Variant report

Variant	rs9632442
Chromosome Location	chr5:95923584-95923585
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	chr5:95922674..95925009-chr5:95925976..95928176,2	K562	blood:

Variant related genes	Relation type
ENSG00000238518	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10066456	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11135477	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13170728	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1457083	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs166356	0.86[ASN][1000 genomes]
rs171869	0.87[ASN][1000 genomes]
rs171870	0.94[ASN][1000 genomes]
rs174415	0.91[ASN][1000 genomes]
rs261217	0.87[ASN][1000 genomes]
rs261218	0.87[ASN][1000 genomes]
rs261219	0.87[ASN][1000 genomes]
rs261220	0.87[ASN][1000 genomes]
rs261221	0.87[ASN][1000 genomes]
rs261222	0.87[ASN][1000 genomes]
rs7706893	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7707269	0.88[ASN][1000 genomes]
rs7718594	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7725567	0.85[ASN][1000 genomes]
rs897746	0.81[ASN][1000 genomes]
rs9314174	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030444	chr5:95353620-95995619	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv537810	chr5:95353620-95995619	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1024964	chr5:95742124-96065492	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv537811	chr5:95742124-96065492	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
5	nsv1026484	chr5:95759910-95961518	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr5:95918400-95924000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:95918400-95926000	Weak transcription	Fetal Intestine Large	intestine
3	chr5:95920000-95923800	Flanking Active TSS	HUVEC	blood vessel
4	chr5:95923400-95931800	Weak transcription	Fetal Intestine Small	intestine

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