Variant report

Variant	rs10164660
Chromosome Location	chr2:9874293-9874294
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:9871478..9874528-chr2:9876144..9879356,3	K562	blood:
2	chr2:9870027..9872978-chr2:9873410..9875751,2	K562	blood:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10202938	0.91[ASN][1000 genomes]
rs10929596	0.88[ASN][1000 genomes]
rs10929597	0.88[ASN][1000 genomes]
rs10929598	0.88[ASN][1000 genomes]
rs10929600	0.91[ASN][1000 genomes]
rs10929602	0.91[ASN][1000 genomes]
rs10929605	0.91[ASN][1000 genomes]
rs10929607	0.86[ASN][1000 genomes]
rs10929608	0.86[ASN][1000 genomes]
rs10929609	0.86[ASN][1000 genomes]
rs11695437	0.91[ASN][1000 genomes]
rs11892176	0.91[ASN][1000 genomes]
rs11901380	0.90[ASN][1000 genomes]
rs11902412	0.91[ASN][1000 genomes]
rs11902608	0.84[ASN][1000 genomes]
rs12472594	0.91[ASN][1000 genomes]
rs12991432	0.96[ASN][1000 genomes]
rs12993968	0.83[ASN][1000 genomes]
rs13024852	0.89[ASN][1000 genomes]
rs1877949	0.95[ASN][1000 genomes]
rs1877950	0.96[ASN][1000 genomes]
rs1877951	0.96[ASN][1000 genomes]
rs1877953	0.91[ASN][1000 genomes]
rs2357264	0.90[ASN][1000 genomes]
rs2357265	0.90[ASN][1000 genomes]
rs28542885	0.82[ASN][1000 genomes]
rs4459704	0.90[ASN][1000 genomes]
rs4507070	0.87[ASN][1000 genomes]
rs4668636	0.84[ASN][1000 genomes]
rs4668637	0.87[ASN][1000 genomes]
rs4668638	0.91[ASN][1000 genomes]
rs4668639	0.91[ASN][1000 genomes]
rs4668640	0.91[ASN][1000 genomes]
rs4668641	0.93[ASN][1000 genomes]
rs4668642	0.95[ASN][1000 genomes]
rs4668643	0.95[ASN][1000 genomes]
rs4669427	0.88[ASN][1000 genomes]
rs4669428	0.88[ASN][1000 genomes]
rs4669429	0.88[ASN][1000 genomes]
rs4669430	0.88[ASN][1000 genomes]
rs4669432	0.91[ASN][1000 genomes]
rs4669433	0.91[ASN][1000 genomes]
rs4669435	0.91[ASN][1000 genomes]
rs4669437	0.90[ASN][1000 genomes]
rs4669441	0.91[ASN][1000 genomes]
rs4669445	0.95[ASN][1000 genomes]
rs4669446	0.95[ASN][1000 genomes]
rs4669447	0.86[ASN][1000 genomes]
rs5020306	0.88[ASN][1000 genomes]
rs58961346	0.91[ASN][1000 genomes]
rs6432033	0.88[ASN][1000 genomes]
rs6724483	0.90[ASN][1000 genomes]
rs6727688	0.96[ASN][1000 genomes]
rs6736421	0.91[ASN][1000 genomes]
rs6752842	0.97[ASN][1000 genomes]
rs7592044	0.90[ASN][1000 genomes]
rs7602784	0.83[ASN][1000 genomes]
rs7605675	0.83[ASN][1000 genomes]
rs885572	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469405	chr2:9814374-9964947	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
2	nsv580930	chr2:9814374-9964947	Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1003026	chr2:9854939-10012516	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv470443	chr2:9857018-9975557	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv1014911	chr2:9863969-9905959	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv873618	chr2:9870631-9919759	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv873619	chr2:9870631-9956981	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
8	esv3349790	chr2:9873557-9874404	Weak transcription	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	chr2:9869600-9875800	Weak transcription	Fetal Thymus	thymus

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