Variant report

Variant	nsv1001094
Chromosome Location	chr4:55131860-55189739
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:688)
CpG islands
(count:429)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:688 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:55162862-55163089	HepG2	liver:	n/a	n/a
2	ATF2	chr4:55181588-55182175	GM12878	blood:	n/a	n/a
3	ATF2	chr4:55181558-55182409	GM12878	blood:	n/a	n/a
4	BACH1	chr4:55143445-55143674	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:55181689-55182109	GM12878	blood:	n/a	n/a
6	BATF	chr4:55141318-55141540	GM12878	blood:	n/a	n/a
7	BATF	chr4:55143876-55144294	GM12878	blood:	n/a	chr4:55144109-55144120
8	BATF	chr4:55142251-55142554	GM12878	blood:	n/a	n/a
9	BATF	chr4:55143891-55144132	GM12878	blood:	n/a	chr4:55144109-55144120
10	BATF	chr4:55181674-55182115	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:55181702-55182144	GM12878	blood:	n/a	chr4:55181946-55181955
12	BCL11A	chr4:55181711-55182026	GM12878	blood:	n/a	chr4:55181946-55181955
13	BCL3	chr4:55181745-55182079	GM12878	blood:	n/a	chr4:55181946-55181955
14	BCLAF1	chr4:55181591-55182237	GM12878	blood:	n/a	chr4:55181946-55181955 chr4:55182172-55182181
15	BCLAF1	chr4:55181640-55182170	GM12878	blood:	n/a	chr4:55181946-55181955
16	BHLHE40	chr4:55181644-55182222	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:55188978-55189397	K562	blood:	n/a	n/a
18	CEBPB	chr4:55144434-55144651	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:55142669-55142969	IMR90	lung:	n/a	chr4:55142791-55142802
20	CEBPB	chr4:55142615-55142975	H1-hESC	embryonic stem cell:	n/a	chr4:55142791-55142802
21	CEBPB	chr4:55185113-55185347	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:55131574-55131910	IMR90	lung:	n/a	n/a
23	CEBPB	chr4:55131571-55131910	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:55147486-55147838	IMR90	lung:	n/a	chr4:55147567-55147578
25	CEBPB	chr4:55142705-55142836	HepG2	liver:	n/a	chr4:55142791-55142802
26	CEBPB	chr4:55142786-55142870	K562	blood:	n/a	chr4:55142791-55142802
27	CEBPB	chr4:55134357-55134635	IMR90	lung:	n/a	n/a
28	CEBPD	chr4:55179465-55179869	K562	blood:	n/a	n/a
29	CHD2	chr4:55134157-55134167	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr4:55143144-55143717	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:55185200-55185350	GM12867	blood:	n/a	chr4:55185255-55185276 chr4:55185256-55185269
32	CTCF	chr4:55185200-55185350	GM12801	blood:	n/a	chr4:55185255-55185276 chr4:55185256-55185269
33	CTCF	chr4:55188966-55189412	K562	blood:	n/a	chr4:55189176-55189197 chr4:55189174-55189192
34	CTCF	chr4:55189100-55189250	GM12866	blood:	n/a	chr4:55189176-55189197 chr4:55189174-55189192
35	CTCF	chr4:55189220-55189370	WI-38	lung:	n/a	n/a
36	CTCF	chr4:55189080-55189230	GM12868	blood:	n/a	chr4:55189176-55189197 chr4:55189174-55189192
37	CTCF	chr4:55189080-55189230	HEK293	kidney:	n/a	chr4:55189176-55189197 chr4:55189174-55189192
38	CTCF	chr4:55189100-55189250	AG09319	gingival:	n/a	chr4:55189176-55189197 chr4:55189174-55189192
39	CTCF	chr4:55185519-55185571	GM10266	blood:	n/a	n/a
40	CTCF	chr4:55185200-55185350	HEK293	kidney:	n/a	chr4:55185255-55185276 chr4:55185256-55185269
41	CTCF	chr4:55185200-55185350	GM12866	blood:	n/a	chr4:55185255-55185276 chr4:55185256-55185269
42	CTCF	chr4:55185180-55185330	GM12869	blood:	n/a	chr4:55185255-55185276 chr4:55185256-55185269
43	CTCF	chr4:55189050-55189319	Fibrobl	skin:	n/a	chr4:55189176-55189197 chr4:55189174-55189192
44	CTCF	chr4:55189070-55189302	MCF-7	breast:	n/a	chr4:55189176-55189197 chr4:55189174-55189192
45	CTCF	chr4:55189120-55189270	Hela-S3	cervix:	n/a	chr4:55189176-55189197 chr4:55189174-55189192
46	CTCF	chr4:55185160-55185310	HAc	cerebellar:	n/a	chr4:55185255-55185276 chr4:55185256-55185269
47	CTCF	chr4:55185082-55185444	K562	blood:	n/a	chr4:55185255-55185276 chr4:55185256-55185269
48	CTCF	chr4:55189081-55189299	Kidney_OC	kidney:	n/a	chr4:55189176-55189197 chr4:55189174-55189192
49	CTCF	chr4:55185200-55185350	SK-N-SH_RA	brain:	n/a	chr4:55185255-55185276 chr4:55185256-55185269
50	CTCF	chr4:55185132-55185389	MCF-7	breast:	n/a	chr4:55185255-55185276 chr4:55185256-55185269

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:55144066-55144116	AG04449	skin:	fetal
2	chr4:55144066-55144116	HRE	kidney:	n/a
3	chr4:55144066-55144116	AG04449	skin:	fetal
4	chr4:55144066-55144116	HRE	kidney:	n/a
5	chr4:55142142-55142192	ProgFib	skin:	n/a
6	chr4:55142142-55142192	CMK	blood:	n/a
7	chr4:55134316-55134366	SKMC	muscle:	n/a
8	chr4:55144066-55144116	MCF-7	breast:	n/a
9	chr4:55139873-55139923	HEK293	kidney:	embryo
10	chr4:55144066-55144116	GM19239	blood:	n/a
11	chr4:55142142-55142192	NB4	blood:	n/a
12	chr4:55143269-55143319	PrEC	prostate:	n/a
13	chr4:55134316-55134366	MCF10A-Er-Src	breast:	n/a
14	chr4:55143269-55143319	ovcar-3	ovarian:	n/a
15	chr4:55142142-55142192	AoSMC	blood vessel:	n/a
16	chr4:55143269-55143319	HCM	heart:	n/a
17	chr4:55142142-55142192	K562	blood:	n/a
18	chr4:55142142-55142192	HCM	heart:	n/a
19	chr4:55143285-55143335	A549	lung:	n/a
20	chr4:55134316-55134366	AG04449	skin:	fetal
21	chr4:55139873-55139923	HMEC	breast:	n/a
22	chr4:55143285-55143335	Hepatocyte	liver:	n/a
23	chr4:55142142-55142192	NHBE	bronchial:	n/a
24	chr4:55139873-55139923	GM06990	blood:	n/a
25	chr4:55143285-55143335	HCF	heart:	n/a
26	chr4:55143285-55143335	CMK	blood:	n/a
27	chr4:55142142-55142192	GM19239	blood:	n/a
28	chr4:55143269-55143319	HL-60	blood:	n/a
29	chr4:55143557-55143607	HAEpiC	amniotic membrane:	n/a
30	chr4:55143285-55143335	HL-60	blood:	n/a
31	chr4:55143285-55143335	HCT-116	colon:	n/a
32	chr4:55143557-55143607	CMK	blood:	n/a
33	chr4:55134316-55134366	CMK	blood:	n/a
34	chr4:55143557-55143607	ProgFib	skin:	n/a
35	chr4:55134316-55134366	SK-N-MC	brain:	n/a
36	chr4:55143557-55143607	MCF10A-Er-Src	breast:	n/a
37	chr4:55143285-55143335	GM12878	blood:	n/a
38	chr4:55143269-55143319	RPTEC	kidney:	n/a
39	chr4:55139873-55139923	Hepatocyte	liver:	n/a
40	chr4:55142142-55142192	AG09309	skin:	n/a
41	chr4:55144066-55144116	AG04450	lung:	fetal
42	chr4:55139873-55139923	HCT-116	colon:	n/a
43	chr4:55142142-55142192	GM12892	blood:	n/a
44	chr4:55143285-55143335	NHDF-neo	bronchial:	n/a
45	chr4:55134316-55134366	AG10803	skin:	n/a
46	chr4:55134316-55134366	HMEC	breast:	n/a
47	chr4:55143557-55143607	SKMC	muscle:	n/a
48	chr4:55144066-55144116	AG10803	skin:	n/a
49	chr4:55143285-55143335	HCM	heart:	n/a
50	chr4:55143557-55143607	NHBE	bronchial:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:55188935..55189678-chr4:55232967..55233845,2	MCF-7	breast:
2	chr4:55185299..55185879-chr4:55250478..55251050,2	MCF-7	breast:
3	chr4:55188871..55189578-chr4:55299616..55300145,2	K562	blood:
4	chr4:55184744..55185734-chr4:55306461..55307691,6	MCF-7	breast:
5	chr4:55188891..55189478-chr4:55307244..55307822,2	MCF-7	breast:
6	chr4:55188918..55189432-chr4:55241699..55242360,2	MCF-7	breast:
7	chr4:55184812..55185387-chr4:55827256..55827776,2	K562	blood:
8	chr4:55188742..55189647-chr4:55306683..55307683,5	K562	blood:
9	chr4:55189198..55189880-chr4:55837437..55838307,2	MCF-7	breast:
10	chr4:55188790..55189653-chr4:55306542..55307230,3	MCF-7	breast:
11	chr4:55184839..55185711-chr4:55827240..55827767,2	MCF-7	breast:
12	chr4:55133319..55135360-chr4:55145191..55147587,2	MCF-7	breast:
13	chr4:55130972..55133707-chr4:55137155..55139847,2	MCF-7	breast:
14	chr4:55184800..55185406-chr4:55706810..55707325,2	MCF-7	breast:
15	chr4:55188876..55189604-chr4:55241739..55242312,2	MCF-7	breast:
16	chr4:55188651..55189879-chr4:55299577..55300637,10	MCF-7	breast:
17	chr4:55139472..55141383-chr4:55141730..55143677,2	MCF-7	breast:
18	chr4:55133319..55135360-chr4:55145191..55147587,2	MCF-7	breast:
19	chr4:55184927..55185737-chr4:55306931..55307659,2	K562	blood:
20	chr4:55188829..55189372-chr4:55706928..55707723,2	MCF-7	breast:
21	chr4:55135740..55138560-chr4:55139917..55141829,2	MCF-7	breast:
22	chr4:55135740..55138560-chr4:55139917..55141829,2	MCF-7	breast:
23	chr4:55188990..55189633-chr4:55827285..55828214,3	K562	blood:
24	chr4:55130972..55133707-chr4:55137155..55139847,2	MCF-7	breast:
25	chr4:55188755..55189636-chr4:55299369..55300499,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHIC2-5	chr4:55167807-55168055	ucscGeneNc_uc003hap_2
2	lnc-CHIC2-5	chr4:55164137-55166101	ucscGeneNc_uc003hap_2

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PDGFRA	hsa-miR-34a-5p	chr4:55164138-55164144
2	PDGFRA	hsa-miR-34a-5p	chr4:55164109-55164115
3	PDGFRA	hsa-miR-140-5p	chr4:55161498-55161504
4	PDGFRA	hsa-miR-34a-5p	chr4:55164095-55164115
5	PDGFRA	hsa-miR-140-5p	chr4:55161485-55161505
6	PDGFRA	hsa-miR-34a-5p	chr4:55164124-55164145
7	PDGFRA	hsa-miR-26b-5p	chr4:55163465-55163485

Variant related genes	Relation type
PDGFRA	TF binding region
PDGFRA	CpG island
ENSG00000248518	chromatin interactions
ENSG00000134853	chromatin interactions

Extended variants
information (count: 2105 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2105 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578088909	chr4:55131867-55131868	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs543665607	chr4:55131877-55131878	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563769630	chr4:55131887-55131888	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531907436	chr4:55131911-55131912	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142413369	chr4:55131918-55131919	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146008102	chr4:55131932-55131933	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186066671	chr4:55131953-55131954	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537974499	chr4:55132138-55132139	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs67600360	chr4:55132162-55132163	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs547664294	chr4:55132195-55132196	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528823780	chr4:55132212-55132213	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564224611	chr4:55132217-55132218	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533110126	chr4:55132231-55132232	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs75201529	chr4:55132255-55132256	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543978675	chr4:55132298-55132299	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4864864	chr4:55132325-55132326	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs200164097	chr4:55132344-55132345	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189655730	chr4:55132366-55132367	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182102200	chr4:55132399-55132400	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187099333	chr4:55132425-55132426	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191499755	chr4:55132426-55132427	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565333469	chr4:55132454-55132455	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183482424	chr4:55132470-55132471	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376745290	chr4:55132502-55132503	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534320172	chr4:55132503-55132504	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188613012	chr4:55132562-55132563	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs578197442	chr4:55132566-55132567	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565413888	chr4:55132569-55132570	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552308043	chr4:55132578-55132579	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11403706	chr4:55132579-55132580	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537622388	chr4:55132583-55132584	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs201240830	chr4:55132590-55132591	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76686173	chr4:55132591-55132592	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115209298	chr4:55132615-55132616	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574315540	chr4:55132683-55132684	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113190864	chr4:55132723-55132724	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs58382319	chr4:55132734-55132735	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559936366	chr4:55132748-55132749	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs148913531	chr4:55132776-55132777	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545084991	chr4:55132834-55132835	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564373275	chr4:55132867-55132868	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4864865	chr4:55132878-55132879	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs569879775	chr4:55132888-55132889	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547156501	chr4:55132889-55132890	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs193147093	chr4:55132946-55132947	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563127523	chr4:55132963-55132964	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529099907	chr4:55132976-55132977	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77751678	chr4:55132988-55132989	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548620425	chr4:55133008-55133009	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536857120	chr4:55133072-55133073	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164920	CNVD
Rhabdomyosarcoma	20807811	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:767 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55119000-55138600	Weak transcription	Fetal Intestine Small	intestine
2	chr4:55119400-55148000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr4:55121000-55147600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr4:55121000-55153200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:55121200-55133400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr4:55121200-55147200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr4:55122400-55133400	Weak transcription	Fetal Muscle Leg	muscle
8	chr4:55122400-55142600	Strong transcription	Cortex derived primary cultured neurospheres	brain
9	chr4:55124400-55140400	Weak transcription	Placenta	Placenta
10	chr4:55124400-55147800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:55124800-55134000	Weak transcription	Fetal Brain Male	brain
12	chr4:55124800-55138600	Weak transcription	NH-A	brain
13	chr4:55125400-55140600	Strong transcription	Ovary	ovary
14	chr4:55125800-55135800	Strong transcription	Fetal Lung	lung
15	chr4:55126000-55132600	Strong transcription	NHLF	lung
16	chr4:55126000-55133400	Strong transcription	Osteobl	bone
17	chr4:55126400-55140800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:55126600-55134400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr4:55127000-55138600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:55127200-55133400	Weak transcription	Fetal Intestine Large	intestine
21	chr4:55127200-55135600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr4:55127800-55140600	Weak transcription	Left Ventricle	heart
23	chr4:55129200-55139000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr4:55129200-55142400	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr4:55129600-55132600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr4:55129800-55136000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr4:55130000-55135400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:55130000-55139000	Weak transcription	Esophagus	oesophagus
29	chr4:55130000-55139000	Weak transcription	Stomach Smooth Muscle	stomach
30	chr4:55130200-55142800	Weak transcription	Gastric	stomach
31	chr4:55130200-55143000	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr4:55130400-55132000	Genic enhancers	NHDF-Ad	bronchial
33	chr4:55130400-55134200	Strong transcription	Fetal Kidney	kidney
34	chr4:55130600-55142400	Weak transcription	Right Ventricle	heart
35	chr4:55130800-55132000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr4:55131200-55132000	Strong transcription	Fetal Stomach	stomach
37	chr4:55131200-55132200	Strong transcription	Aorta	Aorta
38	chr4:55131400-55132000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr4:55131400-55132400	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:55131600-55132000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr4:55131600-55148000	Weak transcription	Duodenum Mucosa	Duodenum
42	chr4:55131800-55132200	Enhancers	Liver	Liver
43	chr4:55131800-55133200	Weak transcription	Fetal Muscle Trunk	muscle
44	chr4:55131800-55134200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr4:55131800-55137200	Weak transcription	Spleen	Spleen
46	chr4:55132000-55133400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr4:55132000-55133400	Weak transcription	Fetal Stomach	stomach
48	chr4:55132000-55133400	Strong transcription	NHDF-Ad	bronchial
49	chr4:55132000-55133600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr4:55132000-55134200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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