Variant report

Variant	nsv1026679
Chromosome Location	chr9:9919783-10069385
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	chr9:10059064-10059467	MCF-7	breast:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
4	CEBPB	chr9:9983589-9983789	A549	lung:	n/a	n/a
5	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
6	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
7	CEBPB	chr9:9961634-9961840	IMR90	lung:	n/a	n/a
8	CEBPB	chr9:9955926-9956152	IMR90	lung:	n/a	n/a
9	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
10	CEBPB	chr9:10000141-10000327	H1-hESC	embryonic stem cell:	n/a	chr9:10000229-10000240
11	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
12	CEBPB	chr9:10000119-10000362	A549	lung:	n/a	chr9:10000229-10000240
13	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
14	CEBPB	chr9:9960562-9960826	HepG2	liver:	n/a	chr9:9960692-9960703
15	CEBPB	chr9:9975513-9975767	HepG2	liver:	n/a	chr9:9975624-9975635
16	CEBPB	chr9:10050102-10050399	IMR90	lung:	n/a	n/a
17	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
18	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
19	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
20	CEBPB	chr9:10000093-10000360	HepG2	liver:	n/a	chr9:10000229-10000240
21	CEBPB	chr9:10000095-10000401	IMR90	lung:	n/a	chr9:10000229-10000240
22	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
23	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
24	CEBPB	chr9:9960643-9960771	H1-hESC	embryonic stem cell:	n/a	chr9:9960692-9960703
25	CEBPB	chr9:9955899-9956091	A549	lung:	n/a	n/a
26	CEBPB	chr9:9997246-9997453	H1-hESC	embryonic stem cell:	n/a	n/a
27	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
28	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
29	CEBPB	chr9:9955856-9956112	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:9982174-9982447	IMR90	lung:	n/a	chr9:9982310-9982323
31	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
32	CEBPZ	chr9:9942914-9943090	HepG2	liver:	n/a	n/a
33	CHD2	chr9:10008242-10008651	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr9:9942900-9943050	HRE	kidney:	n/a	chr9:9942981-9942991 chr9:9942978-9942996 chr9:9942984-9942993 chr9:9942980-9942993 chr9:9942979-9942995 chr9:9942973-9942994
35	CTCF	chr9:9942940-9943090	WERI-Rb-1	eye:	n/a	chr9:9942981-9942991 chr9:9942978-9942996 chr9:9942984-9942993 chr9:9942980-9942993 chr9:9942979-9942995 chr9:9942973-9942994
36	CTCF	chr9:9998580-9998730	GM12872	blood:	n/a	n/a
37	CTCF	chr9:10045666-10045919	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr9:10060363-10060643	SK-N-SH_RA	brain:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
39	CTCF	chr9:9942893-9943091	SK-N-SH_RA	brain:	n/a	chr9:9942981-9942991 chr9:9942978-9942996 chr9:9942984-9942993 chr9:9942980-9942993 chr9:9942979-9942995 chr9:9942973-9942994
40	CTCF	chr9:9942667-9943366	A549	lung:	n/a	chr9:9942981-9942991 chr9:9942978-9942996 chr9:9942984-9942993 chr9:9942980-9942993 chr9:9942979-9942995 chr9:9942973-9942994
41	CTCF	chr9:9998100-9998250	GM12866	blood:	n/a	n/a
42	CTCF	chr9:10060420-10060570	GM12873	blood:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
43	CTCF	chr9:9942900-9943050	GM12869	blood:	n/a	chr9:9942981-9942991 chr9:9942978-9942996 chr9:9942984-9942993 chr9:9942980-9942993 chr9:9942979-9942995 chr9:9942973-9942994
44	CTCF	chr9:9920558-9920697	Gliobla	brain:	n/a	chr9:9920610-9920628 chr9:9920605-9920626 chr9:9920616-9920625
45	CTCF	chr9:9942900-9943050	Caco-2	colon:	n/a	chr9:9942981-9942991 chr9:9942978-9942996 chr9:9942984-9942993 chr9:9942980-9942993 chr9:9942979-9942995 chr9:9942973-9942994
46	CTCF	chr9:10060420-10060570	HVMF	connective:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
47	CTCF	chr9:9971580-9971730	NHEK	skin:	n/a	n/a
48	CTCF	chr9:10026619-10026648	GM12878	blood:	n/a	chr9:10026619-10026640
49	CTCF	chr9:9942920-9943070	HFF	foreskin:	n/a	chr9:9942981-9942991 chr9:9942978-9942996 chr9:9942984-9942993 chr9:9942980-9942993 chr9:9942979-9942995 chr9:9942973-9942994
50	CTCF	chr9:9942787-9943150	Pancreas_OC	pancreas:	n/a	chr9:9942981-9942991 chr9:9942978-9942996 chr9:9942984-9942993 chr9:9942980-9942993 chr9:9942979-9942995 chr9:9942973-9942994

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:9998791-9998841	AG10803	skin:	n/a
2	chr9:9998791-9998841	H1-hESC	embryonic stem cell:	embryo
3	chr9:9998791-9998841	HIPEpiC	eye:	n/a
4	chr9:9998791-9998841	ovcar-3	ovarian:	n/a
5	chr9:9998791-9998841	GM12891	blood:	n/a
6	chr9:9998791-9998841	NHDF-neo	bronchial:	n/a
7	chr9:9998791-9998841	PrEC	prostate:	n/a
8	chr9:9998791-9998841	GM06990	blood:	n/a
9	chr9:9998791-9998841	AG04450	lung:	fetal
10	chr9:9998791-9998841	HRPEpiC	eye:	n/a
11	chr9:9998791-9998841	K562	blood:	n/a
12	chr9:9998791-9998841	HEK293	kidney:	embryo
13	chr9:9998791-9998841	Hela-S3	cervix:	n/a
14	chr9:9998791-9998841	MCF10A-Er-Src	breast:	n/a
15	chr9:9998791-9998841	AG09319	gingival:	n/a
16	chr9:9998791-9998841	MCF-7	breast:	n/a
17	chr9:9998791-9998841	BJ	skin:	n/a
18	chr9:9998791-9998841	HUVEC	blood vessel:	n/a
19	chr9:9998791-9998841	LNCaP	prostate:	n/a
20	chr9:9998791-9998841	GM12878	blood:	n/a
21	chr9:9998791-9998841	NT2-D1	testis:	n/a
22	chr9:9998791-9998841	Jurkat	blood:	n/a
23	chr9:9998791-9998841	CMK	blood:	n/a
24	chr9:9998791-9998841	HCPEpiC	choroid plexus:	n/a
25	chr9:9998791-9998841	BE2_C	brain:	n/a
26	chr9:9998791-9998841	GM12892	blood:	n/a
27	chr9:9998791-9998841	T-47D	breast:	n/a
28	chr9:9998791-9998841	HNPCEpiC	eye:	n/a
29	chr9:9998791-9998841	AoSMC	blood vessel:	n/a
30	chr9:9998791-9998841	NH-A	brain:	n/a
31	chr9:9998791-9998841	SAEC	small airway:	n/a
32	chr9:9998791-9998841	HL-60	blood:	n/a
33	chr9:9998791-9998841	HAEpiC	amniotic membrane:	n/a
34	chr9:9998791-9998841	ProgFib	skin:	n/a
35	chr9:9998791-9998841	HRE	kidney:	n/a
36	chr9:9998791-9998841	SK-N-SH	brain:	n/a
37	chr9:9998791-9998841	IMR90	lung:	fetal
38	chr9:9998791-9998841	HepG2	liver:	n/a
39	chr9:9998791-9998841	Hepatocyte	liver:	n/a
40	chr9:9998791-9998841	GM19239	blood:	n/a
41	chr9:9998791-9998841	AG04449	skin:	fetal
42	chr9:9998791-9998841	HRCEpiC	kidney:	n/a
43	chr9:9998791-9998841	HCM	heart:	n/a
44	chr9:9998791-9998841	SK-N-SH_RA	brain:	n/a
45	chr9:9998791-9998841	HMEC	breast:	n/a
46	chr9:9998791-9998841	SKMC	muscle:	n/a
47	chr9:9998791-9998841	RPTEC	kidney:	n/a
48	chr9:9998791-9998841	U87	brain:	n/a
49	chr9:9998791-9998841	ECC-1	luminal epithelium:	n/a
50	chr9:9998791-9998841	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:9910391..9912203-chr9:9917426..9920377,2	K562	blood:
2	chr9:10053198..10055670-chr9:10065089..10066974,2	K562	blood:
3	chr9:10060352..10060896-chr9:10268535..10269397,2	MCF-7	breast:
4	chr9:10045409..10046174-chr9:10268540..10269128,2	MCF-7	breast:
5	chr9:10053198..10055670-chr9:10065089..10066974,2	K562	blood:

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

Extended variants
information (count: 4805 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:4805 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78809942	chr9:9919790-9919791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76311415	chr9:9919799-9919800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567869030	chr9:9919802-9919803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10978089	chr9:9919881-9919882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530293465	chr9:9919884-9919885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547278079	chr9:9919887-9919888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138189303	chr9:9919894-9919895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534652426	chr9:9919898-9919899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190670721	chr9:9919912-9919913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571400419	chr9:9919924-9919925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181772421	chr9:9919929-9919930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10816233	chr9:9919941-9919942	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs576279564	chr9:9919949-9919950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573790359	chr9:9919951-9919952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542511213	chr9:9919955-9919956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553282086	chr9:9919977-9919978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572895792	chr9:9920016-9920017	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs545036722	chr9:9920018-9920019	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs186589038	chr9:9920021-9920022	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs530883358	chr9:9920036-9920037	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs544707312	chr9:9920049-9920050	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs149590246	chr9:9920050-9920051	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs530317126	chr9:9920058-9920059	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs528687029	chr9:9920065-9920066	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs546973988	chr9:9920066-9920067	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs10816234	chr9:9920089-9920090	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs528076405	chr9:9920123-9920124	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs147232229	chr9:9920124-9920125	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs571280447	chr9:9920145-9920146	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs571379326	chr9:9920148-9920149	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs537103900	chr9:9920171-9920172	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs189799267	chr9:9920182-9920183	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs140760608	chr9:9920205-9920206	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs536489738	chr9:9920214-9920215	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs537177217	chr9:9920223-9920224	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs143306601	chr9:9920227-9920228	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs147544757	chr9:9920236-9920237	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs10816235	chr9:9920242-9920243	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs376763830	chr9:9920243-9920244	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs148554091	chr9:9920244-9920245	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs544330803	chr9:9920253-9920254	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs182698871	chr9:9920270-9920271	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs561476642	chr9:9920275-9920276	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs574924960	chr9:9920284-9920285	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs568373521	chr9:9920301-9920302	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs10816236	chr9:9920345-9920346	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs79454954	chr9:9920395-9920396	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs142906191	chr9:9920401-9920402	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs552915629	chr9:9920415-9920416	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs113250515	chr9:9920417-9920418	Enhancers Active TSS	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
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:9918600-9920800	Enhancers	Brain Germinal Matrix	brain
2	chr9:9919200-9920400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr9:9919200-9920400	Enhancers	Fetal Brain Male	brain
4	chr9:9919400-9919800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr9:9919400-9919800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr9:9919400-9920400	Enhancers	Fetal Brain Female	brain
7	chr9:9919600-9920200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr9:9919800-9920000	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr9:9919800-9920400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr9:9920000-9920200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr9:9920200-9921000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr9:9920200-9921000	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr9:9920600-9921000	Enhancers	Brain Cingulate Gyrus	brain
14	chr9:9921000-9921200	Enhancers	Duodenum Mucosa	Duodenum
15	chr9:9922000-9922200	Enhancers	Primary hematopoietic stem cells	blood
16	chr9:9922000-9922400	Active TSS	Duodenum Mucosa	Duodenum
17	chr9:9922000-9924000	Enhancers	Small Intestine	intestine
18	chr9:9922000-9924200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr9:9922200-9924200	Weak transcription	Primary hematopoietic stem cells	blood
20	chr9:9922400-9922600	Enhancers	Duodenum Mucosa	Duodenum
21	chr9:9922400-9924000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:9922600-9923600	Weak transcription	Duodenum Mucosa	Duodenum
23	chr9:9923600-9924800	Active TSS	Duodenum Mucosa	Duodenum
24	chr9:9924000-9924400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:9924000-9924800	Active TSS	Primary T cells fromperipheralblood	blood
26	chr9:9924000-9924800	Active TSS	Fetal Lung	lung
27	chr9:9924000-9926800	Weak transcription	Small Intestine	intestine
28	chr9:9924200-9924400	Flanking Active TSS	Primary hematopoietic stem cells	blood
29	chr9:9924200-9924600	Active TSS	Primary monocytes fromperipheralblood	blood
30	chr9:9924200-9924600	Active TSS	Cortex derived primary cultured neurospheres	brain
31	chr9:9924200-9924600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr9:9924200-9924600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
33	chr9:9924200-9924600	Active TSS	Rectal Mucosa Donor 31	rectum
34	chr9:9924200-9924800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr9:9924200-9924800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr9:9924200-9924800	Active TSS	Adipose Nuclei	Adipose
37	chr9:9924200-9924800	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr9:9924200-9924800	Active TSS	Placenta	Placenta
39	chr9:9924200-9924800	Active TSS	Fetal Stomach	stomach
40	chr9:9924200-9925000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
41	chr9:9924400-9924600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr9:9924400-9924800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr9:9924400-9924800	Active TSS	Fetal Kidney	kidney
44	chr9:9924400-9924800	Active TSS	Ovary	ovary
45	chr9:9924400-9925000	Active TSS	Primary hematopoietic stem cells	blood
46	chr9:9924600-9925000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr9:9924800-9925000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr9:9931400-9931800	Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr9:9939400-9939800	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr9:9942600-9943000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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