Variant report

Variant	rs1566941
Chromosome Location	chr3:51991251-51991252
allele	C/T
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:51991130..51993001-chr3:51999490..52001486,2	MCF-7	breast:
2	chr3:51989698..51992601-chr3:51995625..51997375,2	MCF-7	breast:
3	chr3:51985563..51987517-chr3:51990241..51992502,2	MCF-7	breast:
4	chr3:51987928..51991924-chr3:52001407..52003695,4	MCF-7	breast:
5	chr3:51988009..51992311-chr3:51992660..51997455,6	K562	blood:
6	chr3:51976311..51979172-chr3:51989239..51992217,2	K562	blood:
7	chr3:51988573..51991523-chr3:52028412..52030001,2	K562	blood:
8	chr3:51985305..51989166-chr3:51989564..51992012,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000162244	Chromatin interaction
ENSG00000090097	Chromatin interaction
ENSG00000041880	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11926611	0.89[ASN][1000 genomes]
rs1876052	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs188953	0.85[EUR][1000 genomes]
rs2271069	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs323864	0.86[ASN][1000 genomes]
rs323868	0.89[ASN][1000 genomes]
rs323871	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs323873	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs323874	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs323879	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs323881	0.89[ASN][1000 genomes]
rs323885	0.89[ASN][1000 genomes]
rs323886	0.89[ASN][1000 genomes]
rs323887	0.89[ASN][1000 genomes]
rs323893	0.89[ASN][1000 genomes]
rs323894	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs323895	0.89[ASN][1000 genomes]
rs323898	0.89[ASN][1000 genomes]
rs3755797	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3774344	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs411209	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4986825	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56715917	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59682660	0.86[ASN][1000 genomes]
rs61546679	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520211	chr3:51772347-52166147	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1012847	chr3:51811062-52056727	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	68 gene(s)	inside rSNPs	diseases
3	nsv536571	chr3:51811062-52056727	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	68 gene(s)	inside rSNPs	diseases
4	nsv1003453	chr3:51962081-52099441	Active TSS Genic enhancers Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	esv1804090	chr3:51962081-52140591	Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
6	esv1835339	chr3:51962081-52140591	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
7	nsv1003581	chr3:51973395-52108645	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
8	nsv1001062	chr3:51973395-52134638	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
9	nsv876780	chr3:51981021-52101799	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
10	nsv876781	chr3:51985664-52009612	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv876782	chr3:51985664-52022779	Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
12	nsv876783	chr3:51987224-52009612	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv876784	chr3:51987224-52013242	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	esv3438711	chr3:51987612-51992410	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51977200-51992000	Weak transcription	Aorta	Aorta
2	chr3:51986200-51993400	Weak transcription	HepG2	liver
3	chr3:51987600-51992000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr3:51988000-51992400	Weak transcription	HSMMtube	muscle
5	chr3:51988400-52000600	Weak transcription	Hela-S3	cervix
6	chr3:51989200-51991400	Enhancers	Liver	Liver
7	chr3:51989200-51991400	Enhancers	Fetal Heart	heart
8	chr3:51989400-51991800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr3:51989400-51997000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr3:51990200-51991800	Weak transcription	Lung	lung
11	chr3:51990400-51991800	Bivalent Enhancer	Placenta	Placenta
12	chr3:51990400-51992400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:51990600-51991400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
14	chr3:51990600-51991400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr3:51990600-51991400	Enhancers	Fetal Lung	lung
16	chr3:51990600-51991400	Genic enhancers	Fetal Muscle Leg	muscle
17	chr3:51990600-51991800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
18	chr3:51990600-51992000	Weak transcription	Left Ventricle	heart
19	chr3:51990600-51993200	Weak transcription	Osteobl	bone
20	chr3:51990600-52000200	Weak transcription	NHDF-Ad	bronchial
21	chr3:51990600-52000400	Weak transcription	Small Intestine	intestine
22	chr3:51990600-52000400	Weak transcription	HUVEC	blood vessel
23	chr3:51990600-52000800	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr3:51990800-51991400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
25	chr3:51990800-51991400	Enhancers	Primary hematopoietic stem cells	blood
26	chr3:51990800-51991400	Transcr. at gene 5' and 3'	Brain Hippocampus Middle	brain
27	chr3:51990800-51991400	Genic enhancers	HSMM	muscle
28	chr3:51990800-51991600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
29	chr3:51990800-51991600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr3:51990800-51991600	Weak transcription	Gastric	stomach
31	chr3:51990800-51991800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr3:51990800-51991800	Transcr. at gene 5' and 3'	Brain Substantia Nigra	brain
33	chr3:51990800-51991800	Genic enhancers	Fetal Muscle Trunk	muscle
34	chr3:51990800-51992400	Weak transcription	Rectal Smooth Muscle	rectum
35	chr3:51990800-51992800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr3:51990800-51995000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:51990800-51996000	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr3:51990800-51997200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr3:51990800-51999600	Weak transcription	NH-A	brain
40	chr3:51990800-52000400	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr3:51991000-51991400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr3:51991000-51991600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr3:51991000-51991600	Weak transcription	Brain Germinal Matrix	brain
44	chr3:51991000-51991600	Weak transcription	Right Ventricle	heart
45	chr3:51991000-51991800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr3:51991000-51991800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr3:51991000-51991800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr3:51991000-51992000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
49	chr3:51991000-51992200	Weak transcription	Stomach Smooth Muscle	stomach
50	chr3:51991000-51992400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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