Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160262208-160262288 | Rare:23 | ||||
chr1:160343151-160343405 | Rare:97 | ||||
chr1:161021074-161021201 | Common:5; Rare:48 | ||||
chr1:161045887-161046050 | Common:1; Rare:44 | ||||
chr1:161098348-161098395 | Rare:8 | ||||
chr1:161117982-161118141 | Rare:83 | ||||
chr1:161132410-161132872 | Common:2; Rare:139 | ||||
chr1:161159466-161159520 | Rare:16 | ||||
chr1:161166268-161166489 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161199049-161199298 | Rare:40 | ||||
chr1:161225768-161226076 | Common:10; Rare:44 | ||||
chr1:161314359-161314417 | Common:2; Rare:26; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161367858-161367890 | Rare:8 | ||||
chr1:161549789-161549885 | Rare:33 | ||||
chr1:161766232-161766363 | Common:3; Rare:43 |