Variant report

Variant	rs9551592
Chromosome Location	chr13:29593369-29593370
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1358937	0.98[ASN][1000 genomes]
rs1407438	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs226904	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs226905	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2475539	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2475540	1.00[ASN][1000 genomes]
rs2475541	1.00[ASN][1000 genomes]
rs2475542	1.00[ASN][1000 genomes]
rs2475543	1.00[ASN][1000 genomes]
rs2479759	1.00[ASN][1000 genomes]
rs2479760	1.00[ASN][1000 genomes]
rs2479764	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2479765	1.00[ASN][1000 genomes]
rs2479766	1.00[ASN][1000 genomes]
rs2479767	1.00[ASN][1000 genomes]
rs2479768	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2484464	1.00[ASN][1000 genomes]
rs2484465	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2484466	1.00[ASN][1000 genomes]
rs28434554	0.98[ASN][1000 genomes]
rs2987343	1.00[ASN][1000 genomes]
rs2987346	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs326509	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs326510	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs326511	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4238114	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4769660	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4769669	1.00[ASN][1000 genomes]
rs60782582	1.00[ASN][1000 genomes]
rs7318626	1.00[ASN][1000 genomes]
rs74041703	0.98[ASN][1000 genomes]
rs74045518	0.98[ASN][1000 genomes]
rs7984343	0.98[ASN][1000 genomes]
rs9506076	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9550433	1.00[ASN][1000 genomes]
rs9550434	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9551587	0.98[ASN][1000 genomes]
rs9551588	0.98[ASN][1000 genomes]
rs9551589	0.98[ASN][1000 genomes]
rs9551590	0.98[ASN][1000 genomes]
rs9551591	0.98[ASN][1000 genomes]
rs9578069	0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 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	chr13:29585000-29609600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr13:29589400-29599000	Weak transcription	Aorta	Aorta
3	chr13:29593000-29593400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr13:29593000-29594600	Enhancers	Fetal Heart	heart

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