| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:23800753-23800959 | Common:1; Rare:71 | ||||
| chr1:23959608-23959916 | Common:2; Rare:81 | ||||
| chr1:24413697-24413903 | Common:1; Rare:49 | ||||
| chr1:24415653-24415835 | Common:1; Rare:50 | ||||
| chr1:24642890-24643329 | Common:2; Rare:146 | ||||
| chr1:24745290-24745623 | Common:2; Rare:117 | ||||
| chr1:25232442-25232667 | Rare:92 | ||||
| chr1:25247314-25247621 | Common:2; Rare:115 | ||||
| chr1:25338214-25338500 | Common:2; Rare:93 | ||||
| chr1:25819882-25820019 | Common:2; Rare:42 | ||||
| chr1:26279847-26280201 | Rare:191 | ||||
| chr1:26432119-26432403 | Common:4; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:26472194-26472627 | Common:4; Rare:150 | ||||
| chr1:26695722-26696047 | Common:1; Rare:105 | ||||
| chr1:26787865-26788201 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):2 |