| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:153536214-153536296 | Common:1; Rare:12 | ||||
| chr1:153628230-153628473 | Common:1; Rare:55 | ||||
| chr1:153633884-153634142 | Common:4; Rare:79 | ||||
| chr1:153658575-153658756 | Common:2; Rare:51 | ||||
| chr1:153727739-153728097 | Common:1; Rare:110 | ||||
| chr1:153958568-153958877 | Common:1; Rare:93 | ||||
| chr1:153963479-153963745 | Common:2; Rare:72 | ||||
| chr1:153967619-153967908 | Common:1; Rare:52 | ||||
| chr1:153986223-153986456 | Rare:61 | ||||
| chr1:153990618-153990968 | Common:2; Rare:139 | ||||
| chr1:154182945-154183277 | Rare:106 | ||||
| chr1:154206326-154206496 | Common:1; Rare:41 | ||||
| chr1:154220509-154221188 | Common:1; Rare:217 | ||||
| chr1:154221252-154221372 | Rare:30 | ||||
| chr1:154272533-154272791 | Common:4; Rare:76; Clinvar:3; Clinvar (benign):4 |