| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44218464-44218690 | Rare:70 | ||||
| chr1:44674413-44674744 | Common:3; Rare:88 | ||||
| chr1:44739667-44739872 | Common:1; Rare:74 | ||||
| chr1:44775447-44775599 | Rare:58 | ||||
| chr1:44777604-44778115 | Common:2; Rare:127 | ||||
| chr1:44986532-44986738 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr1:45339936-45340178 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr1:45340381-45340502 | Common:1; Rare:33; Clinvar:1 | ||||
| chr1:45500083-45500335 | Common:1; Rare:61; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr1:45550699-45551110 | Common:3; Rare:105 | ||||
| chr1:45687059-45687312 | Common:1; Rare:69 | ||||
| chr1:45688091-45688247 | Common:1; Rare:49 | ||||
| chr1:45750596-45750800 | Rare:75 | ||||
| chr1:46132614-46132782 | Rare:63 | ||||
| chr1:46198403-46198522 | Common:1; Rare:46; Clinvar:1 |