Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:3846744-3846885 | Rare:42 | ||||
chr20:5126701-5127045 | Common:3; Rare:110 | ||||
chr20:5610881-5611167 | Common:2; Rare:102 | ||||
chr20:5950410-5950656 | Common:8; Rare:75 | ||||
chr20:13784878-13785080 | Common:2; Rare:90; Clinvar (benign):3 | ||||
chr20:13995246-13995566 | Rare:88 | ||||
chr20:16573308-16573540 | Common:1; Rare:63 | ||||
chr20:16729922-16730064 | Rare:40 | ||||
chr20:17226780-17227053 | Common:1; Rare:78 | ||||
chr20:17569755-17570202 | Common:5; Rare:152 | ||||
chr20:17682112-17682193 | Common:1; Rare:23 | ||||
chr20:17968453-17968613 | Common:4; Rare:72 | ||||
chr20:17968789-17969119 | Common:3; Rare:117 | ||||
chr20:18137744-18137953 | Common:1; Rare:78 | ||||
chr20:18467072-18467448 | Common:1; Rare:78 |