| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:130110466-130110587 | Common:2; Rare:45 | ||||
| chr10:132065860-132065952 | Common:1; Rare:15 | ||||
| chr10:132633179-132633500 | Common:3; Rare:57 | ||||
| chr10:132781888-132782195 | Common:1; Rare:115 | ||||
| chr11:311138-311317 | Rare:13 | ||||
| chr11:318420-318651 | Rare:23 | ||||
| chr11:319540-319797 | Common:1; Rare:71 | ||||
| chr11:319868-320157 | Common:1; Rare:86 | ||||
| chr11:1753465-1753900 | Common:3; Rare:180; Clinvar:12; Clinvar (benign):21; Clinvar (pathogenic):2 | ||||
| chr11:9758172-9758347 | Rare:51 | ||||
| chr11:10581867-10582179 | Common:5; Rare:82 | ||||
| chr11:10600916-10601269 | Common:1; Rare:90 | ||||
| chr11:11920182-11920492 | Common:2; Rare:72 | ||||
| chr11:12086311-12086524 | Common:2; Rare:32 | ||||
| chr11:12086690-12086924 | Common:2; Rare:39 |