Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26233898-26234284 | Common:5; Rare:208 | ||||
chr1:26279945-26280169 | Rare:220 | ||||
chr1:26305960-26306540 | Common:3; Rare:173 | ||||
chr1:26306550-26306860 | Common:26; Rare:172 | ||||
chr1:26432067-26432441 | Common:10; Rare:190; Clinvar:4; Clinvar (benign):2 | ||||
chr1:26471680-26472110 | Common:5; Rare:171 | ||||
chr1:26472244-26472546 | Common:8; Rare:188 | ||||
chr1:26472620-26473440 | Common:7; Rare:373 | ||||
chr1:26529666-26529844 | Rare:104 | ||||
chr1:26695130-26695720 | Common:4; Rare:251 | ||||
chr1:26695876-26696149 | Rare:137 | ||||
chr1:26696227-26696389 | Common:1; Rare:52 | ||||
chr1:26787865-26788243 | Common:6; Rare:215; Clinvar:4; Clinvar (benign):4 | ||||
chr1:26826525-26826755 | Rare:149 | ||||
chr1:26862868-26863207 | Rare:117 |