| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44030798-44031198 | Common:3; Rare:124 | ||||
| chr1:44031292-44031696 | Common:6; Rare:155 | ||||
| chr1:44213244-44213552 | Common:8; Rare:176 | ||||
| chr1:44355160-44355422 | Common:1; Rare:68 | ||||
| chr1:44631550-44632101 | Common:11; Rare:281 | ||||
| chr1:44632040-44632654 | Common:14; Rare:585 | ||||
| chr1:44674237-44674814 | Common:9; Rare:363 | ||||
| chr1:44739551-44739962 | Common:8; Rare:394 | ||||
| chr1:44775358-44775913 | Common:9; Rare:458 | ||||
| chr1:44776399-44776820 | Rare:200 | ||||
| chr1:44799690-44800071 | Common:6; Rare:107 | ||||
| chr1:44800096-44800497 | Common:4; Rare:211 | ||||
| chr1:44986487-44986875 | Common:7; Rare:199; Clinvar:1; Clinvar (benign):3 | ||||
| chr1:45011200-45011355 | Rare:43 | ||||
| chr1:45011262-45012303 | Common:20; Rare:474; Clinvar:12; Clinvar (benign):3 |