Variant report

Variant	nsv873075
Chromosome Location	chr1:197464448-197714851
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1877)
CpG islands
(count:368)
Chromatin interactive
region (count:172)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1877 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:197554837-197555391	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:197611757-197611859	K562	blood:	n/a	n/a
3	ARID3A	chr1:197646598-197647338	K562	blood:	n/a	n/a
4	ARID3A	chr1:197490303-197490638	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:197584280-197585143	HepG2	liver:	n/a	chr1:197584674-197584690 chr1:197584673-197584689
6	ARID3A	chr1:197526524-197526799	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:197694163-197694562	K562	blood:	n/a	n/a
8	ARID3A	chr1:197495983-197496342	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:197573620-197573856	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:197495910-197496335	K562	blood:	n/a	n/a
11	ARID3A	chr1:197588227-197588560	HepG2	liver:	n/a	n/a
12	ARID3A	chr1:197589421-197590390	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:197684109-197684259	HepG2	liver:	n/a	chr1:197684219-197684235
14	ARID3A	chr1:197490328-197490619	K562	blood:	n/a	n/a
15	ARID3A	chr1:197644643-197644869	K562	blood:	n/a	n/a
16	ARID3A	chr1:197488868-197489133	HepG2	liver:	n/a	n/a
17	ARID3A	chr1:197588203-197588456	K562	blood:	n/a	n/a
18	ARID3A	chr1:197694328-197694543	HepG2	liver:	n/a	n/a
19	ATF1	chr1:197584346-197584582	K562	blood:	n/a	n/a
20	ATF1	chr1:197607591-197607763	K562	blood:	n/a	n/a
21	ATF1	chr1:197659216-197659501	K562	blood:	n/a	n/a
22	ATF1	chr1:197707446-197707646	K562	blood:	n/a	n/a
23	ATF1	chr1:197701427-197701605	K562	blood:	n/a	n/a
24	ATF1	chr1:197608561-197608593	K562	blood:	n/a	n/a
25	ATF1	chr1:197628585-197628753	K562	blood:	n/a	n/a
26	ATF1	chr1:197662155-197662348	K562	blood:	n/a	n/a
27	ATF1	chr1:197692747-197692775	K562	blood:	n/a	n/a
28	ATF3	chr1:197659190-197659476	K562	blood:	n/a	n/a
29	BACH1	chr1:197564687-197564784	K562	blood:	n/a	n/a
30	BACH1	chr1:197709644-197709758	K562	blood:	n/a	n/a
31	BACH1	chr1:197510664-197510913	H1-hESC	embryonic stem cell:	n/a	n/a
32	BHLHE40	chr1:197644677-197645357	K562	blood:	n/a	n/a
33	BHLHE40	chr1:197564505-197564788	K562	blood:	n/a	n/a
34	BHLHE40	chr1:197675686-197675706	GM12878	blood:	n/a	n/a
35	BRCA1	chr1:197583197-197583208	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr1:197558816-197558975	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr1:197688042-197688145	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr1:197662092-197662375	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr1:197637535-197637557	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr1:197694101-197694561	K562	blood:	n/a	n/a
41	CBX3	chr1:197659156-197659567	K562	blood:	n/a	n/a
42	CBX3	chr1:197536610-197536899	K562	blood:	n/a	n/a
43	CBX3	chr1:197657426-197657826	K562	blood:	n/a	n/a
44	CBX3	chr1:197536588-197536949	K562	blood:	n/a	n/a
45	CBX3	chr1:197694049-197694638	K562	blood:	n/a	n/a
46	CBX3	chr1:197694170-197694549	HCT-116	colon:	n/a	n/a
47	CBX3	chr1:197657398-197657712	K562	blood:	n/a	n/a
48	CBX3	chr1:197694104-197694578	HCT-116	colon:	n/a	n/a
49	CCNT2	chr1:197564397-197564676	K562	blood:	n/a	n/a
50	CCNT2	chr1:197628837-197629021	K562	blood:	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	chr1:197704881-197704931	AG09309	skin:	n/a
2	chr1:197511177-197511227	H1-hESC	embryonic stem cell:	embryo
3	chr1:197704881-197704931	AG09309	skin:	n/a
4	chr1:197511177-197511227	H1-hESC	embryonic stem cell:	embryo
5	chr1:197564458-197564508	RPTEC	kidney:	n/a
6	chr1:197704774-197704824	ECC-1	luminal epithelium:	n/a
7	chr1:197511177-197511227	SK-N-SH_RA	brain:	n/a
8	chr1:197523608-197523658	Caco-2	colon:	n/a
9	chr1:197704774-197704824	HEEpiC	esophagus:	n/a
10	chr1:197511177-197511227	Caco-2	colon:	n/a
11	chr1:197511177-197511227	NHDF-neo	bronchial:	n/a
12	chr1:197564458-197564508	GM12891	blood:	n/a
13	chr1:197511177-197511227	HCM	heart:	n/a
14	chr1:197704837-197704887	PrEC	prostate:	n/a
15	chr1:197564458-197564508	PANC-1	pancreas:	n/a
16	chr1:197511177-197511227	HCF	heart:	n/a
17	chr1:197511177-197511227	MCF-7	breast:	n/a
18	chr1:197523608-197523658	NT2-D1	testis:	n/a
19	chr1:197523608-197523658	GM06990	blood:	n/a
20	chr1:197511177-197511227	IMR90	lung:	fetal
21	chr1:197704837-197704887	LNCaP	prostate:	n/a
22	chr1:197704837-197704887	HCT-116	colon:	n/a
23	chr1:197523608-197523658	HNPCEpiC	eye:	n/a
24	chr1:197523608-197523658	A549	lung:	n/a
25	chr1:197704881-197704931	HCM	heart:	n/a
26	chr1:197704774-197704824	HL-60	blood:	n/a
27	chr1:197704774-197704824	GM19239	blood:	n/a
28	chr1:197704837-197704887	GM19239	blood:	n/a
29	chr1:197704881-197704931	RPTEC	kidney:	n/a
30	chr1:197564458-197564508	AG10803	skin:	n/a
31	chr1:197704837-197704887	SK-N-SH	brain:	n/a
32	chr1:197704774-197704824	NH-A	brain:	n/a
33	chr1:197704881-197704931	NHBE	bronchial:	n/a
34	chr1:197704881-197704931	HCPEpiC	choroid plexus:	n/a
35	chr1:197704774-197704824	SK-N-SH	brain:	n/a
36	chr1:197704837-197704887	NHDF-neo	bronchial:	n/a
37	chr1:197511177-197511227	HEEpiC	esophagus:	n/a
38	chr1:197704881-197704931	AG10803	skin:	n/a
39	chr1:197564458-197564508	Caco-2	colon:	n/a
40	chr1:197704881-197704931	NH-A	brain:	n/a
41	chr1:197523608-197523658	SK-N-SH	brain:	n/a
42	chr1:197704774-197704824	HMEC	breast:	n/a
43	chr1:197704881-197704931	HCT-116	colon:	n/a
44	chr1:197511177-197511227	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:197704774-197704824	IMR90	lung:	fetal
46	chr1:197564458-197564508	SK-N-SH_RA	brain:	n/a
47	chr1:197523608-197523658	HIPEpiC	eye:	n/a
48	chr1:197523608-197523658	GM12891	blood:	n/a
49	chr1:197704837-197704887	Jurkat	blood:	n/a
50	chr1:197704881-197704931	Jurkat	blood:	n/a

(count:172 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:197583975..197584970-chr1:197837652..197838487,2	MCF-7	breast:
2	chr1:197685915..197688050-chr1:197690516..197693253,2	MCF-7	breast:
3	chr1:197495623..197496560-chr1:197884402..197885121,2	MCF-7	breast:
4	chr1:197572087..197573946-chr1:197577397..197579065,2	K562	blood:
5	chr1:197522501..197524212-chr1:197524469..197526321,2	MCF-7	breast:
6	chr1:197583852..197585003-chr1:197884312..197885694,6	MCF-7	breast:
7	chr1:197466870..197468517-chr1:197480625..197483174,2	K562	blood:
8	chr1:197706025..197708268-chr1:197708751..197710407,2	MCF-7	breast:
9	chr1:197517467..197519003-chr1:197519782..197522301,2	MCF-7	breast:
10	chr1:197631236..197632754-chr1:197743996..197746221,2	K562	blood:
11	chr1:197683448..197686429-chr1:197686441..197688273,2	K562	blood:
12	chr1:197561680..197564518-chr1:198126144..198127682,2	K562	blood:
13	chr1:197688429..197690737-chr1:197693121..197696010,2	MCF-7	breast:
14	chr1:197468068..197470896-chr1:197476662..197478717,2	K562	blood:
15	chr1:197485830..197487622-chr1:197488513..197491078,2	MCF-7	breast:
16	chr1:197536074..197537804-chr1:197566047..197569001,2	MCF-7	breast:
17	chr1:197665354..197667881-chr1:197692912..197694722,2	K562	blood:
18	chr1:197555789..197558080-chr1:197564045..197566228,2	K562	blood:
19	chr1:197706625..197709400-chr1:197710251..197713580,3	MCF-7	breast:
20	chr1:197486893..197488949-chr1:197506821..197509108,2	K562	blood:
21	chr1:197686076..197688310-chr1:197699419..197702157,2	K562	blood:
22	chr1:197613381..197615580-chr1:197616479..197618755,2	K562	blood:
23	chr1:197627378..197633637-chr1:197637134..197640584,7	K562	blood:
24	chr1:197583946..197585840-chr1:197589474..197591778,2	MCF-7	breast:
25	chr1:197661931..197662561-chr1:197836633..197837195,2	MCF-7	breast:
26	chr1:197592165..197594401-chr1:197873722..197876108,2	MCF-7	breast:
27	chr1:197544507..197547050-chr1:197552662..197555146,2	K562	blood:
28	chr1:197497659..197500919-chr1:197504865..197507867,5	K562	blood:
29	chr1:197530060..197532285-chr1:197534124..197535773,2	K562	blood:
30	chr1:197692208..197693791-chr1:197705575..197708266,2	K562	blood:
31	chr1:197497659..197501669-chr1:197502330..197509273,8	K562	blood:
32	chr1:197496825..197498646-chr1:197892256..197894438,2	MCF-7	breast:
33	chr1:197544507..197547050-chr1:197552662..197555146,2	K562	blood:
34	chr1:197581999..197584839-chr1:197586901..197591270,6	K562	blood:
35	chr1:197686781..197688463-chr1:197690334..197692928,2	K562	blood:
36	chr1:197685201..197688463-chr1:197690125..197692928,4	K562	blood:
37	chr1:197498873..197501706-chr1:197501990..197505731,4	MCF-7	breast:
38	chr1:197481645..197483938-chr1:197564288..197566094,2	K562	blood:
39	chr1:197707242..197709785-chr1:197870248..197872414,2	MCF-7	breast:
40	chr1:197623895..197625439-chr1:197644828..197646522,2	K562	blood:
41	chr1:197525937..197528139-chr1:197530420..197533860,3	K562	blood:
42	chr1:197644483..197647407-chr1:197649632..197652293,2	K562	blood:
43	chr1:197486893..197488949-chr1:197506821..197509108,2	K562	blood:
44	chr1:197662721..197665578-chr1:197743679..197745656,2	MCF-7	breast:
45	chr1:197490113..197490959-chr1:197837878..197838660,2	K562	blood:
46	chr1:197485878..197487638-chr1:197491783..197494614,2	MCF-7	breast:
47	chr1:197701490..197704107-chr1:197709565..197711301,2	K562	blood:
48	chr1:197706625..197709400-chr1:197710251..197713580,3	MCF-7	breast:
49	chr1:197530060..197532285-chr1:197534124..197535773,2	K562	blood:
50	chr1:197570884..197572523-chr1:197584581..197587498,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZBTB41-6	chr1:197704380-197704926	NONHSAT008631
2	lnc-ZBTB41-4	chr1:197475064-197476148	NONHSAT008627
3	lnc-ZBTB41-4	chr1:197473881-197475058	NONHSAT008627

No data

Variant related genes	Relation type
ENSG00000235582	TF binding region
DENND1B	TF binding region
ENSG00000207139	TF binding region
EEF1A1P32	TF binding region
ENSG00000235582	CpG island
DENND1B	CpG island
ENSG00000207139	CpG island
EEF1A1P32	CpG island
ENSG00000233040	chromatin interactions
ENSG00000207139	chromatin interactions
ENSG00000151414	chromatin interactions
ENSG00000143355	chromatin interactions
ENSG00000203724	chromatin interactions
ENSG00000213047	chromatin interactions
ENSG00000213046	chromatin interactions
ENSG00000235582	chromatin interactions
ENSG00000196850	chromatin interactions

Extended variants
information (count: 8156 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:8156 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535575712	chr1:197466430-197466431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549574804	chr1:197466434-197466435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567887974	chr1:197466452-197466453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538524886	chr1:197466528-197466529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114160920	chr1:197466622-197466623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142166465	chr1:197466662-197466663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188299673	chr1:197466672-197466673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs151211262	chr1:197466689-197466690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566380763	chr1:197466695-197466696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs193176987	chr1:197466696-197466697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184576446	chr1:197466700-197466701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554732213	chr1:197466728-197466729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530280231	chr1:197466812-197466813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548014908	chr1:197466829-197466830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575871046	chr1:197466833-197466834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543307252	chr1:197466875-197466876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564836593	chr1:197466908-197466909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189365954	chr1:197466977-197466978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545400889	chr1:197467027-197467028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563376032	chr1:197467037-197467038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560354400	chr1:197467053-197467054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34012100	chr1:197467064-197467065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527763209	chr1:197467070-197467071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139207833	chr1:197467091-197467092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567851801	chr1:197467109-197467110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531991600	chr1:197467111-197467112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550450759	chr1:197467118-197467119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571981627	chr1:197467152-197467153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114589811	chr1:197467193-197467194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6428405	chr1:197467200-197467201	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs139272773	chr1:197467215-197467216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533758277	chr1:197467255-197467256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114591858	chr1:197467290-197467291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144590123	chr1:197467300-197467301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373981007	chr1:197467310-197467311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575784314	chr1:197467316-197467317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs6428406	chr1:197467340-197467341	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs534625566	chr1:197467420-197467421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558395992	chr1:197467455-197467456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576747404	chr1:197467464-197467465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs33992990	chr1:197467466-197467467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs386369245	chr1:197467470-197467471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs386369246	chr1:197467473-197467474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs58578946	chr1:197467476-197467477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375234691	chr1:197467620-197467621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147870521	chr1:197467621-197467622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141582373	chr1:197467622-197467623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543106106	chr1:197467655-197467656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561372679	chr1:197467670-197467671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs180679371	chr1:197467680-197467681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung adenocarcinoma	21935476	CNVD
Glioblastoma multiforme	20472715	CNVD
Multiple myeloma	16461302	CNVD
Leukoplakia	24403051	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2063 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197466400-197467200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:197467000-197467800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr1:197467200-197499000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:197472200-197477800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr1:197473800-197479200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr1:197474000-197481600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr1:197475000-197484800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr1:197475200-197479000	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr1:197475400-197478800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr1:197475800-197478200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr1:197476200-197479600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr1:197476400-197478000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:197476400-197478000	Weak transcription	Dnd41	blood
14	chr1:197476400-197478800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:197476600-197477000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr1:197476600-197478200	Weak transcription	Primary B cells from cord blood	blood
17	chr1:197476600-197478200	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr1:197476600-197478200	Weak transcription	Adipose Nuclei	Adipose
19	chr1:197476600-197478800	Weak transcription	Primary hematopoietic stem cells	blood
20	chr1:197476600-197479600	Weak transcription	Ovary	ovary
21	chr1:197476800-197477400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr1:197476800-197477400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr1:197476800-197478400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:197476800-197478400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr1:197476800-197479200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr1:197476800-197479200	Weak transcription	Fetal Lung	lung
27	chr1:197476800-197479200	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr1:197476800-197479600	Weak transcription	Primary T cells from cord blood	blood
29	chr1:197476800-197479600	Weak transcription	Esophagus	oesophagus
30	chr1:197476800-197479600	Weak transcription	Left Ventricle	heart
31	chr1:197476800-197479600	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr1:197476800-197482600	Weak transcription	Hela-S3	cervix
33	chr1:197476800-197483400	Weak transcription	Small Intestine	intestine
34	chr1:197476800-197484600	Weak transcription	Fetal Intestine Large	intestine
35	chr1:197477000-197479000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:197477200-197478800	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr1:197477200-197479200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr1:197477400-197479000	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr1:197477400-197479600	Weak transcription	Primary B cells from peripheral blood	blood
40	chr1:197477600-197479200	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr1:197477600-197479200	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr1:197477600-197479200	Weak transcription	Brain Anterior Caudate	brain
43	chr1:197477600-197479200	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr1:197477800-197479400	Weak transcription	Liver	Liver
45	chr1:197477800-197479600	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr1:197477800-197480400	Weak transcription	Fetal Kidney	kidney
47	chr1:197477800-197481000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr1:197478000-197479600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr1:197478000-197479600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:197478000-197479600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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