Variant report

Variant	rs6102995
Chromosome Location	chr20:41327706-41327707
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs11905283	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11908546	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs16987202	0.94[EUR][1000 genomes]
rs16987229	0.94[EUR][1000 genomes]
rs16987276	0.94[EUR][1000 genomes]
rs2206430	0.96[EUR][1000 genomes]
rs2425504	0.86[JPT][hapmap]
rs2425505	1.00[JPT][hapmap]
rs2425506	1.00[JPT][hapmap]
rs4140493	0.94[EUR][1000 genomes]
rs4560192	0.94[EUR][1000 genomes]
rs4810370	0.92[EUR][1000 genomes]
rs4812615	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4812617	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4812618	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4812633	1.00[EUR][1000 genomes]
rs4812635	0.94[EUR][1000 genomes]
rs4812637	0.92[EUR][1000 genomes]
rs4812638	0.89[EUR][1000 genomes]
rs59581792	0.94[EUR][1000 genomes]
rs6030404	0.94[EUR][1000 genomes]
rs6030405	0.92[EUR][1000 genomes]
rs6030407	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6030408	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs6030409	0.94[EUR][1000 genomes]
rs6030410	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6030432	0.94[EUR][1000 genomes]
rs6030433	0.94[EUR][1000 genomes]
rs6030434	0.94[EUR][1000 genomes]
rs6030435	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs60886646	1.00[EUR][1000 genomes]
rs6093718	0.98[EUR][1000 genomes]
rs6093719	1.00[EUR][1000 genomes]
rs6102978	0.94[EUR][1000 genomes]
rs6102979	0.94[EUR][1000 genomes]
rs6102986	0.94[EUR][1000 genomes]
rs6102990	0.94[EUR][1000 genomes]
rs6102993	1.00[EUR][1000 genomes]
rs6102994	1.00[EUR][1000 genomes]
rs6102997	1.00[EUR][1000 genomes]
rs6103000	0.87[EUR][1000 genomes]
rs6103005	0.94[EUR][1000 genomes]
rs6103008	0.96[EUR][1000 genomes]
rs6103012	0.89[EUR][1000 genomes]
rs7268336	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs7362290	0.94[EUR][1000 genomes]
rs742419	0.89[EUR][1000 genomes]
rs8114061	0.81[CHB][hapmap]
rs8115740	0.94[EUR][1000 genomes]
rs8120378	0.94[EUR][1000 genomes]
rs969262	1.00[JPT][hapmap]
rs976248	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs976249	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064253	chr20:41120425-41379706	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915994	chr20:41180550-41464507	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv532517	chr20:41188651-41342196	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv949644	chr20:41207365-41333541	Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv912878	chr20:41222480-41361424	Strong transcription Bivalent Enhancer Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv833988	chr20:41227788-41379921	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1058990	chr20:41289969-41543912	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv544277	chr20:41289969-41543912	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv586028	chr20:41296994-41381215	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1060878	chr20:41317182-41342290	Weak transcription Strong transcription Enhancers ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41319600-41329200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr20:41327600-41330400	Weak transcription	Liver	Liver

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