Variant report

Variant	rs7837520
Chromosome Location	chr8:10300132-10300133
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10090800	0.85[EUR][1000 genomes]
rs10095788	0.80[ASN][1000 genomes]
rs10106098	0.82[ASN][1000 genomes]
rs10903327	0.95[CHD][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs11250010	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11250011	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11250012	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11250013	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11774291	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11774920	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11781243	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11782465	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11783249	0.88[CEU][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12546721	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12546910	0.82[CHD][hapmap]
rs13257718	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13266986	0.89[CEU][hapmap];0.92[CHB][hapmap];0.95[JPT][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1986358	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34675714	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34975042	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35073964	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35335292	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35479789	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4410951	0.92[ASN][1000 genomes]
rs4471098	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4840484	0.82[EUR][1000 genomes]
rs4841337	0.82[JPT][hapmap]
rs4841342	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs57759396	0.84[EUR][1000 genomes]
rs61510468	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6601462	0.87[ASN][1000 genomes]
rs6601466	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67173113	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6980700	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6989757	0.93[CHB][hapmap];0.97[CHD][hapmap];0.81[JPT][hapmap];0.96[ASN][1000 genomes]
rs6995374	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7007383	0.80[EUR][1000 genomes]
rs7464508	0.82[ASN][1000 genomes]
rs9792321	0.82[ASN][1000 genomes]
rs9792329	0.82[ASN][1000 genomes]
rs9792356	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030934	chr8:10065169-10561161	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv890347	chr8:10153082-10331636	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv527326	chr8:10199548-10320019	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1025557	chr8:10216726-10555187	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv610267	chr8:10268736-10526742	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	nsv890349	chr8:10294330-10355302	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs7837520	PRSS55	cis	cerebellum	SCAN
rs7837520	C8orf79	cis	cerebellum	SCAN
rs7837520	PPP1R3B	cis	cerebellum	SCAN
rs7837520	TNKS	cis	cerebellum	SCAN
rs7837520	BLK	Cis_chr	lymphoblastoid	RTeQTL
rs7837520	FLJ10661	cis	cerebellum	SCAN

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10285800-10305200	Weak transcription	Lung	lung
2	chr8:10291400-10301200	Weak transcription	Pancreas	Pancrea
3	chr8:10292200-10321400	Weak transcription	Fetal Brain Male	brain
4	chr8:10294000-10302400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr8:10294000-10304000	Weak transcription	Fetal Brain Female	brain
6	chr8:10294200-10302800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr8:10294200-10306600	Weak transcription	Liver	Liver
8	chr8:10294400-10301400	Weak transcription	Left Ventricle	heart
9	chr8:10294400-10303200	Weak transcription	Primary T cells from cord blood	blood
10	chr8:10294400-10304800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr8:10295200-10301200	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr8:10300000-10303200	Weak transcription	Aorta	Aorta

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