Variant report

Variant	rs12137796
Chromosome Location	chr1:215988310-215988311
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11120645	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs11120650	0.92[EUR][1000 genomes]
rs12117370	0.92[EUR][1000 genomes]
rs12123296	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs12126346	1.00[CEU][hapmap]
rs12126534	0.96[EUR][1000 genomes]
rs12129576	1.00[CEU][hapmap]
rs12130528	1.00[CEU][hapmap]
rs12132110	1.00[CEU][hapmap]
rs12132798	1.00[CEU][hapmap]
rs12133551	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs12135237	0.96[EUR][1000 genomes]
rs12137445	1.00[YRI][hapmap];0.96[EUR][1000 genomes]
rs12138094	0.92[EUR][1000 genomes]
rs12139361	0.92[EUR][1000 genomes]
rs12141208	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12141340	0.92[EUR][1000 genomes]
rs12144789	1.00[CEU][hapmap]
rs12402107	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs12409223	0.92[EUR][1000 genomes]
rs1416842	0.92[EUR][1000 genomes]
rs1934430	0.92[EUR][1000 genomes]
rs41277194	0.89[EUR][1000 genomes]
rs4314861	0.86[EUR][1000 genomes]
rs4453013	0.92[EUR][1000 genomes]
rs7416880	1.00[CEU][hapmap];0.96[EUR][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	nsv430324	chr1:215649163-216082605	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1006504	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv535288	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv949671	chr1:215942740-216120815	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv549192	chr1:215967857-216034753	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1012279	chr1:215982058-216035558	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv832548	chr1:215987089-216175724	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215987200-216007400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:215988200-215988600	Enhancers	H1 Cell Line	embryonic stem cell

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