Variant report

Variant	rs10457002
Chromosome Location	chr6:133388232-133388233
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10457001	0.81[ASN][1000 genomes]
rs10457599	0.81[ASN][1000 genomes]
rs10457600	0.82[EUR][1000 genomes]
rs12192002	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12192605	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12193118	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12194836	0.81[ASN][1000 genomes]
rs12197849	0.81[ASN][1000 genomes]
rs12198619	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12199138	0.82[EUR][1000 genomes]
rs12199972	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12205139	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12210093	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12212715	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12213350	0.82[EUR][1000 genomes]
rs12213452	0.82[EUR][1000 genomes]
rs12215217	0.82[EUR][1000 genomes]
rs28538690	0.89[EUR][1000 genomes]
rs4077767	0.96[EUR][1000 genomes]
rs4077768	0.92[EUR][1000 genomes]
rs4257872	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4273707	0.90[EUR][1000 genomes]
rs4273708	0.90[EUR][1000 genomes]
rs4895949	0.83[ASN][1000 genomes]
rs4895952	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57161827	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58835706	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62428455	0.81[ASN][1000 genomes]
rs62428563	0.81[EUR][1000 genomes]
rs62430561	0.83[ASN][1000 genomes]
rs62430562	0.96[EUR][1000 genomes]
rs62430580	0.86[EUR][1000 genomes]
rs62430581	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62430582	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62430588	0.90[EUR][1000 genomes]
rs62430590	0.90[EUR][1000 genomes]
rs6569863	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6902225	0.84[EUR][1000 genomes]
rs6902347	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6908361	0.81[ASN][1000 genomes]
rs6911954	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6915521	0.83[ASN][1000 genomes]
rs6927627	0.90[EUR][1000 genomes]
rs6933214	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6935070	0.90[EUR][1000 genomes]
rs6935480	0.90[EUR][1000 genomes]
rs6935677	0.83[ASN][1000 genomes]
rs6936410	0.90[EUR][1000 genomes]
rs6937029	0.90[EUR][1000 genomes]
rs6939899	0.96[EUR][1000 genomes]
rs6940959	0.90[EUR][1000 genomes]
rs72557636	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7738156	0.90[EUR][1000 genomes]
rs7738592	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7745056	0.81[ASN][1000 genomes]
rs7750279	0.81[EUR][1000 genomes]
rs7756171	0.90[CHB][hapmap];0.95[EUR][1000 genomes]
rs7756963	0.81[EUR][1000 genomes]
rs7761372	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9321388	0.96[EUR][1000 genomes]
rs9321389	0.96[EUR][1000 genomes]
rs9483529	0.90[EUR][1000 genomes]
rs9483530	0.90[EUR][1000 genomes]
rs9483535	0.93[EUR][1000 genomes]
rs9493513	0.88[EUR][1000 genomes]
rs9493514	0.82[EUR][1000 genomes]
rs9493515	0.90[EUR][1000 genomes]
rs9493517	0.90[EUR][1000 genomes]
rs9493518	0.90[EUR][1000 genomes]
rs957183	0.81[EUR][1000 genomes]
rs975225	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9791374	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv428154	chr6:133271975-133522803	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	esv3445931	chr6:133347824-133434532	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv519475	chr6:133350936-133474673	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133384400-133388600	Weak transcription	Fetal Heart	heart

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