Variant report

Variant	rs6731674
Chromosome Location	chr2:186300310-186300311
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs11675192	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11675629	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11676655	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11681517	0.94[EUR][1000 genomes]
rs11681870	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11683123	0.94[EUR][1000 genomes]
rs11686018	0.85[EUR][1000 genomes]
rs11686861	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11691490	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11691615	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11691687	0.87[EUR][1000 genomes]
rs11691944	0.87[EUR][1000 genomes]
rs11693233	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11695761	0.87[EUR][1000 genomes]
rs12988744	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12991386	0.85[EUR][1000 genomes]
rs13002265	0.94[EUR][1000 genomes]
rs13007661	0.94[EUR][1000 genomes]
rs13011116	0.94[EUR][1000 genomes]
rs13014616	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13014885	0.90[ASN][1000 genomes]
rs13015041	0.94[EUR][1000 genomes]
rs13015110	0.90[ASN][1000 genomes]
rs13030807	0.86[EUR][1000 genomes]
rs17206943	0.85[EUR][1000 genomes]
rs17331619	0.90[ASN][1000 genomes]
rs17331682	0.90[ASN][1000 genomes]
rs17403498	0.90[ASN][1000 genomes]
rs17403547	0.90[ASN][1000 genomes]
rs17403638	0.90[ASN][1000 genomes]
rs34000575	0.88[EUR][1000 genomes]
rs34087779	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34093449	0.88[EUR][1000 genomes]
rs34113655	0.88[EUR][1000 genomes]
rs34152682	0.94[EUR][1000 genomes]
rs34191961	0.88[EUR][1000 genomes]
rs34221764	0.88[EUR][1000 genomes]
rs34420134	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34449658	0.88[EUR][1000 genomes]
rs34537855	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34571837	0.94[EUR][1000 genomes]
rs34661485	0.94[EUR][1000 genomes]
rs34826735	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34877204	0.87[EUR][1000 genomes]
rs34879834	0.88[EUR][1000 genomes]
rs34969380	0.88[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35047001	0.88[EUR][1000 genomes]
rs35062319	0.88[EUR][1000 genomes]
rs35066265	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35110878	0.84[EUR][1000 genomes]
rs35165452	0.88[EUR][1000 genomes]
rs35201815	0.94[EUR][1000 genomes]
rs35207414	0.94[EUR][1000 genomes]
rs35289321	0.88[EUR][1000 genomes]
rs35320505	0.83[EUR][1000 genomes]
rs35537030	0.88[EUR][1000 genomes]
rs35630311	0.90[ASN][1000 genomes]
rs35638932	0.88[EUR][1000 genomes]
rs35781787	0.88[EUR][1000 genomes]
rs35815004	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35847686	0.88[EUR][1000 genomes]
rs35871462	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35920523	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36012390	0.94[EUR][1000 genomes]
rs36065595	0.94[EUR][1000 genomes]
rs61459829	0.88[EUR][1000 genomes]
rs66508949	0.88[EUR][1000 genomes]
rs66759141	0.90[ASN][1000 genomes]
rs66941454	0.90[ASN][1000 genomes]
rs67035495	0.93[EUR][1000 genomes]
rs6708098	0.91[EUR][1000 genomes]
rs6739732	0.94[EUR][1000 genomes]
rs67432566	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67629903	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67638453	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67784166	0.94[EUR][1000 genomes]
rs67992386	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71430186	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71432404	0.83[EUR][1000 genomes]
rs72892419	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72892423	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72892438	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72892443	0.90[ASN][1000 genomes]
rs72896456	0.94[EUR][1000 genomes]
rs7556993	0.88[EUR][1000 genomes]
rs7599251	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv584009	chr2:186203397-186345148	Active TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv459982	chr2:186213755-186475590	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv584012	chr2:186213755-186475590	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv875525	chr2:186223503-186434458	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv470502	chr2:186245653-186309738	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv459983	chr2:186245653-186377253	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv584013	chr2:186245653-186377253	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv875526	chr2:186272059-186434458	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv875527	chr2:186272059-186475590	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv459985	chr2:186293335-186422662	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv584014	chr2:186293335-186422662	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv459986	chr2:186297074-186413124	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv584015	chr2:186297074-186413124	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186298200-186315800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:186298600-186300400	Active TSS	HMEC	breast
3	chr2:186298600-186315800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:186298800-186314800	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:186299200-186301400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr2:186300000-186301600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:186300000-186302200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:186300200-186300800	Weak transcription	NHEK	skin

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