| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44213315-44213498 | Common:1; Rare:39 | ||||
| chr1:44674425-44674734 | Common:3; Rare:76 | ||||
| chr1:44739655-44739878 | Common:1; Rare:84 | ||||
| chr1:44775457-44775599 | Rare:56 | ||||
| chr1:44986543-44986665 | Common:2; Rare:24; Clinvar (benign):1 | ||||
| chr1:45340117-45340174 | Rare:21 | ||||
| chr1:45340408-45340470 | Common:1; Rare:16; Clinvar:1 | ||||
| chr1:45499998-45500358 | Common:2; Rare:83; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521859-45522093 | Common:1; Rare:88 | ||||
| chr1:45550698-45551098 | Common:3; Rare:101 | ||||
| chr1:45583816-45584066 | Common:1; Rare:82 | ||||
| chr1:45687059-45687318 | Common:1; Rare:70 | ||||
| chr1:45688078-45688222 | Common:1; Rare:41 | ||||
| chr1:46132865-46133157 | Common:1; Rare:89 | ||||
| chr1:46198420-46198506 | Common:1; Rare:32; Clinvar:1 |