Variant report

Variant	rs6551637
Chromosome Location	chr4:62502358-62502359
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10001410	0.82[JPT][hapmap];0.82[YRI][hapmap]
rs10434219	0.82[JPT][hapmap]
rs11131329	0.96[CEU][hapmap]
rs11131334	0.89[CEU][hapmap]
rs11939481	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12504607	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.84[MKK][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13123468	1.00[CEU][hapmap];0.92[JPT][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13123888	0.92[CEU][hapmap]
rs1391321	0.92[CEU][hapmap]
rs1497896	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1497901	0.89[CEU][hapmap]
rs1497906	0.89[CEU][hapmap]
rs1497907	0.92[CEU][hapmap]
rs1497909	0.96[CEU][hapmap];0.92[JPT][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1497916	0.89[CEU][hapmap]
rs1497921	1.00[CEU][hapmap];0.89[GIH][hapmap];0.92[JPT][hapmap];0.84[MKK][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17239080	0.89[CEU][hapmap]
rs1909077	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34538250	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4484334	0.81[JPT][hapmap]
rs4585337	0.82[JPT][hapmap]
rs6551634	0.89[CEU][hapmap]
rs6551640	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6551645	0.82[JPT][hapmap]
rs6817476	0.96[CEU][hapmap]
rs6825200	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6835374	0.89[CEU][hapmap]
rs6840548	0.83[JPT][hapmap]
rs6843311	0.96[CEU][hapmap]
rs6851424	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.84[MKK][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7656051	1.00[CEU][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7669283	0.96[CEU][hapmap]
rs7670950	0.82[JPT][hapmap]
rs7678046	0.82[JPT][hapmap]
rs9312082	0.82[JPT][hapmap]
rs958862	0.92[CEU][hapmap]
rs9997427	0.82[JPT][hapmap]
rs9998713	0.82[JPT][hapmap]

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	nsv461377	chr4:62368762-62883431	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv594328	chr4:62368762-62883431	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1004815	chr4:62398737-62553769	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv537110	chr4:62398737-62553769	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv879077	chr4:62419426-62545435	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv594331	chr4:62498946-62502358	Enhancers	n/a	n/a	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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