Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44899367-44899736 | Common:2; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
chr17:45060964-45061359 | Common:2; Rare:111 | ||||
chr17:45132333-45132626 | Common:2; Rare:83 | ||||
chr17:45148159-45148479 | Common:1; Rare:93 | ||||
chr17:45160529-45160748 | Rare:49 | ||||
chr17:46923091-46923204 | Common:3; Rare:56; Clinvar:3; Clinvar (benign):8 | ||||
chr17:47188839-47189036 | Common:1; Rare:38 | ||||
chr17:47189103-47189374 | Common:1; Rare:77 | ||||
chr17:47530891-47531279 | Common:2; Rare:104 | ||||
chr17:47896191-47896270 | Rare:29 | ||||
chr17:47941335-47941732 | Rare:106; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:48048069-48048460 | Rare:106 | ||||
chr17:48048599-48048862 | Common:4; Rare:41 | ||||
chr17:48908300-48908407 | Common:1; Rare:25 | ||||
chr17:48944781-48944884 | Common:1; Rare:32 |