Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9555712-9555992 | Common:2; Rare:95 | ||||
chr2:9843250-9843539 | Common:6; Rare:86 | ||||
chr2:10689917-10689997 | Common:2; Rare:26 | ||||
chr2:11746449-11746648 | Common:1; Rare:58; Clinvar:2 | ||||
chr2:17753721-17754174 | Common:4; Rare:143; Clinvar (benign):1 | ||||
chr2:19901937-19902049 | Common:1; Rare:38 | ||||
chr2:19990079-19990211 | Rare:34 | ||||
chr2:20051529-20051870 | Common:1; Rare:93 | ||||
chr2:20446887-20447074 | Common:2; Rare:62 | ||||
chr2:20823056-20823186 | Common:1; Rare:47 | ||||
chr2:23940366-23940514 | Common:3; Rare:52 | ||||
chr2:24049620-24049741 | Rare:33 | ||||
chr2:24076205-24076574 | Rare:100 | ||||
chr2:24123272-24123501 | Common:1; Rare:60 | ||||
chr2:25878435-25878772 | Common:4; Rare:99 |