Variant report

Variant	rs7780623
Chromosome Location	chr7:147708432-147708433
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10261595	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10261693	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10264988	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10269138	0.81[EUR][1000 genomes]
rs10269250	0.81[EUR][1000 genomes]
rs10269257	0.81[EUR][1000 genomes]
rs10270437	0.81[AFR][1000 genomes]
rs10270778	0.81[AFR][1000 genomes]
rs10273493	0.93[AFR][1000 genomes]
rs10276996	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10279557	0.88[AFR][1000 genomes]
rs11972972	0.93[AFR][1000 genomes]
rs11974390	0.87[AFR][1000 genomes]
rs11976838	0.91[AFR][1000 genomes]
rs12539425	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12540218	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13225246	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13228553	0.92[ASN][1000 genomes]
rs13236734	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17170792	0.90[ASN][1000 genomes]
rs17170793	0.90[ASN][1000 genomes]
rs17170794	0.90[ASN][1000 genomes]
rs28377968	0.87[AFR][1000 genomes]
rs28394241	0.87[AFR][1000 genomes]
rs28554472	0.87[AFR][1000 genomes]
rs28594409	0.87[AFR][1000 genomes]
rs28693625	0.81[AFR][1000 genomes]
rs34024797	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34378091	0.90[ASN][1000 genomes]
rs34910390	0.92[ASN][1000 genomes]
rs34987081	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35100395	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35294118	0.97[ASN][1000 genomes]
rs35631331	0.92[ASN][1000 genomes]
rs36041591	0.90[ASN][1000 genomes]
rs57783871	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58092267	0.93[AFR][1000 genomes]
rs58526779	0.93[AFR][1000 genomes]
rs58848818	0.86[AFR][1000 genomes]
rs60119393	0.89[AFR][1000 genomes]
rs60692572	0.92[AFR][1000 genomes]
rs62473287	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62473289	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62473290	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6955458	0.89[ASN][1000 genomes]
rs6970931	0.86[AFR][1000 genomes]
rs719310	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs719311	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs719312	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73464297	0.81[AFR][1000 genomes]
rs73466110	0.87[AFR][1000 genomes]
rs73466115	0.85[AFR][1000 genomes]
rs73466190	0.86[AFR][1000 genomes]
rs7781064	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]

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:1 , 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

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