Variant report

Variant	rs4894360
Chromosome Location	chr3:138595927-138595928
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:138595085..138598590-chr3:138606326..138610145,3	K562	blood:
2	chr3:138593800..138596548-chr3:138596877..138598908,3	K562	blood:
3	chr3:138552112..138555391-chr3:138593368..138596315,4	K562	blood:
4	chr3:138593952..138596417-chr3:138628861..138630984,2	K562	blood:
5	chr3:138552826..138554457-chr3:138595104..138599059,3	MCF-7	breast:
6	chr3:138593690..138596327-chr3:138610684..138613648,2	K562	blood:
7	chr3:138593490..138596609-chr3:138597250..138600269,4	K562	blood:
8	chr3:138593342..138595996-chr3:138632596..138634736,2	K562	blood:
9	chr3:138550738..138557068-chr3:138593213..138598902,11	K562	blood:
10	chr3:138581454..138585634-chr3:138592021..138596158,7	K562	blood:
11	chr3:138580257..138585634-chr3:138593415..138596528,8	K562	blood:

No data

Variant related genes	Relation type
ENSG00000051382	Chromatin interaction
ENSG00000242244	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1021135	1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap];0.83[ASN][1000 genomes]
rs11718698	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11915166	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11919625	0.82[AMR][1000 genomes]
rs13099621	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1400267	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1812664	0.82[ASN][1000 genomes]
rs2037192	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2046287	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2046288	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2348148	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2348384	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2348388	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4508810	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4894327	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4894328	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4894361	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4894365	1.00[CEU][hapmap];0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs4894366	1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap];0.90[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4894367	1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap];0.95[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4894369	1.00[CEU][hapmap];0.88[JPT][hapmap];0.82[AMR][1000 genomes]
rs4894370	0.82[AMR][1000 genomes]
rs59509299	0.83[ASN][1000 genomes]
rs59510253	0.95[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs60261131	0.81[ASN][1000 genomes]
rs62282208	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6439820	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6771671	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6781102	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6784503	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6790195	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6793997	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72975145	0.84[AMR][1000 genomes]
rs72975149	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs72975151	0.90[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs72975160	0.90[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs72975167	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs72975192	0.82[AMR][1000 genomes]
rs7621576	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7627822	1.00[CEU][hapmap];0.88[JPT][hapmap]
rs7628753	0.83[ASN][1000 genomes]
rs7632382	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7637710	0.95[AMR][1000 genomes]
rs7646026	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9289568	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9289569	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs966264	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs966265	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9827663	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9833876	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530057	chr3:138014877-138734390	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1013074	chr3:138213166-138737688	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1002612	chr3:138213274-138831792	Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv536726	chr3:138213274-138831792	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv1009726	chr3:138219923-138737688	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv869205	chr3:138248190-138775288	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv868955	chr3:138248190-138848947	Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv591854	chr3:138348081-138764229	Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv1010514	chr3:138365640-138737688	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
10	nsv1000927	chr3:138423543-138632596	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
11	nsv917964	chr3:138440701-138699084	Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138594600-138596400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:138594800-138596000	Enhancers	HMEC	breast
3	chr3:138595000-138596200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:138595200-138598200	Weak transcription	Stomach Mucosa	stomach
5	chr3:138595200-138598400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr3:138595200-138598400	Weak transcription	HepG2	liver
7	chr3:138595400-138596600	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr3:138595400-138598200	Weak transcription	Fetal Intestine Small	intestine
9	chr3:138595400-138600200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr3:138595400-138604600	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr3:138595800-138596600	Flanking Active TSS	K562	blood
12	chr3:138595800-138596800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr3:138595800-138597200	Enhancers	NHEK	skin

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