Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:75724641-75724780 | Common:2; Rare:70; Clinvar:4; Clinvar (benign):2 | ||||
chr1:77219404-77219496 | Rare:41 | ||||
chr1:77370976-77371311 | Common:1; Rare:48 | ||||
chr1:77979046-77979275 | Common:2; Rare:72 | ||||
chr1:84506549-84506752 | Common:3; Rare:41 | ||||
chr1:84574413-84574551 | Common:1; Rare:44 | ||||
chr1:85062204-85062377 | Common:2; Rare:38 | ||||
chr1:85708354-85708541 | Common:2; Rare:68 | ||||
chr1:86704732-86704882 | Common:2; Rare:57 | ||||
chr1:86914325-86914692 | Common:1; Rare:104 | ||||
chr1:87329010-87329194 | Common:2; Rare:42 | ||||
chr1:88992596-88992981 | Common:3; Rare:99 | ||||
chr1:89632905-89633156 | Rare:69 | ||||
chr1:91886082-91886327 | Rare:102 | ||||
chr1:92298972-92299064 | Common:1; Rare:46; Clinvar:1 |