| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11273430-11273510 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chr1:11654833-11654914 | Common:1; Rare:19 | ||||
| chr1:11805896-11806265 | Common:2; Rare:102; Clinvar:1 | ||||
| chr1:11980069-11980383 | Common:4; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:12617202-12617747 | Common:1; Rare:114 | ||||
| chr1:12618123-12618444 | Common:2; Rare:68 | ||||
| chr1:15526553-15526917 | Common:2; Rare:117 | ||||
| chr1:15584862-15584937 | Common:1; Rare:27 | ||||
| chr1:15617243-15617451 | Common:1; Rare:61 | ||||
| chr1:16352419-16352606 | Common:3; Rare:100 | ||||
| chr1:16440538-16440793 | Common:2; Rare:80 | ||||
| chr1:17053976-17054348 | Common:3; Rare:113; Clinvar:12; Clinvar (benign):10 | ||||
| chr1:17439669-17439887 | Rare:71 | ||||
| chr1:17580314-17580621 | Common:2; Rare:59 | ||||
| chr1:18902478-18902842 | Common:2; Rare:112; Clinvar:9; Clinvar (pathogenic):1 |