Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:208266116-208266286 | Common:6; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210002439-210002643 | Common:3; Rare:71 | ||||
chr2:210477548-210477690 | Rare:41 | ||||
chr2:216081757-216081916 | Common:1; Rare:56 | ||||
chr2:216498685-216498875 | Common:6; Rare:73 | ||||
chr2:216633811-216633957 | Rare:33 | ||||
chr2:216694581-216694683 | Rare:27 | ||||
chr2:218270107-218270378 | Common:5; Rare:81 | ||||
chr2:218568767-218568861 | Rare:18 | ||||
chr2:218659338-218659756 | Common:4; Rare:101 | ||||
chr2:218671943-218672339 | Common:2; Rare:109 | ||||
chr2:219177804-219177929 | Common:6; Rare:25 | ||||
chr2:219178162-219178284 | Common:6; Rare:81 | ||||
chr2:219229549-219229829 | Common:1; Rare:79 | ||||
chr2:219245420-219245535 | Common:1; Rare:34 |