Variant report

Variant	rs7054839
Chromosome Location	chr1:171113134-171113135
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10489229	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1080197	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10910879	0.82[AMR][1000 genomes]
rs11809504	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11812044	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11812061	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12402295	0.84[CHB][hapmap];0.82[AMR][1000 genomes]
rs12403297	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12404455	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12405599	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12406572	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17564980	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17565336	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17565579	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17565766	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17565793	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17565983	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs17565990	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs17566256	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17623477	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17623598	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs17623833	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17640463	1.00[CHB][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2066529	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2142630	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2266780	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2272797	1.00[CHB][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2272799	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2272800	1.00[CHB][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2281006	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2281007	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2281008	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28363530	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28363536	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28363537	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28363541	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28363571	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28745586	0.82[AMR][1000 genomes]
rs28745588	0.82[AMR][1000 genomes]
rs35156637	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3817765	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs55639094	0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs57147275	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs57519348	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs57678907	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs58044560	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs58374074	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs58509777	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs59184216	0.96[ASN][1000 genomes]
rs6608452	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6608453	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6608454	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7051747	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7061710	0.91[ASN][1000 genomes]
rs7063044	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7066454	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72712649	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72712658	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72712685	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7879557	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7885569	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7886938	1.00[CHB][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7887142	1.00[CHB][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7889807	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7889839	1.00[CHB][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs909531	0.95[EUR][1000 genomes];0.91[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	nsv1001228	chr1:170885787-171452579	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
2	esv14617	chr1:171016086-171726961	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv1005902	chr1:171036690-171254916	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
4	nsv535203	chr1:171036690-171254916	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171110800-171114600	Enhancers	Fetal Lung	lung
2	chr1:171112200-171120600	Weak transcription	Fetal Kidney	kidney
3	chr1:171112400-171121800	Weak transcription	Aorta	Aorta
4	chr1:171112600-171114000	Enhancers	Adipose Nuclei	Adipose
5	chr1:171112800-171118400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:171112800-171121000	Weak transcription	Psoas Muscle	Psoas
7	chr1:171113000-171113200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:171113000-171113200	Enhancers	Stomach Mucosa	stomach

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