Variant report

Variant	rs62421533
Chromosome Location	chr6:118706096-118706097
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10484289	1.00[ASN][1000 genomes]
rs12333080	0.88[ASN][1000 genomes]
rs1319987	0.88[ASN][1000 genomes]
rs1319988	0.88[ASN][1000 genomes]
rs17080082	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17080124	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17080292	0.88[ASN][1000 genomes]
rs17080302	0.88[ASN][1000 genomes]
rs17424234	1.00[ASN][1000 genomes]
rs25422	0.88[ASN][1000 genomes]
rs4551203	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4593396	0.88[ASN][1000 genomes]
rs4599686	0.88[ASN][1000 genomes]
rs55899435	0.88[ASN][1000 genomes]
rs56082110	0.83[ASN][1000 genomes]
rs56130945	1.00[ASN][1000 genomes]
rs56255677	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62421532	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62421535	0.88[ASN][1000 genomes]
rs62421536	1.00[ASN][1000 genomes]
rs62421538	0.88[ASN][1000 genomes]
rs62421539	0.88[ASN][1000 genomes]
rs62422189	0.83[ASN][1000 genomes]
rs62422190	0.83[ASN][1000 genomes]
rs62422193	0.83[ASN][1000 genomes]
rs62424172	0.88[ASN][1000 genomes]
rs62424173	0.88[ASN][1000 genomes]
rs62424175	1.00[ASN][1000 genomes]
rs62424176	0.88[ASN][1000 genomes]
rs62424195	0.88[ASN][1000 genomes]
rs62424198	0.88[ASN][1000 genomes]
rs62424199	0.88[ASN][1000 genomes]
rs62424200	0.88[ASN][1000 genomes]
rs62424202	1.00[ASN][1000 genomes]
rs62424204	0.85[ASN][1000 genomes]
rs724868	1.00[ASN][1000 genomes]
rs72952733	1.00[ASN][1000 genomes]
rs72952761	0.88[ASN][1000 genomes]
rs72952793	0.83[ASN][1000 genomes]
rs72954806	0.83[ASN][1000 genomes]
rs72967573	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72967581	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72969531	0.88[ASN][1000 genomes]
rs7356858	0.88[ASN][1000 genomes]
rs7356947	0.88[ASN][1000 genomes]
rs9320652	0.88[ASN][1000 genomes]
rs9320655	0.88[ASN][1000 genomes]
rs9481789	0.88[ASN][1000 genomes]
rs9481808	0.88[ASN][1000 genomes]
rs9481811	0.88[ASN][1000 genomes]
rs9481821	0.88[ASN][1000 genomes]
rs9481825	0.80[ASN][1000 genomes]
rs9481826	0.80[ASN][1000 genomes]
rs9489369	0.88[ASN][1000 genomes]
rs9489371	0.88[ASN][1000 genomes]
rs9489372	0.81[ASN][1000 genomes]
rs9489381	0.88[ASN][1000 genomes]
rs9489383	0.88[ASN][1000 genomes]
rs9489399	0.88[ASN][1000 genomes]
rs9489407	0.88[ASN][1000 genomes]
rs9489409	0.88[ASN][1000 genomes]
rs9489416	0.88[ASN][1000 genomes]
rs9489428	0.88[ASN][1000 genomes]
rs9489433	0.88[ASN][1000 genomes]
rs9489436	0.88[ASN][1000 genomes]
rs9489442	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv532051	chr6:118551027-119044197	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1020463	chr6:118593028-119146363	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv604554	chr6:118631282-118716318	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv830787	chr6:118631902-118805106	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1025403	chr6:118635123-119122551	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv1025456	chr6:118669672-119058789	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv1027444	chr6:118687556-119121660	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv538428	chr6:118687556-119121660	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
10	nsv949321	chr6:118692304-119137658	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
11	nsv432958	chr6:118692307-119010307	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
12	nsv604555	chr6:118695049-118856822	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
13	nsv1034448	chr6:118698169-119016383	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
14	nsv1025097	chr6:118699752-119058789	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118699600-118707600	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr6:118699600-118716400	Weak transcription	Psoas Muscle	Psoas
3	chr6:118700800-118708800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:118705000-118706200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:118705200-118706200	Enhancers	HUVEC	blood vessel
6	chr6:118706000-118707600	Weak transcription	NHLF	lung
7	chr6:118706000-118708600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr6:118706000-118708800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:118706000-118708800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:118706000-118708800	Weak transcription	NHDF-Ad	bronchial
11	chr6:118706000-118708800	Weak transcription	Osteobl	bone
12	chr6:118706000-118710400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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