Variant report

Variant	rs11690392
Chromosome Location	chr2:30479545-30479546
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NFIC	chr2:30478888-30479545	ECC-1	luminal epithelium:	n/a	chr2:30479193-30479210
2	POLR2A	chr2:30477119-30482747	SK-N-MC	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:30451092..30457677-chr2:30474497..30480716,15	K562	blood:
2	chr2:30475438..30481096-chr2:30481124..30485591,9	K562	blood:
3	chr2:30475603..30478549-chr2:30478723..30480577,2	K562	blood:
4	chr2:30475984..30481096-chr2:30481124..30486276,10	K562	blood:

Variant related genes	Relation type
ENSG00000256261	TF binding region
ENSG00000256261	Chromatin interaction
ENSG00000213626	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1001202	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1001203	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11127261	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11127262	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11675079	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11679132	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11679137	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11681350	1.00[ASN][1000 genomes]
rs11687193	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11688651	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11690435	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11690629	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11690883	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11694534	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11694679	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12714304	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12996578	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13027149	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13030064	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13030740	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13422834	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34097147	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35163883	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4952114	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62141090	1.00[ASN][1000 genomes]
rs62141122	1.00[ASN][1000 genomes]
rs6736034	0.83[EUR][1000 genomes]
rs829585	1.00[ASN][1000 genomes]
rs906864	1.00[ASN][1000 genomes]
rs9967840	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533886	chr2:30130019-31068764	ZNF genes & repeats Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv1002657	chr2:30339312-30516535	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv2662	chr2:30462905-30495134	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:30457800-30481000	Weak transcription	Gastric	stomach
2	chr2:30461000-30479800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr2:30465400-30480000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr2:30466200-30480400	Weak transcription	Fetal Brain Male	brain
5	chr2:30467600-30479600	Weak transcription	Fetal Brain Female	brain
6	chr2:30470400-30479600	Genic enhancers	Fetal Thymus	thymus
7	chr2:30471000-30484400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr2:30471200-30479600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr2:30471200-30482000	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
10	chr2:30471800-30481600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr2:30472200-30480400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr2:30472600-30480000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr2:30472600-30483400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr2:30473000-30479600	Enhancers	Fetal Heart	heart
15	chr2:30473200-30480000	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr2:30473400-30480800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr2:30473400-30480800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:30474200-30480800	Enhancers	Pancreas	Pancrea
19	chr2:30474400-30481400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr2:30476000-30480200	Weak transcription	GM12878-XiMat	blood
21	chr2:30476200-30479600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr2:30476200-30479800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:30476200-30480000	Genic enhancers	Primary T cells fromperipheralblood	blood
24	chr2:30476200-30480200	Weak transcription	Fetal Muscle Trunk	muscle
25	chr2:30476200-30481200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:30476200-30481400	Weak transcription	Esophagus	oesophagus
27	chr2:30476200-30483400	Weak transcription	Brain Anterior Caudate	brain
28	chr2:30476400-30481400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr2:30476600-30481400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr2:30476600-30496000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr2:30476800-30479800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
32	chr2:30476800-30480000	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr2:30476800-30480400	Weak transcription	Colon Smooth Muscle	Colon
34	chr2:30476800-30480400	Weak transcription	Rectal Smooth Muscle	rectum
35	chr2:30476800-30480600	Weak transcription	Colonic Mucosa	Colon
36	chr2:30476800-30481400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr2:30476800-30485600	Weak transcription	Fetal Kidney	kidney
38	chr2:30477000-30479600	Weak transcription	NH-A	brain
39	chr2:30477000-30479800	Weak transcription	NHDF-Ad	bronchial
40	chr2:30477000-30481000	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr2:30477000-30484200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:30477000-30488800	Weak transcription	Primary hematopoietic stem cells	blood
43	chr2:30477200-30480000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
44	chr2:30477200-30483800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr2:30477400-30481800	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr2:30477600-30479600	Genic enhancers	Thymus	Thymus
47	chr2:30477600-30480000	Genic enhancers	Fetal Intestine Small	intestine
48	chr2:30477600-30480400	Weak transcription	Small Intestine	intestine
49	chr2:30477600-30483600	Strong transcription	Fetal Stomach	stomach
50	chr2:30477800-30479600	Weak transcription	Sigmoid Colon	Sigmoid Colon

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