Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs17085568	1.00[JPT][hapmap]
rs17085570	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1888898	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2210447	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs2325251	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2325252	1.00[CEU][hapmap]
rs2482565	1.00[CEU][hapmap]
rs4883847	1.00[EUR][1000 genomes]
rs6562597	1.00[CEU][hapmap]
rs7319892	1.00[CEU][hapmap]
rs7325546	1.00[CEU][hapmap]
rs7325599	1.00[CEU][hapmap]
rs7328510	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7332783	1.00[JPT][hapmap]
rs7985539	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7985990	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs7990121	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7995380	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7995799	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9529650	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9564629	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9572305	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

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	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
2	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
3	nsv832643	chr13:70324440-70486661	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv900487	chr13:70327693-70548643	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv530724	chr13:70393680-71164323	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1045918	chr13:70409675-70615997	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70478600-70479200	Enhancers	Stomach Mucosa	stomach

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