Variant report

Variant	rs7655160
Chromosome Location	chr4:160536978-160536979
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10012657	0.90[ASN][1000 genomes]
rs10033206	0.90[ASN][1000 genomes]
rs10517699	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10517704	0.94[ASN][1000 genomes]
rs1105951	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11730807	0.85[AMR][1000 genomes]
rs11929746	0.93[ASN][1000 genomes]
rs11930091	0.96[ASN][1000 genomes]
rs11934172	0.93[ASN][1000 genomes]
rs11934253	0.93[ASN][1000 genomes]
rs11934257	0.93[ASN][1000 genomes]
rs11935849	0.96[ASN][1000 genomes]
rs11942089	0.94[ASN][1000 genomes]
rs11943118	0.93[ASN][1000 genomes]
rs11943190	0.93[ASN][1000 genomes]
rs11943255	0.93[ASN][1000 genomes]
rs11946960	0.93[ASN][1000 genomes]
rs12331504	0.96[ASN][1000 genomes]
rs12499316	0.87[EUR][1000 genomes]
rs12641842	0.82[AMR][1000 genomes]
rs12641886	0.82[AMR][1000 genomes]
rs12647153	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12648608	0.88[EUR][1000 genomes]
rs12711318	0.82[EUR][1000 genomes]
rs13103444	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13112184	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13119461	0.93[ASN][1000 genomes]
rs13127518	0.94[ASN][1000 genomes]
rs13135870	0.94[ASN][1000 genomes]
rs13137527	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13138857	0.81[AMR][1000 genomes]
rs13141299	0.93[ASN][1000 genomes]
rs13143542	0.96[ASN][1000 genomes]
rs13144697	0.94[ASN][1000 genomes]
rs13340212	0.80[AMR][1000 genomes]
rs13340269	0.80[AMR][1000 genomes]
rs1502721	0.90[ASN][1000 genomes]
rs1502742	0.86[EUR][1000 genomes]
rs1502743	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1604579	0.94[ASN][1000 genomes]
rs1847201	0.81[AMR][1000 genomes]
rs2088978	0.93[ASN][1000 genomes]
rs2088979	0.93[ASN][1000 genomes]
rs2102180	0.93[ASN][1000 genomes]
rs28797928	0.93[ASN][1000 genomes]
rs28815883	0.93[ASN][1000 genomes]
rs34078024	0.96[ASN][1000 genomes]
rs34493942	0.96[ASN][1000 genomes]
rs35134080	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35720115	0.94[ASN][1000 genomes]
rs35894513	0.96[ASN][1000 genomes]
rs4499661	0.85[EUR][1000 genomes]
rs4579071	0.82[EUR][1000 genomes]
rs4691581	0.81[EUR][1000 genomes]
rs4691582	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4691584	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4691589	0.80[AMR][1000 genomes]
rs4691593	0.82[AMR][1000 genomes]
rs4691597	0.86[EUR][1000 genomes]
rs5013975	0.85[EUR][1000 genomes]
rs62337280	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6536449	0.96[ASN][1000 genomes]
rs6811908	0.93[ASN][1000 genomes]
rs6828419	0.93[ASN][1000 genomes]
rs6833693	0.93[ASN][1000 genomes]
rs6834320	0.93[ASN][1000 genomes]
rs6835283	0.91[ASN][1000 genomes]
rs6835542	0.93[ASN][1000 genomes]
rs6849152	0.86[ASN][1000 genomes]
rs6852085	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6855621	0.86[ASN][1000 genomes]
rs7659355	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7677200	0.83[ASN][1000 genomes]
rs871419	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9990633	0.94[ASN][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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160536200-160537400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:160536400-160537000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
3	chr4:160536400-160537000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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