Variant report

Variant	rs2137866
Chromosome Location	chr4:128409302-128409303
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11098924	0.83[ASN][1000 genomes]
rs11937218	0.91[ASN][1000 genomes]
rs12499018	0.91[ASN][1000 genomes]
rs12500373	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12502458	0.92[ASN][1000 genomes]
rs12505420	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12505574	0.91[ASN][1000 genomes]
rs12506112	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12506317	0.91[ASN][1000 genomes]
rs12508021	0.92[ASN][1000 genomes]
rs12513002	0.91[ASN][1000 genomes]
rs12513073	0.91[ASN][1000 genomes]
rs12513077	0.91[ASN][1000 genomes]
rs12641215	0.82[ASN][1000 genomes]
rs13136353	0.83[ASN][1000 genomes]
rs13147738	0.82[ASN][1000 genomes]
rs1355927	0.80[ASN][1000 genomes]
rs1373026	0.90[EUR][1000 genomes]
rs1443165	0.90[EUR][1000 genomes]
rs1443167	0.90[EUR][1000 genomes]
rs1514304	0.81[ASN][1000 genomes]
rs1514306	0.82[ASN][1000 genomes]
rs1514307	0.82[ASN][1000 genomes]
rs1514308	0.83[ASN][1000 genomes]
rs1514309	0.83[ASN][1000 genomes]
rs17012484	0.92[ASN][1000 genomes]
rs17012500	0.91[ASN][1000 genomes]
rs17012503	0.89[ASN][1000 genomes]
rs1913463	0.80[ASN][1000 genomes]
rs2002543	0.85[ASN][1000 genomes]
rs2090103	0.85[ASN][1000 genomes]
rs56077955	0.91[ASN][1000 genomes]
rs57872398	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58348395	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59695248	0.92[ASN][1000 genomes]
rs61143634	0.91[ASN][1000 genomes]
rs6817525	0.83[ASN][1000 genomes]
rs6851269	0.81[ASN][1000 genomes]
rs72621856	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72621859	0.91[ASN][1000 genomes]
rs72621860	0.91[ASN][1000 genomes]
rs72621861	0.91[ASN][1000 genomes]
rs72621862	0.91[ASN][1000 genomes]
rs72621863	0.80[ASN][1000 genomes]
rs7435603	0.92[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	nsv879915	chr4:128167093-129150590	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv1029214	chr4:128292215-128683123	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv537247	chr4:128292215-128683123	Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv817326	chr4:128292216-128915201	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers 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	nsv1015564	chr4:128394657-128506962	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1017325	chr4:128408370-128509276	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128407400-128410600	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr4:128407600-128409400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr4:128407600-128409400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr4:128407600-128409600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:128407600-128409600	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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