Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:148951858-148952172 | Common:5; Rare:76 | ||||
chr1:148952264-148952406 | Common:2; Rare:48 | ||||
chr1:149390431-149390630 | Rare:23 | ||||
chr1:149886563-149887268 | Common:3; Rare:263 | ||||
chr1:149887494-149887660 | Rare:92 | ||||
chr1:149887894-149888215 | Rare:99 | ||||
chr1:149927755-149927872 | Rare:51; Clinvar (benign):4 | ||||
chr1:149936839-149936951 | Rare:23 | ||||
chr1:150067614-150067844 | Common:1; Rare:63 | ||||
chr1:150268362-150268463 | Rare:20 | ||||
chr1:150282140-150282611 | Common:3; Rare:106 | ||||
chr1:150321421-150321599 | Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150364584-150364724 | Rare:47 | ||||
chr1:150487247-150487445 | Common:3; Rare:46; Clinvar (benign):3 | ||||
chr1:150549150-150549417 | Rare:68 |