| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:23778287-23778537 | Common:9; Rare:121 | ||||
| chr1:23800730-23800929 | Common:1; Rare:65 | ||||
| chr1:23825411-23825490 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:23959479-23959854 | Common:5; Rare:90 | ||||
| chr1:23980210-23980493 | Rare:78 | ||||
| chr1:24415538-24415820 | Common:2; Rare:75 | ||||
| chr1:24642890-24643242 | Rare:109 | ||||
| chr1:25232444-25232672 | Rare:93 | ||||
| chr1:25247070-25247132 | Rare:17 | ||||
| chr1:25247449-25247630 | Common:2; Rare:63 | ||||
| chr1:25338214-25338479 | Common:2; Rare:87 | ||||
| chr1:25819889-25820013 | Common:2; Rare:38 | ||||
| chr1:25906392-25906590 | Rare:76 | ||||
| chr1:26279736-26280167 | Common:1; Rare:221 | ||||
| chr1:26432091-26432414 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 |