Variant report

Variant	rs2339352
Chromosome Location	chr15:34327821-34327822
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:34325247..34329253-chr15:34329844..34332256,3	MCF-7	breast:
2	chr15:34299066..34301596-chr15:34326883..34329699,2	MCF-7	breast:
3	chr15:34314027..34315859-chr15:34326232..34328519,2	MCF-7	breast:
4	chr15:34327076..34328752-chr15:34329743..34331266,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000169857	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11072868	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11635479	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11638109	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12898898	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12903907	0.95[CEU][hapmap];0.85[YRI][hapmap];0.97[EUR][1000 genomes]
rs12913747	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2684940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34474029	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34773983	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35531038	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35804445	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4477671	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4779652	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4779656	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4780203	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs532720	0.85[CEU][hapmap]
rs536345	1.00[CEU][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs602302	1.00[CEU][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs618868	0.88[EUR][1000 genomes]
rs62014670	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62014671	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs632591	1.00[CEU][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6495442	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6495443	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66530874	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67739072	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71462883	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71464844	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7162140	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7168640	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7169003	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7173183	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7175823	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7178075	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7178446	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72718678	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72718682	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8030094	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8033781	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
rs2339352	AVEN	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34309400-34330000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr15:34309600-34330000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr15:34316600-34329400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr15:34320200-34329800	Weak transcription	Hela-S3	cervix
5	chr15:34323000-34328000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr15:34323000-34330000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr15:34324800-34329800	Weak transcription	Brain Angular Gyrus	brain
8	chr15:34325200-34329400	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr15:34326400-34328000	Enhancers	Fetal Lung	lung
10	chr15:34326600-34330200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr15:34327000-34328200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr15:34327000-34328200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr15:34327000-34328200	Enhancers	Fetal Stomach	stomach
14	chr15:34327000-34330000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr15:34327200-34329800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr15:34327200-34330000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr15:34327400-34330000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr15:34327400-34330000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr15:34327400-34330000	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr15:34327600-34329800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr15:34327600-34330000	Weak transcription	Fetal Heart	heart
22	chr15:34327600-34330000	Weak transcription	Fetal Kidney	kidney
23	chr15:34327800-34328200	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr15:34327800-34328200	Weak transcription	NHDF-Ad	bronchial
25	chr15:34327800-34329400	Weak transcription	GM12878-XiMat	blood
26	chr15:34327800-34330000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr15:34327800-34330000	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr15:34327800-34330000	Weak transcription	Colon Smooth Muscle	Colon
29	chr15:34327800-34330000	Weak transcription	Fetal Brain Male	brain

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