Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70257682-70257731 | Common:1; Rare:7 | ||||
chr2:70258022-70258215 | Common:2; Rare:69 | ||||
chr2:70293405-70293504 | Rare:36 | ||||
chr2:70293645-70293912 | Common:3; Rare:87 | ||||
chr2:70301956-70302183 | Common:4; Rare:111 | ||||
chr2:70994742-70995002 | Common:4; Rare:85 | ||||
chr2:71068519-71068711 | Rare:90 | ||||
chr2:71130215-71130671 | Common:6; Rare:128; Clinvar:1; Clinvar (benign):2 | ||||
chr2:71226966-71227422 | Common:2; Rare:110 | ||||
chr2:72825854-72826108 | Rare:83 | ||||
chr2:73214134-73214362 | Common:1; Rare:85 | ||||
chr2:73214481-73214554 | Rare:29 | ||||
chr2:73233174-73233468 | Common:2; Rare:83 | ||||
chr2:73234170-73234361 | Common:2; Rare:56 | ||||
chr2:73284309-73284424 | Common:1; Rare:29 |