Variant report

Variant	rs10508567
Chromosome Location	chr10:19021387-19021388
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA3	chr10:19021056-19021485	SH-SY5Y	brain:	n/a	chr10:19021128-19021149 chr10:19021130-19021146 chr10:19021130-19021146 chr10:19021135-19021142 chr10:19021135-19021142 chr10:19021135-19021142

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:19019982..19021935-chr10:19023921..19026277,3	MCF-7	breast:

Variant related genes	Relation type
AIFM1P1	TF binding region
ENSG00000225509	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10508566	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10764727	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10826351	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10829309	0.92[ASN][1000 genomes]
rs11006702	0.94[ASN][1000 genomes]
rs11007325	0.89[AMR][1000 genomes]
rs11015955	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11015970	0.94[ASN][1000 genomes]
rs11015971	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11015972	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11015976	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11015978	0.91[ASN][1000 genomes]
rs11015979	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11591419	1.00[CHB][hapmap]
rs11819657	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12354939	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12355074	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12359830	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12570499	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2130533	0.94[ASN][1000 genomes]
rs55931411	0.91[ASN][1000 genomes]
rs61033847	0.89[ASN][1000 genomes]
rs7074856	0.94[ASN][1000 genomes]
rs7076492	0.94[ASN][1000 genomes]
rs7077749	0.93[ASN][1000 genomes]
rs7093661	0.95[ASN][1000 genomes]
rs7095167	0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7095319	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72777173	0.96[AMR][1000 genomes]
rs7895597	0.94[ASN][1000 genomes]
rs7897030	0.94[ASN][1000 genomes]
rs7901044	0.91[ASN][1000 genomes]
rs7908403	0.93[AMR][1000 genomes]
rs7912006	0.93[AMR][1000 genomes]
rs9919358	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[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	nsv894915	chr10:18984571-19257664	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19019400-19024200	Weak transcription	K562	blood
2	chr10:19021000-19021800	Enhancers	Fetal Lung	lung
3	chr10:19021200-19021800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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