Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:208255019-208255234 | Common:2; Rare:56 | ||||
chr2:208266121-208266302 | Common:6; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210225094-210225178 | Rare:22 | ||||
chr2:210225259-210225415 | Rare:36 | ||||
chr2:210225417-210225516 | Rare:15 | ||||
chr2:210477568-210477684 | Rare:36 | ||||
chr2:213284146-213284493 | Rare:106 | ||||
chr2:215409635-215409988 | Rare:92 | ||||
chr2:215435656-215436254 | Common:4; Rare:162 | ||||
chr2:216081737-216081925 | Common:1; Rare:66 | ||||
chr2:216498721-216498876 | Common:6; Rare:61 | ||||
chr2:216694437-216694506 | Rare:12 | ||||
chr2:216694511-216694858 | Rare:89 | ||||
chr2:216695359-216695736 | Rare:72 | ||||
chr2:217903792-217903813 | Rare:2 |