| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66268404-66268682 | Common:3; Rare:81 | ||||
| chr11:66289058-66289419 | Common:1; Rare:92 | ||||
| chr11:66345049-66345203 | Common:1; Rare:43 | ||||
| chr11:66347564-66347930 | Common:6; Rare:86 | ||||
| chr11:66438744-66439144 | Common:2; Rare:102 | ||||
| chr11:66480222-66480462 | Common:2; Rare:65 | ||||
| chr11:66510551-66510677 | Common:1; Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr11:66593036-66593223 | Common:1; Rare:69 | ||||
| chr11:66616422-66616689 | Common:2; Rare:81 | ||||
| chr11:66638393-66638747 | Common:4; Rare:156 | ||||
| chr11:66677769-66678015 | Common:1; Rare:98 | ||||
| chr11:66744639-66744829 | Common:1; Rare:78 | ||||
| chr11:67317446-67317515 | Rare:16 | ||||
| chr11:67317767-67317877 | Rare:19 | ||||
| chr11:67353493-67353706 | Common:1; Rare:57 |