Variant report

Variant	rs11902326
Chromosome Location	chr2:182659893-182659894
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:182659802..182662232-chr2:182760144..182763028,2	MCF-7	breast:
2	chr2:182655124..182657474-chr2:182657876..182660662,2	K562	blood:
3	chr2:182658638..182660215-chr2:182682406..182684395,2	MCF-7	breast:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10183937	0.83[CHB][hapmap];0.88[JPT][hapmap]
rs10497586	0.81[ASN][1000 genomes]
rs10803953	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs11891680	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11898530	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12612058	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12618902	0.84[ASN][1000 genomes]
rs12620901	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12622894	0.87[ASN][1000 genomes]
rs13387144	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1427333	0.85[ASN][1000 genomes]
rs1528028	0.84[ASN][1000 genomes]
rs16867494	0.93[CHB][hapmap]
rs16867496	0.81[ASN][1000 genomes]
rs16867502	0.88[JPT][hapmap]
rs16867503	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs16867504	0.88[JPT][hapmap]
rs16867506	0.87[ASN][1000 genomes]
rs1991374	0.85[ASN][1000 genomes]
rs4018749	0.83[CHB][hapmap];0.88[JPT][hapmap]
rs4597474	0.86[CHB][hapmap]
rs57000426	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57281910	0.84[ASN][1000 genomes]
rs57971040	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59159077	0.84[ASN][1000 genomes]
rs59956987	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60200067	0.84[ASN][1000 genomes]
rs61246630	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6720578	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7567399	0.99[ASN][1000 genomes]
rs7567560	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7581484	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7584725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005870	chr2:181968637-182921439	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv536063	chr2:181968637-182921439	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1001558	chr2:182590009-182732738	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv834478	chr2:182654811-182843201	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182657200-182661400	Weak transcription	Osteobl	bone
2	chr2:182657200-182669800	Weak transcription	NHDF-Ad	bronchial

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