Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:191846486-191846542 | Common:1; Rare:28 | ||||
chr2:197488447-197488551 | Common:2; Rare:21; Clinvar:1; Clinvar (benign):1 | ||||
chr2:198491023-198491151 | Common:2; Rare:22 | ||||
chr2:198494739-198494752 | |||||
chr2:198501825-198502108 | Common:2; Rare:58 | ||||
chr2:198541023-198541212 | Rare:32 | ||||
chr2:198541741-198541774 | Rare:7 | ||||
chr2:198564540-198564717 | Rare:44 | ||||
chr2:198697281-198697511 | Common:2; Rare:39 | ||||
chr2:198769167-198769442 | Rare:48 | ||||
chr2:199408972-199409073 | Rare:15 | ||||
chr2:199456892-199457036 | Common:2; Rare:28 | ||||
chr2:199459665-199459792 | Rare:44 | ||||
chr2:199460661-199460910 | Rare:41 | ||||
chr2:199462157-199462322 | Rare:28 |