Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156767735-156767857 | Rare:46 | ||||
chr1:156767931-156768240 | Common:1; Rare:117 | ||||
chr1:156813941-156814226 | Rare:70 | ||||
chr1:157138337-157138444 | Common:1; Rare:26 | ||||
chr1:159780825-159781036 | Common:4; Rare:54 | ||||
chr1:159900132-159900258 | Rare:39 | ||||
chr1:159925452-159925621 | Common:1; Rare:44 | ||||
chr1:159945493-159945769 | Common:2; Rare:72 | ||||
chr1:159945953-159946139 | Rare:45 | ||||
chr1:160031767-160032040 | Common:2; Rare:70 | ||||
chr1:160115551-160115779 | Common:1; Rare:56 | ||||
chr1:160205327-160205459 | Common:1; Rare:46 | ||||
chr1:160262418-160262635 | Common:1; Rare:67 | ||||
chr1:160285091-160285256 | Common:3; Rare:60; Clinvar:2; Clinvar (benign):4 | ||||
chr1:160343181-160343461 | Rare:119 |