Variant report

Variant	rs7463151
Chromosome Location	chr8:113406923-113406924
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10086302	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs10089136	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10089402	0.85[CEU][hapmap];0.86[CHB][hapmap]
rs10090328	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs10094970	0.89[CEU][hapmap];1.00[CHB][hapmap];0.86[CHD][hapmap];0.93[GIH][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap];0.82[AMR][1000 genomes]
rs10097860	0.86[CEU][hapmap];1.00[CHB][hapmap]
rs10099418	0.82[AMR][1000 genomes]
rs1026285	0.89[CEU][hapmap];0.86[CHB][hapmap];0.93[GIH][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap]
rs1026286	0.89[CHB][hapmap]
rs1026287	0.89[CEU][hapmap];0.86[CHB][hapmap];0.93[GIH][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap]
rs1032406	1.00[ASW][hapmap];0.89[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.93[GIH][hapmap];0.91[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];0.82[YRI][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10755908	0.89[CEU][hapmap];0.86[CHB][hapmap];0.93[GIH][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap]
rs1125202	0.81[CEU][hapmap];1.00[CHB][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11776765	0.90[JPT][hapmap]
rs11777694	0.84[JPT][hapmap]
rs12115016	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs12115151	0.89[CEU][hapmap];0.86[CHB][hapmap];0.93[GIH][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap]
rs12155729	0.81[JPT][hapmap]
rs12155759	0.91[JPT][hapmap]
rs12156373	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12676848	0.90[ASW][hapmap];0.96[CEU][hapmap];0.86[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.95[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12678407	0.84[JPT][hapmap]
rs1352993	0.85[CEU][hapmap];0.86[CHB][hapmap]
rs1388959	0.87[MEX][hapmap]
rs1388960	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs1388961	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs1388963	0.86[JPT][hapmap]
rs1388965	0.91[JPT][hapmap]
rs1472166	0.91[JPT][hapmap]
rs1492660	0.89[CEU][hapmap];0.86[CHB][hapmap];0.93[GIH][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap]
rs1492661	0.88[CEU][hapmap];0.94[CHB][hapmap]
rs1492662	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs1492665	0.82[AMR][1000 genomes]
rs1492666	0.89[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes]
rs1492670	0.91[JPT][hapmap]
rs1492673	0.82[JPT][hapmap]
rs1492674	0.82[JPT][hapmap]
rs1492678	0.86[JPT][hapmap]
rs1552785	0.88[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1602703	0.91[JPT][hapmap]
rs16883510	0.91[JPT][hapmap]
rs1873746	0.91[JPT][hapmap]
rs1993208	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs2012465	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs2035895	0.91[JPT][hapmap]
rs2035896	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs2123492	0.82[AMR][1000 genomes]
rs2131298	0.86[JPT][hapmap]
rs2167776	0.86[CHB][hapmap]
rs2883427	0.89[CEU][hapmap];0.86[CHB][hapmap];0.93[GIH][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap]
rs3860881	1.00[CHB][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3950676	0.86[JPT][hapmap]
rs41340951	0.91[JPT][hapmap]
rs41467949	0.82[CEU][hapmap];0.86[JPT][hapmap]
rs4469486	0.89[JPT][hapmap]
rs4563913	0.91[JPT][hapmap]
rs4577984	0.85[JPT][hapmap]
rs4876281	0.85[CEU][hapmap];0.91[JPT][hapmap]
rs4876283	0.84[CEU][hapmap];0.91[JPT][hapmap]
rs4876467	0.90[JPT][hapmap]
rs4876468	0.91[JPT][hapmap]
rs4876469	0.91[JPT][hapmap]
rs4876470	0.90[JPT][hapmap]
rs6469413	0.84[CEU][hapmap];0.86[JPT][hapmap]
rs6469415	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6469416	0.82[AMR][1000 genomes]
rs6994009	0.96[CEU][hapmap];0.86[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7003500	0.85[JPT][hapmap]
rs768095	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs7818132	0.89[CEU][hapmap];1.00[CHB][hapmap];0.82[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7832317	0.91[JPT][hapmap]
rs7838852	0.86[JPT][hapmap]
rs7840922	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7843346	0.89[CEU][hapmap];0.86[CHB][hapmap];0.91[GIH][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap]
rs7844160	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs7845628	0.86[JPT][hapmap]
rs7845794	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs9297474	0.89[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.93[GIH][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9649933	0.96[CEU][hapmap];0.86[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9650044	0.96[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9886643	0.90[ASW][hapmap];0.96[CEU][hapmap];0.86[CHB][hapmap];0.95[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.82[LWK][hapmap];0.92[MEX][hapmap];0.98[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533857	chr8:112819659-113801258	Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1022457	chr8:113071774-113811177	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	esv2755868	chr8:113282795-113634842	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2753595	chr8:113283214-114190390	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
5	esv2754232	chr8:113294967-113634842	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113399400-113410600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:113406400-113408000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
3	chr8:113406600-113408200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
4	chr8:113406800-113407400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell

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