Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:231712455-231712911 | Common:5; Rare:141 | ||||
chr2:233868351-233868424 | Common:1; Rare:34 | ||||
chr2:240762775-240763046 | Rare:48; Clinvar (benign):2 | ||||
chr20:3784861-3785083 | Common:1; Rare:73 | ||||
chr20:6054756-6054914 | Common:2; Rare:26 | ||||
chr20:10419700-10419909 | Rare:29 | ||||
chr20:18793966-18794086 | Rare:39 | ||||
chr20:19757959-19758282 | Common:4; Rare:114 | ||||
chr20:23349964-23350184 | Common:5; Rare:55 | ||||
chr20:25751087-25751215 | Rare:28 | ||||
chr20:32475274-32475611 | Common:1; Rare:78 | ||||
chr20:35263146-35263434 | Common:2; Rare:44 | ||||
chr20:35320502-35320607 | Common:1; Rare:9 | ||||
chr20:36050322-36050729 | Common:2; Rare:142 | ||||
chr20:36050897-36051156 | Common:3; Rare:91 |