Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156591678-156591835 | Common:4; Rare:85 | ||||
chr1:156705569-156705777 | Common:3; Rare:42 | ||||
chr1:156728417-156728460 | Rare:11 | ||||
chr1:156741082-156741417 | Common:1; Rare:84 | ||||
chr1:159924582-159924704 | Rare:30 | ||||
chr1:160343163-160343391 | Rare:91 | ||||
chr1:161021078-161021463 | Common:5; Rare:101 | ||||
chr1:161045888-161046042 | Common:1; Rare:39 | ||||
chr1:161118012-161118137 | Rare:59 | ||||
chr1:161153849-161153995 | Common:1; Rare:40 | ||||
chr1:161199053-161199354 | Rare:47 | ||||
chr1:161314268-161314403 | Common:3; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
chr1:161766125-161766358 | Common:3; Rare:66 | ||||
chr1:162632375-162632488 | Rare:18 | ||||
chr1:163321723-163322007 | Common:1; Rare:76 |