Variant report

Variant	rs7017451
Chromosome Location	chr8:4811774-4811775
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:4805755..4808307-chr8:4809361..4811905,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10110206	0.90[CHB][hapmap]
rs10448110	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11136809	0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11136810	0.89[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs11783540	0.90[CHB][hapmap]
rs11783663	0.90[CHB][hapmap]
rs11986686	0.91[CHB][hapmap]
rs11996410	0.90[CHB][hapmap]
rs11997499	0.90[CHB][hapmap]
rs11997657	0.91[CHB][hapmap]
rs11998341	0.90[CHB][hapmap]
rs11998370	0.89[CHB][hapmap]
rs12056859	0.91[CHB][hapmap]
rs12675859	0.87[ASN][1000 genomes]
rs12676776	0.87[ASN][1000 genomes]
rs12681508	0.91[CHB][hapmap]
rs12682272	0.80[ASN][1000 genomes]
rs13282812	0.80[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs34021868	0.88[ASN][1000 genomes]
rs4360312	0.90[CHB][hapmap]
rs4427198	0.90[CHB][hapmap]
rs4584160	0.90[CHB][hapmap]
rs4620305	0.90[CHB][hapmap]
rs4875416	0.90[CHB][hapmap]
rs4875418	0.90[CHB][hapmap]
rs6988034	0.90[CHB][hapmap]
rs7013186	0.90[CHB][hapmap]
rs7840102	0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.84[ASN][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	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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4811200-4813000	Enhancers	Adipose Nuclei	Adipose
2	chr8:4811400-4811800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr8:4811600-4811800	Flanking Active TSS	Liver	Liver

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