Variant report

Variant	rs72651930
Chromosome Location	chr4:69604491-69604492
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs12500065	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1355806	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1588708	0.90[ASN][1000 genomes]
rs1828697	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1913322	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2090000	0.90[EUR][1000 genomes]
rs28836845	0.94[EUR][1000 genomes]
rs293404	0.94[EUR][1000 genomes]
rs293405	0.94[EUR][1000 genomes]
rs3113331	0.95[EUR][1000 genomes]
rs34355592	0.88[EUR][1000 genomes]
rs35345766	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs384038	0.94[EUR][1000 genomes]
rs387460	0.93[EUR][1000 genomes]
rs3934038	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs406668	0.94[EUR][1000 genomes]
rs418081	0.93[EUR][1000 genomes]
rs436876	0.94[EUR][1000 genomes]
rs4694072	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4694073	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4694288	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72651926	0.91[ASN][1000 genomes]
rs7657065	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757061	chr4:69178920-69631668	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv870075	chr4:69218674-69608683	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1005513	chr4:69446718-69890307	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	esv2763366	chr4:69592847-69661427	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1013885	chr4:69592847-69667996	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv829961	chr4:69592847-69695467	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv594579	chr4:69597175-69665970	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1014042	chr4:69599853-69667996	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69602800-69613400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:69603800-69604600	ZNF genes & repeats	HepG2	liver

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