Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:122077107-122077309 | Common:1; Rare:36 | ||||
chr5:129094468-129094762 | Common:3; Rare:118 | ||||
chr5:133968598-133968698 | Rare:39 | ||||
chr5:134004627-134004893 | Common:1; Rare:94 | ||||
chr5:134226039-134226412 | Common:1; Rare:118 | ||||
chr5:134371036-134371184 | Common:1; Rare:38 | ||||
chr5:134648726-134648848 | Rare:31 | ||||
chr5:135033412-135033495 | Rare:16 | ||||
chr5:136029005-136029187 | Rare:63 | ||||
chr5:136046969-136047382 | Common:2; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
chr5:138178614-138178717 | Rare:26 | ||||
chr5:138178949-138179181 | Common:3; Rare:48 | ||||
chr5:138213292-138213544 | Rare:57 | ||||
chr5:138543096-138543424 | Common:2; Rare:94 | ||||
chr5:139561685-139561794 | Rare:42 |