| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:205121895-205122573 | Common:6; Rare:183 | ||||
| chr1:205211411-205211832 | Common:1; Rare:146; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr1:205591975-205592124 | Rare:36 | ||||
| chr1:205631386-205631510 | Common:1; Rare:41 | ||||
| chr1:205631806-205632190 | Common:4; Rare:137 | ||||
| chr1:205679888-205680105 | Common:2; Rare:52 | ||||
| chr1:205749518-205749880 | Common:6; Rare:150 | ||||
| chr1:205750123-205750242 | Rare:37 | ||||
| chr1:205750558-205750666 | Rare:21 | ||||
| chr1:205775037-205775175 | Common:1; Rare:26 | ||||
| chr1:205775201-205775235 | Common:1; Rare:6 | ||||
| chr1:205775360-205775385 | Rare:1 | ||||
| chr1:205775406-205775568 | Common:2; Rare:38 | ||||
| chr1:205813093-205813422 | Common:3; Rare:138 | ||||
| chr1:205850067-205850338 | Common:1; Rare:68 |