Variant report

Variant	rs1323432
Chromosome Location	chr9:104362937-104362938
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:104355931..104357895-chr9:104361066..104363280,2	K562	blood:

Variant related genes	Relation type
ENSG00000188386	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10512282	0.88[CEU][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11788114	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11789610	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11790230	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11790832	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11791337	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11793752	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16920462	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17188758	0.88[CEU][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs57596144	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59782949	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs61051202	0.83[EUR][1000 genomes]
rs62575839	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62575842	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62575844	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62575845	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62575846	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62575847	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62575848	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62575849	0.97[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62575850	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62575851	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62575852	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62577397	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67248872	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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	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
3	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
4	nsv831672	chr9:104300755-104480849	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104362000-104387400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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