Variant report

Variant	rs4687887
Chromosome Location	chr3:119515585-119515586
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:119510909..119513953-chr3:119514986..119517424,3	K562	blood:
2	chr3:119514298..119516694-chr3:119519777..119521864,2	K562	blood:
3	chr3:119513257..119518482-chr3:119518835..119521864,6	K562	blood:
4	chr3:119512757..119515605-chr3:119516397..119518859,2	MCF-7	breast:
5	chr3:119215696..119217904-chr3:119512821..119515742,3	K562	blood:
6	chr3:119514787..119516289-chr3:119811879..119814364,2	MCF-7	breast:
7	chr3:119217125..119218663-chr3:119514473..119516155,2	K562	blood:

Variant related genes	Relation type
ENSG00000242622	Chromatin interaction
ENSG00000113845	Chromatin interaction
ENSG00000082701	Chromatin interaction
ENSG00000272662	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12721597	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs13323135	1.00[EUR][1000 genomes]
rs16830505	1.00[JPT][hapmap];0.88[LWK][hapmap];0.95[MKK][hapmap];0.88[YRI][hapmap];0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs4687884	0.81[LWK][hapmap];0.87[MKK][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4687885	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4687886	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4688041	1.00[EUR][1000 genomes]
rs55907307	1.00[ASN][1000 genomes]
rs55987931	0.94[AFR][1000 genomes]
rs56155951	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59162145	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59953121	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60822858	1.00[ASN][1000 genomes]
rs61211594	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6438545	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6773295	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6775566	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72552100	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72554005	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72554006	1.00[ASN][1000 genomes]
rs72554009	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72554015	1.00[ASN][1000 genomes]
rs73854707	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73854708	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73854714	1.00[ASN][1000 genomes]
rs73854716	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9828996	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011178	chr3:119437192-119589116	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers 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	12 gene(s)	inside rSNPs	diseases
2	nsv536703	chr3:119437192-119589116	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119512000-119515800	Genic enhancers	Fetal Intestine Small	intestine
2	chr3:119513600-119515800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:119513800-119516200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:119513800-119516200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:119513800-119516200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr3:119514000-119515800	Flanking Active TSS	HepG2	liver
7	chr3:119514200-119515800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr3:119514200-119516000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:119514400-119516200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr3:119514400-119526800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr3:119514600-119516200	Enhancers	Stomach Mucosa	stomach
12	chr3:119514600-119516800	Enhancers	Fetal Intestine Large	intestine
13	chr3:119514800-119515600	Enhancers	Hela-S3	cervix
14	chr3:119514800-119518200	Enhancers	Liver	Liver
15	chr3:119515000-119526000	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr3:119515200-119515600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr3:119515200-119515600	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr3:119515200-119516200	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr3:119515200-119516400	Enhancers	K562	blood
20	chr3:119515200-119516800	Enhancers	A549	lung
21	chr3:119515400-119526000	Weak transcription	Duodenum Mucosa	Duodenum
22	chr3:119515400-119527200	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr3:119515400-119528600	Weak transcription	Colonic Mucosa	Colon

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