Variant report

Variant	rs11871364
Chromosome Location	chr17:45183152-45183153
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11079748	0.84[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11079750	1.00[ASW][hapmap];0.89[CEU][hapmap];0.91[TSI][hapmap];0.89[YRI][hapmap];0.86[EUR][1000 genomes]
rs11079752	0.84[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11649887	0.83[EUR][1000 genomes]
rs11653589	0.92[YRI][hapmap]
rs11654517	0.80[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11658350	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12939753	0.91[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs12942936	0.87[EUR][1000 genomes]
rs12949929	0.84[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs12950276	0.82[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs12950699	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs1476498	0.81[CHB][hapmap]
rs1634265	0.81[CHB][hapmap]
rs1713493	0.81[CHB][hapmap]
rs34038545	0.87[EUR][1000 genomes]
rs34314554	0.86[EUR][1000 genomes]
rs35721448	0.82[EUR][1000 genomes]
rs3851792	0.80[TSI][hapmap]
rs4074247	0.82[EUR][1000 genomes]
rs4074249	0.88[CEU][hapmap];0.97[LWK][hapmap];0.89[MKK][hapmap];0.95[YRI][hapmap];0.87[EUR][1000 genomes]
rs4968253	0.87[EUR][1000 genomes]
rs4968304	0.88[CEU][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs7207418	0.82[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs7214785	0.85[EUR][1000 genomes]
rs7215573	0.91[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs7215903	0.89[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7215907	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7219544	0.87[EUR][1000 genomes]
rs7219899	0.87[EUR][1000 genomes]
rs7220777	0.80[AFR][1000 genomes]
rs7222781	0.86[EUR][1000 genomes]
rs8068715	0.92[YRI][hapmap]
rs8077021	0.87[EUR][1000 genomes]
rs858670	0.81[CHB][hapmap]
rs858677	0.81[CHB][hapmap]

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	nsv833466	chr17:45020360-45204537	Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv1062983	chr17:45030095-45789543	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
3	nsv833467	chr17:45063935-45252624	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv522797	chr17:45084279-45183152	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	esv3332795	chr17:45116212-45209297	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers 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	13 gene(s)	inside rSNPs	diseases
6	esv3386521	chr17:45116232-45209267	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv1059766	chr17:45130765-45203468	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	esv2760450	chr17:45130777-45225222	Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
9	nsv521632	chr17:45151549-45196190	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
10	nsv908563	chr17:45158537-45230311	ZNF genes & repeats Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
11	nsv962456	chr17:45163689-45212872	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs11871364	GOSR2	cis	normal skin	skin_eQTL
rs11871364	STAT5A	cis	cerebellum	SCAN
rs11871364	IFI35	cis	parietal	SCAN
rs11871364	GOSR2	Cis_1M	lymphoblastoid	RTeQTL
rs11871364	CD300LG	cis	cerebellum	SCAN

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45178000-45192600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr17:45182400-45183400	Enhancers	HSMM	muscle
3	chr17:45182400-45183400	Enhancers	HSMMtube	muscle
4	chr17:45182800-45194000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr17:45183000-45183800	Enhancers	K562	blood

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