Variant report

Variant	rs9704013
Chromosome Location	chr11:8165736-8165737
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11041767	0.81[EUR][1000 genomes]
rs2049684	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6578932	0.82[EUR][1000 genomes]
rs6578934	0.82[EUR][1000 genomes]
rs7119468	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829170	chr11:8068594-8216369	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv428249	chr11:8068594-8216369	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv1048537	chr11:8137353-8196203	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv896981	chr11:8152080-8227964	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1054339	chr11:8153582-8263173	Bivalent Enhancer Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8132600-8172200	Weak transcription	Pancreas	Pancrea
2	chr11:8148400-8169200	Weak transcription	Brain Anterior Caudate	brain
3	chr11:8148800-8170200	Weak transcription	Colon Smooth Muscle	Colon
4	chr11:8149800-8179600	Weak transcription	Brain Substantia Nigra	brain
5	chr11:8155200-8166800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr11:8156000-8189800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr11:8158000-8169600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:8158400-8166800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr11:8159600-8166800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr11:8160800-8166800	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr11:8160800-8168000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr11:8160800-8188600	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr11:8161800-8167000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr11:8162000-8172400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr11:8162000-8189400	Weak transcription	Primary B cells from peripheral blood	blood
16	chr11:8162400-8183200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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