Variant report

Variant	rs7859904
Chromosome Location	chr9:95810629-95810630
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11790147	0.94[ASN][1000 genomes]
rs11790662	0.94[ASN][1000 genomes]
rs11794425	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs56868344	0.85[AMR][1000 genomes]
rs57408424	0.85[AMR][1000 genomes]
rs57974003	0.85[AMR][1000 genomes]
rs59221745	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs60481048	0.94[ASN][1000 genomes]
rs62573565	0.91[AFR][1000 genomes];0.96[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	nsv526296	chr9:95708192-96030392	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1054767	chr9:95738134-95875977	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1035230	chr9:95770249-95934982	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv893575	chr9:95781040-95854013	Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv893576	chr9:95789960-96158277	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95799800-95815600	Weak transcription	Thymus	Thymus
2	chr9:95803600-95812600	Weak transcription	Spleen	Spleen
3	chr9:95805600-95817200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr9:95806600-95811000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr9:95806600-95814600	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr9:95806600-95815400	Weak transcription	Primary T cells from cord blood	blood
7	chr9:95806800-95810800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr9:95806800-95815600	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr9:95807400-95811200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr9:95808400-95812800	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr9:95808400-95815200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr9:95809600-95816200	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr9:95809800-95811000	Weak transcription	Ovary	ovary
14	chr9:95809800-95816200	Weak transcription	Primary monocytes fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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