| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66438750-66439210 | Common:2; Rare:113 | ||||
| chr11:66466679-66466921 | Rare:69 | ||||
| chr11:66480215-66480480 | Common:3; Rare:71 | ||||
| chr11:66510539-66510687 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:66545980-66546450 | Common:5; Rare:118 | ||||
| chr11:66593036-66593220 | Common:1; Rare:67 | ||||
| chr11:66616323-66616679 | Common:2; Rare:112 | ||||
| chr11:66618987-66619624 | Common:6; Rare:203 | ||||
| chr11:66638389-66638727 | Common:3; Rare:150 | ||||
| chr11:66677796-66678130 | Common:1; Rare:115 | ||||
| chr11:66728273-66728579 | Rare:84 | ||||
| chr11:66744603-66744781 | Common:1; Rare:65 | ||||
| chr11:66842767-66843167 | Common:2; Rare:232 | ||||
| chr11:66843287-66843491 | Common:5; Rare:105 | ||||
| chr11:66856166-66856588 | Common:1; Rare:139 |