Variant report

Variant	rs10770051
Chromosome Location	chr11:9669384-9669385
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:9647120..9648829-chr11:9667561..9670506,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10770049	0.95[ASN][1000 genomes]
rs10770050	0.93[ASN][1000 genomes]
rs10840277	0.94[ASN][1000 genomes]
rs10840283	0.86[EUR][1000 genomes]
rs10840284	0.86[EUR][1000 genomes]
rs10840286	0.87[EUR][1000 genomes]
rs11042457	0.89[EUR][1000 genomes]
rs11042462	1.00[EUR][1000 genomes]
rs11042464	0.89[EUR][1000 genomes]
rs11042466	0.83[EUR][1000 genomes]
rs11601008	0.99[EUR][1000 genomes]
rs11607321	0.88[EUR][1000 genomes]
rs11607776	0.94[EUR][1000 genomes]
rs11607900	0.99[EUR][1000 genomes]
rs12362879	0.89[EUR][1000 genomes]
rs12364089	0.95[EUR][1000 genomes]
rs12807017	0.93[EUR][1000 genomes]
rs1865557	0.82[ASN][1000 genomes]
rs2099465	0.83[ASN][1000 genomes]
rs35806232	1.00[EUR][1000 genomes]
rs36089180	0.95[EUR][1000 genomes]
rs4243950	0.95[ASN][1000 genomes]
rs4910486	0.93[EUR][1000 genomes]
rs4910487	0.86[EUR][1000 genomes]
rs7112156	0.81[ASN][1000 genomes]
rs7123629	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv896986	chr11:9636854-9679145	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv933855	chr11:9645441-10130519	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv1053369	chr11:9647837-9876054	Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv972945	chr11:9660423-9684250	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv553468	chr11:9667828-9827871	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv521528	chr11:9667917-9672214	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv526210	chr11:9669363-9672214	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9660600-9670400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr11:9666400-9669400	Weak transcription	Lung	lung
3	chr11:9666400-9670000	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr11:9667600-9670000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:9668000-9673200	Weak transcription	Small Intestine	intestine
6	chr11:9668000-9673200	Weak transcription	Spleen	Spleen

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