Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173868534-173868820 | Common:2; Rare:90 | ||||
chr1:174022319-174022501 | Rare:45 | ||||
chr1:174159164-174159657 | Common:6; Rare:168 | ||||
chr1:174964620-174964838 | Rare:37 | ||||
chr1:174999344-174999436 | Rare:27 | ||||
chr1:174999621-175000141 | Common:2; Rare:164 | ||||
chr1:176207224-176207345 | Common:1; Rare:62 | ||||
chr1:178093561-178093807 | Common:5; Rare:81 | ||||
chr1:178341353-178341477 | Common:1; Rare:23 | ||||
chr1:178724946-178725354 | Common:12; Rare:134 | ||||
chr1:178869219-178869279 | Common:1; Rare:10 | ||||
chr1:178871016-178871176 | Rare:28 | ||||
chr1:179081793-179082114 | Common:4; Rare:84 | ||||
chr1:179882205-179882361 | Rare:31 | ||||
chr1:179882502-179882884 | Rare:190; Clinvar:9; Clinvar (benign):2 |