Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:74442768-74443067 | Common:7; Rare:67 | ||||
chr17:74466575-74466698 | Rare:36 | ||||
chr17:74748434-74748693 | Common:4; Rare:98 | ||||
chr17:74749123-74749240 | Common:1; Rare:40; Clinvar:1 | ||||
chr17:74776272-74776550 | Common:4; Rare:92 | ||||
chr17:74860467-74860588 | Common:2; Rare:47 | ||||
chr17:74972652-74972983 | Common:3; Rare:85 | ||||
chr17:75012565-75012719 | Common:2; Rare:46 | ||||
chr17:75046923-75047421 | Common:2; Rare:158 | ||||
chr17:75109878-75109981 | Common:1; Rare:25 | ||||
chr17:75130760-75131110 | Common:2; Rare:127 | ||||
chr17:75205356-75205749 | Common:1; Rare:126 | ||||
chr17:75261583-75261959 | Common:4; Rare:123; Clinvar (benign):3 | ||||
chr17:75271146-75271410 | Common:3; Rare:49 | ||||
chr17:75289387-75289630 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 |