Variant report

Variant	rs73702325
Chromosome Location	chr8:111703251-111703252
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	chr8:111689286..111692174-chr8:111701872..111704181,2	MCF-7	breast:
2	chr8:111702766..111704836-chr8:111705809..111708776,2	MCF-7	breast:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10505150	1.00[EUR][1000 genomes]
rs16880962	1.00[EUR][1000 genomes]
rs16880978	1.00[EUR][1000 genomes]
rs28548303	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28562519	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56144217	1.00[EUR][1000 genomes]
rs56409630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61260614	1.00[EUR][1000 genomes]
rs73700909	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73700910	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73700911	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73700913	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73700914	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702315	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702316	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702317	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702741	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702762	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702869	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702873	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702874	1.00[EUR][1000 genomes]
rs73702875	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702918	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7828396	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv611882	chr8:111342240-111722469	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1031119	chr8:111367939-111720763	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv831422	chr8:111578949-111755170	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv1027659	chr8:111585843-111875753	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1025390	chr8:111605571-111806020	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv539718	chr8:111605571-111806020	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv831423	chr8:111672801-111869818	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	esv1817780	chr8:111694657-111711197	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
9	esv1851720	chr8:111694657-111754075	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111699800-111704400	Weak transcription	Fetal Intestine Small	intestine
2	chr8:111702800-111703400	Enhancers	Primary hematopoietic stem cells short term culture	blood

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