Variant report

Variant	rs58656176
Chromosome Location	chr1:119355707-119355708
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10494215	1.00[ASN][1000 genomes]
rs10494216	1.00[ASN][1000 genomes]
rs1361208	1.00[ASN][1000 genomes]
rs1361209	1.00[ASN][1000 genomes]
rs1416142	1.00[ASN][1000 genomes]
rs17022627	1.00[ASN][1000 genomes]
rs17022643	1.00[ASN][1000 genomes]
rs17022688	1.00[ASN][1000 genomes]
rs4623744	1.00[ASN][1000 genomes]
rs55907232	1.00[ASN][1000 genomes]
rs56176006	1.00[ASN][1000 genomes]
rs56389242	0.96[AFR][1000 genomes]
rs56809525	1.00[ASN][1000 genomes]
rs56957037	1.00[ASN][1000 genomes]
rs58907106	1.00[ASN][1000 genomes]
rs59731249	1.00[ASN][1000 genomes]
rs60114958	0.92[AFR][1000 genomes]
rs6655966	1.00[ASN][1000 genomes]
rs6660769	1.00[ASN][1000 genomes]
rs6665851	1.00[ASN][1000 genomes]
rs73005657	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73005660	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73007524	1.00[ASN][1000 genomes]
rs73007529	1.00[ASN][1000 genomes]
rs73007534	1.00[ASN][1000 genomes]
rs74114542	1.00[ASN][1000 genomes]
rs7532756	1.00[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	esv3494191	chr1:118772550-119719548	Enhancers Strong transcription Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	esv3494192	chr1:118772550-119719548	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv997707	chr1:119199568-119595949	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	esv2750799	chr1:119229257-119382227	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv831181	chr1:119340175-119529347	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:119353800-119356000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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