Variant report

Variant	rs2065334
Chromosome Location	chr21:47258045-47258046
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:47257190..47260005-chr21:47265923..47268414,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000183570	Chromatin interaction

Extended variants
information (count: 99 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs1014446	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs10854472	0.96[ASN][1000 genomes]
rs11089024	0.84[CHB][hapmap];0.85[JPT][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12481867	0.80[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12481913	0.80[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12481970	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12481977	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12482010	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12482094	0.80[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12482377	0.87[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12482750	0.80[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap]
rs12482853	0.80[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1467758	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs17351419	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17351433	0.80[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2183595	1.00[JPT][hapmap]
rs2183596	1.00[JPT][hapmap]
rs2838973	1.00[JPT][hapmap]
rs2838974	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs2838976	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs2838982	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs2838989	1.00[JPT][hapmap]
rs2838991	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs2838992	1.00[JPT][hapmap]
rs2838993	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs2838994	1.00[JPT][hapmap]
rs2839003	0.83[ASN][1000 genomes]
rs2839004	0.80[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2839005	0.80[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2839009	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2839013	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2839014	0.80[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2839026	0.81[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2839029	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2839032	0.80[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs3367	1.00[JPT][hapmap]
rs3788208	0.81[JPT][hapmap];0.93[ASN][1000 genomes]
rs3788209	0.96[ASN][1000 genomes]
rs3788211	0.87[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3788215	0.94[ASN][1000 genomes]
rs3788216	0.80[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3788220	0.87[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3788224	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs3788227	0.80[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3920695	1.00[JPT][hapmap]
rs4434082	1.00[JPT][hapmap]
rs4818801	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs4818802	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4818803	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4818805	0.93[ASN][1000 genomes]
rs4819154	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4819155	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4819156	0.81[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4819157	0.80[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs55780126	0.83[ASN][1000 genomes]
rs55856400	0.96[ASN][1000 genomes]
rs55875620	0.83[ASN][1000 genomes]
rs55912352	0.96[ASN][1000 genomes]
rs55927540	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57688476	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61063225	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61276251	0.91[ASN][1000 genomes]
rs62211883	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62211885	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62211886	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62211895	0.96[ASN][1000 genomes]
rs62211925	0.96[ASN][1000 genomes]
rs62211926	0.96[ASN][1000 genomes]
rs62214604	0.83[ASN][1000 genomes]
rs62214608	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66523344	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67055992	0.96[ASN][1000 genomes]
rs67878041	0.96[ASN][1000 genomes]
rs7280173	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8127369	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs8127428	0.80[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs882668	0.90[ASN][1000 genomes]
rs882669	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs914241	1.00[JPT][hapmap]
rs9306139	1.00[JPT][hapmap]
rs9637208	0.80[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs964975	0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs9977908	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs9978740	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs9983770	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531546	chr21:46504151-47411772	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
2	nsv1058665	chr21:46719445-47634282	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	91 gene(s)	inside rSNPs	diseases
3	nsv544486	chr21:46719445-47634282	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	91 gene(s)	inside rSNPs	diseases
4	nsv1059230	chr21:46956877-47907990	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	n/a
5	nsv544491	chr21:46956877-47907990	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	n/a
6	nsv1058472	chr21:47027823-47797326	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	n/a
7	nsv544492	chr21:47027823-47797326	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	n/a
8	nsv428043	chr21:47179244-47471971	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	n/a
9	nsv1065959	chr21:47188878-48091343	Bivalent Enhancer Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	n/a
10	nsv914078	chr21:47218744-47311686	Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
11	nsv531580	chr21:47221774-48090317	Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	n/a
12	esv2756755	chr21:47243032-47319768	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
13	esv2758821	chr21:47243032-47319768	Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
14	nsv914079	chr21:47243074-47650362	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2065334	PCBP3	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47217800-47260400	Weak transcription	Right Atrium	heart
2	chr21:47251000-47258800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr21:47253200-47258600	Weak transcription	NHEK	skin
4	chr21:47253400-47259000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr21:47253800-47258200	Weak transcription	HSMM	muscle
6	chr21:47254000-47258200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr21:47254200-47259200	Weak transcription	HMEC	breast
8	chr21:47255200-47259800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr21:47256200-47258200	Enhancers	NHDF-Ad	bronchial
10	chr21:47256400-47259200	Weak transcription	HSMMtube	muscle
11	chr21:47256600-47259200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr21:47256600-47260600	Weak transcription	Fetal Brain Male	brain
13	chr21:47257000-47258200	Enhancers	Brain Cingulate Gyrus	brain
14	chr21:47257200-47258200	Enhancers	Brain Angular Gyrus	brain
15	chr21:47257200-47258200	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr21:47257200-47258200	Enhancers	Brain Substantia Nigra	brain
17	chr21:47257200-47259800	Enhancers	NH-A	brain
18	chr21:47257200-47260800	Weak transcription	Fetal Kidney	kidney
19	chr21:47257400-47259400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr21:47257400-47260400	Weak transcription	Primary T cells from cord blood	blood
21	chr21:47257600-47258200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr21:47257800-47258800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr21:47257800-47259000	Weak transcription	Fetal Thymus	thymus
24	chr21:47257800-47259600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr21:47257800-47259600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr21:47257800-47260400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr21:47257800-47260600	Weak transcription	Thymus	Thymus
28	chr21:47258000-47259200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr21:47258000-47259800	Enhancers	Muscle Satellite Cultured Cells	--

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