Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:35664862-35665000 | Common:1; Rare:40 | ||||
chr20:35699292-35699460 | Rare:58; Clinvar (benign):3 | ||||
chr20:35742146-35742649 | Common:5; Rare:157 | ||||
chr20:36236403-36236493 | Common:1; Rare:19 | ||||
chr20:36746051-36746299 | Common:2; Rare:89 | ||||
chr20:36773733-36773965 | Common:3; Rare:79 | ||||
chr20:37178865-37179165 | Rare:86 | ||||
chr20:37289601-37289669 | Common:1; Rare:20 | ||||
chr20:37527830-37528196 | Common:5; Rare:132 | ||||
chr20:38033410-38033818 | Common:2; Rare:123 | ||||
chr20:38472653-38472863 | Common:1; Rare:70 | ||||
chr20:38962158-38962383 | Common:1; Rare:94 | ||||
chr20:41028534-41028887 | Rare:127 | ||||
chr20:41340569-41340842 | Rare:71 | ||||
chr20:43457805-43457907 | Rare:45 |