Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149812343-149812579 | Rare:75 | ||||
chr1:149886519-149887058 | Common:3; Rare:205 | ||||
chr1:149887732-149888243 | Rare:175 | ||||
chr1:149888346-149888502 | Rare:39 | ||||
chr1:149899522-149899675 | Rare:37 | ||||
chr1:149917785-149917961 | Common:2; Rare:46 | ||||
chr1:149927736-149928018 | Common:2; Rare:103; Clinvar:1; Clinvar (benign):6 | ||||
chr1:149928227-149928411 | Common:1; Rare:36 | ||||
chr1:149936320-149936460 | Rare:32 | ||||
chr1:150010617-150010915 | Common:2; Rare:80 | ||||
chr1:150066940-150067430 | Common:5; Rare:93 | ||||
chr1:150067512-150067847 | Common:1; Rare:81 | ||||
chr1:150148918-150149013 | Rare:16 | ||||
chr1:150149026-150149074 | Rare:8 | ||||
chr1:150149440-150149542 | Rare:14 |