Variant report

Variant	rs11763966
Chromosome Location	chr7:119919905-119919906
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	chr7:119918513..119920126-chr7:119921372..119923072,2	K562	blood:
2	chr7:119915799..119917690-chr7:119919772..119921442,2	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10488286	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11487122	0.90[ASN][1000 genomes]
rs11760262	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11767260	0.99[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs11768610	0.95[ASN][1000 genomes]
rs11769340	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11773232	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11982510	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17374849	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17594101	0.80[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs17594220	0.95[ASN][1000 genomes]
rs34850246	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55680276	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55963403	0.88[ASN][1000 genomes]
rs56244901	0.90[ASN][1000 genomes]
rs62469500	0.83[ASN][1000 genomes]
rs62469501	0.83[ASN][1000 genomes]
rs62469503	0.90[ASN][1000 genomes]
rs62469505	0.90[ASN][1000 genomes]
rs62469506	0.90[ASN][1000 genomes]
rs62469507	0.90[ASN][1000 genomes]
rs62470461	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62470532	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62470539	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6466742	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6942451	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6942755	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6969916	0.90[ASN][1000 genomes]
rs6978586	0.95[ASN][1000 genomes]
rs73213448	0.83[ASN][1000 genomes]
rs73213458	0.95[ASN][1000 genomes]
rs7777091	0.83[ASN][1000 genomes]
rs7786492	0.83[ASN][1000 genomes]
rs7800545	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv608326	chr7:119828331-119995890	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv1843078	chr7:119909603-119934006	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119914600-119920200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:119914600-119921000	Weak transcription	Ovary	ovary
3	chr7:119916000-119920000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:119916200-119922400	Active TSS	GM12878-XiMat	blood

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