Variant report

Variant	rs7832847
Chromosome Location	chr8:4803828-4803829
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10448110	0.84[ASN][1000 genomes]
rs11136810	1.00[CHB][hapmap]
rs11783540	0.96[CEU][hapmap];0.84[CHB][hapmap];0.90[YRI][hapmap]
rs11783663	0.84[CHB][hapmap];0.90[YRI][hapmap]
rs11986686	0.84[CHB][hapmap];0.90[YRI][hapmap]
rs11996410	0.84[CHB][hapmap];0.90[YRI][hapmap]
rs11997499	0.82[CHB][hapmap];0.89[YRI][hapmap]
rs11997657	0.84[CHB][hapmap];0.90[YRI][hapmap]
rs11998341	0.84[CHB][hapmap];0.90[YRI][hapmap]
rs11998370	0.90[YRI][hapmap]
rs12056859	0.84[CHB][hapmap];0.88[YRI][hapmap]
rs12541538	0.85[CEU][hapmap];0.90[YRI][hapmap]
rs12681508	0.84[CHB][hapmap];0.95[YRI][hapmap]
rs13248460	0.85[CEU][hapmap]
rs4360312	0.96[CEU][hapmap];0.84[CHB][hapmap];0.90[YRI][hapmap]
rs4427198	0.96[CEU][hapmap];0.84[CHB][hapmap];0.90[YRI][hapmap]
rs4584160	0.96[CEU][hapmap];0.84[CHB][hapmap];0.90[YRI][hapmap]
rs4620305	0.96[CEU][hapmap];0.84[CHB][hapmap];0.85[YRI][hapmap]
rs4875416	0.84[CHB][hapmap];0.88[JPT][hapmap];0.90[YRI][hapmap]
rs4875418	0.84[CHB][hapmap]
rs6988034	1.00[CEU][hapmap];0.84[CHB][hapmap];0.90[YRI][hapmap]
rs7004552	0.86[CEU][hapmap];0.89[EUR][1000 genomes]
rs7013186	1.00[CEU][hapmap];0.84[CHB][hapmap]

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	nsv609876	chr8:4494811-5092970	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1029480	chr8:4497596-5081032	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv498130	chr8:4532988-5176376	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv889976	chr8:4750266-4824335	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1028542	chr8:4758159-4824005	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1031026	chr8:4771072-5054326	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv889977	chr8:4802438-4820177	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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