Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160030885-160031106 | Rare:70; Clinvar (benign):1 | ||||
chr1:160124665-160124733 | Common:1; Rare:9 | ||||
chr1:160124923-160125159 | Common:1; Rare:43; Clinvar (benign):1 | ||||
chr1:160149338-160149449 | Common:1; Rare:19 | ||||
chr1:160149848-160149969 | Rare:18 | ||||
chr1:160206078-160206281 | Rare:42 | ||||
chr1:160206488-160206626 | Rare:21 | ||||
chr1:160261089-160261222 | Rare:29 | ||||
chr1:160726293-160726351 | Rare:13 | ||||
chr1:160726623-160726721 | Common:2; Rare:13 | ||||
chr1:160767766-160767971 | Common:5; Rare:37 | ||||
chr1:160768032-160768121 | Common:1; Rare:8 | ||||
chr1:160768427-160768470 | Rare:10 | ||||
chr1:160826563-160826723 | Rare:25 | ||||
chr1:160827514-160827796 | Common:4; Rare:59 |