| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:231040036-231040419 | Common:1; Rare:152 | ||||
| chr1:231238512-231238766 | Common:1; Rare:45 | ||||
| chr1:231240642-231240946 | Common:2; Rare:49 | ||||
| chr1:231241019-231241423 | Common:4; Rare:183; Clinvar:5; Clinvar (benign):3 | ||||
| chr1:231337461-231337621 | Common:1; Rare:34 | ||||
| chr1:231337734-231338105 | Common:5; Rare:133 | ||||
| chr1:231338158-231338339 | Rare:46 | ||||
| chr1:231528231-231528820 | Common:4; Rare:155 | ||||
| chr1:231626535-231626887 | Common:5; Rare:88 | ||||
| chr1:232950215-232950313 | Common:1; Rare:17 | ||||
| chr1:232950401-232950674 | Common:4; Rare:101 | ||||
| chr1:232951032-232951302 | Common:2; Rare:44 | ||||
| chr1:233295637-233295800 | Common:1; Rare:54 | ||||
| chr1:233327230-233327806 | Common:5; Rare:105 | ||||
| chr1:234373239-234373788 | Common:1; Rare:229; Clinvar (benign):7 |