Variant report

Variant	rs73498851
Chromosome Location	chr11:77249783-77249784
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs35216705	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56709311	1.00[AMR][1000 genomes]
rs57008614	1.00[AMR][1000 genomes]
rs57229097	1.00[AMR][1000 genomes]
rs57544945	1.00[AMR][1000 genomes]
rs58758035	1.00[AMR][1000 genomes]
rs59231807	1.00[AMR][1000 genomes]
rs59293034	1.00[AMR][1000 genomes]
rs60695213	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61186004	1.00[AMR][1000 genomes]
rs73492001	1.00[AMR][1000 genomes]
rs73493813	1.00[AMR][1000 genomes]
rs73498844	1.00[AMR][1000 genomes]
rs73498845	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73498854	1.00[AMR][1000 genomes]
rs73498869	1.00[AMR][1000 genomes]
rs73498882	1.00[AMR][1000 genomes]
rs73498884	1.00[AMR][1000 genomes]
rs73500705	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73500729	1.00[AMR][1000 genomes]
rs73500735	1.00[AMR][1000 genomes]
rs73500750	1.00[AMR][1000 genomes]
rs73500752	1.00[AMR][1000 genomes]
rs73500756	1.00[AMR][1000 genomes]
rs73500773	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73504713	1.00[AMR][1000 genomes]
rs73504718	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73504734	1.00[AMR][1000 genomes]
rs73504744	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73504765	1.00[AMR][1000 genomes]
rs73504777	1.00[AMR][1000 genomes]
rs73504800	1.00[AMR][1000 genomes]
rs73506711	1.00[AMR][1000 genomes]
rs73506717	1.00[AMR][1000 genomes]
rs73506724	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73506730	1.00[AMR][1000 genomes]
rs73506734	1.00[AMR][1000 genomes]
rs73506737	1.00[AMR][1000 genomes]
rs73506741	1.00[AMR][1000 genomes]
rs73506742	1.00[AMR][1000 genomes]
rs73506754	1.00[AMR][1000 genomes]
rs73506778	1.00[AMR][1000 genomes]
rs73508705	1.00[AMR][1000 genomes]
rs73508715	1.00[AMR][1000 genomes]
rs73508720	1.00[AMR][1000 genomes]
rs73508749	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048360	chr11:76900813-77387933	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv541089	chr11:76900813-77387933	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1049603	chr11:76900813-77520411	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv541090	chr11:76900813-77520411	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	esv3424135	chr11:76961603-77277087	Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1037724	chr11:77061945-77250391	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv541091	chr11:77061945-77250391	Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	esv3437433	chr11:77101280-77291686	Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	esv2752651	chr11:77211136-77318279	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr11:77237400-77249800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr11:77249200-77258600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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