Variant report

Variant	rs7017687
Chromosome Location	chr8:104883379-104883380
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:104776221..104777249-chr8:104883194..104884184,4	MCF-7	breast:
2	chr8:104719474..104720086-chr8:104883273..104884095,3	MCF-7	breast:
3	chr8:104720101..104721082-chr8:104883258..104883794,2	MCF-7	breast:
4	chr8:104807612..104809857-chr8:104883134..104884151,8	MCF-7	breast:
5	chr8:104788640..104789427-chr8:104883229..104884125,2	MCF-7	breast:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12114257	1.00[AMR][1000 genomes]
rs12115119	1.00[AMR][1000 genomes]
rs55738066	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56773931	1.00[AMR][1000 genomes]
rs58032159	1.00[AMR][1000 genomes]
rs60299412	1.00[AMR][1000 genomes]
rs60412815	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60552383	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61042766	1.00[AMR][1000 genomes]
rs61589769	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6990477	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6993163	1.00[AMR][1000 genomes]
rs7004346	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7006816	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7018117	0.89[AFR][1000 genomes]
rs73697653	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697657	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697662	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697668	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697673	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697683	1.00[AMR][1000 genomes]
rs73697684	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697688	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697690	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697694	1.00[AMR][1000 genomes]
rs73697695	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697696	1.00[AMR][1000 genomes]
rs73697698	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7826206	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7841801	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9918740	0.89[AFR][1000 genomes];1.00[AMR][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	nsv1020476	chr8:104312212-104924482	Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv539704	chr8:104312212-104924482	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	esv2752692	chr8:104520824-105123824	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1016387	chr8:104578389-104931853	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1031195	chr8:104601231-105194208	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
6	esv1841024	chr8:104872512-104908099	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 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	chr8:104859400-104897200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:104882400-104884200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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