Variant report

Variant	nsv539652
Chromosome Location	chr8:79287819-79434844
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	chr8:79420431-79420703	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:79305734-79306031	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:79305710-79305995	K562	blood:	n/a	n/a
4	ARID3A	chr8:79419872-79420116	HepG2	liver:	n/a	n/a
5	ATF2	chr8:79428058-79428740	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr8:79423002-79423385	GM12878	blood:	n/a	n/a
7	ATF2	chr8:79427804-79429036	GM12878	blood:	n/a	n/a
8	ATF2	chr8:79428163-79428746	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr8:79427804-79428739	GM12878	blood:	n/a	n/a
10	BACH1	chr8:79428037-79428824	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr8:79422965-79423234	GM12878	blood:	n/a	n/a
12	BATF	chr8:79422932-79423247	GM12878	blood:	n/a	n/a
13	BCL3	chr8:79328410-79328728	GM12878	blood:	n/a	n/a
14	BCL3	chr8:79332085-79332449	GM12878	blood:	n/a	n/a
15	BCL3	chr8:79332070-79332351	GM12878	blood:	n/a	n/a
16	BCLAF1	chr8:79428496-79428958	GM12878	blood:	n/a	chr8:79428576-79428585 chr8:79428639-79428648 chr8:79428569-79428582
17	BCLAF1	chr8:79427859-79428353	GM12878	blood:	n/a	chr8:79428244-79428251 chr8:79428113-79428122
18	BCLAF1	chr8:79428291-79428889	GM12878	blood:	n/a	chr8:79428576-79428585 chr8:79428639-79428648 chr8:79428569-79428582
19	BHLHE40	chr8:79428270-79428630	K562	blood:	n/a	chr8:79428607-79428623 chr8:79428566-79428582
20	BHLHE40	chr8:79427849-79429013	GM12878	blood:	n/a	chr8:79428607-79428623 chr8:79428566-79428582
21	BHLHE40	chr8:79428202-79428677	HepG2	liver:	n/a	chr8:79428607-79428623 chr8:79428566-79428582
22	BRCA1	chr8:79428176-79428885	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr8:79428011-79428879	GM12878	blood:	n/a	n/a
24	CCNT2	chr8:79428312-79428721	K562	blood:	n/a	n/a
25	CEBPB	chr8:79310795-79311219	MCF-7	breast:	n/a	n/a
26	CEBPB	chr8:79304280-79304592	A549	lung:	n/a	chr8:79304419-79304430
27	CEBPB	chr8:79305597-79305954	HepG2	liver:	n/a	chr8:79305775-79305786 chr8:79305774-79305787
28	CEBPB	chr8:79305610-79305953	IMR90	lung:	n/a	chr8:79305775-79305786 chr8:79305774-79305787
29	CEBPB	chr8:79422797-79423160	MCF-7	breast:	n/a	chr8:79423015-79423026 chr8:79423017-79423026 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423017-79423028
30	CEBPB	chr8:79369507-79369707	A549	lung:	n/a	n/a
31	CEBPB	chr8:79305670-79305916	ECC-1	luminal epithelium:	n/a	chr8:79305775-79305786 chr8:79305774-79305787
32	CEBPB	chr8:79310838-79311162	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:79305526-79305936	MCF-7	breast:	n/a	chr8:79305775-79305786 chr8:79305774-79305787
34	CEBPB	chr8:79350473-79350698	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:79393442-79393551	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr8:79314015-79314077	H1-hESC	embryonic stem cell:	n/a	chr8:79314047-79314058
37	CEBPB	chr8:79305599-79306033	Hela-S3	cervix:	n/a	chr8:79305775-79305786 chr8:79305774-79305787
38	CEBPB	chr8:79382933-79383110	MCF-7	breast:	n/a	n/a
39	CEBPB	chr8:79350506-79350601	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr8:79296917-79297204	A549	lung:	n/a	chr8:79297038-79297049
41	CEBPB	chr8:79310760-79311286	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr8:79305597-79305942	K562	blood:	n/a	chr8:79305775-79305786 chr8:79305774-79305787
43	CEBPB	chr8:79305647-79305936	A549	lung:	n/a	chr8:79305775-79305786 chr8:79305774-79305787
44	CEBPB	chr8:79304281-79304595	HepG2	liver:	n/a	chr8:79304419-79304430
45	CEBPB	chr8:79305678-79305962	MCF-7	breast:	n/a	chr8:79305775-79305786 chr8:79305774-79305787
46	CEBPB	chr8:79427811-79428596	GM12878	blood:	n/a	n/a
47	CEBPB	chr8:79296932-79297192	IMR90	lung:	n/a	chr8:79297038-79297049
48	CEBPB	chr8:79383005-79383219	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr8:79296994-79297129	HepG2	liver:	n/a	chr8:79297038-79297049
50	CEBPB	chr8:79422829-79423174	Hela-S3	cervix:	n/a	chr8:79423015-79423026 chr8:79423017-79423026 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423017-79423028

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:79428325-79428375	HMEC	breast:	n/a
2	chr8:79428325-79428375	ProgFib	skin:	n/a
3	chr8:79428444-79428494	AG09309	skin:	n/a
4	chr8:79429818-79429868	GM12891	blood:	n/a
5	chr8:79428313-79428363	GM12892	blood:	n/a
6	chr8:79428313-79428363	CMK	blood:	n/a
7	chr8:79428313-79428363	NHBE	bronchial:	n/a
8	chr8:79429818-79429868	Hepatocyte	liver:	n/a
9	chr8:79428444-79428494	HIPEpiC	eye:	n/a
10	chr8:79429818-79429868	SAEC	small airway:	n/a
11	chr8:79428325-79428375	MCF-7	breast:	n/a
12	chr8:79428117-79428167	AG09319	gingival:	n/a
13	chr8:79428313-79428363	SK-N-MC	brain:	n/a
14	chr8:79428434-79428484	ProgFib	skin:	n/a
15	chr8:79428117-79428167	U87	brain:	n/a
16	chr8:79428325-79428375	MCF10A-Er-Src	breast:	n/a
17	chr8:79428313-79428363	AG09309	skin:	n/a
18	chr8:79428725-79428775	MCF10A-Er-Src	breast:	n/a
19	chr8:79427993-79428043	NHBE	bronchial:	n/a
20	chr8:79428444-79428494	MCF10A-Er-Src	breast:	n/a
21	chr8:79428434-79428484	HPAEpiC	pulmonary alveolar:	n/a
22	chr8:79428325-79428375	HNPCEpiC	eye:	n/a
23	chr8:79429818-79429868	NHDF-neo	bronchial:	n/a
24	chr8:79427993-79428043	SKMC	muscle:	n/a
25	chr8:79428569-79428619	PANC-1	pancreas:	n/a
26	chr8:79428569-79428619	NB4	blood:	n/a
27	chr8:79429818-79429868	HPAEpiC	pulmonary alveolar:	n/a
28	chr8:79428434-79428484	AoSMC	blood vessel:	n/a
29	chr8:79428444-79428494	GM12892	blood:	n/a
30	chr8:79428569-79428619	PFSK-1	brain:	n/a
31	chr8:79427993-79428043	IMR90	lung:	fetal
32	chr8:79428569-79428619	GM06990	blood:	n/a
33	chr8:79428325-79428375	HUVEC	blood vessel:	n/a
34	chr8:79428725-79428775	ProgFib	skin:	n/a
35	chr8:79428434-79428484	HCM	heart:	n/a
36	chr8:79427993-79428043	LNCaP	prostate:	n/a
37	chr8:79427993-79428043	U87	brain:	n/a
38	chr8:79428725-79428775	AG04450	lung:	fetal
39	chr8:79428325-79428375	ovcar-3	ovarian:	n/a
40	chr8:79428325-79428375	U87	brain:	n/a
41	chr8:79429818-79429868	HCT-116	colon:	n/a
42	chr8:79429818-79429868	HEK293	kidney:	embryo
43	chr8:79428434-79428484	H1-hESC	embryonic stem cell:	embryo
44	chr8:79428725-79428775	HRE	kidney:	n/a
45	chr8:79429818-79429868	MCF-7	breast:	n/a
46	chr8:79428725-79428775	HRPEpiC	eye:	n/a
47	chr8:79428325-79428375	GM12892	blood:	n/a
48	chr8:79428434-79428484	HEEpiC	esophagus:	n/a
49	chr8:79428444-79428494	PFSK-1	brain:	n/a
50	chr8:79428434-79428484	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:79420594..79422389-chr8:79424976..79426839,2	MCF-7	breast:
2	chr8:79420413..79426569-chr8:79426863..79431107,5	MCF-7	breast:
3	chr8:79419078..79420072-chr8:79441781..79442729,2	MCF-7	breast:
4	chr8:79420594..79422389-chr8:79424976..79426839,2	MCF-7	breast:
5	chr8:79418638..79421599-chr8:79440731..79442586,3	MCF-7	breast:
6	chr8:79423442..79426104-chr8:79439954..79442867,2	MCF-7	breast:
7	chr8:79304240..79306156-chr8:79340487..79342636,2	MCF-7	breast:
8	chr8:79410893..79411697-chr8:79419823..79420388,2	K562	blood:
9	chr8:79304240..79306156-chr8:79340487..79342636,2	MCF-7	breast:
10	chr8:79298959..79299694-chr8:79310894..79311484,2	MCF-7	breast:
11	chr8:79420915..79422835-chr8:79428460..79430735,2	MCF-7	breast:
12	chr8:79305386..79305931-chr8:79343758..79344739,2	MCF-7	breast:
13	chr8:79323753..79325262-chr8:79328733..79331284,2	MCF-7	breast:
14	chr8:79298959..79299694-chr8:79310894..79311484,2	MCF-7	breast:
15	chr8:79300813..79303665-chr8:79516158..79519095,2	MCF-7	breast:
16	chr8:79433865..79436951-chr8:79440425..79443949,3	MCF-7	breast:
17	chr8:79410893..79411697-chr8:79419823..79420388,2	K562	blood:
18	chr8:79423918..79426841-chr8:79427285..79430314,3	MCF-7	breast:
19	chr8:79419518..79421514-chr8:79518015..79520151,2	MCF-7	breast:
20	chr8:79419499..79420416-chr8:79442084..79442972,6	MCF-7	breast:
21	chr8:79162917..79163612-chr8:79343717..79344374,3	MCF-7	breast:
22	chr8:79402266..79404340-chr8:79413420..79415402,2	MCF-7	breast:
23	chr8:79310990..79313753-chr8:79324129..79327439,3	MCF-7	breast:
24	chr8:79402266..79404340-chr8:79413420..79415402,2	MCF-7	breast:
25	chr8:79419533..79420037-chr8:79764408..79765064,2	MCF-7	breast:
26	chr8:79305220..79306244-chr8:79343794..79344725,3	MCF-7	breast:
27	chr22:39640025..39642519-chr8:79419690..79422250,2	MCF-7	breast:
28	chr8:79305893..79307637-chr8:79308532..79312236,3	MCF-7	breast:
29	chr8:79419743..79422501-chr8:79439751..79442069,2	MCF-7	breast:
30	chr8:79419785..79420445-chr8:79527063..79528030,4	MCF-7	breast:
31	chr8:79419378..79420481-chr8:79527083..79528366,7	MCF-7	breast:
32	chr8:79310990..79313753-chr8:79324129..79327439,3	MCF-7	breast:
33	chr8:79428435..79430204-chr8:79516996..79519469,2	MCF-7	breast:
34	chr20:56283155..56284954-chr8:79396075..79397773,2	MCF-7	breast:
35	chr8:79305220..79306244-chr8:79343794..79344725,3	MCF-7	breast:
36	chr8:79305386..79305931-chr8:79343758..79344739,2	MCF-7	breast:
37	chr8:79426480..79431052-chr8:79432809..79439382,7	MCF-7	breast:
38	chr8:79323753..79325262-chr8:79328733..79331284,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL7-1	chr8:79343091-79343183	ENSG00000254266
2	lnc-IL7-1	chr8:79338338-79338683	ENSG00000254266
3	lnc-IL7-1	chr8:79392489-79392570	ENSG00000254266

Variant related genes	Relation type
PKIA	TF binding region
RNU6-1220P	TF binding region
PKIA	CpG island
RNU6-1220P	CpG island
ENSG00000252935	chromatin interactions
ENSG00000171033	chromatin interactions
ENSG00000100311	chromatin interactions
ENSG00000260398	chromatin interactions
ENSG00000124225	chromatin interactions

Extended variants
information (count: 2285 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2285 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529192571	chr8:79287843-79287844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541055600	chr8:79287849-79287850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10504667	chr8:79287852-79287853	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs142696795	chr8:79287954-79287955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13438827	chr8:79287955-79287956	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs377554645	chr8:79287965-79287966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150999488	chr8:79288024-79288025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190958131	chr8:79288040-79288041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12674695	chr8:79288057-79288058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139927707	chr8:79288078-79288079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183400812	chr8:79288090-79288091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535723587	chr8:79288107-79288108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554170286	chr8:79288113-79288114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565898734	chr8:79288114-79288115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539943815	chr8:79288131-79288132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529842784	chr8:79288165-79288166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557917495	chr8:79288184-79288185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576313410	chr8:79288191-79288192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537377768	chr8:79288221-79288222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs61698353	chr8:79288234-79288235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs67031472	chr8:79288235-79288236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111307508	chr8:79288243-79288244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs13252205	chr8:79288247-79288248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372558190	chr8:79288250-79288251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187529277	chr8:79288267-79288268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115020799	chr8:79288309-79288310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541299747	chr8:79288343-79288344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113862184	chr8:79288405-79288406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577521971	chr8:79288410-79288411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545099025	chr8:79288434-79288435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146586921	chr8:79288440-79288441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541980421	chr8:79288464-79288465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191209132	chr8:79288470-79288471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561928179	chr8:79288496-79288497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141291121	chr8:79288555-79288556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113005591	chr8:79288577-79288578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75962695	chr8:79288629-79288630	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs547743376	chr8:79288685-79288686	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs566066586	chr8:79288689-79288690	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs150204296	chr8:79288699-79288700	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs182952903	chr8:79288701-79288702	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs570209185	chr8:79288704-79288705	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs537527905	chr8:79288732-79288733	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs555616357	chr8:79288746-79288747	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs199652490	chr8:79288751-79288752	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs573853506	chr8:79288762-79288763	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs534922620	chr8:79288788-79288789	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs145706690	chr8:79288831-79288832	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs577863106	chr8:79288916-79288917	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs555131430	chr8:79288943-79288944	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Colorectal cancer	19455253	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	21251322	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:951 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:79287200-79289600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr8:79287400-79288400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:79287400-79289200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr8:79287800-79290000	Enhancers	Fetal Stomach	stomach
5	chr8:79288400-79288800	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr8:79288400-79289000	Enhancers	Brain Substantia Nigra	brain
7	chr8:79288400-79289400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:79288400-79290000	Enhancers	Fetal Kidney	kidney
9	chr8:79288600-79289200	Enhancers	Fetal Lung	lung
10	chr8:79288600-79289400	Active TSS	Brain Hippocampus Middle	brain
11	chr8:79288600-79289600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr8:79288600-79289600	Enhancers	Fetal Muscle Leg	muscle
13	chr8:79289000-79289400	Flanking Active TSS	Brain Substantia Nigra	brain
14	chr8:79289000-79289600	Enhancers	Fetal Muscle Trunk	muscle
15	chr8:79289000-79290200	Enhancers	HMEC	breast
16	chr8:79289200-79289400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr8:79289200-79289600	Enhancers	Brain Anterior Caudate	brain
18	chr8:79289200-79289600	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr8:79289400-79289600	Enhancers	Brain Hippocampus Middle	brain
20	chr8:79297200-79297600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:79299200-79299600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr8:79299400-79299800	Enhancers	GM12878-XiMat	blood
23	chr8:79314400-79314800	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr8:79315200-79315400	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr8:79318200-79318600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr8:79326000-79326400	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr8:79326400-79331800	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr8:79328400-79329400	Enhancers	Brain Germinal Matrix	brain
29	chr8:79328800-79329400	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr8:79329600-79330000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:79330000-79330400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr8:79330000-79330400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:79330400-79331400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:79331800-79332200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr8:79331800-79332200	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr8:79342000-79343000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr8:79342000-79343200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr8:79342000-79343200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr8:79342400-79343200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr8:79342600-79343000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr8:79342800-79357200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:79349600-79351000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr8:79349600-79351800	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr8:79350000-79351200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr8:79350000-79351400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr8:79350000-79351400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr8:79350000-79351800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr8:79350400-79351600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr8:79350600-79351200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr8:79350800-79351400	Enhancers	H1 Cell Line	embryonic stem cell

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