Variant report

Variant	rs17103106
Chromosome Location	chr11:104694577-104694578
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs12276274	1.00[EUR][1000 genomes]
rs12286054	1.00[EUR][1000 genomes]
rs17093742	1.00[AMR][1000 genomes]
rs17102890	1.00[AMR][1000 genomes]
rs17103039	1.00[AMR][1000 genomes]
rs17103307	1.00[EUR][1000 genomes]
rs17103313	1.00[EUR][1000 genomes]
rs2114368	1.00[EUR][1000 genomes]
rs2114369	1.00[EUR][1000 genomes]
rs2114370	1.00[EUR][1000 genomes]
rs2162342	1.00[EUR][1000 genomes]
rs3181337	1.00[AMR][1000 genomes]
rs34464472	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3888096	1.00[EUR][1000 genomes]
rs4258348	1.00[EUR][1000 genomes]
rs4540818	1.00[EUR][1000 genomes]
rs45516397	1.00[AMR][1000 genomes]
rs45539433	1.00[AMR][1000 genomes]
rs477993	1.00[EUR][1000 genomes]
rs482385	1.00[EUR][1000 genomes]
rs484438	1.00[EUR][1000 genomes]
rs488928	1.00[YRI][hapmap]
rs5000899	1.00[EUR][1000 genomes]
rs508916	1.00[EUR][1000 genomes]
rs517153	1.00[EUR][1000 genomes]
rs520766	1.00[EUR][1000 genomes]
rs521107	1.00[EUR][1000 genomes]
rs525020	1.00[EUR][1000 genomes]
rs527522	1.00[EUR][1000 genomes]
rs530398	1.00[EUR][1000 genomes]
rs532089	1.00[EUR][1000 genomes]
rs550051	1.00[EUR][1000 genomes]
rs556062	1.00[EUR][1000 genomes]
rs556589	1.00[EUR][1000 genomes]
rs557069	1.00[EUR][1000 genomes]
rs566945	1.00[EUR][1000 genomes]
rs571407	1.00[YRI][hapmap]
rs579353	1.00[EUR][1000 genomes]
rs59301970	1.00[EUR][1000 genomes]
rs606399	1.00[EUR][1000 genomes]
rs608655	1.00[EUR][1000 genomes]
rs619515	1.00[EUR][1000 genomes]
rs623114	1.00[YRI][hapmap]
rs626354	1.00[EUR][1000 genomes]
rs640857	1.00[EUR][1000 genomes]
rs652377	1.00[EUR][1000 genomes]
rs655884	1.00[EUR][1000 genomes]
rs693506	1.00[EUR][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	nsv1046098	chr11:104207210-105003661	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1054456	chr11:104358924-104805251	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv531430	chr11:104380924-105194452	Genic enhancers Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv826072	chr11:104662708-104768357	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv832255	chr11:104674918-104846961	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 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	chr11:104691600-104707600	Weak transcription	Fetal Brain Male	brain
2	chr11:104694400-104694800	Enhancers	Brain Hippocampus Middle	brain

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