Variant report

Variant	rs719312
Chromosome Location	chr7:147708820-147708821
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10227736	1.00[CEU][hapmap]
rs10229688	1.00[CEU][hapmap]
rs10253762	1.00[CEU][hapmap]
rs10261595	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10261693	0.94[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10264988	0.93[ASN][1000 genomes]
rs10269138	1.00[CEU][hapmap]
rs10269257	1.00[CEU][hapmap]
rs10276996	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10281326	1.00[CEU][hapmap]
rs10452891	1.00[CEU][hapmap]
rs10485853	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10500194	1.00[CEU][hapmap]
rs12530525	1.00[CEU][hapmap]
rs12532080	1.00[CEU][hapmap]
rs12532103	1.00[CEU][hapmap]
rs12532213	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12536135	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12536614	1.00[CEU][hapmap]
rs12539425	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12539685	1.00[CEU][hapmap];0.95[JPT][hapmap];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12540014	1.00[CEU][hapmap]
rs12540049	1.00[CEU][hapmap];0.89[JPT][hapmap];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12540218	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12667420	1.00[CEU][hapmap];0.95[JPT][hapmap];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13225246	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13225250	1.00[CEU][hapmap]
rs13225815	1.00[CEU][hapmap]
rs13228312	1.00[CEU][hapmap];0.90[JPT][hapmap];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13228553	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13228704	1.00[CEU][hapmap]
rs13233277	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap]
rs13236734	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13236937	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13238527	1.00[CEU][hapmap]
rs17170767	1.00[CEU][hapmap]
rs17170789	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs17170792	0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17170793	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17170794	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2373278	1.00[CEU][hapmap]
rs2373280	1.00[CEU][hapmap]
rs2373286	1.00[CEU][hapmap]
rs34024797	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34378091	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34910390	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34987081	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35100395	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35294118	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35442317	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35631331	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36041591	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57783871	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62473287	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62473288	0.87[EUR][1000 genomes]
rs62473289	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62473290	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6947287	1.00[CEU][hapmap]
rs6947595	1.00[CEU][hapmap]
rs6955458	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6957073	1.00[CEU][hapmap];0.95[JPT][hapmap]
rs6962266	1.00[CEU][hapmap]
rs719310	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs719311	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7779961	0.85[JPT][hapmap]
rs7780623	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7781064	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7781680	0.80[JPT][hapmap]
rs7785350	0.85[JPT][hapmap]
rs7789579	1.00[CEU][hapmap]
rs7797584	1.00[CEU][hapmap]
rs7800075	0.85[JPT][hapmap]
rs7805706	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023913	chr7:147521075-147806318	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1026058	chr7:147521109-147783042	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv539179	chr7:147521109-147783042	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv934002	chr7:147521110-147807705	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1017610	chr7:147523752-147806427	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv889399	chr7:147643923-147712471	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv889400	chr7:147650411-147712471	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147708200-147709000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:147708600-147709200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:147708800-147709000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:147708800-147709200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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