| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:203626664-203626859 | Common:1; Rare:45 | ||||
| chr1:203795411-203795738 | Common:1; Rare:96 | ||||
| chr1:203796016-203796199 | Common:1; Rare:39 | ||||
| chr1:204151594-204152268 | Common:3; Rare:190 | ||||
| chr1:204411413-204411471 | Rare:21 | ||||
| chr1:204411810-204412085 | Common:9; Rare:85 | ||||
| chr1:204494714-204494955 | Common:1; Rare:74 | ||||
| chr1:204516266-204516536 | Common:1; Rare:75 | ||||
| chr1:204516648-204516703 | Common:1; Rare:9 | ||||
| chr1:204828566-204828707 | Rare:66 | ||||
| chr1:205043175-205043286 | Rare:29 | ||||
| chr1:205121937-205122304 | Common:5; Rare:105 | ||||
| chr1:205211314-205211488 | Common:1; Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr1:205211537-205211612 | Rare:30 | ||||
| chr1:205211665-205211753 | Rare:21 |