Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20656163-20656247 | Rare:22 | ||||
chr1:21857176-21857324 | Common:1; Rare:39; Clinvar:2 | ||||
chr1:21884818-21885149 | Common:1; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
chr1:22025450-22025535 | Common:4; Rare:33 | ||||
chr1:23088981-23089339 | Common:4; Rare:83 | ||||
chr1:23217498-23217599 | Rare:25 | ||||
chr1:24127641-24127915 | Common:3; Rare:35 | ||||
chr1:24321904-24321976 | Common:1; Rare:11 | ||||
chr1:25890436-25890636 | Common:1; Rare:47 | ||||
chr1:26188657-26188836 | Common:2; Rare:55 | ||||
chr1:26225369-26225599 | Common:1; Rare:42 | ||||
chr1:26539214-26539268 | Rare:10 | ||||
chr1:26569600-26569673 | Rare:12 | ||||
chr1:28581849-28582027 | Common:1; Rare:58 | ||||
chr1:28648330-28648618 | Common:4; Rare:99 |