Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23369791-23369938 | Rare:27 | ||||
chr1:23424611-23424898 | Common:1; Rare:82 | ||||
chr1:23559340-23559653 | Common:1; Rare:137 | ||||
chr1:23691744-23691826 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23778269-23778383 | Common:5; Rare:60 | ||||
chr1:23791047-23791241 | Rare:59 | ||||
chr1:23800745-23800929 | Common:1; Rare:58 | ||||
chr1:23825405-23825563 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23868238-23868430 | Common:6; Rare:65; Clinvar:2; Clinvar (benign):5 | ||||
chr1:23959641-23959877 | Common:2; Rare:66 | ||||
chr1:23980244-23980514 | Rare:84 | ||||
chr1:24112122-24112276 | Rare:36 | ||||
chr1:24413697-24413855 | Common:1; Rare:36 | ||||
chr1:24415526-24415829 | Common:3; Rare:77 | ||||
chr1:24642874-24643335 | Common:2; Rare:152 |