Variant report

Variant	rs11986432
Chromosome Location	chr8:5069324-5069325
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11774126	1.00[ASN][1000 genomes]
rs11774842	1.00[ASN][1000 genomes]
rs11781233	1.00[ASN][1000 genomes]
rs11782170	1.00[ASN][1000 genomes]
rs11782556	1.00[ASN][1000 genomes]
rs11785693	1.00[ASN][1000 genomes]
rs11986801	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11995108	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11995153	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11997836	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11997861	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11998551	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12542814	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12543184	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12549617	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62491168	1.00[ASN][1000 genomes]
rs62491191	1.00[ASN][1000 genomes]
rs62491199	1.00[ASN][1000 genomes]
rs62491200	1.00[ASN][1000 genomes]
rs7002179	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7011584	1.00[ASN][1000 genomes]
rs73183606	1.00[ASN][1000 genomes]
rs73183633	1.00[ASN][1000 genomes]
rs73188811	1.00[ASN][1000 genomes]
rs7815024	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7838806	1.00[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	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	nsv889978	chr8:4853197-5460166	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1028846	chr8:4907673-5128665	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv889980	chr8:4940320-5112194	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv831217	chr8:5007449-5210093	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1016696	chr8:5040671-5089101	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
9	nsv1019369	chr8:5057818-5102396	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
10	nsv1028841	chr8:5065445-5094981	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
11	nsv539407	chr8:5065445-5094981	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
12	esv3384268	chr8:5067394-5071292	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv2761177	chr8:5069057-5076672	Weak transcription Enhancers Active TSS	n/a	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	chr8:5065000-5070000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:5066200-5070000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr8:5069200-5069600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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