Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:76103712-76103867 | Common:4; Rare:49 | ||||
chr17:76353612-76353677 | Rare:27 | ||||
chr17:76585814-76586167 | Common:5; Rare:79 | ||||
chr17:76726478-76726886 | Common:5; Rare:153 | ||||
chr17:76737306-76737525 | Common:3; Rare:88 | ||||
chr17:76737894-76738034 | Common:3; Rare:40 | ||||
chr17:77140660-77141045 | Common:2; Rare:136 | ||||
chr17:78187029-78187371 | Common:3; Rare:112 | ||||
chr17:78782255-78782525 | Common:5; Rare:80 | ||||
chr17:78840751-78841114 | Common:2; Rare:137 | ||||
chr17:79009784-79009924 | Common:7; Rare:35 | ||||
chr17:80220325-80220459 | Common:1; Rare:52; Clinvar:1 | ||||
chr17:80415105-80415191 | Common:1; Rare:58 | ||||
chr17:81239036-81239343 | Common:3; Rare:97 | ||||
chr17:81512715-81513186 | Common:8; Rare:234; Clinvar (benign):14 |