Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:155644357-155644719 | Common:2; Rare:126 | ||||
chr7:156640554-156640685 | Common:2; Rare:68 | ||||
chr7:157336790-157337085 | Common:2; Rare:137; Clinvar:2 | ||||
chr8:232180-232403 | Common:3; Rare:83 | ||||
chr8:6406527-6406670 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
chr8:9151537-9151814 | Common:2; Rare:99 | ||||
chr8:10839819-10839996 | Rare:72 | ||||
chr8:11802450-11802799 | Common:6; Rare:188 | ||||
chr8:13514834-13515018 | Rare:45 | ||||
chr8:17246795-17247053 | Common:2; Rare:108 | ||||
chr8:17801202-17801344 | Common:4; Rare:59 | ||||
chr8:17922613-17922923 | Common:4; Rare:114 | ||||
chr8:19817381-19817491 | Common:3; Rare:49 | ||||
chr8:22245026-22245436 | Common:2; Rare:144 | ||||
chr8:23457613-23457782 | Common:3; Rare:62 |