Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228083061-228083164 | Rare:34 | ||||
chr1:228103317-228103477 | Common:1; Rare:52 | ||||
chr1:228139856-228140083 | Common:1; Rare:56 | ||||
chr1:228146593-228146918 | Common:3; Rare:68 | ||||
chr1:228457865-228458113 | Common:1; Rare:78 | ||||
chr1:229271027-229271307 | Rare:93 | ||||
chr1:229508222-229508489 | Common:1; Rare:106 | ||||
chr1:229625962-229626261 | Rare:97 | ||||
chr1:231241063-231241362 | Common:2; Rare:146; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337813-231338056 | Common:2; Rare:88 | ||||
chr1:231528515-231528738 | Common:2; Rare:79 | ||||
chr1:234373347-234373792 | Common:1; Rare:200; Clinvar (benign):7 | ||||
chr1:234608023-234608283 | Common:1; Rare:85 | ||||
chr1:235866874-235867174 | Common:3; Rare:96 | ||||
chr1:236065072-236065335 | Common:2; Rare:104; Clinvar (pathogenic):1 |