Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:225882757-225882928 | Common:6; Rare:40 | ||||
chr1:225922469-225922793 | Common:1; Rare:60 | ||||
chr1:225923554-225923783 | Rare:63; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:225923829-225923916 | Common:1; Rare:23 | ||||
chr1:225924003-225924780 | Common:12; Rare:210 | ||||
chr1:225924830-225924882 | Common:1; Rare:8 | ||||
chr1:225998759-225999104 | Rare:61 | ||||
chr1:225999143-225999661 | Common:2; Rare:197 | ||||
chr1:226061224-226061683 | Rare:80 | ||||
chr1:226061761-226062757 | Common:2; Rare:323 | ||||
chr1:226062760-226063335 | Common:2; Rare:181 | ||||
chr1:226063508-226063780 | Common:2; Rare:68 | ||||
chr1:226186122-226186288 | Rare:37 | ||||
chr1:226186298-226186394 | Rare:34 | ||||
chr1:226186398-226186558 | Rare:42 |