Variant report

Variant	nsv819303
Chromosome Location	chr2:113044722-113050345
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOS	chr2:113047644-113048174	HUVEC	blood vessel:	n/a	n/a
2	FOXA2	chr2:113047778-113048013	HepG2	liver:	n/a	n/a
3	GATA2	chr2:113047658-113048118	HUVEC	blood vessel:	n/a	n/a
4	POLR2A	chr2:113048979-113049662	K562	blood:	n/a	n/a
5	POLR2A	chr2:113046366-113046460	K562	blood:	n/a	n/a
6	POLR2A	chr2:113050052-113050304	K562	blood:	n/a	n/a
7	POLR2A	chr2:113047656-113048146	HUVEC	blood vessel:	n/a	n/a
8	POLR2A	chr2:113045271-113045432	K562	blood:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:113031677..113034717-chr2:113042895..113047019,4	K562	blood:
2	chr2:113033844..113035666-chr2:113048299..113050198,2	K562	blood:
3	chr2:113032383..113034533-chr2:113048360..113050723,3	MCF-7	breast:
4	chr2:113031383..113033830-chr2:113044346..113047264,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000235258	TF binding region
ENSG00000188177	chromatin interactions

Extended variants
information (count: 329 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530330510	chr2:113044802-113044803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs558917518	chr2:113044820-113044821	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs566140081	chr2:113044862-113044863	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs534826592	chr2:113044872-113044873	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187253993	chr2:113044896-113044897	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs192006250	chr2:113044913-113044914	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs77536235	chr2:113044932-113044933	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs547231453	chr2:113044976-113044977	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs182546139	chr2:113045014-113045015	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs556040303	chr2:113045066-113045067	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs375453810	chr2:113045095-113045096	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541851385	chr2:113045102-113045103	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140406909	chr2:113045106-113045107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566965460	chr2:113045107-113045108	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113263467	chr2:113045121-113045122	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs575973642	chr2:113045168-113045169	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs544789025	chr2:113045185-113045186	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs143583138	chr2:113045186-113045187	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs75825271	chr2:113045208-113045209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs372584695	chr2:113045215-113045216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs79257134	chr2:113045217-113045218	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs78009253	chr2:113045240-113045241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs113358068	chr2:113045241-113045242	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs76124611	chr2:113045242-113045243	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs74609797	chr2:113045248-113045249	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs564961333	chr2:113045272-113045273	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs78444467	chr2:113045279-113045280	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs527354351	chr2:113045280-113045281	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs80070124	chr2:113045283-113045284	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs74574788	chr2:113045305-113045306	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs76367993	chr2:113045306-113045307	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376850195	chr2:113045316-113045317	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs77409298	chr2:113045328-113045329	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs540786419	chr2:113045330-113045331	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs79287397	chr2:113045335-113045336	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs80038539	chr2:113045340-113045341	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs371234420	chr2:113045355-113045356	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs560893881	chr2:113045364-113045365	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs74789274	chr2:113045370-113045371	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs56735089	chr2:113045415-113045416	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs201012322	chr2:113045420-113045421	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs59409635	chr2:113045421-113045422	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529709250	chr2:113045430-113045431	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs61151133	chr2:113045444-113045445	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs60598653	chr2:113045446-113045447	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs549843032	chr2:113045456-113045457	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs570347849	chr2:113045459-113045460	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532881138	chr2:113045475-113045476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs561832128	chr2:113045496-113045497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs58001268	chr2:113045566-113045567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance

Variant related diseases (count:66)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113034200-113058200	Weak transcription	Ovary	ovary
2	chr2:113034400-113047800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr2:113034400-113051400	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr2:113034400-113097000	Weak transcription	Psoas Muscle	Psoas
5	chr2:113035000-113046000	Weak transcription	Fetal Kidney	kidney
6	chr2:113035000-113057800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr2:113035000-113057800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:113035000-113057800	Weak transcription	Fetal Intestine Small	intestine
9	chr2:113035400-113047600	Weak transcription	Osteobl	bone
10	chr2:113035600-113047600	Weak transcription	NHDF-Ad	bronchial
11	chr2:113035600-113058200	Weak transcription	Primary B cells from cord blood	blood
12	chr2:113035800-113058000	Weak transcription	Primary T cells from cord blood	blood
13	chr2:113035800-113060400	Weak transcription	Fetal Thymus	thymus
14	chr2:113035800-113067400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr2:113036600-113058000	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr2:113037000-113054200	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr2:113040000-113081800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:113040600-113054400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr2:113041200-113058600	Weak transcription	Fetal Heart	heart
20	chr2:113041400-113058600	Weak transcription	K562	blood
21	chr2:113041800-113047800	Weak transcription	Liver	Liver
22	chr2:113042400-113051600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr2:113042600-113047600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr2:113045600-113051400	Weak transcription	Aorta	Aorta
25	chr2:113045800-113046200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:113045800-113046200	Enhancers	Thymus	Thymus
27	chr2:113046000-113046200	ZNF genes & repeats	Fetal Kidney	kidney
28	chr2:113046000-113046200	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr2:113046000-113052600	Weak transcription	Fetal Lung	lung
30	chr2:113046200-113047800	Weak transcription	Fetal Kidney	kidney
31	chr2:113046200-113057800	Weak transcription	Thymus	Thymus
32	chr2:113046600-113047600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr2:113046600-113079800	Weak transcription	Fetal Stomach	stomach
34	chr2:113046800-113065000	Weak transcription	HSMMtube	muscle
35	chr2:113047000-113048000	Weak transcription	Brain Cingulate Gyrus	brain
36	chr2:113047200-113048600	Enhancers	HUVEC	blood vessel
37	chr2:113047200-113058200	Weak transcription	Primary B cells from peripheral blood	blood
38	chr2:113047400-113048200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr2:113047400-113048600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr2:113047600-113047800	Enhancers	NHDF-Ad	bronchial
41	chr2:113047600-113048000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr2:113047600-113048000	Enhancers	NH-A	brain
43	chr2:113047600-113048200	Enhancers	Osteobl	bone
44	chr2:113047600-113058400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr2:113047800-113048000	ZNF genes & repeats	Fetal Kidney	kidney
46	chr2:113047800-113048000	Enhancers	Spleen	Spleen
47	chr2:113047800-113048200	Genic enhancers	Brain Inferior Temporal Lobe	brain
48	chr2:113047800-113048600	Enhancers	Duodenum Mucosa	Duodenum
49	chr2:113047800-113049000	Enhancers	Liver	Liver
50	chr2:113047800-113050400	Weak transcription	NHDF-Ad	bronchial

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