Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:203627000-203627109 | Rare:26 | ||||
chr1:204494806-204494910 | Rare:40 | ||||
chr1:204516237-204516440 | Rare:56 | ||||
chr1:205121934-205122295 | Common:4; Rare:102 | ||||
chr1:205211332-205211643 | Common:2; Rare:143; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:205456352-205456443 | Rare:20 | ||||
chr1:205750146-205750408 | Common:3; Rare:63 | ||||
chr1:205813181-205813421 | Common:3; Rare:99 | ||||
chr1:206612432-206612633 | Common:3; Rare:55 | ||||
chr1:207050980-207051105 | Common:1; Rare:49 | ||||
chr1:207052957-207053285 | Common:1; Rare:82 | ||||
chr1:207751933-207752149 | Common:1; Rare:69 | ||||
chr1:209784531-209784721 | Common:1; Rare:62 | ||||
chr1:209937960-209938262 | Common:3; Rare:99; Clinvar (pathogenic):1 | ||||
chr1:211259075-211259399 | Common:1; Rare:104 |