Variant report

Variant	rs34968446
Chromosome Location	chr5:113101995-113101996
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11740330	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12187174	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12188752	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12514754	0.95[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs13155514	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13159664	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs13188515	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1384285	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1384286	0.89[ASN][1000 genomes]
rs1482368	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs1482369	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs1482373	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs1825205	0.86[AMR][1000 genomes]
rs1905135	0.95[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2220023	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2416333	0.85[AMR][1000 genomes]
rs2900076	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs34358509	0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs34635281	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs34956734	0.95[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs35346716	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs35540152	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3891925	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs66857996	0.91[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6869773	0.94[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7703513	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7703664	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7710947	0.95[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7734857	0.95[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7737167	0.95[AMR][1000 genomes];0.91[ASN][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	nsv462390	chr5:113076095-113181289	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv471041	chr5:113076095-113181289	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv599408	chr5:113076095-113181289	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv432799	chr5:113077017-113150101	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv599409	chr5:113079354-113184211	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1018938	chr5:113080567-113185361	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1027940	chr5:113091513-113185361	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113099800-113111800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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