| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45206352-45206677 | Common:2; Rare:203 | ||||
| chr1:45339898-45340277 | Common:1; Rare:205; Clinvar:23; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr1:45340320-45340610 | Common:3; Rare:120; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:45499902-45500389 | Common:4; Rare:237; Clinvar:10; Clinvar (pathogenic):6 | ||||
| chr1:45521814-45522089 | Common:2; Rare:203 | ||||
| chr1:45550668-45551131 | Common:7; Rare:226 | ||||
| chr1:45583924-45584050 | Rare:87 | ||||
| chr1:45584520-45584880 | Common:1; Rare:122 | ||||
| chr1:45686499-45686702 | Rare:108 | ||||
| chr1:45686994-45687369 | Common:4; Rare:189 | ||||
| chr1:45688023-45688253 | Common:2; Rare:116 | ||||
| chr1:45688304-45688704 | Common:5; Rare:104 | ||||
| chr1:45750604-45750856 | Rare:169 | ||||
| chr1:45803317-45803688 | Common:3; Rare:190 | ||||
| chr1:46132840-46133220 | Common:4; Rare:198 |