Variant report

Variant	rs6556933
Chromosome Location	chr5:95882436-95882437
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs11135467	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11135468	0.97[ASN][1000 genomes]
rs11135469	0.97[ASN][1000 genomes]
rs11742038	0.97[ASN][1000 genomes]
rs11742044	0.97[ASN][1000 genomes]
rs11742063	0.97[ASN][1000 genomes]
rs11948144	0.92[ASN][1000 genomes]
rs13173434	0.96[ASN][1000 genomes]
rs13175874	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs13177618	0.96[ASN][1000 genomes]
rs13184161	0.97[ASN][1000 genomes]
rs1380500	0.97[ASN][1000 genomes]
rs1380501	0.97[ASN][1000 genomes]
rs1824425	0.94[ASN][1000 genomes]
rs2117142	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2117144	0.97[ASN][1000 genomes]
rs2117145	0.97[ASN][1000 genomes]
rs2217718	0.96[ASN][1000 genomes]
rs2350241	0.97[ASN][1000 genomes]
rs2570469	0.97[ASN][1000 genomes]
rs2611738	0.97[ASN][1000 genomes]
rs261974	0.96[ASN][1000 genomes]
rs261978	0.97[ASN][1000 genomes]
rs261979	0.97[ASN][1000 genomes]
rs35057722	0.94[ASN][1000 genomes]
rs35190022	0.97[ASN][1000 genomes]
rs35283841	0.97[ASN][1000 genomes]
rs4267885	0.97[ASN][1000 genomes]
rs4634375	0.97[ASN][1000 genomes]
rs4869143	0.94[ASN][1000 genomes]
rs4869144	0.97[ASN][1000 genomes]
rs4869290	0.97[ASN][1000 genomes]
rs62365724	0.92[ASN][1000 genomes]
rs62365725	0.90[ASN][1000 genomes]
rs6556928	0.97[ASN][1000 genomes]
rs6859191	0.97[ASN][1000 genomes]
rs6867933	0.80[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs6870000	0.97[ASN][1000 genomes]
rs6870152	0.97[ASN][1000 genomes]
rs6873005	0.97[ASN][1000 genomes]
rs6877870	0.97[ASN][1000 genomes]
rs6878046	0.97[ASN][1000 genomes]
rs6878234	0.96[ASN][1000 genomes]
rs6889388	0.97[ASN][1000 genomes]
rs71580786	0.92[ASN][1000 genomes]
rs7713454	0.97[ASN][1000 genomes]
rs7714425	0.96[ASN][1000 genomes]
rs7734121	0.97[ASN][1000 genomes]
rs7734417	0.97[ASN][1000 genomes]
rs7736659	0.92[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	nsv1030444	chr5:95353620-95995619	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv537810	chr5:95353620-95995619	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1024964	chr5:95742124-96065492	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv537811	chr5:95742124-96065492	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
5	nsv1026484	chr5:95759910-95961518	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr5:95873800-95884200	Weak transcription	Aorta	Aorta
2	chr5:95881000-95885000	Enhancers	Hela-S3	cervix
3	chr5:95882000-95884400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:95882200-95883000	Enhancers	Stomach Mucosa	stomach

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