Variant report

Variant	rs724308
Chromosome Location	chr13:39705796-39705797
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11616492	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11616952	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11620166	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11841097	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1409439	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1409440	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17443849	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17444010	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs1926472	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1977396	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4142497	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4142498	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4264268	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4383024	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4485232	0.98[EUR][1000 genomes]
rs4495996	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4941906	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4941907	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4941908	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4943627	0.86[ASN][1000 genomes]
rs4943633	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs5013353	0.96[EUR][1000 genomes]
rs5013354	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs5013355	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs5013356	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs5013357	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs5013358	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6563679	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6563681	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7322680	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7325562	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7327588	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7332696	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7337509	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7337925	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7339411	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73463894	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs767	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs768	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs769	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7984240	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7984252	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7994388	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7995665	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754118	chr13:39347702-40222644	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1035255	chr13:39618302-39715336	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39701400-39706800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:39702200-39706400	Weak transcription	Fetal Intestine Large	intestine
3	chr13:39703400-39706000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr13:39704800-39706600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr13:39705000-39706400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr13:39705000-39706600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr13:39705200-39706800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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