Variant report

Variant	rs4535756
Chromosome Location	chr8:4788361-4788362
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11985845	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11989036	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs11998370	0.80[CEU][hapmap]
rs12334427	0.91[CEU][hapmap]
rs12334744	0.91[CEU][hapmap]
rs12334748	0.91[CEU][hapmap]
rs12334931	0.91[CEU][hapmap]
rs13249466	0.85[CEU][hapmap]
rs13250150	0.82[EUR][1000 genomes]
rs13250626	0.89[CEU][hapmap]
rs13259602	0.91[CEU][hapmap]
rs13269117	0.91[CEU][hapmap]
rs13280124	0.86[CEU][hapmap]
rs4875129	0.91[CEU][hapmap]
rs5001120	0.91[CEU][hapmap]
rs5001124	0.91[CEU][hapmap]
rs5001125	0.90[CEU][hapmap]
rs5001126	0.85[CEU][hapmap]
rs57424708	0.89[EUR][1000 genomes]
rs6981938	0.90[CEU][hapmap]
rs6990414	0.91[CEU][hapmap]
rs6990769	0.91[CEU][hapmap]
rs7011210	0.89[CEU][hapmap]
rs7825060	0.91[CEU][hapmap]
rs7829151	0.91[CEU][hapmap]
rs7840682	0.91[CEU][hapmap]
rs7841154	0.83[CEU][hapmap]
rs7841741	0.91[CEU][hapmap]
rs7842153	0.90[CEU][hapmap]
rs9657371	0.87[CEU][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	nsv1020907	chr8:4693024-4801941	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv889976	chr8:4750266-4824335	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1028542	chr8:4758159-4824005	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	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

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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