Variant report

Variant	esv2755136
Chromosome Location	chr9:9995882-10065206
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	chr9:10000093-10000360	HepG2	liver:	n/a	chr9:10000229-10000240
4	CEBPB	chr9:9997246-9997453	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr9:10000141-10000327	H1-hESC	embryonic stem cell:	n/a	chr9:10000229-10000240
6	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
7	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
8	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
9	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
10	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
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	chr9:10000095-10000401	IMR90	lung:	n/a	chr9:10000229-10000240
13	CEBPB	chr9:10050102-10050399	IMR90	lung:	n/a	n/a
14	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
15	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
16	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
17	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
18	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
19	CEBPB	chr9:10000119-10000362	A549	lung:	n/a	chr9:10000229-10000240
20	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
21	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
22	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
23	CHD2	chr9:10008242-10008651	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr9:9998580-9998730	HRE	kidney:	n/a	n/a
25	CTCF	chr9:10045771-10045798	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr9:10026619-10026648	GM12878	blood:	n/a	chr9:10026619-10026640
27	CTCF	chr9:10060440-10060590	HMEC	breast:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
28	CTCF	chr9:10060440-10060590	GM12874	blood:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
29	CTCF	chr9:9998564-9998737	MCF-7	breast:	n/a	n/a
30	CTCF	chr9:10045720-10045870	AG09319	gingival:	n/a	n/a
31	CTCF	chr9:10060420-10060570	GM12869	blood:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
32	CTCF	chr9:10045720-10045870	HEK293	kidney:	n/a	n/a
33	CTCF	chr9:10045666-10045929	Medullo	brain:	n/a	n/a
34	CTCF	chr9:10060620-10060770	AG09309	skin:	n/a	n/a
35	CTCF	chr9:10060560-10060710	RPTEC	kidney:	n/a	n/a
36	CTCF	chr9:10045740-10045890	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr9:10060413-10060623	Hela-S3	cervix:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
38	CTCF	chr9:10060420-10060570	HRE	kidney:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
39	CTCF	chr9:10060960-10061110	AG10803	skin:	n/a	n/a
40	CTCF	chr9:10060380-10060530	SK-N-SH_RA	brain:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521
41	CTCF	chr9:10045680-10045830	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr9:10060420-10060570	HBMEC	blood vessel:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
43	CTCF	chr9:10060460-10060610	HMF	breast:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
44	CTCF	chr9:10060420-10060570	AG10803	skin:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
45	CTCF	chr9:9998640-9998790	GM12870	blood:	n/a	n/a
46	CTCF	chr9:9998560-9998710	SAEC	small airway:	n/a	n/a
47	CTCF	chr9:10026640-10026790	HMEC	breast:	n/a	n/a
48	CTCF	chr9:9998540-9998690	HEK293	kidney:	n/a	n/a
49	CTCF	chr9:10060338-10060638	GM12878	blood:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
50	CTCF	chr9:10060440-10060590	HCFaa	heart:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:9998791-9998841	AoSMC	blood vessel:	n/a
2	chr9:9998791-9998841	U87	brain:	n/a
3	chr9:9998791-9998841	SKMC	muscle:	n/a
4	chr9:9998791-9998841	MCF10A-Er-Src	breast:	n/a
5	chr9:9998791-9998841	ECC-1	luminal epithelium:	n/a
6	chr9:9998791-9998841	PANC-1	pancreas:	n/a
7	chr9:9998791-9998841	HRE	kidney:	n/a
8	chr9:9998791-9998841	LNCaP	prostate:	n/a
9	chr9:9998791-9998841	ProgFib	skin:	n/a
10	chr9:9998791-9998841	NB4	blood:	n/a
11	chr9:9998791-9998841	HRCEpiC	kidney:	n/a
12	chr9:9998791-9998841	HCF	heart:	n/a
13	chr9:9998791-9998841	SK-N-SH	brain:	n/a
14	chr9:9998791-9998841	BE2_C	brain:	n/a
15	chr9:9998791-9998841	GM19239	blood:	n/a
16	chr9:9998791-9998841	Jurkat	blood:	n/a
17	chr9:9998791-9998841	GM12878	blood:	n/a
18	chr9:9998791-9998841	HCM	heart:	n/a
19	chr9:9998791-9998841	AG04450	lung:	fetal
20	chr9:9998791-9998841	CMK	blood:	n/a
21	chr9:9998791-9998841	NT2-D1	testis:	n/a
22	chr9:9998791-9998841	AG09309	skin:	n/a
23	chr9:9998791-9998841	HPAEpiC	pulmonary alveolar:	n/a
24	chr9:9998791-9998841	PrEC	prostate:	n/a
25	chr9:9998791-9998841	HNPCEpiC	eye:	n/a
26	chr9:9998791-9998841	H1-hESC	embryonic stem cell:	embryo
27	chr9:9998791-9998841	SK-N-SH_RA	brain:	n/a
28	chr9:9998791-9998841	T-47D	breast:	n/a
29	chr9:9998791-9998841	PFSK-1	brain:	n/a
30	chr9:9998791-9998841	AG04449	skin:	fetal
31	chr9:9998791-9998841	HCPEpiC	choroid plexus:	n/a
32	chr9:9998791-9998841	Hepatocyte	liver:	n/a
33	chr9:9998791-9998841	MCF-7	breast:	n/a
34	chr9:9998791-9998841	HCT-116	colon:	n/a
35	chr9:9998791-9998841	K562	blood:	n/a
36	chr9:9998791-9998841	AG10803	skin:	n/a
37	chr9:9998791-9998841	SK-N-MC	brain:	n/a
38	chr9:9998791-9998841	HMEC	breast:	n/a
39	chr9:9998791-9998841	RPTEC	kidney:	n/a
40	chr9:9998791-9998841	NH-A	brain:	n/a
41	chr9:9998791-9998841	IMR90	lung:	fetal
42	chr9:9998791-9998841	A549	lung:	n/a
43	chr9:9998791-9998841	HUVEC	blood vessel:	n/a
44	chr9:9998791-9998841	Caco-2	colon:	n/a
45	chr9:9998791-9998841	HEK293	kidney:	embryo
46	chr9:9998791-9998841	HepG2	liver:	n/a
47	chr9:9998791-9998841	NHDF-neo	bronchial:	n/a
48	chr9:9998791-9998841	GM12892	blood:	n/a
49	chr9:9998791-9998841	ovcar-3	ovarian:	n/a
50	chr9:9998791-9998841	HAEpiC	amniotic membrane:	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: 2726 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:2726 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10759122	chr9:9995882-9995883	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115286852	chr9:9995889-9995890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112577895	chr9:9995891-9995892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10816273	chr9:9995938-9995939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144167654	chr9:9995970-9995971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573979702	chr9:9995977-9995978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543334468	chr9:9995995-9995996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561517088	chr9:9996067-9996068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs66777826	chr9:9996096-9996097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571966394	chr9:9996134-9996135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574049692	chr9:9996139-9996140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79473237	chr9:9996141-9996142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573516096	chr9:9996170-9996171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540977964	chr9:9996171-9996172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72692773	chr9:9996211-9996212	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs187055438	chr9:9996226-9996227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372307591	chr9:9996320-9996321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191825568	chr9:9996328-9996329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527818926	chr9:9996382-9996383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149078502	chr9:9996430-9996431	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs545994621	chr9:9996437-9996438	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs534972516	chr9:9996438-9996439	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs551508874	chr9:9996472-9996473	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs182878998	chr9:9996503-9996504	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs537184192	chr9:9996511-9996512	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs188380039	chr9:9996528-9996529	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs369205009	chr9:9996587-9996588	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs573943510	chr9:9996625-9996626	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs536455077	chr9:9996704-9996705	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs143140560	chr9:9996731-9996732	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs573479753	chr9:9996748-9996749	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs193252457	chr9:9996749-9996750	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs533226124	chr9:9996756-9996757	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs185722595	chr9:9996760-9996761	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs577788414	chr9:9996805-9996806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543586882	chr9:9996825-9996826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542039411	chr9:9996841-9996842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529046937	chr9:9996887-9996888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151050296	chr9:9996924-9996925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79119056	chr9:9996947-9996948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75799737	chr9:9996960-9996961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561719661	chr9:9996969-9996970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376246195	chr9:9997056-9997057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141014848	chr9:9997094-9997095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189406649	chr9:9997153-9997154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146349064	chr9:9997180-9997181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78480133	chr9:9997248-9997249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550620174	chr9:9997250-9997251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs60029845	chr9:9997285-9997286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577314023	chr9:9997286-9997287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:9989800-10000400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:9990000-9999000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:9995000-9998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr9:9995200-9996200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr9:9995200-9998000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr9:9995200-9998200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr9:9995200-9999200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr9:9995200-9999200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr9:9995200-9999400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr9:9995200-10001000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr9:9995400-9997200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr9:9995600-9996200	Weak transcription	Primary hematopoietic stem cells	blood
13	chr9:9995600-9996400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr9:9995600-9996400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr9:9995600-9997200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr9:9995800-9996400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr9:9996200-9997600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:9996200-9999000	Enhancers	Primary hematopoietic stem cells	blood
19	chr9:9996400-9996600	Enhancers	H1 Cell Line	embryonic stem cell
20	chr9:9996400-9996600	Enhancers	H9 Cell Line	embryonic stem cell
21	chr9:9996400-9996800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr9:9996400-9996800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr9:9996400-9996800	Enhancers	Stomach Mucosa	stomach
24	chr9:9996400-9997000	Enhancers	Fetal Kidney	kidney
25	chr9:9996400-9997200	Enhancers	HUVEC	blood vessel
26	chr9:9996600-9997400	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr9:9996600-9997400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr9:9996800-9998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr9:9996800-9999200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr9:9997200-9997600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr9:9997200-9998200	Weak transcription	HUVEC	blood vessel
32	chr9:9997200-9999000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:9997200-9999200	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr9:9997400-9997800	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr9:9997400-9998600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr9:9997400-9998600	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr9:9997400-9999400	Enhancers	H9 Cell Line	embryonic stem cell
38	chr9:9997600-9997800	Enhancers	Fetal Heart	heart
39	chr9:9997600-9998000	Enhancers	Brain Germinal Matrix	brain
40	chr9:9997600-10000400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr9:9997600-10000800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr9:9997800-9998200	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr9:9997800-9998800	Weak transcription	Fetal Heart	heart
44	chr9:9997800-9999000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr9:9998000-9998800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr9:9998200-9998800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr9:9998200-9998800	Enhancers	HUVEC	blood vessel
48	chr9:9998200-9999800	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr9:9998400-9998800	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr9:9998600-9999000	Weak transcription	H1 Cell Line	embryonic stem cell

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