Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:226939933-226940357 | Rare:150; Clinvar:3 | ||||
chr1:227318291-227318350 | Common:2; Rare:31 | ||||
chr1:227318359-227318789 | Common:2; Rare:147 | ||||
chr1:227735241-227735498 | Common:4; Rare:151 | ||||
chr1:228082498-228082803 | Common:3; Rare:117 | ||||
chr1:228103209-228103494 | Common:1; Rare:109 | ||||
chr1:228107802-228108114 | Common:4; Rare:101 | ||||
chr1:228109223-228109485 | Rare:88 | ||||
chr1:228139876-228140381 | Common:4; Rare:155 | ||||
chr1:228165870-228166147 | Common:2; Rare:143; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):5 | ||||
chr1:228457786-228458130 | Common:2; Rare:152 | ||||
chr1:229270983-229271363 | Rare:121 | ||||
chr1:229342527-229342690 | Rare:56 | ||||
chr1:229508017-229508113 | Rare:41 | ||||
chr1:229508184-229508513 | Common:1; Rare:131 |