 | Common:3; Rare:48 | ||||
| chr11:108664848-108665142 | Common:5; Rare:122 | ||||
| chr11:110296466-110296741 | Common:1; Rare:125; Clinvar:9 | ||||
| chr11:110430006-110430180 | Common:4; Rare:43 | ||||
| chr11:111602247-111602579 | Common:1; Rare:110 | ||||
| chr11:111766345-111766459 | Common:1; Rare:70 | ||||
| chr11:111871266-111871391 | Rare:38; Clinvar:1 | ||||
| chr11:111878871-111879016 | Common:2; Rare:60 | ||||
| chr11:111879158-111879554 | Common:1; Rare:118 | ||||
| chr11:111912057-111912236 | Common:2; Rare:27 | ||||
| chr11:111912712-111912847 | Rare:22 | ||||
| chr11:111913128-111913300 | Rare:46 |