Variant report

Variant	rs7832671
Chromosome Location	chr8:122446747-122446748
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:122437593..122440678-chr8:122446025..122448409,3	MCF-7	breast:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10094084	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10107573	0.82[EUR][1000 genomes]
rs10481070	0.86[ASN][1000 genomes]
rs10481147	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10505401	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10956035	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10956038	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10956039	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10956040	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11993674	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12545486	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13265234	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13265478	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13267289	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13269889	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1386442	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1487158	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1487170	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2046570	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2385927	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2891939	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4144692	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4282581	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6469998	0.82[EUR][1000 genomes]
rs6470000	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6985415	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6988724	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7004666	0.81[ASN][1000 genomes]
rs7006642	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7006650	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7008446	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7008769	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7015873	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7017097	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73332335	0.92[ASN][1000 genomes]
rs7824421	0.82[EUR][1000 genomes]
rs7824450	0.82[EUR][1000 genomes]
rs7838314	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7846340	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9643156	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs982818	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][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	nsv831445	chr8:122336877-122509300	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv465793	chr8:122405097-122452320	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
3	nsv612132	chr8:122405097-122452320	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv891427	chr8:122411349-122472297	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv527877	chr8:122426082-122472297	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv1033501	chr8:122436332-122758651	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:122444200-122448600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr8:122444600-122447800	Weak transcription	Fetal Muscle Leg	muscle

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