Variant report

Variant	rs56236202
Chromosome Location	chr3:59902988-59902989
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1666058	1.00[EUR][1000 genomes]
rs35342045	1.00[EUR][1000 genomes]
rs55802039	1.00[EUR][1000 genomes]
rs58999901	1.00[EUR][1000 genomes]
rs72884777	1.00[EUR][1000 genomes]
rs73839552	1.00[EUR][1000 genomes]
rs73839553	1.00[EUR][1000 genomes]
rs73839556	1.00[EUR][1000 genomes]
rs73839560	1.00[EUR][1000 genomes]
rs73839561	1.00[EUR][1000 genomes]
rs73839564	1.00[EUR][1000 genomes]
rs73839599	1.00[EUR][1000 genomes]
rs73841803	1.00[EUR][1000 genomes]
rs73841806	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73841807	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7616048	1.00[EUR][1000 genomes]
rs7649319	1.00[EUR][1000 genomes]
rs780343	1.00[EUR][1000 genomes]
rs9855365	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428085	chr3:59782509-60070116	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv460564	chr3:59821071-59927727	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv590384	chr3:59821071-59927727	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv590386	chr3:59846067-59912377	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1002104	chr3:59875996-59907597	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1014983	chr3:59884024-60558331	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv590387	chr3:59890976-60481459	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:59873200-59904200	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr3:59890600-59903600	Weak transcription	Fetal Thymus	thymus
3	chr3:59893000-59915800	Weak transcription	Thymus	Thymus
4	chr3:59894400-59903200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr3:59898200-59903600	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr3:59899600-59915800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr3:59901000-59904000	Weak transcription	Pancreas	Pancrea
8	chr3:59902600-59903800	Genic enhancers	Primary T cells from cord blood	blood
9	chr3:59902600-59904200	Strong transcription	Dnd41	blood
10	chr3:59902600-59907000	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr3:59902600-59908000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr3:59902800-59907400	Enhancers	Primary T helper naive cells from peripheral blood	blood

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

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