Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44775847-44776140 | Common:2; Rare:108 | ||||
chr1:45339984-45340041 | Rare:17 | ||||
chr1:45340090-45340178 | Rare:31 | ||||
chr1:45340386-45340457 | Common:1; Rare:16; Clinvar:1 | ||||
chr1:45500056-45500356 | Common:1; Rare:74; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521679-45521742 | Rare:19 | ||||
chr1:45521827-45522077 | Common:1; Rare:99 | ||||
chr1:45550741-45551086 | Common:3; Rare:83 | ||||
chr1:45583931-45584164 | Rare:93 | ||||
chr1:45687050-45687351 | Common:1; Rare:79 | ||||
chr1:45688055-45688272 | Common:1; Rare:60 | ||||
chr1:45750599-45750800 | Rare:73 | ||||
chr1:46133037-46133195 | Common:1; Rare:41 | ||||
chr1:46198384-46198525 | Common:1; Rare:56; Clinvar:1 | ||||
chr1:46203239-46203374 | Rare:30 |