| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11012170-11012460 | Common:1; Rare:74 | ||||
| chr1:11012545-11012707 | Common:2; Rare:88; Clinvar:6; Clinvar (benign):2 | ||||
| chr1:11013000-11013450 | Common:2; Rare:199 | ||||
| chr1:11059901-11060401 | Common:5; Rare:248 | ||||
| chr1:11099170-11099500 | Rare:130 | ||||
| chr1:11099753-11099977 | Common:5; Rare:145 | ||||
| chr1:11262463-11262817 | Common:4; Rare:204 | ||||
| chr1:11654401-11654561 | Rare:74 | ||||
| chr1:11654631-11654931 | Common:8; Rare:151 | ||||
| chr1:11663723-11664306 | Common:6; Rare:250 | ||||
| chr1:11735964-11736274 | Common:6; Rare:161 | ||||
| chr1:11736355-11736787 | Common:2; Rare:133 | ||||
| chr1:11805474-11805671 | Common:2; Rare:36 | ||||
| chr1:11805835-11806280 | Common:4; Rare:234; Clinvar:4 | ||||
| chr1:11926371-11926585 | Common:12; Rare:116 |