Variant report

Variant	rs6709865
Chromosome Location	chr2:50669861-50669862
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10048731	1.00[CEU][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1005431	0.91[CEU][hapmap];0.84[JPT][hapmap];0.94[MEX][hapmap];0.89[TSI][hapmap];0.92[EUR][1000 genomes]
rs10181475	0.91[EUR][1000 genomes]
rs10181522	0.85[GIH][hapmap];0.83[TSI][hapmap];0.85[EUR][1000 genomes]
rs10182951	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10190857	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10205311	0.85[EUR][1000 genomes]
rs10209627	0.81[EUR][1000 genomes]
rs11125306	1.00[CEU][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12473243	0.95[CEU][hapmap];0.91[CHB][hapmap];0.89[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12475335	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12613343	0.95[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12619946	0.86[CEU][hapmap];0.91[CHB][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12620045	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12713100	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12994492	0.85[GIH][hapmap]
rs13014251	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13032292	0.82[EUR][1000 genomes]
rs13032775	0.81[EUR][1000 genomes]
rs13390864	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13392422	0.85[GIH][hapmap];0.86[TSI][hapmap]
rs13396103	1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.97[TSI][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13407013	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13407657	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[CHD][hapmap];0.90[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13407788	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13430295	0.80[TSI][hapmap]
rs1402124	0.86[TSI][hapmap]
rs1520437	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1520438	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1520439	1.00[CEU][hapmap];0.91[CHB][hapmap];0.81[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.97[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1533692	0.88[EUR][1000 genomes]
rs17040600	0.85[GIH][hapmap];0.86[TSI][hapmap]
rs17040640	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1818715	0.83[TSI][hapmap]
rs1818716	0.80[TSI][hapmap]
rs1851012	0.95[CEU][hapmap];0.91[CHB][hapmap];0.89[JPT][hapmap]
rs1971698	0.92[EUR][1000 genomes]
rs2160443	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs34846571	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57564327	0.82[EUR][1000 genomes]
rs6711307	0.95[CEU][hapmap];0.91[CHB][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.81[MKK][hapmap];0.97[TSI][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6717441	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6718809	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6738086	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6743117	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6743562	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6743584	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6744418	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6747128	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6747258	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6756081	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6756219	0.95[CEU][hapmap];0.91[CHB][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];0.94[MEX][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6756479	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7423850	1.00[CEU][hapmap];0.91[CHB][hapmap];0.89[JPT][hapmap]
rs7585229	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7585534	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9309182	1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.81[LWK][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.85[AMR][1000 genomes];0.97[EUR][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	nsv492164	chr2:50399251-51029090	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1000653	chr2:50417660-51083470	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv535693	chr2:50417660-51083470	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv948548	chr2:50569117-50695100	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv948361	chr2:50611076-50785178	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv933786	chr2:50628354-50780185	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1010510	chr2:50649641-51011565	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv535694	chr2:50649641-51011565	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50665000-50670400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr2:50666400-50671000	Weak transcription	Brain Germinal Matrix	brain
3	chr2:50669600-50673000	Enhancers	Hela-S3	cervix

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