| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18526847-18527063 | Common:2; Rare:102 | ||||
| chr11:18588667-18588777 | Rare:43 | ||||
| chr11:18634332-18634619 | Common:2; Rare:98 | ||||
| chr11:20387394-20387725 | Common:8; Rare:104 | ||||
| chr11:27506739-27506859 | Common:1; Rare:51 | ||||
| chr11:31509575-31509806 | Common:1; Rare:76 | ||||
| chr11:33161449-33161624 | Common:5; Rare:46 | ||||
| chr11:33736384-33736586 | Common:2; Rare:65 | ||||
| chr11:34916286-34916676 | Common:10; Rare:158; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35943892-35944110 | Common:3; Rare:72 | ||||
| chr11:36510235-36510350 | Rare:31 | ||||
| chr11:45804965-45805189 | Common:3; Rare:57; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45917865-45918180 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46277921-46278073 | Rare:42 | ||||
| chr11:46700559-46700818 | Common:1; Rare:66 |