Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:28405729-28405883 | Rare:40 | ||||
chr17:28406123-28406335 | Rare:49; Clinvar:1 | ||||
chr17:28547732-28547875 | Rare:43; Clinvar:3 | ||||
chr17:28549750-28550064 | Common:1; Rare:60 | ||||
chr17:28570910-28571117 | Rare:70; Clinvar (pathogenic):1 | ||||
chr17:28571454-28571788 | Rare:98 | ||||
chr17:28576840-28577117 | Common:2; Rare:70 | ||||
chr17:28598939-28599241 | Common:3; Rare:102 | ||||
chr17:28599552-28599773 | Rare:41 | ||||
chr17:28645030-28645429 | Common:1; Rare:161 | ||||
chr17:28661574-28661733 | Rare:41 | ||||
chr17:28661834-28662296 | Common:1; Rare:171 | ||||
chr17:28711211-28711641 | Common:3; Rare:144 | ||||
chr17:28712254-28712403 | Rare:38 | ||||
chr17:28717237-28717312 | Common:1; Rare:27 |