Variant report

Variant	rs13295809
Chromosome Location	chr9:104278123-104278124
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10125893	0.83[ASN][1000 genomes]
rs12342991	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12343288	0.84[ASN][1000 genomes]
rs13284984	1.00[CHB][hapmap];0.85[JPT][hapmap];0.80[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13290720	1.00[CHB][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs16920473	0.90[CHB][hapmap];0.84[ASN][1000 genomes]
rs1885977	0.86[ASN][1000 genomes]
rs1929496	1.00[CHB][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs28533545	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs34153995	0.89[ASN][1000 genomes]
rs34727333	0.84[ASN][1000 genomes]
rs36004060	0.84[ASN][1000 genomes]
rs3903804	0.97[ASN][1000 genomes]
rs4119332	0.98[ASN][1000 genomes]
rs45488691	0.88[ASN][1000 genomes]
rs56205348	0.87[ASN][1000 genomes]
rs59770438	0.98[ASN][1000 genomes]
rs7034754	0.90[CHB][hapmap];0.84[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	nsv1046975	chr9:104167583-104659873	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats 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	nsv893626	chr9:104172936-104324545	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv949579	chr9:104229820-104512923	Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv1052492	chr9:104263419-104387782	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	nsv893627	chr9:104268342-104334333	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104276200-104286400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:104277200-104279600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr9:104277400-104278600	Weak transcription	Brain Anterior Caudate	brain
4	chr9:104277400-104278600	Weak transcription	NHDF-Ad	bronchial
5	chr9:104277600-104279000	Weak transcription	Fetal Heart	heart
6	chr9:104277800-104286200	Weak transcription	HUES64 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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