Variant report

Variant	rs6802658
Chromosome Location	chr3:118630798-118630799
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs11927719	0.89[ASW][hapmap];0.89[CEU][hapmap];0.81[LWK][hapmap];0.85[MKK][hapmap];0.96[TSI][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12487299	0.83[EUR][1000 genomes]
rs12489856	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1474231	0.83[CHB][hapmap];0.89[YRI][hapmap];0.86[AFR][1000 genomes]
rs1521293	0.86[AFR][1000 genomes]
rs1581374	0.81[AFR][1000 genomes]
rs16829163	0.89[CEU][hapmap];0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1879552	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2110368	0.89[CEU][hapmap];0.96[TSI][hapmap];0.91[EUR][1000 genomes]
rs2110369	1.00[ASW][hapmap];1.00[CEU][hapmap];0.89[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.95[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2160052	1.00[CEU][hapmap];0.89[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2215811	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2866317	1.00[CEU][hapmap];0.89[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs36052974	0.91[EUR][1000 genomes]
rs4687958	0.84[AFR][1000 genomes]
rs58464946	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs66601488	0.82[AFR][1000 genomes]
rs6765168	0.89[TSI][hapmap];0.82[EUR][1000 genomes]
rs6782002	0.89[CHB][hapmap];0.88[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.96[MEX][hapmap];0.89[MKK][hapmap];0.90[TSI][hapmap];0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6795936	0.89[CEU][hapmap];0.96[TSI][hapmap];0.88[EUR][1000 genomes]
rs73183699	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73185803	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7610212	0.88[CEU][hapmap];0.92[YRI][hapmap];0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs9821861	0.82[AFR][1000 genomes]
rs9848979	1.00[CEU][hapmap];0.84[CHB][hapmap];0.88[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9854506	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3487859	chr3:118570588-119419623	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv3487860	chr3:118570588-119419623	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6802658	IGSF11	cis	parietal	SCAN

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118619800-118651400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr3:118620200-118663200	Weak transcription	Pancreas	Pancrea
3	chr3:118622000-118644600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:118624000-118631200	Weak transcription	Brain Anterior Caudate	brain
5	chr3:118625400-118631200	Weak transcription	Ovary	ovary
6	chr3:118625400-118639800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr3:118627600-118632400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr3:118627800-118632600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr3:118627800-118632600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr3:118627800-118642200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr3:118629400-118631000	Weak transcription	Brain Hippocampus Middle	brain
12	chr3:118629600-118631400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr3:118630000-118630800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:118630000-118641600	Weak transcription	Brain Angular Gyrus	brain
15	chr3:118630200-118630800	Enhancers	Brain Substantia Nigra	brain
16	chr3:118630600-118631200	Enhancers	K562	blood
17	chr3:118630600-118631800	Enhancers	Brain Cingulate Gyrus	brain

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