Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42958858-42959046 | Common:1; Rare:50; Clinvar:4; Clinvar (benign):2 | ||||
chr1:43368013-43368212 | Rare:55 | ||||
chr1:45688055-45688202 | Common:1; Rare:34 | ||||
chr1:46303609-46303730 | Common:1; Rare:33 | ||||
chr1:52056119-52056334 | Common:1; Rare:62 | ||||
chr1:53946306-53946385 | Rare:32 | ||||
chr1:54053398-54053670 | Common:5; Rare:88 | ||||
chr1:54200020-54200184 | Rare:32 | ||||
chr1:63593643-63593687 | Rare:23; Clinvar (pathogenic):1 | ||||
chr1:70205549-70205726 | Rare:53 | ||||
chr1:74733009-74733169 | Common:4; Rare:46 | ||||
chr1:93345806-93345971 | Common:2; Rare:66 | ||||
chr1:101025760-101025857 | Rare:28 | ||||
chr1:101236614-101236920 | Common:2; Rare:53 | ||||
chr1:111140076-111140243 | Common:1; Rare:54 |