Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:77918624-77919132 | Common:3; Rare:114 | ||||
chr13:77919431-77919510 | Rare:36; Clinvar:1 | ||||
chr13:77919520-77919672 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
chr13:78659097-78659235 | Common:2; Rare:100 | ||||
chr13:79405792-79405901 | Rare:38 | ||||
chr13:79406161-79406374 | Common:4; Rare:67 | ||||
chr13:79481003-79481511 | Common:2; Rare:194 | ||||
chr13:80340781-80340988 | Rare:39 | ||||
chr13:80341068-80341175 | Rare:39 | ||||
chr13:80341277-80341405 | Rare:42 | ||||
chr13:83882274-83882413 | Rare:37; Clinvar:1 | ||||
chr13:93226768-93226900 | Common:2; Rare:28; Clinvar (benign):1 | ||||
chr13:93227014-93227474 | Common:2; Rare:105; Clinvar:6; Clinvar (benign):2 | ||||
chr13:94596105-94596369 | Common:2; Rare:93 | ||||
chr13:94712507-94712717 | Common:1; Rare:39 |