Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:20651054-20651234 | Rare:51 | ||||
chr2:20823064-20823176 | Rare:41 | ||||
chr2:23927057-23927339 | Common:3; Rare:98 | ||||
chr2:24076238-24076523 | Rare:82 | ||||
chr2:24123252-24123526 | Common:1; Rare:73 | ||||
chr2:24360394-24360658 | Common:3; Rare:91 | ||||
chr2:24971597-24971836 | Common:2; Rare:83 | ||||
chr2:24971900-24972145 | Common:1; Rare:80 | ||||
chr2:25878289-25878498 | Rare:50 | ||||
chr2:26033792-26034250 | Common:3; Rare:162 | ||||
chr2:26195177-26195295 | Rare:50; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr2:26244564-26244971 | Common:2; Rare:150; Clinvar:6; Clinvar (benign):9 | ||||
chr2:26345831-26346189 | Common:1; Rare:104 | ||||
chr2:26764188-26764337 | Common:1; Rare:61 | ||||
chr2:27032867-27033004 | Rare:51 |