Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39738725-39738935 | Common:2; Rare:50 | ||||
chr1:39955004-39955199 | Common:1; Rare:51 | ||||
chr1:40040457-40040890 | Common:4; Rare:132 | ||||
chr1:40097228-40097318 | Rare:36; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:40161255-40161402 | Rare:38 | ||||
chr1:40257898-40258313 | Common:4; Rare:115; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40315908-40316208 | Common:1; Rare:60 | ||||
chr1:40450047-40450416 | Common:7; Rare:110 | ||||
chr1:40477190-40477325 | Common:1; Rare:40 | ||||
chr1:40508655-40508796 | Common:3; Rare:38 | ||||
chr1:40531487-40531674 | Rare:47 | ||||
chr1:40665663-40665828 | Common:2; Rare:48 | ||||
chr1:40691369-40691874 | Common:3; Rare:203 | ||||
chr1:40692022-40692203 | Common:2; Rare:63 | ||||
chr1:40709124-40709457 | Rare:78 |