Variant report

Variant	rs13291749
Chromosome Location	chr9:116888818-116888819
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs13291169	1.00[ASN][1000 genomes]
rs13291434	1.00[ASN][1000 genomes]
rs13300086	1.00[ASN][1000 genomes]
rs13300798	1.00[ASN][1000 genomes]
rs1808630	1.00[ASN][1000 genomes]
rs35719524	1.00[ASN][1000 genomes]
rs62556537	1.00[ASN][1000 genomes]
rs62556538	1.00[ASN][1000 genomes]
rs62556540	1.00[ASN][1000 genomes]
rs62560767	1.00[ASN][1000 genomes]
rs62560772	1.00[ASN][1000 genomes]
rs7857688	1.00[ASN][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	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	esv2422396	chr9:116792944-117354862	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh 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	155 gene(s)	inside rSNPs	diseases
3	esv2422492	chr9:116811294-117366643	Genic enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS 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 miRNA target site	155 gene(s)	inside rSNPs	diseases
4	esv2761285	chr9:116811897-117103268	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
5	nsv870215	chr9:116842614-117070344	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	124 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116882800-116889200	Weak transcription	Gastric	stomach
2	chr9:116885400-116889000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:116886800-116889000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:116888600-116891200	Weak transcription	Stomach Mucosa	stomach
5	chr9:116888800-116889000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr9:116888800-116889000	Enhancers	Placenta	Placenta
7	chr9:116888800-116889200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr9:116888800-116892800	Weak transcription	Fetal Heart	heart

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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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