Variant report

Variant	nsv975149
Chromosome Location	chr11:9466591-9468624
allele	n/a
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:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

No data

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:9461359..9463552-chr11:9468544..9471104,2	K562	blood:
2	chr11:9465547..9467985-chr11:9478686..9481606,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	IPO7	hsa-miR-16-5p	chr11:9467545-9467566
2	IPO7	hsa-miR-106b-5p	chr11:9467329-9467352
3	IPO7	hsa-miR-9-5p	chr11:9467118-9467140
4	IPO7	hsa-miR-92a-3p	chr11:9467728-9467749
5	IPO7	hsa-miR-204-5p	chr11:9468530-9468552
6	IPO7	hsa-miR-16-5p	chr11:9467559-9467566
7	IPO7	hsa-miR-106b-5p	chr11:9467345-9467351
8	IPO7	hsa-let-7a-5p	chr11:9467488-9467510

Extended variants
information (count: 68 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:68 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370850304	chr11:9466628-9466629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs374264509	chr11:9466633-9466634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371155574	chr11:9466768-9466769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535881443	chr11:9466803-9466804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11042357	chr11:9466836-9466837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11042358	chr11:9466838-9466839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs61876790	chr11:9466881-9466882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183668627	chr11:9466897-9466898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371660574	chr11:9466922-9466923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs60115807	chr11:9466936-9466937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs398015313	chr11:9466943-9466944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539072383	chr11:9467034-9467035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369428057	chr11:9467039-9467040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559009096	chr11:9467065-9467066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572446132	chr11:9467066-9467067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533846194	chr11:9467089-9467090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553992229	chr11:9467102-9467103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573791351	chr11:9467179-9467180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542801590	chr11:9467196-9467197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149600432	chr11:9467313-9467314	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373742051	chr11:9467429-9467430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373327209	chr11:9467437-9467438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369916744	chr11:9467499-9467500	Weak transcription Strong transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
24	rs538526617	chr11:9467528-9467529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144275708	chr11:9467579-9467580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189553736	chr11:9467640-9467641	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192445437	chr11:9467661-9467662	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561623258	chr11:9467674-9467675	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184831886	chr11:9467697-9467698	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542927430	chr11:9467762-9467763	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550385178	chr11:9467816-9467817	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570231300	chr11:9467864-9467865	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148726795	chr11:9467876-9467877	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373860169	chr11:9467903-9467904	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76664366	chr11:9467916-9467917	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558368922	chr11:9467928-9467929	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189764583	chr11:9467935-9467936	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571904441	chr11:9468077-9468078	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553826150	chr11:9468094-9468095	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142280670	chr11:9468098-9468099	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs370505639	chr11:9468110-9468111	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536091947	chr11:9468133-9468134	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181543508	chr11:9468140-9468141	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575803071	chr11:9468151-9468152	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185872782	chr11:9468155-9468156	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556452036	chr11:9468170-9468171	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553857317	chr11:9468179-9468180	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147869424	chr11:9468181-9468182	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189157722	chr11:9468199-9468200	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181912047	chr11:9468213-9468214	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9419600-9471000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr11:9421000-9471200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:9423000-9470400	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr11:9424200-9470400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr11:9424800-9468600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
6	chr11:9424800-9469000	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr11:9424800-9470600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:9425000-9468200	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr11:9425000-9468400	Strong transcription	H1 Cell Line	embryonic stem cell
10	chr11:9425200-9467200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:9425800-9468000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:9426200-9471600	Strong transcription	Dnd41	blood
13	chr11:9426800-9468400	Strong transcription	Primary B cells from peripheral blood	blood
14	chr11:9426800-9470600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr11:9427200-9466800	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr11:9427600-9471000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr11:9429800-9469000	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr11:9430200-9470200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr11:9430400-9468200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr11:9431800-9468800	Weak transcription	Stomach Mucosa	stomach
21	chr11:9434800-9470400	Strong transcription	Osteobl	bone
22	chr11:9435400-9466600	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr11:9435400-9470400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:9439400-9468200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr11:9439600-9467600	Strong transcription	Placenta	Placenta
26	chr11:9439600-9468000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:9439600-9472000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr11:9439800-9467000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr11:9439800-9468200	Strong transcription	Duodenum Smooth Muscle	Duodenum
30	chr11:9439800-9470200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:9439800-9470600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr11:9440000-9470800	Strong transcription	Fetal Thymus	thymus
33	chr11:9440200-9466600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr11:9440200-9468200	Strong transcription	Duodenum Mucosa	Duodenum
35	chr11:9440200-9468400	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr11:9440200-9470400	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr11:9441600-9466800	Strong transcription	Skeletal Muscle Female	skeletal muscle
38	chr11:9441600-9468200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr11:9442000-9466800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr11:9443600-9470200	Strong transcription	HSMM	muscle
41	chr11:9443800-9466600	Strong transcription	Rectal Mucosa Donor 29	rectum
42	chr11:9443800-9470200	Strong transcription	HUVEC	blood vessel
43	chr11:9445400-9467000	Strong transcription	Fetal Muscle Leg	muscle
44	chr11:9445400-9468600	Strong transcription	Fetal Intestine Large	intestine
45	chr11:9445800-9467000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr11:9445800-9468200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr11:9450600-9468600	Strong transcription	Liver	Liver
48	chr11:9452800-9480000	Weak transcription	Fetal Brain Male	brain
49	chr11:9453400-9466600	Strong transcription	Sigmoid Colon	Sigmoid Colon
50	chr11:9453400-9467000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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