Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:164841763-164841933 | Common:1; Rare:48 | ||||
chr2:164955484-164955654 | Rare:40 | ||||
chr2:166375877-166376117 | Common:4; Rare:70; Clinvar:1; Clinvar (benign):5 | ||||
chr2:168456129-168456432 | Rare:105 | ||||
chr2:169584600-169584630 | Rare:6 | ||||
chr2:169584764-169584816 | Rare:17 | ||||
chr2:169694354-169694615 | Common:5; Rare:90 | ||||
chr2:170928907-170929334 | Common:5; Rare:127 | ||||
chr2:171160346-171160646 | Common:1; Rare:98 | ||||
chr2:171433973-171434239 | Common:2; Rare:67 | ||||
chr2:171434546-171434670 | Rare:40; Clinvar:1 | ||||
chr2:171434746-171434824 | Rare:18 | ||||
chr2:171922283-171922490 | Rare:78 | ||||
chr2:171999831-171999985 | Common:1; Rare:63 | ||||
chr2:172427044-172427432 | Common:5; Rare:67 |