Variant report

Variant	rs7763022
Chromosome Location	chr6:54245857-54245858
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:54239793..54241712-chr6:54244311..54245976,2	MCF-7	breast:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10080851	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1508634	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1508635	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17755505	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17828461	0.80[ASN][1000 genomes]
rs17828521	0.84[EUR][1000 genomes]
rs3736352	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3736353	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3777636	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3822894	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs41413844	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55868486	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56257351	0.81[EUR][1000 genomes]
rs57614124	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57677324	0.80[ASN][1000 genomes]
rs61162221	0.84[EUR][1000 genomes]
rs6902402	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6907037	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72965255	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7739948	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7746042	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7758586	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7767253	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9296755	0.82[ASN][1000 genomes]
rs9370292	0.88[ASN][1000 genomes]
rs9382330	0.88[ASN][1000 genomes]
rs9395950	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9464067	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9464068	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9464070	0.88[ASN][1000 genomes]
rs9474815	0.81[ASN][1000 genomes]
rs9474821	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9474827	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9474829	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9474831	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs949469	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067663	chr6:53796341-54449718	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv529158	chr6:53796341-54449718	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv885888	chr6:54132353-54266032	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3369021	chr6:54244893-54247041	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54211800-54256200	Weak transcription	Fetal Intestine Large	intestine
2	chr6:54212000-54257400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr6:54243000-54250800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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