Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1330943	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs178345	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap]
rs1888743	0.95[JPT][hapmap]
rs2134802	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2348563	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs2781300	0.83[ASN][1000 genomes]
rs314527	0.88[ASN][1000 genomes]
rs314533	1.00[CEU][hapmap];0.96[CHB][hapmap];0.95[JPT][hapmap]
rs314537	0.80[ASN][1000 genomes]
rs314538	0.80[ASN][1000 genomes]
rs314539	0.80[ASN][1000 genomes]
rs314543	0.80[ASN][1000 genomes]
rs314545	0.80[ASN][1000 genomes]
rs314546	0.80[ASN][1000 genomes]
rs314547	0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs314548	0.96[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs314549	1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs314554	1.00[CEU][hapmap];0.91[CHB][hapmap];0.96[JPT][hapmap]
rs314560	0.80[ASN][1000 genomes]
rs314566	0.81[ASN][1000 genomes]
rs314569	0.85[ASN][1000 genomes]
rs314571	0.96[CHB][hapmap];0.96[JPT][hapmap]
rs314577	0.88[ASN][1000 genomes]
rs366604	0.81[ASN][1000 genomes]
rs3803211	1.00[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap]
rs411403	0.82[ASN][1000 genomes]
rs6492421	0.80[ASN][1000 genomes]
rs7335516	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9522473	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs9560285	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9560295	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs9588553	0.95[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915862	chr13:89408920-90118030	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1040210	chr13:89584630-90156186	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1048574	chr13:89650680-90232894	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv832676	chr13:89941212-90090424	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv900859	chr13:89944833-90036166	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr13:89961000-89961400	Enhancers	Fetal Heart	heart

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