Variant report

Variant	rs56162021
Chromosome Location	chr4:160556850-160556851
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10004655	0.89[EUR][1000 genomes]
rs10213093	0.88[EUR][1000 genomes]
rs10517703	0.89[EUR][1000 genomes]
rs11100246	0.88[EUR][1000 genomes]
rs11100247	0.89[EUR][1000 genomes]
rs11721796	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11730807	0.84[EUR][1000 genomes]
rs11737328	0.88[EUR][1000 genomes]
rs12512433	0.88[EUR][1000 genomes]
rs12641814	0.88[EUR][1000 genomes]
rs12641842	0.88[EUR][1000 genomes]
rs12641886	0.88[EUR][1000 genomes]
rs12645511	0.84[EUR][1000 genomes]
rs12647897	0.87[EUR][1000 genomes]
rs12648744	0.89[EUR][1000 genomes]
rs12649393	0.80[EUR][1000 genomes]
rs12711318	0.84[ASN][1000 genomes]
rs13138857	0.84[EUR][1000 genomes]
rs13138862	0.84[EUR][1000 genomes]
rs13147870	0.86[EUR][1000 genomes]
rs13340212	0.84[EUR][1000 genomes]
rs13340269	0.84[EUR][1000 genomes]
rs1502718	0.85[EUR][1000 genomes]
rs1566701	0.90[EUR][1000 genomes]
rs1566702	0.91[EUR][1000 genomes]
rs1566703	0.91[EUR][1000 genomes]
rs1566704	0.91[EUR][1000 genomes]
rs1847201	0.88[EUR][1000 genomes]
rs2047797	0.88[EUR][1000 genomes]
rs2134423	0.89[EUR][1000 genomes]
rs2134424	0.89[EUR][1000 genomes]
rs2221313	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28577259	0.92[EUR][1000 genomes]
rs28713322	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2881907	0.88[EUR][1000 genomes]
rs35903720	0.88[EUR][1000 genomes]
rs3929449	0.91[EUR][1000 genomes]
rs4303932	0.88[EUR][1000 genomes]
rs4303935	0.88[EUR][1000 genomes]
rs4328868	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4346600	0.91[EUR][1000 genomes]
rs4383572	0.87[EUR][1000 genomes]
rs4499662	0.92[EUR][1000 genomes]
rs4536877	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4550866	0.89[EUR][1000 genomes]
rs4579071	0.84[ASN][1000 genomes]
rs4579072	0.88[EUR][1000 genomes]
rs4610292	0.92[EUR][1000 genomes]
rs4613519	0.91[EUR][1000 genomes]
rs4618267	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4690953	0.85[EUR][1000 genomes]
rs4691581	0.81[ASN][1000 genomes]
rs4691589	0.84[EUR][1000 genomes]
rs4691593	0.87[EUR][1000 genomes]
rs4691594	0.89[EUR][1000 genomes]
rs4691595	0.89[EUR][1000 genomes]
rs4691596	0.89[EUR][1000 genomes]
rs4691600	0.85[EUR][1000 genomes]
rs6536449	0.81[EUR][1000 genomes]
rs67111572	0.88[EUR][1000 genomes]
rs6826570	0.91[EUR][1000 genomes]
rs7675005	0.83[EUR][1000 genomes]
rs7677200	0.82[EUR][1000 genomes]
rs7682849	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015469	chr4:160389277-160841619	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537316	chr4:160389277-160841619	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv881205	chr4:160516090-160628006	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160553600-160576200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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