Variant report

Variant	rs9568351
Chromosome Location	chr13:50480207-50480208
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12429041	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12429047	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12430021	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12430731	0.80[ASN][1000 genomes]
rs12584761	0.87[EUR][1000 genomes]
rs12585937	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1609571	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17073758	0.91[EUR][1000 genomes]
rs2407879	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2897794	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4142286	0.89[EUR][1000 genomes]
rs4942896	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4942898	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4942903	0.87[EUR][1000 genomes]
rs7983585	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9562940	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9562941	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9562944	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9562951	0.91[EUR][1000 genomes]
rs9568348	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9568353	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9568359	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9568361	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9568365	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9568371	0.91[EUR][1000 genomes]
rs9568379	0.87[EUR][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	esv1851738	chr13:50474326-50507944	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50468600-50486000	Weak transcription	Liver	Liver
2	chr13:50476400-50497400	Weak transcription	Pancreas	Pancrea
3	chr13:50477800-50499600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr13:50478000-50487200	Weak transcription	Ovary	ovary
5	chr13:50478000-50495200	Weak transcription	Brain Hippocampus Middle	brain
6	chr13:50478600-50491400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:50479200-50489600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr13:50479400-50482200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr13:50479400-50490600	Weak transcription	Esophagus	oesophagus
10	chr13:50479600-50508600	Weak transcription	K562	blood
11	chr13:50479800-50500000	Weak transcription	Colon Smooth Muscle	Colon

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