Variant report

Variant	rs11130714
Chromosome Location	chr3:59492652-59492653
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10510812	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs11130713	0.89[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs11923741	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11925209	0.98[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs11925279	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12486826	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12487257	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12489949	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12492287	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12492308	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12493195	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17275189	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17275950	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4679487	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56197311	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56963895	0.84[AFR][1000 genomes]
rs57042572	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs58664036	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs60365449	0.89[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs60476036	0.96[ASN][1000 genomes]
rs73837348	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73837355	0.93[AMR][1000 genomes];0.85[EUR][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	nsv1011181	chr3:58665373-59542339	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv536574	chr3:58665373-59542339	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv534257	chr3:58855959-59606464	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv998676	chr3:59485915-59519363	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr3:59491200-59492800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr3:59492400-59501000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr3:59492600-59496400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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