Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9843411-9843533 | Common:3; Rare:33 | ||||
chr2:11746403-11746672 | Common:2; Rare:77; Clinvar:4 | ||||
chr2:12716753-12717056 | Common:1; Rare:87 | ||||
chr2:17753759-17753858 | Common:1; Rare:42 | ||||
chr2:19990079-19990211 | Rare:34 | ||||
chr2:20446860-20447074 | Common:3; Rare:80 | ||||
chr2:20823055-20823176 | Rare:47 | ||||
chr2:23927065-23927326 | Common:3; Rare:91 | ||||
chr2:23940379-23940514 | Common:3; Rare:49 | ||||
chr2:24076225-24076493 | Rare:82 | ||||
chr2:24123255-24123489 | Common:1; Rare:59 | ||||
chr2:26033778-26034167 | Common:3; Rare:142 | ||||
chr2:26244592-26244966 | Common:2; Rare:135; Clinvar:5; Clinvar (benign):8 | ||||
chr2:26345819-26346156 | Common:1; Rare:100 | ||||
chr2:27032872-27033004 | Rare:51 |