Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:226870520-226870641 | Common:1; Rare:39; Clinvar (benign):1 | ||||
chr1:226940026-226940313 | Rare:96; Clinvar:2 | ||||
chr1:227735208-227735487 | Common:4; Rare:163 | ||||
chr1:228103317-228103517 | Common:1; Rare:61 | ||||
chr1:228457866-228458147 | Common:1; Rare:107 | ||||
chr1:229271036-229271293 | Rare:87 | ||||
chr1:229508295-229508443 | Common:1; Rare:58 | ||||
chr1:229625970-229626205 | Rare:66 | ||||
chr1:231241107-231241253 | Rare:81; Clinvar:2 | ||||
chr1:231528485-231528698 | Common:2; Rare:68 | ||||
chr1:232950488-232950658 | Common:3; Rare:58 | ||||
chr1:233613885-233614141 | Common:2; Rare:64 | ||||
chr1:234373353-234373458 | Rare:49; Clinvar (benign):1 | ||||
chr1:234608072-234608197 | Common:1; Rare:37 | ||||
chr1:235866893-235867142 | Common:2; Rare:73 |