Variant report

Variant	rs7926512
Chromosome Location	chr11:65464487-65464488
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65462860..65464502-chr11:65486006..65488122,2	MCF-7	breast:
2	chr11:65463670..65466251-chr11:65542574..65544907,2	K562	blood:
3	chr11:65445422..65447498-chr11:65463363..65465929,2	MCF-7	breast:
4	chr11:65464340..65466957-chr11:65635073..65636599,2	MCF-7	breast:
5	chr11:65460118..65463457-chr11:65463620..65467916,5	K562	blood:
6	chr11:65429955..65431628-chr11:65463619..65466319,2	MCF-7	breast:
7	chr11:65429766..65432533-chr11:65462094..65464981,2	MCF-7	breast:
8	chr11:65403783..65405933-chr11:65463116..65465453,2	K562	blood:
9	chr11:65463676..65466407-chr11:65650763..65652793,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000172922	Chromatin interaction
ENSG00000172638	Chromatin interaction
ENSG00000173039	Chromatin interaction
ENSG00000213445	Chromatin interaction
ENSG00000239356	Chromatin interaction
ENSG00000172977	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10400292	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11227259	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11227277	0.87[EUR][1000 genomes]
rs11820062	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12576802	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12787843	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2127507	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2170082	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4244812	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4930305	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7932857	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897716	chr11:65083491-65481166	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	999 gene(s)	inside rSNPs	diseases
2	nsv897718	chr11:65140209-65577516	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1003 gene(s)	inside rSNPs	diseases
3	nsv897723	chr11:65294830-65481166	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
4	nsv897735	chr11:65335705-65481166	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Active TSS ZNF genes & repeats 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 miRNA target site	98 gene(s)	inside rSNPs	diseases
5	nsv897736	chr11:65335705-65676516	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
6	nsv897747	chr11:65353906-65481166	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
7	nsv897748	chr11:65392695-65466911	Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
8	nsv897755	chr11:65405300-65481166	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
9	nsv430401	chr11:65419324-65788024	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65459400-65466200	Enhancers	Stomach Mucosa	stomach
2	chr11:65461200-65465000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:65461800-65465600	Weak transcription	K562	blood
4	chr11:65462000-65465600	Weak transcription	Esophagus	oesophagus
5	chr11:65462000-65465800	Weak transcription	Gastric	stomach
6	chr11:65462400-65468000	Enhancers	Brain Hippocampus Middle	brain
7	chr11:65462600-65464600	Enhancers	Brain Substantia Nigra	brain
8	chr11:65462600-65467800	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr11:65463000-65464600	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr11:65463000-65464600	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr11:65463000-65464600	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr11:65463000-65464800	Enhancers	Brain Angular Gyrus	brain
13	chr11:65463000-65465200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr11:65463400-65465000	Enhancers	Brain Anterior Caudate	brain
15	chr11:65463400-65465600	Weak transcription	Duodenum Mucosa	Duodenum
16	chr11:65463800-65464600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr11:65463800-65474000	Weak transcription	Pancreas	Pancrea
18	chr11:65464000-65467400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr11:65464400-65464600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr11:65464400-65465600	Weak transcription	Brain Cingulate Gyrus	brain
21	chr11:65464400-65465800	Enhancers	Placenta	Placenta

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