Variant report

Variant	rs7864207
Chromosome Location	chr9:9090834-9090835
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:56434645..56437118-chr9:9089375..9092373,2	K562	blood:
2	chr12:56435690..56436195-chr9:9090395..9091395,2	HCT-116	colon:
3	chr12:56435752..56436286-chr9:9090373..9090875,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257449	Chromatin interaction
ENSG00000197728	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10115009	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs10117009	1.00[CHB][hapmap];0.93[CHD][hapmap];0.82[JPT][hapmap]
rs10117634	1.00[CHB][hapmap]
rs10118348	1.00[CHB][hapmap];0.93[CHD][hapmap];0.82[JPT][hapmap]
rs10120781	0.88[CHB][hapmap];0.86[CHD][hapmap];0.82[JPT][hapmap];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10121415	0.88[CHB][hapmap];0.82[JPT][hapmap];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10122888	0.88[CHB][hapmap];0.82[JPT][hapmap];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10124317	0.88[CHB][hapmap];0.82[JPT][hapmap]
rs10125527	1.00[CHB][hapmap];0.82[JPT][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10977508	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs10977509	1.00[CHB][hapmap];0.93[CHD][hapmap];0.82[JPT][hapmap]
rs10977514	1.00[CHB][hapmap];0.93[CHD][hapmap];0.82[JPT][hapmap]
rs10977516	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs10977517	0.88[CHB][hapmap];0.82[JPT][hapmap]
rs12335759	1.00[CHB][hapmap];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12335761	1.00[CHB][hapmap];0.93[CHD][hapmap];0.82[JPT][hapmap];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12336672	1.00[CHB][hapmap];0.82[JPT][hapmap];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12337224	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs12339653	1.00[CHB][hapmap]
rs12341389	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs12349866	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs12350219	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs12351020	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs12352800	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28567443	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56699508	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57688746	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59772000	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60642850	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61192231	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61519553	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72694980	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9886879	0.88[CHB][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv498066	chr9:8961722-9486652	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv892248	chr9:9024254-9176176	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv892249	chr9:9026854-9377679	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv892250	chr9:9032693-9125205	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv1033404	chr9:9058285-9211223	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv831505	chr9:9072216-9277320	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv892251	chr9:9074830-9119229	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv972648	chr9:9090657-9091667	Inactive region	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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