| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66480218-66480455 | Common:3; Rare:63 | ||||
| chr11:66593042-66593209 | Common:1; Rare:59 | ||||
| chr11:66616398-66616646 | Common:1; Rare:67 | ||||
| chr11:66638393-66638772 | Common:4; Rare:161 | ||||
| chr11:66677539-66678019 | Common:1; Rare:169 | ||||
| chr11:66744632-66744892 | Common:3; Rare:104 | ||||
| chr11:67353514-67353730 | Common:1; Rare:59 | ||||
| chr11:67401780-67402076 | Common:3; Rare:111 | ||||
| chr11:67428324-67428537 | Rare:74 | ||||
| chr11:67443451-67443697 | Common:2; Rare:81 | ||||
| chr11:67482906-67483154 | Rare:55; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:68030381-68030764 | Common:3; Rare:104; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271871-68272115 | Common:2; Rare:100 | ||||
| chr11:68460223-68460331 | Common:2; Rare:52 | ||||
| chr11:68903756-68903946 | Common:4; Rare:86; Clinvar (benign):6 |