Variant report

Variant	nsv824840
Chromosome Location	chr9:6762285-6805457
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:359)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6779378-6780217	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6788815-6789003	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6779811-6780274	K562	blood:	n/a	n/a
4	ARID3A	chr9:6781433-6781998	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:6787981-6788483	HepG2	liver:	n/a	n/a
6	ATF1	chr9:6779901-6780225	K562	blood:	n/a	n/a
7	ATF2	chr9:6771687-6772129	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr9:6771753-6772027	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr9:6777168-6777670	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr9:6779898-6780160	K562	blood:	n/a	n/a
11	BACH1	chr9:6765406-6765470	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr9:6764615-6764768	H1-hESC	embryonic stem cell:	n/a	chr9:6764754-6764768
13	BCL11A	chr9:6771770-6772048	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr9:6788713-6789019	HepG2	liver:	n/a	n/a
15	BHLHE40	chr9:6787901-6788385	HepG2	liver:	n/a	n/a
16	BRCA1	chr9:6779743-6780201	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr9:6768480-6768824	IMR90	lung:	n/a	chr9:6768629-6768640
18	CEBPB	chr9:6781443-6781836	HepG2	liver:	n/a	chr9:6781728-6781739
19	CEBPB	chr9:6797447-6797583	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr9:6793793-6794137	IMR90	lung:	n/a	chr9:6793948-6793959
21	CEBPB	chr9:6781514-6781923	HepG2	liver:	n/a	chr9:6781728-6781739
22	CEBPB	chr9:6793884-6794068	H1-hESC	embryonic stem cell:	n/a	chr9:6793948-6793959
23	CEBPB	chr9:6797435-6797552	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:6793835-6794105	HepG2	liver:	n/a	chr9:6793948-6793959
25	CEBPB	chr9:6768513-6768813	A549	lung:	n/a	chr9:6768629-6768640
26	CEBPB	chr9:6793815-6794098	K562	blood:	n/a	chr9:6793948-6793959
27	CEBPB	chr9:6781535-6781913	HepG2	liver:	n/a	chr9:6781728-6781739
28	CEBPB	chr9:6768566-6768901	H1-hESC	embryonic stem cell:	n/a	chr9:6768629-6768640
29	CEBPB	chr9:6797383-6797661	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:6763333-6763545	K562	blood:	n/a	n/a
31	CEBPB	chr9:6768492-6768812	Hela-S3	cervix:	n/a	chr9:6768629-6768640
32	CEBPB	chr9:6781642-6781800	K562	blood:	n/a	chr9:6781728-6781739
33	CEBPB	chr9:6781599-6781805	HepG2	liver:	n/a	chr9:6781728-6781739
34	CEBPB	chr9:6793836-6794137	A549	lung:	n/a	chr9:6793948-6793959
35	CEBPB	chr9:6770729-6770955	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr9:6768477-6768941	K562	blood:	n/a	chr9:6768629-6768640
37	CEBPB	chr9:6791899-6792074	HepG2	liver:	n/a	chr9:6791972-6791983
38	CEBPB	chr9:6797470-6797589	K562	blood:	n/a	n/a
39	CEBPB	chr9:6768480-6768823	HepG2	liver:	n/a	chr9:6768629-6768640
40	CEBPD	chr9:6779829-6780307	K562	blood:	n/a	n/a
41	CEBPD	chr9:6779797-6780313	K562	blood:	n/a	n/a
42	CEBPD	chr9:6781541-6781880	HepG2	liver:	n/a	n/a
43	CHD2	chr9:6771793-6772087	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTBP2	chr9:6771650-6772094	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr9:6802686-6802719	GM10266	blood:	n/a	n/a
46	CTCF	chr9:6785760-6785910	GM12865	blood:	n/a	n/a
47	CTCF	chr9:6775740-6775890	GM12875	blood:	n/a	n/a
48	E2F6	chr9:6776719-6777044	H1-hESC	embryonic stem cell:	n/a	n/a
49	E2F6	chr9:6776657-6777194	H1-hESC	embryonic stem cell:	n/a	n/a
50	ELF1	chr9:6779324-6779645	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6779450-6779500	GM06990	blood:	n/a
2	chr9:6779450-6779500	ECC-1	luminal epithelium:	n/a
3	chr9:6779450-6779500	HAEpiC	amniotic membrane:	n/a
4	chr9:6779450-6779500	MCF-7	breast:	n/a
5	chr9:6779450-6779500	SK-N-SH	brain:	n/a
6	chr9:6779450-6779500	PrEC	prostate:	n/a
7	chr9:6779450-6779500	GM19239	blood:	n/a
8	chr9:6779450-6779500	HCF	heart:	n/a
9	chr9:6779450-6779500	NB4	blood:	n/a
10	chr9:6779450-6779500	ovcar-3	ovarian:	n/a
11	chr9:6779450-6779500	HMEC	breast:	n/a
12	chr9:6779450-6779500	AG09319	gingival:	n/a
13	chr9:6779450-6779500	Hepatocyte	liver:	n/a
14	chr9:6779450-6779500	NH-A	brain:	n/a
15	chr9:6779450-6779500	SKMC	muscle:	n/a
16	chr9:6779450-6779500	T-47D	breast:	n/a
17	chr9:6779450-6779500	HNPCEpiC	eye:	n/a
18	chr9:6779450-6779500	HCT-116	colon:	n/a
19	chr9:6779450-6779500	BE2_C	brain:	n/a
20	chr9:6779450-6779500	SK-N-SH_RA	brain:	n/a
21	chr9:6779450-6779500	K562	blood:	n/a
22	chr9:6779450-6779500	AG04449	skin:	fetal
23	chr9:6779450-6779500	Caco-2	colon:	n/a
24	chr9:6779450-6779500	NHDF-neo	bronchial:	n/a
25	chr9:6779450-6779500	MCF10A-Er-Src	breast:	n/a
26	chr9:6779450-6779500	PANC-1	pancreas:	n/a
27	chr9:6779450-6779500	HCM	heart:	n/a
28	chr9:6779450-6779500	RPTEC	kidney:	n/a
29	chr9:6779450-6779500	HRE	kidney:	n/a
30	chr9:6779450-6779500	HEK293	kidney:	embryo
31	chr9:6779450-6779500	CMK	blood:	n/a
32	chr9:6779450-6779500	NT2-D1	testis:	n/a
33	chr9:6779450-6779500	Hela-S3	cervix:	n/a
34	chr9:6779450-6779500	HEEpiC	esophagus:	n/a
35	chr9:6779450-6779500	A549	lung:	n/a
36	chr9:6779450-6779500	GM12891	blood:	n/a
37	chr9:6779450-6779500	HCPEpiC	choroid plexus:	n/a
38	chr9:6779450-6779500	H1-hESC	embryonic stem cell:	embryo
39	chr9:6779450-6779500	HIPEpiC	eye:	n/a
40	chr9:6779450-6779500	HRCEpiC	kidney:	n/a
41	chr9:6779450-6779500	AG04450	lung:	fetal
42	chr9:6779450-6779500	HL-60	blood:	n/a
43	chr9:6779450-6779500	IMR90	lung:	fetal
44	chr9:6779450-6779500	PFSK-1	brain:	n/a
45	chr9:6779450-6779500	AG10803	skin:	n/a
46	chr9:6779450-6779500	ProgFib	skin:	n/a
47	chr9:6779450-6779500	GM12892	blood:	n/a
48	chr9:6779450-6779500	Jurkat	blood:	n/a
49	chr9:6779450-6779500	GM12878	blood:	n/a
50	chr9:6779450-6779500	SAEC	small airway:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6757021..6759532-chr9:6768470..6771017,3	K562	blood:
2	chr9:6757988..6759532-chr9:6768470..6771009,2	K562	blood:
3	chr9:6766833..6770674-chr9:6780008..6783723,3	K562	blood:
4	chr9:6766833..6770674-chr9:6780008..6783723,3	K562	blood:
5	chr9:6756506..6759336-chr9:6761694..6766158,6	MCF-7	breast:
6	chr9:6757388..6759261-chr9:6764601..6766785,2	MCF-7	breast:
7	chr9:6765179..6766927-chr9:6770237..6771845,2	K562	blood:
8	chr9:6706468..6709007-chr9:6764056..6766511,2	MCF-7	breast:
9	chr9:6765179..6766927-chr9:6770237..6771845,2	K562	blood:
10	chr9:6680103..6682666-chr9:6784102..6786978,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UHRF2-1	chr9:6785601-6785929	ENSG00000236563.1
2	lnc-UHRF2-1	chr9:6780333-6780490	ENSG00000236563.1

No data

Variant related genes	Relation type
KDM4C	TF binding region
KDM4C	CpG island
ENSG00000107077	chromatin interactions

Extended variants
information (count: 2385 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2385 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192539320	chr9:6762308-6762309	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs72699617	chr9:6762349-6762350	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs183709654	chr9:6762355-6762356	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs142066100	chr9:6762364-6762365	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569826112	chr9:6762447-6762448	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112679159	chr9:6762492-6762493	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554939110	chr9:6762542-6762543	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566717034	chr9:6762549-6762550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs189193933	chr9:6762580-6762581	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535418171	chr9:6762590-6762591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547645617	chr9:6762591-6762592	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565583556	chr9:6762625-6762626	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs575164423	chr9:6762630-6762631	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs557744508	chr9:6762641-6762642	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs576228926	chr9:6762642-6762643	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76369055	chr9:6762675-6762676	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs77984839	chr9:6762677-6762678	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552210645	chr9:6762684-6762685	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs556032924	chr9:6762713-6762714	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs574159329	chr9:6762729-6762730	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs111434501	chr9:6762749-6762750	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs559986865	chr9:6762772-6762773	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs139103774	chr9:6762801-6762802	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs145198158	chr9:6762804-6762805	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563313641	chr9:6762857-6762858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530927369	chr9:6762878-6762879	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs549050460	chr9:6762900-6762901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs820511	chr9:6762911-6762912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs181992793	chr9:6762917-6762918	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs117378700	chr9:6762919-6762920	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs553208066	chr9:6762955-6762956	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111673708	chr9:6762956-6762957	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs569656090	chr9:6762983-6762984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537175173	chr9:6763004-6763005	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555498568	chr9:6763027-6763028	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574193756	chr9:6763028-6763029	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545142703	chr9:6763034-6763035	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs147623579	chr9:6763036-6763037	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs553246269	chr9:6763037-6763038	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs578212024	chr9:6763041-6763042	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs545261027	chr9:6763066-6763067	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564946412	chr9:6763071-6763072	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs12001316	chr9:6763072-6763073	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs544230539	chr9:6763086-6763087	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs543873538	chr9:6763093-6763094	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs184265172	chr9:6763104-6763105	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs140130399	chr9:6763120-6763121	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs372381345	chr9:6763149-6763150	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs13290778	chr9:6763162-6763163	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547570264	chr9:6763167-6763168	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
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
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
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:1396 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6759000-6763200	Weak transcription	Spleen	Spleen
2	chr9:6759200-6763200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:6759200-6763800	Weak transcription	Lung	lung
4	chr9:6759400-6767400	Weak transcription	Gastric	stomach
5	chr9:6759600-6763200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr9:6759600-6763200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:6759600-6763200	Weak transcription	Thymus	Thymus
8	chr9:6759600-6764000	Weak transcription	Fetal Heart	heart
9	chr9:6759600-6764400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr9:6759600-6764400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr9:6759600-6764600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr9:6759600-6764600	Weak transcription	Colon Smooth Muscle	Colon
13	chr9:6759600-6764800	Weak transcription	Small Intestine	intestine
14	chr9:6759600-6765800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr9:6759600-6766400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr9:6759600-6769200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr9:6759600-6782200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr9:6759800-6764000	Weak transcription	A549	lung
19	chr9:6759800-6764400	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr9:6759800-6766800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr9:6759800-6771800	Weak transcription	Ovary	ovary
22	chr9:6759800-6778800	Weak transcription	Psoas Muscle	Psoas
23	chr9:6759800-6780000	Weak transcription	Rectal Smooth Muscle	rectum
24	chr9:6759800-6782800	Weak transcription	Primary hematopoietic stem cells	blood
25	chr9:6760000-6763200	Weak transcription	Fetal Thymus	thymus
26	chr9:6760000-6774800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr9:6760200-6762400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr9:6760200-6763000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr9:6760200-6763200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr9:6760200-6763200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr9:6760200-6763200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr9:6760200-6763800	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr9:6760200-6764200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr9:6760200-6764400	Weak transcription	Brain Anterior Caudate	brain
35	chr9:6760200-6764400	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr9:6760200-6764600	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr9:6760400-6762800	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr9:6760400-6763200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr9:6760400-6763200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr9:6760400-6763200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr9:6760400-6763200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr9:6760400-6763200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:6760400-6763200	Weak transcription	Fetal Intestine Small	intestine
44	chr9:6760400-6763200	Weak transcription	Dnd41	blood
45	chr9:6760400-6764000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr9:6760400-6764200	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr9:6760400-6764400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr9:6760400-6764400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr9:6760400-6764400	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr9:6760400-6764800	Weak transcription	Rectal Mucosa Donor 31	rectum

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