Variant report

Variant	nsv892302
Chromosome Location	chr9:9974221-10158866
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	ARID3A	chr9:10146474-10146820	HepG2	liver:	n/a	n/a
3	BACH1	chr9:10008391-10008587	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr9:10130155-10130709	IMR90	lung:	n/a	chr9:10130521-10130533
5	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
6	CEBPB	chr9:10126127-10126248	HepG2	liver:	n/a	chr9:10126189-10126200 chr9:10126147-10126158
7	CEBPB	chr9:9982174-9982447	IMR90	lung:	n/a	chr9:9982310-9982323
8	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
9	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
10	CEBPB	chr9:10000141-10000327	H1-hESC	embryonic stem cell:	n/a	chr9:10000229-10000240
11	CEBPB	chr9:9997246-9997453	H1-hESC	embryonic stem cell:	n/a	n/a
12	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
13	CEBPB	chr9:10156585-10156841	IMR90	lung:	n/a	chr9:10156731-10156742
14	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
15	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
16	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
17	CEBPB	chr9:10000095-10000401	IMR90	lung:	n/a	chr9:10000229-10000240
18	CEBPB	chr9:9975513-9975767	HepG2	liver:	n/a	chr9:9975624-9975635
19	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
20	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
21	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
22	CEBPB	chr9:10000119-10000362	A549	lung:	n/a	chr9:10000229-10000240
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	chr9:10050102-10050399	IMR90	lung:	n/a	n/a
25	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
26	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
27	CEBPB	chr9:10000093-10000360	HepG2	liver:	n/a	chr9:10000229-10000240
28	CEBPB	chr9:10125227-10125411	HepG2	liver:	n/a	chr9:10125267-10125278
29	CEBPB	chr9:10156638-10156842	HepG2	liver:	n/a	chr9:10156731-10156742
30	CEBPB	chr9:10073607-10073661	HepG2	liver:	n/a	n/a
31	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
32	CEBPB	chr9:9983589-9983789	A549	lung:	n/a	n/a
33	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
34	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
35	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
36	CHD2	chr9:10008242-10008651	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr9:10060380-10060530	SK-N-SH_RA	brain:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521
38	CTCF	chr9:9998560-9998710	BE2_C	brain:	n/a	n/a
39	CTCF	chr9:9998580-9998730	MCF-7	breast:	n/a	n/a
40	CTCF	chr9:10060200-10060350	GM12868	blood:	n/a	n/a
41	CTCF	chr9:9998543-9998760	MCF-7	breast:	n/a	n/a
42	CTCF	chr9:10060440-10060590	Caco-2	colon:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
43	CTCF	chr9:10060000-10060150	HVMF	connective:	n/a	n/a
44	CTCF	chr9:10060135-10060196	GM20000	blood:	n/a	n/a
45	CTCF	chr9:9998560-9998710	AG09319	gingival:	n/a	n/a
46	CTCF	chr9:10060480-10060630	NHDF-neo	bronchial:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
47	CTCF	chr9:10060460-10060610	HA-sp	spinal cord:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
48	CTCF	chr9:10045720-10045870	BJ	skin:	n/a	n/a
49	CTCF	chr9:10060325-10060602	HepG2	liver:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
50	CTCF	chr9:10060142-10060259	GM13977	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:9998791-9998841	MCF10A-Er-Src	breast:	n/a
2	chr9:9998791-9998841	HRPEpiC	eye:	n/a
3	chr9:9998791-9998841	GM06990	blood:	n/a
4	chr9:9998791-9998841	HNPCEpiC	eye:	n/a
5	chr9:9998791-9998841	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:9998791-9998841	K562	blood:	n/a
7	chr9:9998791-9998841	NHDF-neo	bronchial:	n/a
8	chr9:9998791-9998841	NB4	blood:	n/a
9	chr9:9998791-9998841	Hela-S3	cervix:	n/a
10	chr9:9998791-9998841	HCPEpiC	choroid plexus:	n/a
11	chr9:9998791-9998841	HMEC	breast:	n/a
12	chr9:9998791-9998841	SK-N-MC	brain:	n/a
13	chr9:9998791-9998841	HRE	kidney:	n/a
14	chr9:9998791-9998841	MCF-7	breast:	n/a
15	chr9:9998791-9998841	HCF	heart:	n/a
16	chr9:9998791-9998841	HCM	heart:	n/a
17	chr9:9998791-9998841	A549	lung:	n/a
18	chr9:9998791-9998841	SKMC	muscle:	n/a
19	chr9:9998791-9998841	RPTEC	kidney:	n/a
20	chr9:9998791-9998841	ECC-1	luminal epithelium:	n/a
21	chr9:9998791-9998841	AG09309	skin:	n/a
22	chr9:9998791-9998841	SK-N-SH	brain:	n/a
23	chr9:9998791-9998841	AoSMC	blood vessel:	n/a
24	chr9:9998791-9998841	GM12878	blood:	n/a
25	chr9:9998791-9998841	HUVEC	blood vessel:	n/a
26	chr9:9998791-9998841	HAEpiC	amniotic membrane:	n/a
27	chr9:9998791-9998841	ovcar-3	ovarian:	n/a
28	chr9:9998791-9998841	ProgFib	skin:	n/a
29	chr9:9998791-9998841	PrEC	prostate:	n/a
30	chr9:9998791-9998841	IMR90	lung:	fetal
31	chr9:9998791-9998841	Jurkat	blood:	n/a
32	chr9:9998791-9998841	AG04449	skin:	fetal
33	chr9:9998791-9998841	GM19239	blood:	n/a
34	chr9:9998791-9998841	LNCaP	prostate:	n/a
35	chr9:9998791-9998841	AG04450	lung:	fetal
36	chr9:9998791-9998841	SAEC	small airway:	n/a
37	chr9:9998791-9998841	BE2_C	brain:	n/a
38	chr9:9998791-9998841	Hepatocyte	liver:	n/a
39	chr9:9998791-9998841	T-47D	breast:	n/a
40	chr9:9998791-9998841	HEEpiC	esophagus:	n/a
41	chr9:9998791-9998841	PANC-1	pancreas:	n/a
42	chr9:9998791-9998841	HIPEpiC	eye:	n/a
43	chr9:9998791-9998841	AG10803	skin:	n/a
44	chr9:9998791-9998841	NT2-D1	testis:	n/a
45	chr9:9998791-9998841	BJ	skin:	n/a
46	chr9:9998791-9998841	HRCEpiC	kidney:	n/a
47	chr9:9998791-9998841	SK-N-SH_RA	brain:	n/a
48	chr9:9998791-9998841	U87	brain:	n/a
49	chr9:9998791-9998841	HL-60	blood:	n/a
50	chr9:9998791-9998841	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:10045409..10046174-chr9:10268540..10269128,2	MCF-7	breast:
2	chr9:10060352..10060896-chr9:10268535..10269397,2	MCF-7	breast:
3	chr9:10053198..10055670-chr9:10065089..10066974,2	K562	blood:
4	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: 5762 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:5762 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531816140	chr9:9989621-9989622	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs192785588	chr9:9989622-9989623	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs10978151	chr9:9989624-9989625	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs527848604	chr9:9989632-9989633	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs574688133	chr9:9989678-9989679	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs548014331	chr9:9989679-9989680	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs571100071	chr9:9989686-9989687	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs374508985	chr9:9989700-9989701	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs371341485	chr9:9989747-9989748	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs367837110	chr9:9989754-9989755	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs539760812	chr9:9989759-9989760	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs373140609	chr9:9989760-9989761	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs2096316	chr9:9989765-9989766	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs568790160	chr9:9989787-9989788	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs113507082	chr9:9989796-9989797	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs573328484	chr9:9989813-9989814	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554282125	chr9:9989814-9989815	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574202747	chr9:9989820-9989821	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150826114	chr9:9989842-9989843	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139409075	chr9:9989858-9989859	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577030567	chr9:9989920-9989921	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545812863	chr9:9989940-9989941	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116030458	chr9:9989963-9989964	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184665103	chr9:9989964-9989965	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542254140	chr9:9989983-9989984	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73406425	chr9:9989987-9989988	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs188152654	chr9:9990001-9990002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547977655	chr9:9990009-9990010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150072232	chr9:9990017-9990018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545540198	chr9:9990051-9990052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192737179	chr9:9990064-9990065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145335042	chr9:9990068-9990069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78699440	chr9:9990071-9990072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199744463	chr9:9990072-9990073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537405812	chr9:9990092-9990093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547784248	chr9:9990104-9990105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567786652	chr9:9990124-9990125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533656568	chr9:9990138-9990139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538162337	chr9:9990141-9990142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553916553	chr9:9990145-9990146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576991663	chr9:9990151-9990152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374136872	chr9:9990173-9990174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530913073	chr9:9990191-9990192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185092597	chr9:9990219-9990220	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556143763	chr9:9990236-9990237	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576409340	chr9:9990286-9990287	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542217855	chr9:9990316-9990317	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562082972	chr9:9990331-9990332	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368069317	chr9:9990345-9990346	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200930709	chr9:9990364-9990365	ZNF genes & repeats 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
Glioma	20126413	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	22183965	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:9989600-9989800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:9989800-9990000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:9989800-10000400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:9990000-9999000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:9990200-9990600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:9994200-9994400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:9994400-9995000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr9:9995000-9995400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr9:9995000-9998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr9:9995200-9995800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr9:9995200-9996200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr9:9995200-9998000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr9:9995200-9998200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr9:9995200-9999200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr9:9995200-9999200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr9:9995200-9999400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr9:9995200-10001000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr9:9995400-9995600	Enhancers	H1 Cell Line	embryonic stem cell
19	chr9:9995400-9995600	Enhancers	H9 Cell Line	embryonic stem cell
20	chr9:9995400-9995600	Enhancers	Primary hematopoietic stem cells	blood
21	chr9:9995400-9995800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:9995400-9997200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr9:9995600-9996200	Weak transcription	Primary hematopoietic stem cells	blood
24	chr9:9995600-9996400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr9:9995600-9996400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr9:9995600-9997200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr9:9995800-9996400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr9:9996200-9997600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr9:9996200-9999000	Enhancers	Primary hematopoietic stem cells	blood
30	chr9:9996400-9996600	Enhancers	H1 Cell Line	embryonic stem cell
31	chr9:9996400-9996600	Enhancers	H9 Cell Line	embryonic stem cell
32	chr9:9996400-9996800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr9:9996400-9996800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr9:9996400-9996800	Enhancers	Stomach Mucosa	stomach
35	chr9:9996400-9997000	Enhancers	Fetal Kidney	kidney
36	chr9:9996400-9997200	Enhancers	HUVEC	blood vessel
37	chr9:9996600-9997400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr9:9996600-9997400	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr9:9996800-9998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr9:9996800-9999200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr9:9997200-9997600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr9:9997200-9998200	Weak transcription	HUVEC	blood vessel
43	chr9:9997200-9999000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr9:9997200-9999200	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr9:9997400-9997800	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr9:9997400-9998600	Enhancers	H1 Cell Line	embryonic stem cell
47	chr9:9997400-9998600	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr9:9997400-9999400	Enhancers	H9 Cell Line	embryonic stem cell
49	chr9:9997600-9997800	Enhancers	Fetal Heart	heart
50	chr9:9997600-9998000	Enhancers	Brain Germinal Matrix	brain

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