| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:705270-705452 | Common:3; Rare:52 | ||||
| chr11:706509-706668 | Rare:30 | ||||
| chr11:709398-709608 | Common:2; Rare:76 | ||||
| chr11:763390-763943 | Rare:237; Clinvar:3; Clinvar (pathogenic):3 | ||||
| chr11:777416-777621 | Common:1; Rare:96 | ||||
| chr11:798233-798457 | Common:1; Rare:72 | ||||
| chr11:809213-809352 | Common:2; Rare:38 | ||||
| chr11:809474-809664 | Common:2; Rare:57 | ||||
| chr11:809758-810354 | Common:3; Rare:248 | ||||
| chr11:832819-833029 | Common:7; Rare:69 | ||||
| chr11:842414-843329 | Common:9; Rare:321 | ||||
| chr11:843953-844153 | Common:1; Rare:51 | ||||
| chr11:844180-844442 | Common:3; Rare:79 | ||||
| chr11:910774-910911 | Common:3; Rare:51 | ||||
| chr11:1309529-1309771 | Common:2; Rare:105 |