| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73876763-73877044 | Common:5; Rare:81 | ||||
| chr11:73982829-73982930 | Common:6; Rare:36 | ||||
| chr11:73983305-73983616 | Common:1; Rare:60 | ||||
| chr11:74170853-74171385 | Common:3; Rare:168 | ||||
| chr11:74398382-74398494 | Common:2; Rare:20 | ||||
| chr11:74493065-74493370 | Common:1; Rare:103; Clinvar (pathogenic):1 | ||||
| chr11:74592470-74592659 | Common:1; Rare:62 | ||||
| chr11:74949089-74949329 | Common:6; Rare:70 | ||||
| chr11:74988785-74988920 | Rare:31 | ||||
| chr11:75351605-75352078 | Common:6; Rare:122 | ||||
| chr11:75352099-75352178 | Rare:19 | ||||
| chr11:75352200-75352489 | Common:1; Rare:60 | ||||
| chr11:75399398-75399584 | Common:4; Rare:80 | ||||
| chr11:76381101-76381409 | Common:4; Rare:100 | ||||
| chr11:76444590-76445088 | Common:1; Rare:123 |