Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:154589420-154589734 | Rare:84; Clinvar:3; Clinvar (pathogenic):2 | ||||
chr4:154605172-154605444 | Rare:40 | ||||
chr4:155909854-155910211 | Common:4; Rare:80; Clinvar (pathogenic):1 | ||||
chr4:158697456-158697709 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):3 | ||||
chr4:168903661-168903890 | Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
chr4:176320512-176320612 | Rare:30 | ||||
chr4:184348807-184349050 | Rare:49 | ||||
chr4:184382194-184382460 | Common:4; Rare:41 | ||||
chr4:184770402-184770563 | Rare:31 | ||||
chr4:184772841-184773158 | Common:1; Rare:68 | ||||
chr4:184813370-184813694 | Common:2; Rare:68 | ||||
chr4:184814151-184814191 | Common:1; Rare:8 | ||||
chr4:184815043-184815266 | Common:2; Rare:52 | ||||
chr4:184899305-184899465 | Common:1; Rare:22 | ||||
chr4:185713378-185713523 | Common:2; Rare:31 |