Variant report

Variant	rs9561341
Chromosome Location	chr13:94063634-94063635
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs17234467	1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.97[ASN][1000 genomes]
rs2813637	0.90[ASN][1000 genomes]
rs57159809	0.85[ASN][1000 genomes]
rs7997987	1.00[CHB][hapmap];0.88[JPT][hapmap];0.96[ASN][1000 genomes]
rs9301878	0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs9301879	0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs9556290	0.92[ASN][1000 genomes]
rs9556295	0.90[ASN][1000 genomes]
rs9556298	0.87[CHB][hapmap]
rs9561333	1.00[YRI][hapmap]
rs9561338	0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs9561343	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs9561349	0.94[CHB][hapmap];0.82[JPT][hapmap];0.94[ASN][1000 genomes]
rs9561356	0.83[CHB][hapmap]

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	nsv869070	chr13:93347616-94286933	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1053035	chr13:93842576-94229732	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv541880	chr13:93842576-94229732	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv530636	chr13:93997311-94281707	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv916039	chr13:94035909-94191105	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:94057600-94066400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr13:94058600-94077600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr13:94062600-94064200	Enhancers	Fetal Heart	heart
4	chr13:94063600-94063800	Enhancers	Psoas Muscle	Psoas
5	chr13:94063600-94066600	Weak transcription	Aorta	Aorta

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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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