Variant report

Variant	rs9572250
Chromosome Location	chr13:70302178-70302179
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12867754	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1364377	0.88[CHB][hapmap]
rs17085275	0.84[CEU][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1895569	0.86[CHB][hapmap];0.91[CHD][hapmap]
rs2018205	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs3904254	0.88[JPT][hapmap]
rs3909551	1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs4304920	1.00[CHB][hapmap]
rs58084677	0.83[AMR][1000 genomes]
rs7321156	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7323633	0.82[CHB][hapmap]
rs7991639	0.88[CHB][hapmap]
rs7999609	0.85[CHD][hapmap]
rs9317837	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9317839	0.94[CHB][hapmap];0.88[JPT][hapmap]
rs9317840	0.80[CHB][hapmap]
rs9529629	0.94[CHB][hapmap];0.91[CHD][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap]
rs9529631	0.88[JPT][hapmap]
rs9542057	0.84[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap]
rs9542068	1.00[CEU][hapmap];0.88[CHB][hapmap];0.86[JPT][hapmap]
rs9542074	0.88[CHB][hapmap]
rs9564595	0.94[CHB][hapmap]
rs9564596	0.94[CHB][hapmap];0.94[CHD][hapmap]
rs9564597	0.87[ASW][hapmap];0.80[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];0.80[LWK][hapmap]
rs9564601	0.94[CHB][hapmap]
rs9564608	0.80[CHB][hapmap]
rs9564609	0.82[CHB][hapmap]
rs9572242	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[GIH][hapmap];0.88[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9572253	0.93[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap]
rs9599499	0.83[CHB][hapmap]
rs9599508	0.88[CHB][hapmap]
rs9599509	0.94[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045844	chr13:70038096-70405435	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1049684	chr13:70126871-70333445	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv900481	chr13:70147851-70560731	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1054554	chr13:70159715-70502956	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv900482	chr13:70186605-70383876	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv1837120	chr13:70209507-70425056	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv482460	chr13:70240630-70419347	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv900483	chr13:70254555-70464234	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv900484	chr13:70298300-70383876	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 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
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