Variant report

Variant	rs7584134
Chromosome Location	chr2:231421964-231421965
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10210885	0.88[ASN][1000 genomes]
rs11676240	0.85[ASN][1000 genomes]
rs11679027	0.86[ASN][1000 genomes]
rs11680387	0.90[ASN][1000 genomes]
rs11682065	0.85[ASN][1000 genomes]
rs11682119	0.81[ASN][1000 genomes]
rs11682758	0.81[ASN][1000 genomes]
rs11687105	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11688621	0.83[ASN][1000 genomes]
rs11693931	0.83[ASN][1000 genomes]
rs11693933	0.83[ASN][1000 genomes]
rs11695625	0.89[ASN][1000 genomes]
rs11695658	0.84[ASN][1000 genomes]
rs11695659	0.89[ASN][1000 genomes]
rs11695666	0.89[ASN][1000 genomes]
rs17276229	1.00[CHB][hapmap]
rs17276271	0.81[CEU][hapmap];0.95[CHB][hapmap];0.87[CHD][hapmap]
rs17276306	0.82[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2288356	0.81[CHB][hapmap]
rs2396763	0.81[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.80[TSI][hapmap]
rs55955122	0.83[ASN][1000 genomes]
rs56295541	0.80[ASN][1000 genomes]
rs57793329	0.80[ASN][1000 genomes]
rs58209772	0.83[ASN][1000 genomes]
rs58541541	0.85[ASN][1000 genomes]
rs59407020	0.83[ASN][1000 genomes]
rs61329403	0.83[ASN][1000 genomes]
rs61579817	0.83[ASN][1000 genomes]
rs62195481	0.85[ASN][1000 genomes]
rs62195483	0.85[ASN][1000 genomes]
rs62195484	0.85[ASN][1000 genomes]
rs62195486	0.83[ASN][1000 genomes]
rs62195489	0.83[ASN][1000 genomes]
rs62195490	0.83[ASN][1000 genomes]
rs62195511	0.81[ASN][1000 genomes]
rs62195512	0.81[ASN][1000 genomes]
rs6436947	0.83[ASN][1000 genomes]
rs66521108	0.83[ASN][1000 genomes]
rs6717191	0.83[ASN][1000 genomes]
rs6720383	0.83[ASN][1000 genomes]
rs6730737	0.83[ASN][1000 genomes]
rs6746779	0.85[ASN][1000 genomes]
rs6749311	0.83[ASN][1000 genomes]
rs6749431	0.83[ASN][1000 genomes]
rs6750183	0.83[ASN][1000 genomes]
rs6759529	0.83[ASN][1000 genomes]
rs6759540	0.83[ASN][1000 genomes]
rs6761716	0.85[ASN][1000 genomes]
rs7561174	0.83[ASN][1000 genomes]
rs7561418	0.83[ASN][1000 genomes]
rs7575130	0.83[ASN][1000 genomes]
rs7587870	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv18000	chr2:231072978-231467847	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv584673	chr2:231385231-231433237	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv875949	chr2:231407663-231434272	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	lncRNA	n/a	inside rSNPs	diseases
4	nsv875950	chr2:231413681-231434272	Enhancers Weak transcription Active TSS Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
5	nsv528220	chr2:231414688-231433237	Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	inside rSNPs	diseases
6	nsv460120	chr2:231414688-231433237	Enhancers Weak transcription Flanking Active TSS Active TSS	lncRNA	n/a	inside rSNPs	diseases
7	nsv584674	chr2:231414688-231433237	Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	inside rSNPs	diseases
8	nsv875951	chr2:231414688-231434272	Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	inside rSNPs	diseases
9	nsv875952	chr2:231415189-231434272	Enhancers Weak transcription Flanking Active TSS Active TSS	lncRNA	n/a	inside rSNPs	diseases
10	nsv875953	chr2:231415189-231457819	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv875954	chr2:231421531-231441828	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7584134	NEU2	cis	parietal	SCAN
rs7584134	POLR2A	cis	cerebellum	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231401000-231430200	Weak transcription	Pancreas	Pancrea
2	chr2:231410200-231428800	Weak transcription	Primary B cells from cord blood	blood

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