Variant report

Variant	rs6735489
Chromosome Location	chr2:141551350-141551351
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10191182	0.95[CHB][hapmap]
rs10209438	0.87[CEU][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1025337	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs11674928	0.94[CHB][hapmap]
rs11677778	0.95[CHB][hapmap]
rs11678482	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs11684411	0.95[CHB][hapmap]
rs11686050	0.94[CHB][hapmap];0.81[JPT][hapmap]
rs11694855	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs11893770	0.95[CHB][hapmap];0.95[CHD][hapmap]
rs12620422	0.95[CHB][hapmap]
rs12621209	0.95[CHB][hapmap]
rs12623466	0.94[CHB][hapmap]
rs12691562	0.82[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs12691568	0.82[GIH][hapmap]
rs12691571	0.95[CHB][hapmap];0.95[CHD][hapmap]
rs13000151	0.97[EUR][1000 genomes]
rs13009144	0.82[CEU][hapmap];0.92[GIH][hapmap];0.81[TSI][hapmap]
rs13010984	0.95[CEU][hapmap];0.97[EUR][1000 genomes]
rs13030928	0.82[CEU][hapmap];0.92[GIH][hapmap];0.82[TSI][hapmap];0.91[EUR][1000 genomes]
rs1429333	0.95[CHB][hapmap]
rs1429356	1.00[CEU][hapmap]
rs1429369	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs1486124	0.84[GIH][hapmap]
rs17514829	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs17515498	0.95[CHB][hapmap];0.95[CHD][hapmap]
rs17515899	0.95[CHB][hapmap];0.81[JPT][hapmap];0.90[ASN][1000 genomes]
rs17517552	0.81[CHB][hapmap]
rs1843585	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs1963394	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs2171173	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs2380889	0.95[CHB][hapmap]
rs3828265	0.89[CHB][hapmap];0.95[CHD][hapmap];0.81[JPT][hapmap]
rs4423546	0.95[CHB][hapmap];0.93[CHD][hapmap]
rs4616417	0.95[CHB][hapmap]
rs4954860	0.90[CHB][hapmap]
rs6720709	0.95[CHB][hapmap]
rs6720793	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs6722632	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[YRI][hapmap]
rs6735583	1.00[CEU][hapmap]
rs6749275	0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap]
rs6749707	0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap]
rs6750270	0.84[EUR][1000 genomes]
rs6757066	0.81[ASN][1000 genomes]
rs7571628	0.95[CHB][hapmap];0.95[CHD][hapmap]
rs7571766	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs7578679	0.95[CHB][hapmap]
rs9287300	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];0.91[JPT][hapmap];0.82[MEX][hapmap];0.82[TSI][hapmap]
rs9653169	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875198	chr2:141409166-141571329	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv875199	chr2:141409166-141600366	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv875201	chr2:141448312-141561255	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv875202	chr2:141448312-141587228	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv875203	chr2:141448312-141592252	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv875204	chr2:141496596-141592252	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv875205	chr2:141500692-141592252	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv875206	chr2:141504719-141571329	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv583198	chr2:141510791-142150620	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv875207	chr2:141517652-141592252	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1003008	chr2:141518795-141763505	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv583199	chr2:141551350-141583206	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	n/a	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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