Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151327520-151327818 | Common:2; Rare:56 | ||||
chr1:151346763-151347091 | Rare:85 | ||||
chr1:151347167-151347487 | Rare:77 | ||||
chr1:151399488-151399808 | Common:4; Rare:102; Clinvar (pathogenic):2 | ||||
chr1:151408100-151408403 | Common:1; Rare:63; Clinvar (benign):1 | ||||
chr1:151441765-151442089 | Common:2; Rare:66 | ||||
chr1:151459135-151459270 | Common:1; Rare:42 | ||||
chr1:151459287-151459626 | Common:2; Rare:119 | ||||
chr1:151611895-151612276 | Common:4; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
chr1:151763465-151763565 | Common:1; Rare:33 | ||||
chr1:151763631-151763717 | Rare:25 | ||||
chr1:151790394-151790863 | Common:3; Rare:112 | ||||
chr1:151851374-151851446 | Rare:11 | ||||
chr1:151909370-151909705 | Common:4; Rare:122 | ||||
chr1:151909832-151910031 | Common:2; Rare:48 |