Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:30581011-30581406 | Common:2; Rare:105 | ||||
chr22:30936271-30936543 | Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
chr22:30968998-30969304 | Common:3; Rare:93 | ||||
chr22:30969793-30970259 | Common:2; Rare:123 | ||||
chr22:30971895-30972071 | Common:1; Rare:42 | ||||
chr22:30972092-30972696 | Common:4; Rare:122 | ||||
chr22:31177961-31178087 | Rare:22 | ||||
chr22:31538092-31538242 | Rare:31 | ||||
chr22:31538311-31538436 | Common:3; Rare:14 | ||||
chr22:31617797-31618169 | Common:3; Rare:100 | ||||
chr22:31647522-31647840 | Common:4; Rare:48 | ||||
chr22:32480668-32480973 | Rare:53 | ||||
chr22:32802352-32802460 | Rare:21 | ||||
chr22:32816414-32816568 | Rare:15 | ||||
chr22:35330269-35330349 | Common:1; Rare:23 |