| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44775388-44776164 | Common:19; Rare:1041 | ||||
| chr1:44776442-44777628 | Common:1; Rare:619 | ||||
| chr1:44777645-44778045 | Common:2; Rare:156 | ||||
| chr1:44778120-44778520 | Common:5; Rare:182 | ||||
| chr1:44799620-44800050 | Common:11; Rare:226 | ||||
| chr1:44800001-44800529 | Common:15; Rare:656 | ||||
| chr1:44807094-44807494 | Common:2; Rare:67 | ||||
| chr1:44807630-44808569 | Common:28; Rare:590 | ||||
| chr1:44808560-44809287 | Common:2; Rare:288 | ||||
| chr1:44842376-44843244 | Common:4; Rare:274; Clinvar:6; Clinvar (benign):2 | ||||
| chr1:44843160-44843520 | Rare:146 | ||||
| chr1:44986454-44986909 | Common:15; Rare:421; Clinvar:3; Clinvar (benign):6 | ||||
| chr1:45010757-45011267 | Common:11; Rare:349 | ||||
| chr1:45011250-45012678 | Common:38; Rare:1061; Clinvar:20; Clinvar (benign):5 | ||||
| chr1:45012583-45013699 | Common:6; Rare:759; Clinvar (pathogenic):1 |