Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:206159389-206159992 | Common:3; Rare:182 | ||||
chr2:206765324-206765615 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
chr2:207165928-207166088 | Rare:29 | ||||
chr2:207529747-207530025 | Common:3; Rare:91 | ||||
chr2:208254408-208254457 | Rare:10 | ||||
chr2:208255048-208255238 | Common:2; Rare:51 | ||||
chr2:210002473-210002664 | Common:5; Rare:65 | ||||
chr2:210303505-210303861 | Common:3; Rare:71 | ||||
chr2:210314898-210315317 | Common:7; Rare:117 | ||||
chr2:215311867-215312112 | Common:6; Rare:94 | ||||
chr2:215436023-215436254 | Common:2; Rare:73 | ||||
chr2:216498740-216498886 | Common:5; Rare:60 | ||||
chr2:216694603-216694656 | Rare:12 | ||||
chr2:217434197-217434341 | Rare:30 | ||||
chr2:218217058-218217247 | Common:1; Rare:67 |