Variant report

Variant	rs575475735
Chromosome Location	chr6:11902698-11902699
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2574880	chr6:11902568-11904153	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11901400-11903000	ZNF genes & repeats	K562	blood
2	chr6:11901800-11903200	Enhancers	Primary T cells from cord blood	blood
3	chr6:11902000-11902800	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr6:11902000-11903200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr6:11902200-11903000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr6:11902400-11903000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr6:11902600-11903000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr6:11902600-11903000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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