Variant report

Variant	rs1647941
Chromosome Location	chr11:85165731-85165732
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:85165504..85168134-chr11:85173876..85175824,2	MCF-7	breast:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs11604028	0.81[EUR][1000 genomes]
rs11607685	0.83[EUR][1000 genomes]
rs1213236	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1354397	0.81[ASN][1000 genomes]
rs1504027	0.81[EUR][1000 genomes]
rs158217	0.83[EUR][1000 genomes]
rs166977	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1793210	0.84[ASN][1000 genomes]
rs1806414	0.83[EUR][1000 genomes]
rs184057	0.83[EUR][1000 genomes]
rs185932	0.83[EUR][1000 genomes]
rs190813	0.86[ASN][1000 genomes]
rs1954757	0.83[EUR][1000 genomes]
rs207060	0.83[EUR][1000 genomes]
rs2113920	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2433016	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2512800	0.83[EUR][1000 genomes]
rs286044	0.86[ASN][1000 genomes]
rs286494	0.83[EUR][1000 genomes]
rs286497	0.82[ASN][1000 genomes]
rs286509	0.83[EUR][1000 genomes]
rs286512	0.83[EUR][1000 genomes]
rs286513	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs286515	0.98[ASN][1000 genomes]
rs286516	0.87[ASN][1000 genomes]
rs286521	0.83[EUR][1000 genomes]
rs286522	0.83[EUR][1000 genomes]
rs286524	0.83[EUR][1000 genomes]
rs286525	0.83[EUR][1000 genomes]
rs286531	0.83[EUR][1000 genomes]
rs286534	0.83[EUR][1000 genomes]
rs286537	0.83[EUR][1000 genomes]
rs286538	0.83[EUR][1000 genomes]
rs286539	0.83[EUR][1000 genomes]
rs286540	0.83[EUR][1000 genomes]
rs286541	0.81[EUR][1000 genomes]
rs2930575	0.82[ASN][1000 genomes]
rs35097455	0.83[EUR][1000 genomes]
rs4943918	0.95[ASN][1000 genomes]
rs4944516	0.95[ASN][1000 genomes]
rs56073783	0.83[EUR][1000 genomes]
rs56238215	0.83[EUR][1000 genomes]
rs57223077	0.83[EUR][1000 genomes]
rs60838923	0.83[EUR][1000 genomes]
rs61286868	0.83[EUR][1000 genomes]
rs62388	0.83[EUR][1000 genomes]
rs7104879	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7108137	0.83[EUR][1000 genomes]
rs7110363	0.93[ASN][1000 genomes]
rs7116340	0.89[ASN][1000 genomes]
rs7122822	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7130198	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7939217	0.83[EUR][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	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv898044	chr11:84895033-85220773	ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
4	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	nsv898045	chr11:85094601-85168570	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1035905	chr11:85130543-85220773	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv1050363	chr11:85163437-85293233	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv541111	chr11:85163437-85293233	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85163600-85173800	Weak transcription	Left Ventricle	heart

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