| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:153953389-153953583 | Rare:42 | ||||
| chr1:153954620-153954890 | Common:1; Rare:57 | ||||
| chr1:153963497-153963745 | Common:2; Rare:67 | ||||
| chr1:153967718-153967956 | Rare:41 | ||||
| chr1:153976958-153977231 | Common:1; Rare:69 | ||||
| chr1:153985353-153985690 | Common:2; Rare:44 | ||||
| chr1:153986268-153986459 | Rare:44 | ||||
| chr1:153990653-153990819 | Common:2; Rare:80 | ||||
| chr1:154170398-154170684 | Rare:61; Clinvar (benign):1 | ||||
| chr1:154172905-154173127 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr1:154183007-154183116 | Rare:26 | ||||
| chr1:154219842-154220230 | Common:5; Rare:107 | ||||
| chr1:154220341-154221035 | Common:1; Rare:231 | ||||
| chr1:154221248-154221379 | Rare:30 | ||||
| chr1:154221431-154221561 | Rare:35 |