Variant report

Variant	rs7081603
Chromosome Location	chr10:96155978-96155979
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:96154206..96156824-chr10:96158509..96161283,2	MCF-7	breast:
2	chr10:96153074..96157080-chr10:96161760..96164291,4	MCF-7	breast:
3	chr10:96122264..96123877-chr10:96154739..96156763,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000173145	Chromatin interaction
ENSG00000108239	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11187855	1.00[AMR][1000 genomes]
rs11187898	1.00[AMR][1000 genomes]
rs11187954	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11188002	1.00[AMR][1000 genomes]
rs11188029	1.00[AMR][1000 genomes]
rs11188035	1.00[AMR][1000 genomes]
rs12243492	1.00[AMR][1000 genomes]
rs12243849	1.00[AMR][1000 genomes]
rs12246731	0.90[AFR][1000 genomes]
rs12247370	0.82[AFR][1000 genomes]
rs12249578	1.00[AMR][1000 genomes]
rs12249709	1.00[AMR][1000 genomes]
rs12250011	1.00[AMR][1000 genomes]
rs12250480	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12254178	1.00[AMR][1000 genomes]
rs12256637	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12259382	1.00[AMR][1000 genomes]
rs12260069	0.87[AFR][1000 genomes]
rs12266679	1.00[AMR][1000 genomes]
rs12266908	1.00[AMR][1000 genomes]
rs12269029	1.00[AMR][1000 genomes]
rs2244404	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57412910	1.00[AMR][1000 genomes]
rs58324538	0.86[AFR][1000 genomes]
rs60996053	1.00[AMR][1000 genomes]
rs6583938	1.00[AMR][1000 genomes]
rs7067896	1.00[AMR][1000 genomes]
rs7082254	1.00[AMR][1000 genomes]
rs7092239	0.81[AFR][1000 genomes]
rs73321857	1.00[AMR][1000 genomes]
rs73323523	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73323528	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73327425	0.81[AFR][1000 genomes]
rs73327452	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73327462	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73327472	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73327486	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73327491	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73327495	1.00[AMR][1000 genomes]
rs73329611	1.00[AMR][1000 genomes]
rs7907525	1.00[AMR][1000 genomes]
rs9665608	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761616	chr10:95966768-96303701	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv831946	chr10:96055190-96226438	Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	esv1819509	chr10:96064300-96361776	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	esv3398177	chr10:96139011-96169931	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	esv3411992	chr10:96139011-96172041	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	nsv551947	chr10:96154267-96162969	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
8	nsv551948	chr10:96154267-96163020	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 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	chr10:96155800-96156200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr10:96155800-96157200	Weak transcription	HepG2	liver
3	chr10:96155800-96161800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:96155800-96162000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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