| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44674406-44674749 | Common:3; Rare:92 | ||||
| chr1:44775462-44775620 | Common:1; Rare:63 | ||||
| chr1:44775848-44776140 | Common:2; Rare:108 | ||||
| chr1:44777584-44778067 | Common:2; Rare:125 | ||||
| chr1:44986532-44986825 | Common:2; Rare:58; Clinvar (benign):1 | ||||
| chr1:45339959-45340178 | Rare:70 | ||||
| chr1:45340381-45340579 | Common:1; Rare:49; Clinvar:1 | ||||
| chr1:45499997-45500345 | Common:2; Rare:80; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521817-45522074 | Common:1; Rare:99 | ||||
| chr1:45550741-45551105 | Common:3; Rare:87 | ||||
| chr1:45583931-45584060 | Rare:47 | ||||
| chr1:45687058-45687312 | Common:1; Rare:69 | ||||
| chr1:45688053-45688216 | Common:1; Rare:41 | ||||
| chr1:45750622-45750821 | Rare:74 | ||||
| chr1:46198338-46198506 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 |