| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:23980249-23980604 | Common:1; Rare:111 | ||||
| chr1:24187221-24187442 | Common:4; Rare:60 | ||||
| chr1:24413714-24413909 | Common:1; Rare:44 | ||||
| chr1:24415531-24415812 | Common:3; Rare:75 | ||||
| chr1:24642890-24643335 | Common:2; Rare:147 | ||||
| chr1:25232442-25232668 | Rare:93 | ||||
| chr1:25247425-25247638 | Common:2; Rare:81 | ||||
| chr1:25338188-25338408 | Common:1; Rare:78 | ||||
| chr1:25819882-25820021 | Common:2; Rare:43 | ||||
| chr1:25859359-25859595 | Common:3; Rare:99 | ||||
| chr1:26279926-26280162 | Rare:132 | ||||
| chr1:26306585-26306836 | Common:9; Rare:67 | ||||
| chr1:26432119-26432365 | Common:4; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:26545722-26545870 | Common:1; Rare:31 | ||||
| chr1:26787859-26788207 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):2 |