Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:24992702-24992827 | Common:3; Rare:56 | ||||
chr20:25195561-25195769 | Common:2; Rare:78 | ||||
chr20:25696782-25697091 | Common:3; Rare:87 | ||||
chr20:31547305-31547438 | Rare:34 | ||||
chr20:31845560-31845710 | Rare:30 | ||||
chr20:32207694-32207944 | Common:3; Rare:99 | ||||
chr20:33401507-33401590 | Rare:22 | ||||
chr20:33731987-33732010 | Rare:13 | ||||
chr20:34516333-34516443 | Rare:40 | ||||
chr20:35542307-35542552 | Rare:81 | ||||
chr20:35664815-35665012 | Common:1; Rare:52 | ||||
chr20:35699295-35699460 | Rare:57; Clinvar (benign):3 | ||||
chr20:35740823-35741088 | Common:3; Rare:80 | ||||
chr20:35742170-35742630 | Common:5; Rare:143 | ||||
chr20:35771796-35772044 | Common:2; Rare:77 |