Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228109239-228109441 | Rare:65 | ||||
chr1:228457859-228458127 | Common:1; Rare:94 | ||||
chr1:229271013-229271307 | Rare:96 | ||||
chr1:229508275-229508453 | Common:1; Rare:73 | ||||
chr1:229625962-229626277 | Rare:108 | ||||
chr1:230978762-230979138 | Common:2; Rare:146 | ||||
chr1:231241089-231241362 | Common:2; Rare:134; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337901-231338057 | Common:1; Rare:57 | ||||
chr1:231528482-231528758 | Common:2; Rare:91 | ||||
chr1:232950488-232950658 | Common:3; Rare:58 | ||||
chr1:233613885-233614118 | Common:2; Rare:56 | ||||
chr1:234373288-234373609 | Common:1; Rare:143; Clinvar (benign):4 | ||||
chr1:234373613-234373775 | Rare:66; Clinvar (benign):3 | ||||
chr1:234608063-234608351 | Common:1; Rare:92 | ||||
chr1:235128750-235129074 | Common:1; Rare:135 |