Variant report

Variant	rs13290171
Chromosome Location	chr9:16876651-16876652
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10756825	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12683916	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34358697	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs34919930	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs35386000	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs35483590	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs36021466	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7021921	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7027849	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7044899	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs71513271	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs71513274	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs71513275	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs71513276	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7864210	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7864745	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7868212	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7868424	0.85[AMR][1000 genomes];0.95[ASN][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	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv892650	chr9:16696187-16950860	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv892652	chr9:16843128-16958312	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
4	nsv892653	chr9:16848790-16895610	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
5	nsv1018615	chr9:16865804-16960970	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
6	nsv540074	chr9:16865804-16960970	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16872000-16885000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:16872200-16879400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:16874000-16883400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:16876600-16877000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

Quick Search:

Input of quick search could be:

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

what's new

Quick links