Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:67159885-67160028 | Rare:23 | ||||
chr16:67170444-67170555 | Common:1; Rare:17 | ||||
chr16:67183559-67183754 | Rare:50 | ||||
chr16:67227008-67227191 | Rare:78 | ||||
chr16:67481028-67481380 | Common:1; Rare:122 | ||||
chr16:67528734-67528897 | Rare:40 | ||||
chr16:67660207-67660366 | Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67660746-67661030 | Common:2; Rare:99 | ||||
chr16:67666728-67666880 | Rare:34 | ||||
chr16:67719264-67719440 | Rare:46 | ||||
chr16:67806511-67806878 | Rare:82 | ||||
chr16:67828478-67828791 | Rare:106 | ||||
chr16:67935662-67935906 | Common:1; Rare:71 | ||||
chr16:67968571-67968863 | Common:2; Rare:97 | ||||
chr16:67999017-67999046 | Rare:10 |