Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161199051-161199254 | Rare:34 | ||||
chr1:161314262-161314405 | Common:3; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
chr1:161750263-161750368 | Rare:23 | ||||
chr1:161766147-161766382 | Common:3; Rare:74 | ||||
chr1:162497735-162497859 | Common:1; Rare:36 | ||||
chr1:162561346-162561724 | Common:4; Rare:144 | ||||
chr1:163321723-163322057 | Common:1; Rare:91 | ||||
chr1:164772808-164772987 | Rare:19 | ||||
chr1:165768732-165769065 | Common:2; Rare:132 | ||||
chr1:165895410-165895610 | Common:1; Rare:29 | ||||
chr1:166839321-166839522 | Rare:57 | ||||
chr1:167935974-167936266 | Common:1; Rare:88 | ||||
chr1:167936546-167936706 | Rare:53 | ||||
chr1:168225925-168226056 | Common:1; Rare:45 | ||||
chr1:169367727-169368261 | Common:3; Rare:115 |