Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161021113-161021314 | Common:1; Rare:54 | ||||
chr1:161045856-161046057 | Common:1; Rare:52 | ||||
chr1:161117952-161118177 | Rare:113 | ||||
chr1:161118230-161118358 | Rare:32 | ||||
chr1:161132417-161132683 | Common:1; Rare:91 | ||||
chr1:161159366-161159520 | Common:2; Rare:41 | ||||
chr1:161209241-161209929 | Common:2; Rare:174; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:161314264-161314403 | Common:3; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
chr1:161749577-161749835 | Common:1; Rare:85 | ||||
chr1:161750254-161750306 | Rare:13 | ||||
chr1:162561509-162561759 | Common:2; Rare:101 | ||||
chr1:163321688-163322148 | Common:1; Rare:123 | ||||
chr1:163322169-163322209 | Rare:8 | ||||
chr1:164558873-164559215 | Common:1; Rare:91 | ||||
chr1:164559288-164559470 | Rare:49 |