Variant report

Variant	nsv892240
Chromosome Location	chr9:8796449-8834108
allele	n/a
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	CEBPB	chr9:8810067-8810317	HepG2	liver:	n/a	chr9:8810172-8810183 chr9:8810174-8810185 chr9:8810174-8810185
2	CEBPB	chr9:8833481-8833697	K562	blood:	n/a	chr9:8833624-8833637 chr9:8833625-8833636 chr9:8833624-8833637 chr9:8833624-8833637
3	CEBPB	chr9:8822586-8822914	HepG2	liver:	n/a	chr9:8822735-8822746
4	CEBPB	chr9:8833554-8833777	HepG2	liver:	n/a	chr9:8833624-8833637 chr9:8833625-8833636 chr9:8833624-8833637 chr9:8833624-8833637
5	CEBPB	chr9:8833571-8833682	H1-hESC	embryonic stem cell:	n/a	chr9:8833624-8833637 chr9:8833625-8833636 chr9:8833624-8833637 chr9:8833624-8833637
6	CEBPB	chr9:8815292-8815726	HepG2	liver:	n/a	chr9:8815612-8815625
7	CTCF	chr9:8817498-8817527	Kidney_OC	kidney:	n/a	n/a
8	CTCF	chr9:8821440-8821590	NHLF	lung:	n/a	n/a
9	CTCF	chr9:8802850-8802921	Lung_OC	lung:	n/a	n/a
10	E2F4	chr9:8817720-8817742	MCF10A-Er-Src	breast:	n/a	n/a
11	E2F4	chr9:8830230-8830429	MCF10A-Er-Src	breast:	n/a	n/a
12	E2F4	chr9:8813801-8813883	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F6	chr9:8823345-8823732	H1-hESC	embryonic stem cell:	n/a	n/a
14	EP300	chr9:8822153-8822160	GM12878	blood:	n/a	n/a
15	FOS	chr9:8802379-8802627	MCF10A-Er-Src	breast:	n/a	chr9:8802560-8802571
16	FOS	chr9:8802394-8802585	MCF10A-Er-Src	breast:	n/a	chr9:8802560-8802571
17	FOS	chr9:8802395-8802596	MCF10A-Er-Src	breast:	n/a	chr9:8802560-8802571
18	GATA2	chr9:8829143-8829743	SH-SY5Y	brain:	n/a	n/a
19	GATA2	chr9:8815892-8816497	SH-SY5Y	brain:	n/a	chr9:8816178-8816199 chr9:8816191-8816201 chr9:8816183-8816192 chr9:8816266-8816277
20	GATA2	chr9:8809608-8810103	SH-SY5Y	brain:	n/a	chr9:8809660-8809667 chr9:8809660-8809669 chr9:8809660-8809667 chr9:8809656-8809672 chr9:8809923-8809932 chr9:8809660-8809667 chr9:8809653-8809674
21	GATA3	chr9:8829231-8829714	SH-SY5Y	brain:	n/a	n/a
22	GATA3	chr9:8809733-8810088	SH-SY5Y	brain:	n/a	chr9:8809923-8809932
23	GATA3	chr9:8815949-8816552	SH-SY5Y	brain:	n/a	chr9:8816178-8816199 chr9:8816191-8816201 chr9:8816183-8816192 chr9:8816266-8816277
24	GATA3	chr9:8832353-8832399	SH-SY5Y	brain:	n/a	n/a
25	JUN	chr9:8820825-8820999	HepG2	liver:	n/a	chr9:8820915-8820928
26	JUND	chr9:8820798-8821079	HepG2	liver:	n/a	n/a
27	MAFF	chr9:8816895-8817063	HepG2	liver:	n/a	chr9:8816991-8817009
28	MAFF	chr9:8821929-8822297	K562	blood:	n/a	chr9:8822110-8822124 chr9:8822111-8822129
29	MAFF	chr9:8806296-8806493	K562	blood:	n/a	chr9:8806334-8806352
30	MAFF	chr9:8806194-8806506	HepG2	liver:	n/a	chr9:8806334-8806352
31	MAFF	chr9:8821910-8822307	HepG2	liver:	n/a	chr9:8822110-8822124 chr9:8822111-8822129
32	MAFK	chr9:8810959-8811016	HepG2	liver:	n/a	chr9:8810965-8810980
33	MAFK	chr9:8821931-8822322	HepG2	liver:	n/a	chr9:8822112-8822128 chr9:8822117-8822128 chr9:8822109-8822125 chr9:8822115-8822129 chr9:8822110-8822124 chr9:8822112-8822127 chr9:8822116-8822127 chr9:8822107-8822127 chr9:8822116-8822127
34	MAFK	chr9:8821912-8822337	Hela-S3	cervix:	n/a	chr9:8822112-8822128 chr9:8822117-8822128 chr9:8822109-8822125 chr9:8822115-8822129 chr9:8822110-8822124 chr9:8822112-8822127 chr9:8822116-8822127 chr9:8822107-8822127 chr9:8822116-8822127
35	MAFK	chr9:8821940-8822315	H1-hESC	embryonic stem cell:	n/a	chr9:8822112-8822128 chr9:8822117-8822128 chr9:8822109-8822125 chr9:8822115-8822129 chr9:8822110-8822124 chr9:8822112-8822127 chr9:8822116-8822127 chr9:8822107-8822127 chr9:8822116-8822127
36	MAFK	chr9:8821928-8822304	IMR90	lung:	n/a	chr9:8822112-8822128 chr9:8822117-8822128 chr9:8822109-8822125 chr9:8822115-8822129 chr9:8822110-8822124 chr9:8822112-8822127 chr9:8822116-8822127 chr9:8822107-8822127 chr9:8822116-8822127
37	MAFK	chr9:8821938-8822301	K562	blood:	n/a	chr9:8822112-8822128 chr9:8822117-8822128 chr9:8822109-8822125 chr9:8822115-8822129 chr9:8822110-8822124 chr9:8822112-8822127 chr9:8822116-8822127 chr9:8822107-8822127 chr9:8822116-8822127
38	MAFK	chr9:8806203-8806506	IMR90	lung:	n/a	chr9:8806336-8806347 chr9:8806339-8806356 chr9:8806336-8806351 chr9:8806336-8806347 chr9:8806335-8806349 chr9:8806337-8806348 chr9:8806336-8806352 chr9:8806337-8806348
39	MAFK	chr9:8816881-8817081	HepG2	liver:	n/a	chr9:8816995-8817009 chr9:8816992-8817007 chr9:8816996-8817007 chr9:8816997-8817008 chr9:8816996-8817007 chr9:8816997-8817008
40	MAFK	chr9:8806219-8806502	HepG2	liver:	n/a	chr9:8806336-8806347 chr9:8806339-8806356 chr9:8806336-8806351 chr9:8806336-8806347 chr9:8806335-8806349 chr9:8806337-8806348 chr9:8806336-8806352 chr9:8806337-8806348
41	MAFK	chr9:8806191-8806524	HepG2	liver:	n/a	chr9:8806336-8806347 chr9:8806339-8806356 chr9:8806336-8806351 chr9:8806336-8806347 chr9:8806335-8806349 chr9:8806337-8806348 chr9:8806336-8806352 chr9:8806337-8806348
42	MAFK	chr9:8821930-8822308	HepG2	liver:	n/a	chr9:8822112-8822128 chr9:8822117-8822128 chr9:8822109-8822125 chr9:8822115-8822129 chr9:8822110-8822124 chr9:8822112-8822127 chr9:8822116-8822127 chr9:8822107-8822127 chr9:8822116-8822127
43	MAFK	chr9:8821864-8822469	GM12878	blood:	n/a	chr9:8822112-8822128 chr9:8822117-8822128 chr9:8822109-8822125 chr9:8822115-8822129 chr9:8822110-8822124 chr9:8822112-8822127 chr9:8822116-8822127 chr9:8822107-8822127 chr9:8822116-8822127
44	MAFK	chr9:8816885-8817116	HepG2	liver:	n/a	chr9:8816995-8817009 chr9:8816992-8817007 chr9:8816996-8817007 chr9:8816997-8817008 chr9:8816996-8817007 chr9:8816997-8817008
45	MAX	chr9:8816351-8816738	H1-hESC	embryonic stem cell:	n/a	chr9:8816553-8816562 chr9:8816549-8816558
46	MAZ	chr9:8817152-8817276	HepG2	liver:	n/a	n/a
47	MYC	chr9:8804515-8804570	H1-hESC	embryonic stem cell:	n/a	n/a
48	MYC	chr9:8828745-8828945	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr9:8815198-8815305	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr9:8809575-8810152	H1-neurons	neurons:	n/a	n/a

Variant related genes	Relation type
RNU7-185P	TF binding region

Extended variants
information (count: 2060 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:2060 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1550004	chr9:8796449-8796450	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115544276	chr9:8796457-8796458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145805819	chr9:8796464-8796465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10124036	chr9:8796484-8796485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189884707	chr9:8796525-8796526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372310330	chr9:8796537-8796538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs13294311	chr9:8796554-8796555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs13294312	chr9:8796555-8796556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568712943	chr9:8796569-8796570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536114657	chr9:8796580-8796581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10124085	chr9:8796643-8796644	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs572745044	chr9:8796673-8796674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140741061	chr9:8796677-8796678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112538387	chr9:8796689-8796690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs13290166	chr9:8796690-8796691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377272654	chr9:8796692-8796693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs13294642	chr9:8796704-8796705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544347922	chr9:8796706-8796707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375401046	chr9:8796711-8796712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563826862	chr9:8796755-8796756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575920560	chr9:8796782-8796783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542943228	chr9:8796783-8796784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145894629	chr9:8796787-8796788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528459463	chr9:8796790-8796791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547029873	chr9:8796834-8796835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546938482	chr9:8796839-8796840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564958658	chr9:8796842-8796843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114043438	chr9:8796848-8796849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs13290674	chr9:8796912-8796913	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs111313342	chr9:8796921-8796922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539163015	chr9:8796931-8796932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200911854	chr9:8796936-8796937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550667558	chr9:8796937-8796938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181156941	chr9:8797021-8797022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529944603	chr9:8797050-8797051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147827610	chr9:8797056-8797057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73640952	chr9:8797070-8797071	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs146623082	chr9:8797073-8797074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533861654	chr9:8797078-8797079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140814637	chr9:8797087-8797088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570467083	chr9:8797100-8797101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556193632	chr9:8797102-8797103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143010408	chr9:8797151-8797152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576171173	chr9:8797155-8797156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556335004	chr9:8797166-8797167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541950153	chr9:8797178-8797179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535679995	chr9:8797191-8797192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575747506	chr9:8797238-8797239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543233901	chr9:8797242-8797243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554880051	chr9:8797248-8797249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	20668451	CNVD
Schizophrenia	20838587	CNVD
Glioblastoma	18772890	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8778800-8798600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr9:8785400-8797400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:8786200-8799000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr9:8786200-8799400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr9:8786400-8799400	Weak transcription	Fetal Kidney	kidney
6	chr9:8793400-8798000	Weak transcription	Brain Anterior Caudate	brain
7	chr9:8794000-8797600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:8794200-8797200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr9:8794200-8798600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:8794200-8799400	Weak transcription	Fetal Lung	lung
11	chr9:8794200-8821800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr9:8794400-8799200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr9:8794800-8799800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr9:8794800-8825600	Weak transcription	Ovary	ovary
15	chr9:8795800-8797600	Enhancers	Brain Hippocampus Middle	brain
16	chr9:8796000-8796600	Enhancers	Brain Substantia Nigra	brain
17	chr9:8796200-8797400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr9:8796600-8797600	Weak transcription	Brain Substantia Nigra	brain
19	chr9:8797200-8800000	Enhancers	Brain Cingulate Gyrus	brain
20	chr9:8797400-8797600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr9:8797400-8797600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr9:8797400-8797800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr9:8797400-8797800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr9:8797400-8797800	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr9:8797600-8797800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr9:8797600-8797800	Enhancers	Brain Angular Gyrus	brain
27	chr9:8797600-8797800	Enhancers	Brain Substantia Nigra	brain
28	chr9:8797600-8798600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr9:8797600-8798600	Weak transcription	Brain Hippocampus Middle	brain
30	chr9:8797600-8798800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr9:8797600-8800600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr9:8797800-8798200	Weak transcription	Brain Substantia Nigra	brain
33	chr9:8797800-8798400	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr9:8797800-8798400	Weak transcription	Brain Angular Gyrus	brain
35	chr9:8797800-8798800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr9:8797800-8799000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr9:8797800-8799200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr9:8798000-8798200	Enhancers	Brain Anterior Caudate	brain
39	chr9:8798200-8799000	Weak transcription	Brain Anterior Caudate	brain
40	chr9:8798200-8799800	Enhancers	Brain Substantia Nigra	brain
41	chr9:8798400-8798600	Enhancers	Fetal Heart	heart
42	chr9:8798400-8800200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr9:8798400-8800800	Enhancers	Brain Angular Gyrus	brain
44	chr9:8798400-8815400	Weak transcription	Fetal Brain Male	brain
45	chr9:8798600-8798800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr9:8798600-8799800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr9:8798600-8799800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr9:8798600-8800000	Weak transcription	Fetal Heart	heart
49	chr9:8798600-8800200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:8798600-8800600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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