Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:120069594-120069920 | Not yet | Common:7; Rare:68 | 190 | ||
chr1:120176350-120176684 | Not yet | Common:1; Rare:61 | 217 | ||
chr1:145823891-145824249 | Not yet | Rare:128 | 177 | ||
chr1:145858996-145859167 | Not yet | Rare:48 | 89 | ||
chr1:145918689-145919013 | Not yet | Common:2; Rare:69 | 231 | ||
chr1:145927394-145927634 | Not yet | Common:1; Rare:63; Clinvar (pathogenic):1 | 198 | ||
chr1:145957974-145958223 | Not yet | Rare:60 | 170 | ||
chr1:145964559-145964742 | Not yet | Rare:47 | 104 | ||
chr1:146228968-146229190 | Not yet | Common:2; Rare:46 | 164 | ||
chr1:147172427-147172786 | Not yet | Common:1; Rare:93 | 163 | ||
chr1:147225303-147225555 | Not yet | Common:3; Rare:49 | 183 | ||
chr1:147242500-147242715 | Not yet | Common:3; Rare:77 | 122 | ||
chr1:148679740-148679929 | Not yet | Rare:17 | 138 | ||
chr1:148844339-148844432 | Not yet | Rare:8 | 108 | ||
chr1:148952273-148952603 | Not yet | Common:5; Rare:99 | 186 |