Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:226870501-226870637 | Common:1; Rare:45; Clinvar (benign):1 | ||||
chr1:226939985-226940345 | Rare:122; Clinvar:3 | ||||
chr1:227735208-227735498 | Common:5; Rare:168 | ||||
chr1:228082487-228082788 | Common:3; Rare:119 | ||||
chr1:228103282-228103442 | Common:1; Rare:59 | ||||
chr1:228109201-228109509 | Rare:97 | ||||
chr1:228139870-228140389 | Common:4; Rare:160 | ||||
chr1:228457848-228458113 | Common:1; Rare:93 | ||||
chr1:228735262-228735480 | Common:1; Rare:63 | ||||
chr1:229271003-229271315 | Rare:101 | ||||
chr1:229508263-229508481 | Common:1; Rare:89 | ||||
chr1:229625962-229626261 | Rare:97 | ||||
chr1:230978753-230979108 | Common:2; Rare:137 | ||||
chr1:231241101-231241269 | Rare:93; Clinvar:3 | ||||
chr1:231337823-231338056 | Common:2; Rare:84 |