Variant report

Variant	rs536345
Chromosome Location	chr15:34291991-34291992
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11072868	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11635479	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11638109	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12898898	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12903907	0.95[CEU][hapmap];0.94[EUR][1000 genomes]
rs12913747	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2339352	1.00[CEU][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2684940	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34474029	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34773983	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35531038	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35804445	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4477671	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4779652	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4779656	1.00[CEU][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4780203	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs532720	0.86[CEU][hapmap]
rs602302	1.00[CEU][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs618868	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs632591	1.00[CEU][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6495442	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6495443	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66530874	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67739072	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71462883	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7162140	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7169003	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7173183	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7175823	1.00[CEU][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7178075	1.00[CEU][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7178446	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72718678	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72718682	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8030094	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043046	chr15:33714908-34321330	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv456789	chr15:34034421-34426618	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv568920	chr15:34034421-34426618	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv471235	chr15:34035529-34421951	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv1044844	chr15:34065524-34296829	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv903985	chr15:34279319-34370487	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs536345	AVEN	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34265200-34299600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr15:34265400-34294200	Weak transcription	Fetal Stomach	stomach
3	chr15:34265400-34311800	Weak transcription	Liver	Liver
4	chr15:34274400-34311000	Weak transcription	Primary B cells from cord blood	blood
5	chr15:34275400-34293200	Weak transcription	Primary T cells from cord blood	blood
6	chr15:34277800-34303200	Weak transcription	Gastric	stomach
7	chr15:34278200-34310000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr15:34278400-34299600	Weak transcription	HSMM	muscle
9	chr15:34280800-34296200	Weak transcription	Pancreas	Pancrea
10	chr15:34281000-34306800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr15:34283000-34294600	Weak transcription	Left Ventricle	heart
12	chr15:34283000-34306000	Weak transcription	Ovary	ovary
13	chr15:34284200-34296800	Weak transcription	Brain Angular Gyrus	brain
14	chr15:34289400-34303800	Weak transcription	Psoas Muscle	Psoas
15	chr15:34289800-34293400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr15:34289800-34299200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr15:34290400-34293400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr15:34291200-34292000	Strong transcription	Aorta	Aorta
19	chr15:34291800-34295200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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