Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228083061-228083164 | Not yet | Rare:34 | 131 | ||
chr1:228103317-228103477 | Not yet | Common:1; Rare:52 | 169 | ||
chr1:228139856-228140083 | Not yet | Common:1; Rare:56 | 239 | ||
chr1:228146593-228146918 | Not yet | Common:3; Rare:68 | 337 | ||
chr1:228457865-228458113 | Not yet | Common:1; Rare:78 | 272 | ||
chr1:229271027-229271307 | Not yet | Rare:93 | 187 | ||
chr1:229508222-229508489 | Not yet | Common:1; Rare:106 | 290 | ||
chr1:229625962-229626261 | Not yet | Rare:97 | 256 | ||
chr1:231241063-231241362 | Not yet | Common:2; Rare:146; Clinvar:4; Clinvar (benign):2 | 232 | ||
chr1:231337813-231338056 | Not yet | Common:2; Rare:88 | 235 | ||
chr1:231528515-231528738 | Not yet | Common:2; Rare:79 | 240 | ||
chr1:234373347-234373792 | Not yet | Common:1; Rare:200; Clinvar (benign):7 | 383 | ||
chr1:234608023-234608283 | Not yet | Common:1; Rare:85 | 375 | ||
chr1:235866874-235867174 | Not yet | Common:3; Rare:96 | 241 | ||
chr1:236065072-236065335 | Not yet | Common:2; Rare:104; Clinvar (pathogenic):1 | 258 |