Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:163735987-163736029 | Rare:6 | ||||
chr2:164841168-164841561 | Rare:113 | ||||
chr2:164841805-164841951 | Common:1; Rare:42 | ||||
chr2:164955484-164955650 | Rare:39 | ||||
chr2:165953748-165954089 | Common:3; Rare:114; Clinvar:6; Clinvar (benign):1 | ||||
chr2:166493988-166494286 | Common:1; Rare:47 | ||||
chr2:166494304-166494380 | Rare:15 | ||||
chr2:168456136-168456437 | Rare:106 | ||||
chr2:169584564-169584630 | Rare:13 | ||||
chr2:169584744-169584819 | Rare:19 | ||||
chr2:169694340-169694597 | Common:5; Rare:87 | ||||
chr2:170928981-170929335 | Common:4; Rare:114 | ||||
chr2:171160293-171160646 | Common:1; Rare:120 | ||||
chr2:171433941-171434248 | Common:3; Rare:79 | ||||
chr2:171434593-171434671 | Rare:24 |