Variant report

Variant	rs342695
Chromosome Location	chr13:92352832-92352833
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:92351988..92354291-chr13:92355999..92358274,2	K562	blood:

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10219980	0.82[EUR][1000 genomes]
rs10492611	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs11619422	0.87[EUR][1000 genomes]
rs11841822	0.84[CEU][hapmap];0.87[EUR][1000 genomes]
rs11843168	0.85[CEU][hapmap]
rs11843202	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs11843298	0.87[EUR][1000 genomes]
rs1326742	0.84[CEU][hapmap];0.88[EUR][1000 genomes]
rs1348663	0.82[EUR][1000 genomes]
rs1365874	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs1365875	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs1373863	0.81[EUR][1000 genomes]
rs1409600	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs1409602	0.82[CEU][hapmap];0.87[EUR][1000 genomes]
rs1409603	0.84[CEU][hapmap];0.87[EUR][1000 genomes]
rs1412311	0.88[EUR][1000 genomes]
rs1412312	0.85[CEU][hapmap];0.88[EUR][1000 genomes]
rs1584154	0.87[EUR][1000 genomes]
rs163929	0.93[EUR][1000 genomes]
rs163930	0.93[EUR][1000 genomes]
rs163932	0.82[CEU][hapmap]
rs163933	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs168216	0.91[EUR][1000 genomes]
rs16946409	0.85[EUR][1000 genomes]
rs16946412	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs16946426	0.84[CEU][hapmap];0.87[EUR][1000 genomes]
rs16946459	0.87[EUR][1000 genomes]
rs1822915	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs1822916	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs182924	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs182925	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1831567	0.85[CEU][hapmap];0.88[EUR][1000 genomes]
rs1831568	0.88[EUR][1000 genomes]
rs184661	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs191479	0.92[CEU][hapmap];0.93[EUR][1000 genomes]
rs191480	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2148530	0.82[EUR][1000 genomes]
rs2882822	0.85[CEU][hapmap];0.88[EUR][1000 genomes]
rs342671	0.92[EUR][1000 genomes]
rs342674	0.91[EUR][1000 genomes]
rs342675	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs342676	0.91[EUR][1000 genomes]
rs342677	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs342678	0.83[CEU][hapmap]
rs342679	0.92[EUR][1000 genomes]
rs342682	0.92[CEU][hapmap]
rs342683	0.90[EUR][1000 genomes]
rs342684	0.92[CEU][hapmap];0.93[EUR][1000 genomes]
rs342685	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs342686	0.95[EUR][1000 genomes]
rs342692	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs342693	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs342694	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs345435	0.92[EUR][1000 genomes]
rs3852116	0.88[EUR][1000 genomes]
rs3864178	0.88[EUR][1000 genomes]
rs3906488	0.85[EUR][1000 genomes]
rs393695	0.92[CEU][hapmap]
rs429039	0.91[EUR][1000 genomes]
rs435417	0.92[CEU][hapmap];0.91[EUR][1000 genomes]
rs457538	0.91[EUR][1000 genomes]
rs461810	0.92[CEU][hapmap];0.92[EUR][1000 genomes]
rs466165	0.91[EUR][1000 genomes]
rs523428	0.90[EUR][1000 genomes]
rs532989	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs536822	0.91[EUR][1000 genomes]
rs538673	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs553717	0.83[CEU][hapmap]
rs554857	0.84[CEU][hapmap];0.92[EUR][1000 genomes]
rs55924226	0.88[EUR][1000 genomes]
rs560759	0.92[CEU][hapmap];0.93[EUR][1000 genomes]
rs58166883	0.82[EUR][1000 genomes]
rs60635585	0.87[EUR][1000 genomes]
rs60790837	0.82[EUR][1000 genomes]
rs6492560	0.88[EUR][1000 genomes]
rs72643220	0.85[EUR][1000 genomes]
rs72643226	0.87[EUR][1000 genomes]
rs72643228	0.87[EUR][1000 genomes]
rs7321165	0.85[EUR][1000 genomes]
rs7337822	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs746612	0.85[CEU][hapmap]
rs914557	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs9583950	0.82[EUR][1000 genomes]
rs9583952	0.87[EUR][1000 genomes]
rs9589322	0.85[CEU][hapmap];0.86[EUR][1000 genomes]
rs9589323	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs9589324	0.85[CEU][hapmap];0.84[EUR][1000 genomes]
rs9589326	0.85[EUR][1000 genomes]
rs9589327	0.84[CEU][hapmap];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042947	chr13:91571040-92416897	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
2	nsv541871	chr13:91571040-92416897	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
3	nsv1049382	chr13:92024240-92521180	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv541873	chr13:92024240-92521180	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv2753383	chr13:92226599-92462699	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv529268	chr13:92267310-92531263	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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