Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:58259547-58259721 | Rare:27 | ||||
chr5:58259724-58259910 | Common:2; Rare:42 | ||||
chr5:64507610-64507743 | Rare:27 | ||||
chr5:77087916-77088111 | Common:2; Rare:41 | ||||
chr5:95752126-95752268 | Rare:36 | ||||
chr5:128083058-128083184 | Common:8; Rare:39 | ||||
chr5:137753164-137753179 | Rare:6 | ||||
chr5:139455052-139455438 | Rare:52 | ||||
chr5:148401801-148402091 | Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
chr5:150600183-150600339 | Rare:25 | ||||
chr5:150778680-150778827 | Rare:62 | ||||
chr5:157564406-157564671 | Common:1; Rare:50 | ||||
chr5:160468057-160468252 | Rare:38 | ||||
chr5:180831582-180831679 | Common:2; Rare:42 | ||||
chr6:2876535-2876832 | Rare:49 |