Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40161272-40161405 | Rare:34 | ||||
chr1:40257904-40258393 | Common:4; Rare:141; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:40304978-40305065 | Common:3; Rare:12 | ||||
chr1:40450040-40450164 | Common:3; Rare:43 | ||||
chr1:40477210-40477325 | Common:1; Rare:32 | ||||
chr1:40508627-40508858 | Common:5; Rare:70 | ||||
chr1:40531502-40531700 | Rare:54 | ||||
chr1:40665669-40665808 | Common:1; Rare:43 | ||||
chr1:40691325-40691861 | Common:3; Rare:210 | ||||
chr1:40709434-40709469 | Rare:11 | ||||
chr1:40979401-40979829 | Common:5; Rare:134 | ||||
chr1:41045754-41045875 | Rare:27 | ||||
chr1:41046588-41046765 | Rare:45 | ||||
chr1:41242090-41242188 | Rare:23 | ||||
chr1:42335169-42335378 | Common:5; Rare:101 |