Variant report

Variant	nsv539989
Chromosome Location	chr9:9943339-10126281
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	ARID3A	chr9:10045783-10045920	HepG2	liver:	n/a	n/a
2	BACH1	chr9:10008391-10008587	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr9:10101598-10101883	A549	lung:	n/a	chr9:10101728-10101739 chr9:10101730-10101739 chr9:10101730-10101739 chr9:10101729-10101740 chr9:10101730-10101739 chr9:10101728-10101741 chr9:10101730-10101739
4	CEBPB	chr9:9983589-9983789	A549	lung:	n/a	n/a
5	CEBPB	chr9:10101562-10101892	HepG2	liver:	n/a	chr9:10101728-10101739 chr9:10101730-10101739 chr9:10101730-10101739 chr9:10101729-10101740 chr9:10101730-10101739 chr9:10101728-10101741 chr9:10101730-10101739
6	CEBPB	chr9:10125227-10125411	HepG2	liver:	n/a	chr9:10125267-10125278
7	CEBPB	chr9:10126127-10126248	HepG2	liver:	n/a	chr9:10126189-10126200 chr9:10126147-10126158
8	CEBPB	chr9:10059043-10059532	A549	lung:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
9	CEBPB	chr9:9975513-9975767	HepG2	liver:	n/a	chr9:9975624-9975635
10	CEBPB	chr9:10059013-10059547	A549	lung:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
11	CEBPB	chr9:10059025-10059505	ECC-1	luminal epithelium:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
12	CEBPB	chr9:10059113-10059428	HepG2	liver:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
13	CEBPB	chr9:10059167-10059392	HepG2	liver:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
14	CEBPB	chr9:10058985-10059505	MCF-7	breast:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
15	CEBPB	chr9:10000093-10000360	HepG2	liver:	n/a	chr9:10000229-10000240
16	CEBPB	chr9:9955856-9956112	HepG2	liver:	n/a	n/a
17	CEBPB	chr9:9997246-9997453	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr9:10000119-10000362	A549	lung:	n/a	chr9:10000229-10000240
19	CEBPB	chr9:9955899-9956091	A549	lung:	n/a	n/a
20	CEBPB	chr9:10050102-10050399	IMR90	lung:	n/a	n/a
21	CEBPB	chr9:9982174-9982447	IMR90	lung:	n/a	chr9:9982310-9982323
22	CEBPB	chr9:10059095-10059476	K562	blood:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
23	CEBPB	chr9:10059063-10059490	H1-hESC	embryonic stem cell:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
24	CEBPB	chr9:10073607-10073661	HepG2	liver:	n/a	n/a
25	CEBPB	chr9:10059095-10059482	A549	lung:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
26	CEBPB	chr9:10000095-10000401	IMR90	lung:	n/a	chr9:10000229-10000240
27	CEBPB	chr9:10059096-10059479	HepG2	liver:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
28	CEBPB	chr9:10000141-10000327	H1-hESC	embryonic stem cell:	n/a	chr9:10000229-10000240
29	CEBPB	chr9:10101585-10101907	IMR90	lung:	n/a	chr9:10101728-10101739 chr9:10101730-10101739 chr9:10101730-10101739 chr9:10101729-10101740 chr9:10101730-10101739 chr9:10101728-10101741 chr9:10101730-10101739
30	CEBPB	chr9:9960562-9960826	HepG2	liver:	n/a	chr9:9960692-9960703
31	CEBPB	chr9:9961634-9961840	IMR90	lung:	n/a	n/a
32	CEBPB	chr9:10059065-10059560	IMR90	lung:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
33	CEBPB	chr9:9960643-9960771	H1-hESC	embryonic stem cell:	n/a	chr9:9960692-9960703
34	CEBPB	chr9:10059096-10059483	Hela-S3	cervix:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
35	CEBPB	chr9:10059029-10059551	ECC-1	luminal epithelium:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
36	CEBPB	chr9:9955926-9956152	IMR90	lung:	n/a	n/a
37	CEBPB	chr9:10059064-10059467	MCF-7	breast:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
38	CHD2	chr9:10008242-10008651	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr9:10026570-10026680	HepG2	liver:	n/a	chr9:10026618-10026634 chr9:10026619-10026640
40	CTCF	chr9:10060400-10060550	NHDF-neo	bronchial:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
41	CTCF	chr9:9998660-9998810	MCF-7	breast:	n/a	n/a
42	CTCF	chr9:9998560-9998710	BE2_C	brain:	n/a	n/a
43	CTCF	chr9:10045666-10045929	Medullo	brain:	n/a	n/a
44	CTCF	chr9:9998497-9998869	MCF-7	breast:	n/a	n/a
45	CTCF	chr9:10060440-10060590	GM06990	blood:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
46	CTCF	chr9:9998580-9998730	HMEC	breast:	n/a	n/a
47	CTCF	chr9:10060413-10060623	Hela-S3	cervix:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
48	CTCF	chr9:9943200-9943350	AG04449	skin:	n/a	n/a
49	CTCF	chr9:10026548-10026679	HUVEC	blood vessel:	n/a	chr9:10026618-10026634 chr9:10026619-10026640
50	CTCF	chr9:9998540-9998690	GM12875	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:9998791-9998841	PFSK-1	brain:	n/a
2	chr9:9998791-9998841	NHBE	bronchial:	n/a
3	chr9:9998791-9998841	SKMC	muscle:	n/a
4	chr9:9998791-9998841	AG04450	lung:	fetal
5	chr9:9998791-9998841	HMEC	breast:	n/a
6	chr9:9998791-9998841	HEK293	kidney:	embryo
7	chr9:9998791-9998841	PrEC	prostate:	n/a
8	chr9:9998791-9998841	BE2_C	brain:	n/a
9	chr9:9998791-9998841	HRE	kidney:	n/a
10	chr9:9998791-9998841	BJ	skin:	n/a
11	chr9:9998791-9998841	AG10803	skin:	n/a
12	chr9:9998791-9998841	AG04449	skin:	fetal
13	chr9:9998791-9998841	GM06990	blood:	n/a
14	chr9:9998791-9998841	MCF10A-Er-Src	breast:	n/a
15	chr9:9998791-9998841	CMK	blood:	n/a
16	chr9:9998791-9998841	HAEpiC	amniotic membrane:	n/a
17	chr9:9998791-9998841	AG09309	skin:	n/a
18	chr9:9998791-9998841	HL-60	blood:	n/a
19	chr9:9998791-9998841	IMR90	lung:	fetal
20	chr9:9998791-9998841	Hela-S3	cervix:	n/a
21	chr9:9998791-9998841	SK-N-MC	brain:	n/a
22	chr9:9998791-9998841	HCT-116	colon:	n/a
23	chr9:9998791-9998841	GM12878	blood:	n/a
24	chr9:9998791-9998841	K562	blood:	n/a
25	chr9:9998791-9998841	T-47D	breast:	n/a
26	chr9:9998791-9998841	HCF	heart:	n/a
27	chr9:9998791-9998841	SK-N-SH_RA	brain:	n/a
28	chr9:9998791-9998841	NB4	blood:	n/a
29	chr9:9998791-9998841	HRCEpiC	kidney:	n/a
30	chr9:9998791-9998841	HUVEC	blood vessel:	n/a
31	chr9:9998791-9998841	Jurkat	blood:	n/a
32	chr9:9998791-9998841	HNPCEpiC	eye:	n/a
33	chr9:9998791-9998841	NT2-D1	testis:	n/a
34	chr9:9998791-9998841	AG09319	gingival:	n/a
35	chr9:9998791-9998841	ovcar-3	ovarian:	n/a
36	chr9:9998791-9998841	H1-hESC	embryonic stem cell:	embryo
37	chr9:9998791-9998841	HRPEpiC	eye:	n/a
38	chr9:9998791-9998841	HCPEpiC	choroid plexus:	n/a
39	chr9:9998791-9998841	PANC-1	pancreas:	n/a
40	chr9:9998791-9998841	Caco-2	colon:	n/a
41	chr9:9998791-9998841	HEEpiC	esophagus:	n/a
42	chr9:9998791-9998841	NHDF-neo	bronchial:	n/a
43	chr9:9998791-9998841	LNCaP	prostate:	n/a
44	chr9:9998791-9998841	GM12891	blood:	n/a
45	chr9:9998791-9998841	HCM	heart:	n/a
46	chr9:9998791-9998841	GM19239	blood:	n/a
47	chr9:9998791-9998841	HIPEpiC	eye:	n/a
48	chr9:9998791-9998841	ProgFib	skin:	n/a
49	chr9:9998791-9998841	U87	brain:	n/a
50	chr9:9998791-9998841	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:10045409..10046174-chr9:10268540..10269128,2	MCF-7	breast:
2	chr9:10053198..10055670-chr9:10065089..10066974,2	K562	blood:
3	chr9:10053198..10055670-chr9:10065089..10066974,2	K562	blood:
4	chr9:10060352..10060896-chr9:10268535..10269397,2	MCF-7	breast:

Variant related genes	Relation type
PTPRD	TF binding region
PTPRD	CpG island

Extended variants
information (count: 6013 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:6013 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191032090	chr9:9943339-9943340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527446468	chr9:9943343-9943344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547588681	chr9:9943352-9943353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570604691	chr9:9943358-9943359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533300700	chr9:9943363-9943364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10514816	chr9:9943367-9943368	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs183304481	chr9:9943379-9943380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs36092810	chr9:9943397-9943398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535541020	chr9:9943400-9943401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs566039478	chr9:9943414-9943415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555407616	chr9:9943417-9943418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370994764	chr9:9943426-9943427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369359363	chr9:9943433-9943434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565858850	chr9:9943461-9943462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534859111	chr9:9943465-9943466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561732202	chr9:9943519-9943520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188185788	chr9:9943521-9943522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532719110	chr9:9943525-9943526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150931999	chr9:9943553-9943554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547351220	chr9:9943556-9943557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576139945	chr9:9943557-9943558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192280594	chr9:9943562-9943563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561735681	chr9:9943571-9943572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141110709	chr9:9943578-9943579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116428156	chr9:9943587-9943588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532778327	chr9:9943601-9943602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184666402	chr9:9943612-9943613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187870061	chr9:9943630-9943631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7854099	chr9:9943631-9943632	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs201020873	chr9:9943648-9943649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113236085	chr9:9943650-9943651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369507866	chr9:9943651-9943652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35261613	chr9:9943653-9943654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569631579	chr9:9943656-9943657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375452010	chr9:9943683-9943684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs16930657	chr9:9943710-9943711	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs192598189	chr9:9943742-9943743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541638971	chr9:9943771-9943772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561964616	chr9:9943772-9943773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144918667	chr9:9943774-9943775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138652002	chr9:9943780-9943781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558065145	chr9:9943820-9943821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183508710	chr9:9943833-9943834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530210293	chr9:9943852-9943853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571837676	chr9:9943871-9943872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537327330	chr9:9943873-9943874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557652478	chr9:9943875-9943876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574405872	chr9:9943906-9943907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552926152	chr9:9943939-9943940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541796930	chr9:9943942-9943943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
abnormal development	18461090	CNVD
Disorders of sex development	21048976	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
Glioblastoma multiforme	21080181	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
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
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	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
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
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21611746	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Glioma	20126413	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	22183965	CNVD

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:9943000-9943400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr9:9943200-9943600	Enhancers	Fetal Heart	heart
3	chr9:9943400-9944400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr9:9943600-9944200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:9943600-9949600	Weak transcription	Fetal Heart	heart
6	chr9:9943800-9944400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:9946400-9946800	Enhancers	Fetal Brain Male	brain
8	chr9:9949600-9949800	Active TSS	Fetal Heart	heart
9	chr9:9949600-9950400	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr9:9949800-9950000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr9:9949800-9950400	Flanking Active TSS	Fetal Heart	heart
12	chr9:9950000-9950400	Enhancers	Left Ventricle	heart
13	chr9:9950000-9951400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr9:9950000-9952400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr9:9950400-9950800	Enhancers	Fetal Heart	heart
16	chr9:9950800-9951200	Flanking Active TSS	Fetal Heart	heart
17	chr9:9950800-9952600	Enhancers	Primary hematopoietic stem cells	blood
18	chr9:9951200-9954200	Enhancers	Fetal Heart	heart
19	chr9:9951400-9951800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr9:9951800-9952200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr9:9962200-9962600	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr9:9963200-9963600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr9:9965000-9965400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:9965200-9967800	Enhancers	Fetal Heart	heart
25	chr9:9969600-9970000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:9970000-9972800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr9:9970600-9971000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr9:9972800-9973000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr9:9972800-9973600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr9:9973200-9973600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr9:9989600-9989800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr9:9989800-9990000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr9:9989800-10000400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr9:9990000-9999000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr9:9990200-9990600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr9:9994200-9994400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:9994400-9995000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr9:9995000-9995400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr9:9995000-9998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr9:9995200-9995800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr9:9995200-9996200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr9:9995200-9998000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr9:9995200-9998200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr9:9995200-9999200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr9:9995200-9999200	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr9:9995200-9999400	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr9:9995200-10001000	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr9:9995400-9995600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr9:9995400-9995600	Enhancers	H9 Cell Line	embryonic stem cell
50	chr9:9995400-9995600	Enhancers	Primary hematopoietic stem cells	blood

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