Variant report

Variant	rs73453052
Chromosome Location	chr7:145502176-145502177
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:145490921..145492885-chr7:145501378..145504321,2	K562	blood:
2	chr7:145496261..145498317-chr7:145500912..145502935,2	K562	blood:
3	chr7:145499268..145500796-chr7:145500851..145503015,2	K562	blood:
4	chr7:145500763..145502459-chr7:145504004..145505820,2	K562	blood:

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs11489480	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12111803	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12112908	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56926166	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57727563	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58978891	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60764366	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61016174	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6951352	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6951353	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6954391	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6954396	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6954685	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6954857	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6958710	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6959043	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6960168	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6960960	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6962759	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6971359	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6973173	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451004	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451006	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451019	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451020	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451022	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451034	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451035	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451038	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451040	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451041	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451043	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451047	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451048	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451056	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451059	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451061	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451063	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451067	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451073	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451076	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73453053	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73453057	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73453075	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73453076	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73456911	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73456916	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73456929	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73456936	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73456974	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73456984	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73456994	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73458806	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73458810	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73458865	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73458867	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73465701	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467313	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467316	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467317	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467318	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467322	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467324	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467325	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467326	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467331	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467335	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467337	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467361	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467362	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467365	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467367	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467370	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73467373	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7778402	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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	nsv889383	chr7:145396141-145549570	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv831182	chr7:145399806-145556489	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	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
6	nsv966740	chr7:145499697-145511328	Weak transcription	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	chr7:145495400-145511400	Weak transcription	K562	blood

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