Variant report

Variant	rs28672970
Chromosome Location	chr7:21892321-21892322
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018133	chr7:21740118-22055283	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv830922	chr7:21793386-21964675	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:21890200-21893000	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr7:21890200-21893000	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr7:21890400-21892600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr7:21890400-21892600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr7:21890600-21892400	Enhancers	Fetal Thymus	thymus
6	chr7:21891000-21892400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr7:21891000-21892400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
8	chr7:21891000-21892600	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr7:21891000-21893000	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr7:21891600-21892800	Enhancers	Primary T cells fromperipheralblood	blood
11	chr7:21891600-21893000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr7:21891800-21893000	Enhancers	Primary T cells from cord blood	blood
13	chr7:21892000-21892400	Weak transcription	HUVEC	blood vessel

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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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