Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:167967051-167967249 | Rare:27 | ||||
chr2:168138408-168138735 | Common:2; Rare:61 | ||||
chr2:170770796-170771108 | Common:2; Rare:55 | ||||
chr2:172484918-172485136 | Rare:41 | ||||
chr2:172995579-172995703 | Common:1; Rare:16 | ||||
chr2:174024174-174024411 | Common:1; Rare:45 | ||||
chr2:176637536-176637749 | Common:2; Rare:71 | ||||
chr2:177117470-177117724 | Common:2; Rare:43 | ||||
chr2:178413899-178414004 | Common:1; Rare:32 | ||||
chr2:181123939-181123957 | Rare:5 | ||||
chr2:187383282-187383482 | Rare:40 | ||||
chr2:188996176-188996456 | Common:12; Rare:64; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:190970600-190970916 | Common:1; Rare:45 | ||||
chr2:191846503-191846542 | Common:1; Rare:16 | ||||
chr2:191846543-191846631 | Common:1; Rare:30 |