Variant report

Variant	rs2076515
Chromosome Location	chr6:38914039-38914040
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:38909328..38913522-chr6:38913862..38917283,4	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10305428	1.00[AMR][1000 genomes]
rs10484848	0.81[JPT][hapmap]
rs10484849	0.81[JPT][hapmap]
rs10947769	0.81[JPT][hapmap]
rs10947775	0.81[JPT][hapmap]
rs12196393	0.81[JPT][hapmap]
rs12202648	0.81[JPT][hapmap]
rs12202878	0.81[JPT][hapmap]
rs12212950	0.81[JPT][hapmap]
rs1332016	0.81[JPT][hapmap]
rs16891346	0.88[CHB][hapmap];0.86[JPT][hapmap];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs16891368	0.82[CHB][hapmap];0.86[JPT][hapmap];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs16891395	1.00[AMR][1000 genomes]
rs16891420	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs16891425	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs16891428	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs16891431	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs16891435	0.82[CHB][hapmap];0.86[JPT][hapmap];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs16891439	1.00[AMR][1000 genomes]
rs2281339	0.82[CHB][hapmap];0.86[JPT][hapmap];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2281341	0.83[ASN][1000 genomes]
rs2281343	0.82[CHB][hapmap];0.86[JPT][hapmap];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2281344	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs58473344	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs60464866	1.00[AMR][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	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1028088	chr6:38821047-39163549	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv538205	chr6:38821047-39163549	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv885821	chr6:38843970-39039503	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv602962	chr6:38907202-38940282	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	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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