Variant report

Variant	rs12331789
Chromosome Location	chr4:63118468-63118469
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10003627	0.85[ASN][1000 genomes]
rs10004423	0.85[ASN][1000 genomes]
rs10008785	0.85[ASN][1000 genomes]
rs10009880	0.85[ASN][1000 genomes]
rs10010463	0.85[ASN][1000 genomes]
rs10012480	0.85[ASN][1000 genomes]
rs10015753	0.85[ASN][1000 genomes]
rs10015844	0.85[ASN][1000 genomes]
rs10015846	0.85[ASN][1000 genomes]
rs10021905	0.85[ASN][1000 genomes]
rs10024048	0.85[ASN][1000 genomes]
rs10026975	0.85[ASN][1000 genomes]
rs10027076	0.85[ASN][1000 genomes]
rs10027411	0.85[ASN][1000 genomes]
rs10027512	0.81[ASN][1000 genomes]
rs10033483	0.85[ASN][1000 genomes]
rs10471114	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs11725609	0.85[ASN][1000 genomes]
rs11726657	0.85[ASN][1000 genomes]
rs11727529	0.85[ASN][1000 genomes]
rs11730751	0.81[ASN][1000 genomes]
rs11940467	0.85[ASN][1000 genomes]
rs11941836	0.85[ASN][1000 genomes]
rs12715709	0.85[ASN][1000 genomes]
rs13123213	0.85[ASN][1000 genomes]
rs13128988	0.85[ASN][1000 genomes]
rs13132164	0.85[ASN][1000 genomes]
rs13140495	0.85[ASN][1000 genomes]
rs13435302	0.85[ASN][1000 genomes]
rs13435561	0.85[ASN][1000 genomes]
rs1459805	0.85[ASN][1000 genomes]
rs17239317	0.85[ASN][1000 genomes]
rs1903219	0.81[ASN][1000 genomes]
rs28393241	0.81[ASN][1000 genomes]
rs28415606	0.85[ASN][1000 genomes]
rs28514681	0.85[ASN][1000 genomes]
rs28564897	0.81[ASN][1000 genomes]
rs28589406	0.85[ASN][1000 genomes]
rs28601846	0.85[ASN][1000 genomes]
rs28602232	0.85[ASN][1000 genomes]
rs28607232	0.90[ASN][1000 genomes]
rs28616274	0.85[ASN][1000 genomes]
rs28668804	0.85[ASN][1000 genomes]
rs28685676	0.85[ASN][1000 genomes]
rs28688720	0.81[ASN][1000 genomes]
rs28721915	0.85[ASN][1000 genomes]
rs28733452	0.85[ASN][1000 genomes]
rs28759106	0.81[ASN][1000 genomes]
rs3811796	0.81[ASN][1000 genomes]
rs4492031	0.85[ASN][1000 genomes]
rs6551687	0.85[ASN][1000 genomes]
rs6551688	0.85[ASN][1000 genomes]
rs6551689	0.85[ASN][1000 genomes]
rs6827087	0.85[ASN][1000 genomes]
rs7658468	0.95[ASN][1000 genomes]
rs7659035	0.85[ASN][1000 genomes]
rs7663425	0.95[ASN][1000 genomes]
rs7665803	0.85[ASN][1000 genomes]
rs7665993	0.85[ASN][1000 genomes]
rs7669709	0.81[ASN][1000 genomes]
rs7676692	0.85[ASN][1000 genomes]
rs7679574	0.85[ASN][1000 genomes]
rs7694238	0.85[ASN][1000 genomes]
rs7695334	0.85[ASN][1000 genomes]
rs7695525	0.81[ASN][1000 genomes]
rs7700012	0.85[ASN][1000 genomes]
rs9312088	0.85[ASN][1000 genomes]
rs9992673	0.85[ASN][1000 genomes]
rs9993083	0.85[ASN][1000 genomes]
rs9993407	0.95[ASN][1000 genomes]
rs9993704	0.85[ASN][1000 genomes]
rs9994116	0.85[ASN][1000 genomes]
rs9996086	0.85[ASN][1000 genomes]
rs9996259	0.85[ASN][1000 genomes]
rs9999000	0.85[ASN][1000 genomes]
rs9999659	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013327	chr4:62989426-63149048	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1012093	chr4:63014592-63568580	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537113	chr4:63014592-63568580	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv534618	chr4:63025655-63568620	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv997505	chr4:63025663-63575696	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv594333	chr4:63025823-63467034	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv461378	chr4:63037324-63158560	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
8	nsv594334	chr4:63037324-63158560	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
9	nsv1013850	chr4:63049885-63568580	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv537114	chr4:63049885-63568580	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv594335	chr4:63054757-63183246	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
12	nsv879079	chr4:63059672-63184850	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
13	nsv594336	chr4:63075414-63183246	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:63118400-63118600	Enhancers	HUES6 Cell Line	embryonic stem cell

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