Variant report

Variant	rs10931319
Chromosome Location	chr2:188825184-188825185
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10178187	0.86[EUR][1000 genomes]
rs10179589	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1400073	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1516118	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1516119	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1516120	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1516130	0.93[EUR][1000 genomes]
rs1850179	0.87[EUR][1000 genomes]
rs1898909	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1992281	0.86[EUR][1000 genomes]
rs2016373	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2118998	0.84[EUR][1000 genomes]
rs2165153	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2350194	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4666747	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4667199	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4667202	0.86[EUR][1000 genomes]
rs6711838	1.00[EUR][1000 genomes]
rs7419931	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7571862	0.86[AMR][1000 genomes];0.87[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	nsv533353	chr2:188498301-189024655	Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv875597	chr2:188573244-188916290	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1011832	chr2:188631943-188896492	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv536087	chr2:188631943-188896492	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv584041	chr2:188644642-188928433	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv523293	chr2:188774681-188928433	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv875599	chr2:188780717-188833306	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188812600-188827400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:188824800-188827200	Weak transcription	Aorta	Aorta
3	chr2:188825000-188827400	Weak transcription	HUVEC	blood vessel

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