Variant report

Variant	nsv934323
Chromosome Location	chr5:89968158-90111853
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1342)
CpG islands
(count:368)
Chromatin interactive
region (count:137)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:90003713-90003798	K562	blood:	n/a	n/a
2	ARID3A	chr5:90005141-90005474	K562	blood:	n/a	n/a
3	ARID3A	chr5:90079524-90079811	K562	blood:	n/a	n/a
4	ARID3A	chr5:90009369-90009462	K562	blood:	n/a	n/a
5	ATF1	chr5:90057649-90057656	K562	blood:	n/a	n/a
6	BACH1	chr5:90036137-90036320	K562	blood:	n/a	n/a
7	BACH1	chr5:90043108-90043170	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:89968291-89968300	K562	blood:	n/a	n/a
9	BATF	chr5:90005602-90005915	GM12878	blood:	n/a	n/a
10	BATF	chr5:90005582-90005917	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:90036161-90036469	K562	blood:	n/a	n/a
12	BHLHE40	chr5:90005339-90005398	K562	blood:	n/a	n/a
13	BRCA1	chr5:90005179-90005502	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr5:90079672-90079809	HepG2	liver:	n/a	n/a
15	BRCA1	chr5:90098539-90098758	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr5:90065882-90066278	K562	blood:	n/a	n/a
17	CBX3	chr5:90092791-90093149	K562	blood:	n/a	n/a
18	CBX3	chr5:90036064-90036560	K562	blood:	n/a	n/a
19	CCNT2	chr5:89991327-89991373	K562	blood:	n/a	n/a
20	CCNT2	chr5:90029382-90029480	K562	blood:	n/a	n/a
21	CCNT2	chr5:90036117-90036427	K562	blood:	n/a	n/a
22	CCNT2	chr5:90079588-90079924	K562	blood:	n/a	n/a
23	CCNT2	chr5:89992229-89992429	K562	blood:	n/a	n/a
24	CEBPB	chr5:89969083-89969305	HepG2	liver:	n/a	chr5:89969225-89969236
25	CEBPB	chr5:89976017-89976285	H1-hESC	embryonic stem cell:	n/a	chr5:89976122-89976133
26	CEBPB	chr5:90079587-90079928	K562	blood:	n/a	n/a
27	CEBPB	chr5:89986281-89986301	K562	blood:	n/a	n/a
28	CEBPB	chr5:90036920-90037137	K562	blood:	n/a	n/a
29	CEBPB	chr5:89981470-89981840	MCF-7	breast:	n/a	chr5:89981633-89981644
30	CEBPB	chr5:89976058-89976275	HepG2	liver:	n/a	chr5:89976122-89976133
31	CEBPB	chr5:89981476-89981981	MCF-7	breast:	n/a	chr5:89981633-89981644
32	CEBPB	chr5:89981529-89981846	A549	lung:	n/a	chr5:89981633-89981644
33	CEBPB	chr5:89981452-89981830	IMR90	lung:	n/a	chr5:89981633-89981644
34	CEBPB	chr5:89981444-89981911	K562	blood:	n/a	chr5:89981633-89981644
35	CEBPB	chr5:89975948-89976259	K562	blood:	n/a	chr5:89976122-89976133
36	CEBPB	chr5:90036961-90037161	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:90099007-90099193	HepG2	liver:	n/a	chr5:90099156-90099167
38	CEBPB	chr5:89981488-89981777	K562	blood:	n/a	chr5:89981633-89981644
39	CEBPB	chr5:89981443-89981945	K562	blood:	n/a	chr5:89981633-89981644
40	CEBPB	chr5:90027860-90027918	H1-hESC	embryonic stem cell:	n/a	chr5:90027873-90027884
41	CEBPB	chr5:90013304-90013324	A549	lung:	n/a	n/a
42	CEBPB	chr5:90013236-90013333	K562	blood:	n/a	n/a
43	CEBPB	chr5:89981456-89981846	ECC-1	luminal epithelium:	n/a	chr5:89981633-89981644
44	CEBPB	chr5:90099090-90099222	Hela-S3	cervix:	n/a	chr5:90099156-90099167
45	CEBPB	chr5:89971002-89971372	HepG2	liver:	n/a	n/a
46	CEBPB	chr5:90079606-90079936	K562	blood:	n/a	n/a
47	CEBPB	chr5:89981462-89981896	ECC-1	luminal epithelium:	n/a	chr5:89981633-89981644
48	CEBPB	chr5:89981442-89981832	H1-hESC	embryonic stem cell:	n/a	chr5:89981633-89981644
49	CEBPB	chr5:89976027-89976306	K562	blood:	n/a	chr5:89976122-89976133
50	CEBPB	chr5:90079576-90079924	Hela-S3	cervix:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:89968232-89968282	SK-N-MC	brain:	n/a
2	chr5:89968232-89968282	K562	blood:	n/a
3	chr5:89968232-89968282	SK-N-MC	brain:	n/a
4	chr5:89968232-89968282	K562	blood:	n/a
5	chr5:90042723-90042773	NHDF-neo	bronchial:	n/a
6	chr5:89968232-89968282	NB4	blood:	n/a
7	chr5:90075932-90075982	RPTEC	kidney:	n/a
8	chr5:90076860-90076910	AG09319	gingival:	n/a
9	chr5:90076860-90076910	HCPEpiC	choroid plexus:	n/a
10	chr5:90042723-90042773	AG04450	lung:	fetal
11	chr5:90042723-90042773	HUVEC	blood vessel:	n/a
12	chr5:90076292-90076342	BE2_C	brain:	n/a
13	chr5:90076860-90076910	HAEpiC	amniotic membrane:	n/a
14	chr5:90076292-90076342	NH-A	brain:	n/a
15	chr5:90075932-90075982	HRE	kidney:	n/a
16	chr5:90036436-90036486	AG09309	skin:	n/a
17	chr5:89968232-89968282	HMEC	breast:	n/a
18	chr5:90076292-90076342	HEK293	kidney:	embryo
19	chr5:89968232-89968282	HCM	heart:	n/a
20	chr5:89968232-89968282	MCF10A-Er-Src	breast:	n/a
21	chr5:90036436-90036486	LNCaP	prostate:	n/a
22	chr5:90036436-90036486	MCF-7	breast:	n/a
23	chr5:90076860-90076910	BE2_C	brain:	n/a
24	chr5:90075932-90075982	MCF-7	breast:	n/a
25	chr5:90075932-90075982	ProgFib	skin:	n/a
26	chr5:89968232-89968282	NHBE	bronchial:	n/a
27	chr5:89968232-89968282	PANC-1	pancreas:	n/a
28	chr5:90076860-90076910	AG10803	skin:	n/a
29	chr5:90076292-90076342	NT2-D1	testis:	n/a
30	chr5:90076860-90076910	ProgFib	skin:	n/a
31	chr5:90036436-90036486	MCF10A-Er-Src	breast:	n/a
32	chr5:90042723-90042773	IMR90	lung:	fetal
33	chr5:89968232-89968282	Jurkat	blood:	n/a
34	chr5:90036436-90036486	Jurkat	blood:	n/a
35	chr5:89968232-89968282	U87	brain:	n/a
36	chr5:90036436-90036486	AG10803	skin:	n/a
37	chr5:90076860-90076910	AG04450	lung:	fetal
38	chr5:90076860-90076910	GM12878	blood:	n/a
39	chr5:90076860-90076910	HCM	heart:	n/a
40	chr5:90042723-90042773	HEEpiC	esophagus:	n/a
41	chr5:90075932-90075982	Hepatocyte	liver:	n/a
42	chr5:90042723-90042773	HEK293	kidney:	embryo
43	chr5:90076860-90076910	SKMC	muscle:	n/a
44	chr5:90076860-90076910	H1-hESC	embryonic stem cell:	embryo
45	chr5:90076860-90076910	IMR90	lung:	fetal
46	chr5:90042723-90042773	Hela-S3	cervix:	n/a
47	chr5:90076860-90076910	AoSMC	blood vessel:	n/a
48	chr5:90042723-90042773	Hepatocyte	liver:	n/a
49	chr5:90036436-90036486	ECC-1	luminal epithelium:	n/a
50	chr5:90076292-90076342	HIPEpiC	eye:	n/a

(count:137 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:90001746..90003482-chr5:90003758..90005802,2	K562	blood:
2	chr5:90004952..90005852-chr5:90079260..90079764,2	K562	blood:
3	chr5:90009460..90011230-chr5:90014685..90016873,2	K562	blood:
4	chr5:90108587..90111561-chr5:90677135..90678808,2	K562	blood:
5	chr5:90046899..90048953-chr5:90056620..90058436,2	K562	blood:
6	chr5:89994085..89995994-chr5:89996980..89998521,2	K562	blood:
7	chr5:89952329..89954940-chr5:90078278..90080126,2	K562	blood:
8	chr5:89976023..89978717-chr5:89988560..89991355,2	K562	blood:
9	chr5:90088753..90091420-chr5:90094556..90098739,3	K562	blood:
10	chr5:90105553..90108677-chr5:90109621..90112137,3	MCF-7	breast:
11	chr5:90004952..90005852-chr5:90079260..90079764,2	K562	blood:
12	chr5:90010535..90012763-chr5:90098417..90101148,2	K562	blood:
13	chr5:89966124..89967960-chr5:89969829..89971642,2	K562	blood:
14	chr5:89769110..89772331-chr5:90086907..90091587,4	K562	blood:
15	chr5:89938091..89940489-chr5:89979242..89981079,3	K562	blood:
16	chr5:90077865..90079674-chr5:90083346..90085514,2	K562	blood:
17	chr5:89985219..89986790-chr5:90677102..90678990,2	K562	blood:
18	chr5:90079294..90080237-chr5:90089325..90090028,2	MCF-7	breast:
19	chr5:89964661..89966273-chr5:89968372..89970736,2	K562	blood:
20	chr5:90045038..90047655-chr5:90049129..90051100,2	K562	blood:
21	chr5:90098765..90101168-chr5:90678671..90680272,2	MCF-7	breast:
22	chr5:90077865..90079674-chr5:90083346..90085514,2	K562	blood:
23	chr5:90066747..90069663-chr5:90070261..90074130,4	K562	blood:
24	chr5:89992042..89994832-chr5:90000512..90002853,3	K562	blood:
25	chr5:89704530..89707367-chr5:90108211..90111116,2	K562	blood:
26	chr5:90076080..90077925-chr5:90078435..90080138,2	K562	blood:
27	chr5:90077865..90080476-chr5:90084014..90086656,2	K562	blood:
28	chr5:90033178..90036416-chr5:90039651..90042855,4	K562	blood:
29	chr5:89989229..89992043-chr5:90052048..90054479,3	K562	blood:
30	chr5:90088753..90091420-chr5:90094556..90098739,3	K562	blood:
31	chr5:90055144..90057508-chr5:90058506..90061459,3	K562	blood:
32	chr5:90098345..90099139-chr5:90145555..90146337,4	MCF-7	breast:
33	chr5:89992042..89994832-chr5:90000512..90002853,2	K562	blood:
34	chr5:90021626..90023836-chr5:90049567..90052309,2	K562	blood:
35	chr5:90045038..90047655-chr5:90049129..90051100,2	K562	blood:
36	chr5:90077865..90080476-chr5:90084014..90086656,2	K562	blood:
37	chr5:90066747..90069663-chr5:90070261..90074130,4	K562	blood:
38	chr5:89989350..89991740-chr5:90000493..90002123,2	K562	blood:
39	chr5:89987591..89990356-chr5:89991172..89993291,2	MCF-7	breast:
40	chr5:90005569..90007151-chr5:90010684..90012354,2	K562	blood:
41	chr5:90105553..90108677-chr5:90109621..90112137,3	MCF-7	breast:
42	chr5:89968653..89971402-chr5:89981382..89983436,3	K562	blood:
43	chr5:89992042..89994832-chr5:90000512..90002853,3	K562	blood:
44	chr5:90055288..90058176-chr5:90059292..90060804,2	MCF-7	breast:
45	chr5:90042349..90044397-chr5:90045490..90049083,3	K562	blood:
46	chr5:90071528..90073103-chr5:90073748..90076241,2	K562	blood:
47	chr5:89996062..89998352-chr5:90001342..90003176,2	K562	blood:
48	chr5:90026342..90028789-chr5:90031725..90034231,3	K562	blood:
49	chr5:90066656..90069234-chr5:90677139..90680259,3	K562	blood:
50	chr5:89973316..89976811-chr5:89977815..89981018,4	K562	blood:

No data

Variant related genes	Relation type
GPR98	TF binding region
GPR98	CpG island
ENSG00000255647	chromatin interactions
ENSG00000113356	chromatin interactions
ENSG00000113369	chromatin interactions
ENSG00000176055	chromatin interactions
ENSG00000164199	chromatin interactions
ENSG00000153140	chromatin interactions

Extended variants
information (count: 5556 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:5556 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114006677	chr5:89968166-89968167	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs192094812	chr5:89968180-89968181	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs148522936	chr5:89968181-89968182	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs115233910	chr5:89968233-89968234	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs183967729	chr5:89968258-89968259	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs374471431	chr5:89968313-89968314	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs199862251	chr5:89968339-89968340	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs368793935	chr5:89968343-89968344	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs144401211	chr5:89968380-89968381	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200592712	chr5:89968384-89968385	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371179945	chr5:89968396-89968397	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375621749	chr5:89968397-89968398	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368303691	chr5:89968461-89968462	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111753827	chr5:89968474-89968475	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376895610	chr5:89968481-89968482	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs367588475	chr5:89968490-89968491	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141346393	chr5:89968495-89968496	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371747319	chr5:89968551-89968552	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs199633024	chr5:89968560-89968561	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1028191	chr5:89968626-89968627	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs577069960	chr5:89968627-89968628	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111986329	chr5:89968636-89968637	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186834527	chr5:89968637-89968638	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569003016	chr5:89968650-89968651	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75196004	chr5:89968659-89968660	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143938603	chr5:89968660-89968661	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376288750	chr5:89968728-89968729	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1028192	chr5:89968773-89968774	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs75397269	chr5:89968783-89968784	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190413493	chr5:89968796-89968797	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571083997	chr5:89968807-89968808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533448522	chr5:89968865-89968866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs151321213	chr5:89968935-89968936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566848641	chr5:89968963-89968964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567420966	chr5:89969001-89969002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555861111	chr5:89969012-89969013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183050201	chr5:89969017-89969018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537206174	chr5:89969037-89969038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556890136	chr5:89969045-89969046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186975753	chr5:89969167-89969168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533234441	chr5:89969217-89969218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77531166	chr5:89969219-89969220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76287917	chr5:89969234-89969235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541441228	chr5:89969242-89969243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561418748	chr5:89969255-89969256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114362193	chr5:89969324-89969325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536289342	chr5:89969348-89969349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs56339400	chr5:89969355-89969356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79912576	chr5:89969360-89969361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566282746	chr5:89969376-89969377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:726 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89936800-89994200	Weak transcription	Brain Germinal Matrix	brain
2	chr5:89950200-89981600	Weak transcription	Fetal Brain Female	brain
3	chr5:89950400-90033400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr5:89950800-89973800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr5:89954800-89972600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr5:89957600-89969400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:89964400-89968600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:89964400-89971000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr5:89964400-89993400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr5:89964600-89968200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr5:89964600-89968600	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr5:89964600-89994800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr5:89964800-89971200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:89965000-89993600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr5:89967000-89968400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:89967000-89969200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr5:89967200-89979000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr5:89967200-89992000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:89967400-89968400	Weak transcription	K562	blood
20	chr5:89967400-89969200	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr5:89967800-89968800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr5:89968000-89980400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr5:89968000-89982000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
24	chr5:89968200-89968600	Genic enhancers	HUES48 Cell Line	embryonic stem cell
25	chr5:89968200-89968800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr5:89968400-89974400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr5:89968400-89982000	Strong transcription	K562	blood
28	chr5:89968600-89969200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:89968600-89982000	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr5:89968600-89982000	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr5:89968800-89971000	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr5:89968800-89971200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr5:89969200-89970400	Strong transcription	H9 Cell Line	embryonic stem cell
34	chr5:89969200-89971200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:89969200-89971600	Strong transcription	H1 Cell Line	embryonic stem cell
36	chr5:89969400-89972600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr5:89970400-89970600	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr5:89970600-89971600	Strong transcription	H9 Cell Line	embryonic stem cell
39	chr5:89971000-89971200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:89971000-89971400	Genic enhancers	HUES6 Cell Line	embryonic stem cell
41	chr5:89971200-89971400	ZNF genes & repeats	Pancreas	Pancrea
42	chr5:89971200-89971600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr5:89971200-89972000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
44	chr5:89971200-89972800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:89971400-89971800	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr5:89971600-89974600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr5:89971600-89978000	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr5:89971600-89978000	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr5:89971800-89979400	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr5:89972000-89985600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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