Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:28335429-28335810 | Common:1; Rare:85 | ||||
chr17:28357444-28357699 | Common:5; Rare:130; Clinvar (pathogenic):1 | ||||
chr17:28571482-28571688 | Rare:54 | ||||
chr17:28645084-28645278 | Common:1; Rare:75 | ||||
chr17:28661881-28661949 | Rare:31 | ||||
chr17:28662122-28662327 | Rare:81 | ||||
chr17:28717839-28718002 | Rare:34 | ||||
chr17:28854971-28855032 | Rare:16 | ||||
chr17:29090530-29090908 | Common:1; Rare:92 | ||||
chr17:29568512-29568740 | Common:2; Rare:72 | ||||
chr17:29761277-29761603 | Common:4; Rare:120 | ||||
chr17:32142351-32142673 | Common:8; Rare:132 | ||||
chr17:32350012-32350228 | Rare:110 | ||||
chr17:34961441-34961569 | Common:1; Rare:61 | ||||
chr17:34980389-34980604 | Common:4; Rare:62 |