Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:207167223-207167371 | Common:2; Rare:36 | ||||
chr2:207529808-207530126 | Common:1; Rare:85 | ||||
chr2:207624569-207624763 | Rare:51 | ||||
chr2:207625167-207625539 | Common:1; Rare:105 | ||||
chr2:208254375-208254490 | Rare:31 | ||||
chr2:208255032-208255234 | Common:2; Rare:52 | ||||
chr2:208266111-208266344 | Common:6; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210002462-210002677 | Common:5; Rare:74 | ||||
chr2:213284210-213284499 | Rare:94 | ||||
chr2:215311993-215312144 | Common:7; Rare:67 | ||||
chr2:215375195-215375720 | Common:2; Rare:142 | ||||
chr2:215435637-215436180 | Common:3; Rare:140 | ||||
chr2:216081756-216081911 | Common:1; Rare:54 | ||||
chr2:216498721-216498894 | Common:7; Rare:72 | ||||
chr2:216694438-216694506 | Rare:12 |