Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150067578-150067912 | Common:1; Rare:97 | ||||
chr1:150268403-150268463 | Rare:10 | ||||
chr1:150272422-150272827 | Common:1; Rare:76 | ||||
chr1:150282180-150282206 | Rare:6 | ||||
chr1:150282291-150282602 | Common:3; Rare:65 | ||||
chr1:150293753-150293920 | Common:1; Rare:57 | ||||
chr1:150321406-150321599 | Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363928-150364206 | Common:4; Rare:98 | ||||
chr1:150364559-150364730 | Common:1; Rare:56 | ||||
chr1:150487247-150487459 | Common:3; Rare:55; Clinvar (benign):3 | ||||
chr1:150578243-150578748 | Common:2; Rare:152 | ||||
chr1:150579588-150579861 | Common:10; Rare:88 | ||||
chr1:150629107-150629398 | Common:1; Rare:88 | ||||
chr1:150629421-150629856 | Common:1; Rare:104 | ||||
chr1:150808227-150808369 | Rare:36; Clinvar:2 |