Variant report

Variant	rs62526711
Chromosome Location	chr8:92191027-92191028
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10091041	1.00[ASN][1000 genomes]
rs10093640	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10094031	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10094656	1.00[ASN][1000 genomes]
rs10099683	0.92[ASN][1000 genomes]
rs10102397	1.00[ASN][1000 genomes]
rs10104912	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10105201	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10109015	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10113232	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13439536	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28539046	0.84[AMR][1000 genomes]
rs28643423	0.83[ASN][1000 genomes]
rs56978897	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57438891	1.00[ASN][1000 genomes]
rs58052832	0.83[ASN][1000 genomes]
rs62526706	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62526731	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7007552	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7009676	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028628	chr8:91680968-92418954	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539672	chr8:91680968-92418954	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	esv2758623	chr8:91974499-92273724	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	esv2759629	chr8:91974499-92273724	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv831390	chr8:92037011-92198605	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
6	esv35058	chr8:92127463-92218776	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:92187800-92192000	Weak transcription	Fetal Intestine Small	intestine
2	chr8:92188400-92192800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr8:92190600-92191800	Enhancers	Colon Smooth Muscle	Colon
4	chr8:92190800-92192200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:92191000-92191200	Enhancers	NHLF	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links