Variant report

Variant	rs6731332
Chromosome Location	chr2:127991170-127991171
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1011019	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10496661	0.90[EUR][1000 genomes]
rs10850	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11680877	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11680949	0.87[AMR][1000 genomes]
rs11691916	0.87[AMR][1000 genomes]
rs11692990	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12105051	0.80[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs1504135	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2404534	0.81[EUR][1000 genomes]
rs2896979	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3958415	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4150402	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4150404	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4150421	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4150471	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4150474	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4150476	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4150499	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4662713	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4662716	0.81[EUR][1000 genomes]
rs4662718	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4662719	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4662720	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59378658	0.85[AMR][1000 genomes]
rs61422716	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62157508	0.89[EUR][1000 genomes]
rs6430933	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6430936	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6733478	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6738690	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6744237	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6757492	0.87[EUR][1000 genomes]
rs72845975	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72845976	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72845991	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72845993	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72845997	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72846002	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72848604	0.87[AMR][1000 genomes]
rs72848615	0.80[AMR][1000 genomes]
rs7556675	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7556756	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7562428	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006112	chr2:127830117-128032546	Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv2757832	chr2:127830943-128006514	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	esv2759090	chr2:127830943-128006514	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1011378	chr2:127841930-128020546	Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv999809	chr2:127841930-128032546	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv1010669	chr2:127848860-128032546	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv1003599	chr2:127871183-128059407	Strong transcription Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	nsv535920	chr2:127871183-128059407	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs6731332	ERCC3	cis	Nerve Tibial	GTEx
rs6731332	ERCC3	cis	Adipose Subcutaneous	GTEx
rs6731332	ERCC3	cis	Thyroid	GTEx
rs6731332	ERCC3	cis	Esophagus Muscularis	GTEx

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127984600-128012800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:127989400-128013000	Weak transcription	Pancreas	Pancrea

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