Variant report

Variant	rs55764478
Chromosome Location	chr7:145633744-145633745
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:145633292..145636880-chr7:145639535..145641924,3	K562	blood:

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10224199	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10271223	0.80[ASN][1000 genomes]
rs10271257	0.80[ASN][1000 genomes]
rs10458274	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11972095	0.95[ASN][1000 genomes]
rs11972487	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11975240	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11975868	0.90[ASN][1000 genomes]
rs11977340	0.93[ASN][1000 genomes]
rs11977410	0.93[ASN][1000 genomes]
rs11982943	0.88[ASN][1000 genomes]
rs12112237	0.92[ASN][1000 genomes]
rs12154288	0.93[ASN][1000 genomes]
rs12666281	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12674186	0.83[ASN][1000 genomes]
rs12703750	0.83[ASN][1000 genomes]
rs1523733	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17169902	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2177748	0.93[ASN][1000 genomes]
rs2372461	0.88[ASN][1000 genomes]
rs28687396	0.83[ASN][1000 genomes]
rs28860008	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4436045	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4534070	0.92[ASN][1000 genomes]
rs55637642	0.93[ASN][1000 genomes]
rs55844645	0.93[ASN][1000 genomes]
rs55910573	0.93[ASN][1000 genomes]
rs56051867	0.93[ASN][1000 genomes]
rs56055653	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56067475	0.83[ASN][1000 genomes]
rs56107552	0.93[ASN][1000 genomes]
rs56198146	0.93[ASN][1000 genomes]
rs56662540	0.85[ASN][1000 genomes]
rs56747015	0.92[ASN][1000 genomes]
rs56775210	0.85[ASN][1000 genomes]
rs57679157	0.95[ASN][1000 genomes]
rs58456605	0.95[ASN][1000 genomes]
rs58546376	0.95[ASN][1000 genomes]
rs58869616	0.92[ASN][1000 genomes]
rs59450195	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61044500	0.90[ASN][1000 genomes]
rs61593228	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6464704	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6946087	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6952571	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs6954312	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6954634	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6956829	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs6960698	0.93[ASN][1000 genomes]
rs6966233	0.85[ASN][1000 genomes]
rs6969543	0.83[ASN][1000 genomes]
rs6978472	0.92[ASN][1000 genomes]
rs6978905	0.92[ASN][1000 genomes]
rs73458832	0.83[ASN][1000 genomes]
rs7781219	0.95[ASN][1000 genomes]
rs7785512	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7788691	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7792245	1.00[ASN][1000 genomes]
rs7795695	0.82[ASN][1000 genomes]
rs7802089	0.85[ASN][1000 genomes]
rs7805756	0.83[ASN][1000 genomes]
rs7805880	0.83[ASN][1000 genomes]
rs7808969	0.83[ASN][1000 genomes]
rs949729	0.93[ASN][1000 genomes]
rs9655578	0.83[EUR][1000 genomes]
rs9655683	0.83[ASN][1000 genomes]
rs9918491	0.82[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	esv2754040	chr7:145303352-145698352	Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2755386	chr7:145303352-145698352	Genic enhancers Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1019118	chr7:145483353-145639795	Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv889384	chr7:145541783-146239545	Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1023861	chr7:145606069-145910049	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv539170	chr7:145606069-145910049	Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv889385	chr7:145617629-145803095	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr7:145630000-145634800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr7:145630000-145634800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr7:145630000-145635000	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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