Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:150685641-150685741 | Rare:21 | ||||
chr7:151059460-151059716 | Common:1; Rare:75 | ||||
chr7:151080793-151080979 | Rare:62 | ||||
chr7:151232310-151232528 | Common:1; Rare:76 | ||||
chr7:151632569-151632576 | Rare:1 | ||||
chr7:151736252-151736621 | Common:6; Rare:67 | ||||
chr7:152676094-152676273 | Common:2; Rare:71; Clinvar (benign):7 | ||||
chr7:155644349-155644718 | Common:2; Rare:128 | ||||
chr7:156640535-156640780 | Common:3; Rare:117 | ||||
chr7:157336776-157337083 | Common:2; Rare:148; Clinvar:2 | ||||
chr7:158856423-158856676 | Common:6; Rare:92 | ||||
chr8:232174-232409 | Common:3; Rare:93 | ||||
chr8:6406527-6406670 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
chr8:6562995-6563471 | Common:4; Rare:111 | ||||
chr8:6708189-6708221 | Rare:9 |