Variant report

Variant	rs61583057
Chromosome Location	chr1:179545769-179545770
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179543200-179546400	Bivalent/Poised TSS	Fetal Kidney	kidney
2	chr1:179544800-179545800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr1:179545200-179546000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
4	chr1:179545400-179545800	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
5	chr1:179545400-179545800	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
6	chr1:179545400-179545800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
7	chr1:179545400-179546000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:179545600-179545800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
9	chr1:179545600-179545800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
10	chr1:179545600-179545800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
11	chr1:179545600-179545800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:179545600-179545800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:179545600-179546000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr1:179545600-179546000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
15	chr1:179545600-179546000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:179545600-179546000	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr1:179545600-179546000	Bivalent Enhancer	Small Intestine	intestine

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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