Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:15999536-15999859 | Common:3; Rare:163; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr17:16215515-16215622 | Rare:46 | ||||
chr17:17237109-17237431 | Common:4; Rare:102; Clinvar:1; Clinvar (benign):3 | ||||
chr17:18039154-18039410 | Common:3; Rare:64; Clinvar (benign):1 | ||||
chr17:18314927-18315325 | Common:1; Rare:114 | ||||
chr17:19378162-19378560 | Common:2; Rare:94 | ||||
chr17:19977820-19977974 | Common:1; Rare:51 | ||||
chr17:21214111-21214307 | Common:2; Rare:82 | ||||
chr17:28318915-28319202 | Common:3; Rare:94 | ||||
chr17:28335376-28335582 | Common:1; Rare:48 | ||||
chr17:28357455-28357667 | Common:5; Rare:105 | ||||
chr17:28661896-28662305 | Common:1; Rare:143 | ||||
chr17:28717866-28718031 | Rare:33 | ||||
chr17:28718378-28718630 | Common:1; Rare:46 | ||||
chr17:29568467-29568740 | Common:4; Rare:92 |