Variant report

Variant	rs9852053
Chromosome Location	chr3:23472006-23472007
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs11922562	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs17013009	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs17013099	0.88[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17013329	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs28548892	1.00[AMR][1000 genomes]
rs28567933	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58047209	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58879825	1.00[AMR][1000 genomes]
rs60014070	1.00[AMR][1000 genomes]
rs61081559	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61500565	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61636332	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6768277	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6795043	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs73138415	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138434	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138436	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138449	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138480	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138490	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138492	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73140509	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73140514	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73141810	1.00[AMR][1000 genomes]
rs73149686	1.00[AMR][1000 genomes]
rs73149689	1.00[AMR][1000 genomes]
rs7611624	1.00[AMR][1000 genomes]
rs7634565	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs7652287	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9310716	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs9681506	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs9809364	1.00[AMR][1000 genomes]
rs9810378	1.00[AMR][1000 genomes]
rs9811442	1.00[AMR][1000 genomes]
rs9819566	0.94[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9819788	0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs9821681	1.00[AMR][1000 genomes]
rs9829577	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9834737	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9842159	1.00[AMR][1000 genomes]
rs9845340	0.94[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9866889	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9869171	0.94[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9878638	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9879132	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9879217	0.88[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][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	nsv1002823	chr3:23277838-23623083	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1007373	chr3:23367952-23710331	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv876624	chr3:23385877-23483536	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv876625	chr3:23390301-23509597	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv533980	chr3:23445901-24311972	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23447000-23479600	Weak transcription	Primary B cells from cord blood	blood
2	chr3:23467200-23472200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr3:23467400-23472200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr3:23467400-23472400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:23467400-23476200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr3:23467400-23476400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr3:23467400-23476400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr3:23467400-23476800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr3:23467600-23478400	Weak transcription	Fetal Heart	heart
10	chr3:23471400-23472200	Enhancers	Psoas Muscle	Psoas
11	chr3:23471800-23472200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr3:23471800-23472600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr3:23471800-23472800	Enhancers	Brain Hippocampus Middle	brain
14	chr3:23471800-23473200	Enhancers	Brain Substantia Nigra	brain
15	chr3:23472000-23472400	Enhancers	Left Ventricle	heart
16	chr3:23472000-23472400	Enhancers	Ovary	ovary
17	chr3:23472000-23472800	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr3:23472000-23473000	Enhancers	Primary B cells from peripheral blood	blood
19	chr3:23472000-23473000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr3:23472000-23473000	Enhancers	Small Intestine	intestine

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