Variant report

Variant	rs4975779
Chromosome Location	chr5:1983619-1983620
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10035144	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10037957	0.88[CHB][hapmap]
rs10038712	0.83[CHB][hapmap]
rs10040620	0.83[CHB][hapmap]
rs10043083	0.97[ASN][1000 genomes]
rs10045683	0.94[ASN][1000 genomes]
rs1017924	0.92[ASN][1000 genomes]
rs10474733	0.90[ASN][1000 genomes]
rs10474734	0.90[ASN][1000 genomes]
rs11133918	0.92[ASN][1000 genomes]
rs1123381	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1123390	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1123391	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11749073	0.90[ASN][1000 genomes]
rs11952205	0.87[ASN][1000 genomes]
rs12188545	0.92[ASN][1000 genomes]
rs12716127	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13166888	0.94[ASN][1000 genomes]
rs1486937	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1601641	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3902820	0.97[ASN][1000 genomes]
rs4246752	0.92[ASN][1000 genomes]
rs4371796	0.94[ASN][1000 genomes]
rs4398680	0.86[ASN][1000 genomes]
rs4407661	0.92[ASN][1000 genomes]
rs4526149	0.97[ASN][1000 genomes]
rs4975777	0.92[ASN][1000 genomes]
rs4975778	0.89[CHB][hapmap]
rs4975786	0.90[ASN][1000 genomes]
rs55860207	0.82[ASN][1000 genomes]
rs57434783	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61656301	0.88[ASN][1000 genomes]
rs62337135	0.88[ASN][1000 genomes]
rs67659713	0.91[ASN][1000 genomes]
rs9312970	0.90[ASN][1000 genomes]
rs965276	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[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	nsv817407	chr5:1495354-2191460	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
2	nsv869236	chr5:1719263-2259100	Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
3	nsv915846	chr5:1891098-2167677	Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1026930	chr5:1898993-2126061	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv427705	chr5:1950467-2115059	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv4681	chr5:1967628-2010091	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	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	chr5:1977200-1997000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr5:1983600-1983800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:1983600-1984200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr5:1983600-1984400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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