Variant report

Variant	rs6815196
Chromosome Location	chr4:128417035-128417036
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10025576	0.82[EUR][1000 genomes]
rs11098924	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11098926	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11737101	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12500373	0.85[ASN][1000 genomes]
rs12505420	0.83[ASN][1000 genomes]
rs12506112	0.83[ASN][1000 genomes]
rs12641215	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12644377	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs13136353	0.98[ASN][1000 genomes]
rs13145532	0.83[EUR][1000 genomes]
rs13147738	0.97[ASN][1000 genomes]
rs1355924	0.84[EUR][1000 genomes]
rs1399215	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1514300	0.82[EUR][1000 genomes]
rs1514301	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1514303	0.91[ASN][1000 genomes]
rs1514304	0.96[ASN][1000 genomes]
rs1514306	0.97[ASN][1000 genomes]
rs1514307	0.97[ASN][1000 genomes]
rs1514308	0.98[ASN][1000 genomes]
rs1514309	0.98[ASN][1000 genomes]
rs1913463	0.95[ASN][1000 genomes]
rs2002543	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2007243	0.85[JPT][hapmap]
rs2090103	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2137866	0.85[ASN][1000 genomes]
rs2203374	0.84[EUR][1000 genomes]
rs4833378	0.86[EUR][1000 genomes]
rs58348395	0.85[ASN][1000 genomes]
rs6817525	0.98[ASN][1000 genomes]
rs6817788	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6851269	0.95[ASN][1000 genomes]
rs72621856	0.85[ASN][1000 genomes]
rs7653949	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs908009	0.85[CEU][hapmap];0.86[EUR][1000 genomes]
rs972329	0.91[EUR][1000 genomes]
rs979051	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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
7	nsv595387	chr4:128410916-128523964	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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