Variant report

Variant	rs686768
Chromosome Location	chr11:86361508-86361509
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	chr11:86360141..86362731-chr11:86373368..86375959,2	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10501626	0.90[ASN][1000 genomes]
rs10792871	0.84[ASN][1000 genomes]
rs12573953	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12575285	0.90[ASN][1000 genomes]
rs12575580	0.82[EUR][1000 genomes]
rs17211458	0.89[ASN][1000 genomes]
rs17211563	0.90[ASN][1000 genomes]
rs17211584	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17818784	0.90[ASN][1000 genomes]
rs17818845	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17819523	0.88[ASN][1000 genomes]
rs17819683	0.90[ASN][1000 genomes]
rs1945142	0.90[ASN][1000 genomes]
rs2226566	0.90[ASN][1000 genomes]
rs471780	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs539214	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56095595	0.82[EUR][1000 genomes]
rs56140354	0.90[ASN][1000 genomes]
rs56935647	0.87[ASN][1000 genomes]
rs581796	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs60229086	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60379752	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs623785	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs659301	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs66878934	0.82[EUR][1000 genomes]
rs66909667	0.90[ASN][1000 genomes]
rs67112634	0.90[ASN][1000 genomes]
rs67655324	0.82[EUR][1000 genomes]
rs687138	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72955481	0.83[ASN][1000 genomes]
rs72957414	0.90[ASN][1000 genomes]
rs72957420	0.90[ASN][1000 genomes]
rs72957437	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72957439	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72957441	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72957457	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72957470	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72957473	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72957476	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72959410	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72959413	0.83[ASN][1000 genomes]
rs72959421	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72959427	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72959431	0.83[EUR][1000 genomes]
rs72961766	0.82[EUR][1000 genomes]
rs7480835	0.90[ASN][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	nsv1044081	chr11:86133641-86868560	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv541118	chr11:86133641-86868560	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv555665	chr11:86230898-86417553	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1055071	chr11:86301240-86465465	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv555704	chr11:86344677-86386784	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv428263	chr11:86357990-86508480	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86344000-86373800	Weak transcription	Rectal Smooth Muscle	rectum
2	chr11:86348800-86361600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:86355600-86370400	Weak transcription	Psoas Muscle	Psoas
4	chr11:86356200-86361800	Weak transcription	Left Ventricle	heart
5	chr11:86356600-86361800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr11:86356800-86369600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr11:86357000-86361800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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