Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:68843230-68843546 | Rare:54 | ||||
chr16:69132521-69132680 | Rare:62 | ||||
chr16:69311102-69311422 | Rare:94 | ||||
chr16:69339559-69339826 | Common:1; Rare:111; Clinvar (benign):1 | ||||
chr16:69424363-69424698 | Common:2; Rare:91 | ||||
chr16:69726511-69726861 | Common:3; Rare:88 | ||||
chr16:69754849-69755116 | Common:1; Rare:101 | ||||
chr16:69762245-69762381 | Common:1; Rare:38 | ||||
chr16:69951196-69951338 | Rare:14 | ||||
chr16:70114138-70114376 | Common:2; Rare:83 | ||||
chr16:70174029-70174236 | Rare:31 | ||||
chr16:70299151-70299292 | Rare:35 | ||||
chr16:70346783-70346961 | Common:1; Rare:92 | ||||
chr16:70523533-70523893 | Common:3; Rare:116; Clinvar (pathogenic):1 | ||||
chr16:71289325-71289745 | Common:4; Rare:137 |