| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44355269-44355472 | Common:1; Rare:46 | ||||
| chr1:44739626-44739934 | Common:3; Rare:123 | ||||
| chr1:44775360-44775620 | Common:2; Rare:103 | ||||
| chr1:44775854-44776151 | Common:1; Rare:110 | ||||
| chr1:44777585-44778074 | Common:2; Rare:126 | ||||
| chr1:44986538-44986708 | Common:2; Rare:29; Clinvar (benign):1 | ||||
| chr1:45339996-45340243 | Rare:87; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr1:45500017-45500384 | Common:2; Rare:98; Clinvar:5; Clinvar (pathogenic):3 | ||||
| chr1:45521809-45522074 | Common:1; Rare:102 | ||||
| chr1:45550733-45550869 | Common:1; Rare:39 | ||||
| chr1:45686508-45686743 | Rare:84 | ||||
| chr1:45687050-45687357 | Common:1; Rare:81 | ||||
| chr1:45688055-45688243 | Common:1; Rare:54 | ||||
| chr1:45750599-45750856 | Rare:92 | ||||
| chr1:46198388-46198534 | Common:1; Rare:61; Clinvar:1 |