Variant report

Variant	rs12272964
Chromosome Location	chr11:108244688-108244689
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11212588	0.83[AFR][1000 genomes]
rs11212611	1.00[AFR][1000 genomes]
rs11212657	0.87[AFR][1000 genomes]
rs11212673	0.87[AFR][1000 genomes]
rs11822807	0.87[AFR][1000 genomes]
rs12270808	1.00[AFR][1000 genomes]
rs12291754	0.87[AFR][1000 genomes]
rs12292677	0.81[AFR][1000 genomes]
rs12293324	0.87[AFR][1000 genomes]
rs4988000	0.83[AFR][1000 genomes]
rs4988009	0.83[AFR][1000 genomes]
rs4988056	0.83[AFR][1000 genomes]
rs4988074	0.83[AFR][1000 genomes]
rs4988096	0.83[AFR][1000 genomes]
rs4988100	0.83[AFR][1000 genomes]
rs59333417	0.87[AFR][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	nsv898383	chr11:108068954-108251211	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv898384	chr11:108097333-108251211	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv1052254	chr11:108122683-108845008	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv541164	chr11:108122683-108845008	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv832262	chr11:108123831-108309350	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv832263	chr11:108183372-108384391	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108226600-108257400	Weak transcription	Right Ventricle	heart
2	chr11:108227600-108245600	Weak transcription	Fetal Brain Female	brain
3	chr11:108227800-108245600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:108236200-108245000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr11:108236800-108245600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr11:108237800-108245200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr11:108237800-108245600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr11:108239600-108245800	Weak transcription	Brain Substantia Nigra	brain
9	chr11:108239600-108260800	Weak transcription	Brain Hippocampus Middle	brain
10	chr11:108240200-108245400	Weak transcription	Primary T cells from cord blood	blood
11	chr11:108244400-108244800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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