Variant report

Variant	rs2577331
Chromosome Location	chr3:53776146-53776147
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1020820	0.92[CEU][hapmap]
rs1020821	0.92[CEU][hapmap]
rs1809282	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs2015263	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2016271	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs2169143	0.92[CEU][hapmap]
rs2169144	0.92[CEU][hapmap]
rs2577325	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs2577327	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2577328	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs2577329	0.97[EUR][1000 genomes]
rs2612023	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs2612024	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs2612025	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs2612026	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs2612029	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2612030	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2612033	0.91[CEU][hapmap]
rs2612034	0.92[CEU][hapmap]
rs2633725	0.91[CEU][hapmap]
rs2633727	0.91[CEU][hapmap]
rs2680649	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs2680651	0.90[EUR][1000 genomes]
rs2680652	0.91[CEU][hapmap]
rs2680664	0.92[CEU][hapmap];0.80[AMR][1000 genomes]
rs2680669	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs2680670	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs3774554	0.85[CEU][hapmap]
rs7373113	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs7373253	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs755886	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs7649275	0.91[CEU][hapmap]
rs877257	0.92[CEU][hapmap];0.96[EUR][1000 genomes]
rs898419	1.00[CEU][hapmap];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003621	chr3:53448934-54425322	Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1001128	chr3:53659570-53927842	Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1013783	chr3:53694418-53934781	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv1002452	chr3:53742148-53802811	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv520027	chr3:53762713-53784625	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53742600-53778000	Weak transcription	Pancreas	Pancrea
2	chr3:53761600-53781800	Weak transcription	Spleen	Spleen
3	chr3:53764200-53779800	Weak transcription	Liver	Liver
4	chr3:53764800-53783400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr3:53765000-53779800	Weak transcription	Brain Anterior Caudate	brain
6	chr3:53765000-53779800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr3:53765000-53788600	Weak transcription	Fetal Kidney	kidney
8	chr3:53765200-53783400	Weak transcription	Brain Angular Gyrus	brain
9	chr3:53765400-53781600	Weak transcription	Brain Hippocampus Middle	brain
10	chr3:53766600-53781200	Weak transcription	Lung	lung
11	chr3:53768600-53801000	Strong transcription	Fetal Lung	lung
12	chr3:53769600-53787400	Weak transcription	Duodenum Mucosa	Duodenum
13	chr3:53770200-53779800	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr3:53773000-53807600	Strong transcription	Fetal Intestine Large	intestine
15	chr3:53774200-53776800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr3:53774200-53789200	Weak transcription	Fetal Brain Male	brain
17	chr3:53774400-53782000	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr3:53774600-53785000	Weak transcription	Brain Cingulate Gyrus	brain
19	chr3:53774800-53776400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr3:53774800-53807200	Strong transcription	Fetal Intestine Small	intestine
21	chr3:53775800-53779400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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