Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:21427823-21428104 | Common:3; Rare:105 | ||||
chr7:21945831-21946199 | Common:3; Rare:119 | ||||
chr7:22726983-22727217 | Common:2; Rare:26 | ||||
chr7:22822757-22822964 | Common:3; Rare:75 | ||||
chr7:23014054-23014393 | Common:6; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
chr7:23105673-23105860 | Common:3; Rare:101; Clinvar:2; Clinvar (benign):3 | ||||
chr7:23181912-23182088 | Rare:75 | ||||
chr7:23467924-23468096 | Common:2; Rare:39 | ||||
chr7:23470316-23470342 | Rare:5 | ||||
chr7:23470345-23470419 | Rare:24 | ||||
chr7:23470435-23470546 | Rare:34 | ||||
chr7:24757409-24757535 | Common:1; Rare:37 | ||||
chr7:25125245-25125660 | Rare:160; Clinvar:3 | ||||
chr7:26200644-26201296 | Common:3; Rare:306 | ||||
chr7:26201411-26201805 | Common:2; Rare:187 |