Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:46797094-46797261 | Common:2; Rare:56 | ||||
chr13:46797278-46797324 | Rare:15 | ||||
chr13:48000744-48000844 | Rare:23 | ||||
chr13:48001218-48001410 | Common:1; Rare:88; Clinvar:4; Clinvar (benign):7 | ||||
chr13:48037686-48037829 | Common:2; Rare:76; Clinvar:2 | ||||
chr13:48037904-48038132 | Common:5; Rare:72 | ||||
chr13:48233060-48233475 | Common:3; Rare:144 | ||||
chr13:48303657-48304047 | Common:1; Rare:128; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr13:48492601-48492702 | Rare:26 | ||||
chr13:48533038-48533153 | Common:2; Rare:36 | ||||
chr13:48975790-48975960 | Common:1; Rare:63 | ||||
chr13:48976539-48976878 | Common:1; Rare:96 | ||||
chr13:49247629-49248035 | Common:1; Rare:85 | ||||
chr13:49401303-49401654 | Common:1; Rare:71 | ||||
chr13:49443997-49444519 | Common:2; Rare:162 |