Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:222654268-222654475 | Common:1; Rare:49 | ||||
chr1:222814968-222815122 | Common:3; Rare:57 | ||||
chr1:223992554-223992830 | Common:4; Rare:99 | ||||
chr1:224219365-224219719 | Common:4; Rare:65 | ||||
chr1:225856661-225856956 | Common:7; Rare:87 | ||||
chr1:226115771-226115833 | Common:1; Rare:22 | ||||
chr1:226133249-226133417 | Common:2; Rare:25 | ||||
chr1:226152343-226152906 | Common:1; Rare:135 | ||||
chr1:228084287-228084323 | Rare:11 | ||||
chr1:228142269-228142364 | Rare:23 | ||||
chr1:229624954-229625149 | Rare:35 | ||||
chr1:231421059-231421399 | Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
chr1:233615138-233615343 | Common:2; Rare:39 | ||||
chr1:234357157-234357209 | Common:1; Rare:13 | ||||
chr1:234600132-234600297 | Common:5; Rare:76 |