Variant report

Variant	nsv881449
Chromosome Location	chr4:174984230-175225452
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2930)
CpG islands
(count:3237)
Chromatin interactive
region (count:165)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:2930 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:175203551-175205192	K562	blood:	n/a	n/a
2	ARID3A	chr4:175117670-175117734	K562	blood:	n/a	n/a
3	ARID3A	chr4:175115893-175116007	K562	blood:	n/a	n/a
4	ARID3A	chr4:175114840-175114857	K562	blood:	n/a	n/a
5	ARID3A	chr4:175162684-175162710	K562	blood:	n/a	n/a
6	ARID3A	chr4:175206493-175207419	K562	blood:	n/a	n/a
7	ARID3A	chr4:175204124-175205672	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:175202419-175202866	K562	blood:	n/a	n/a
9	ARID3A	chr4:175057339-175057515	K562	blood:	n/a	n/a
10	ARID3A	chr4:175075664-175076094	K562	blood:	n/a	n/a
11	ARID3A	chr4:175119912-175120522	K562	blood:	n/a	n/a
12	ARID3A	chr4:175077447-175077665	HepG2	liver:	n/a	n/a
13	ARID3A	chr4:175077338-175078813	K562	blood:	n/a	n/a
14	ARID3A	chr4:175181219-175181666	HepG2	liver:	n/a	n/a
15	ARID3A	chr4:175077006-175077040	K562	blood:	n/a	n/a
16	ATF1	chr4:175204120-175205399	K562	blood:	n/a	n/a
17	ATF1	chr4:175078096-175078762	K562	blood:	n/a	n/a
18	ATF1	chr4:175187439-175187616	K562	blood:	n/a	n/a
19	ATF1	chr4:175077427-175077741	K562	blood:	n/a	n/a
20	ATF1	chr4:175094579-175094782	K562	blood:	n/a	n/a
21	ATF2	chr4:175204176-175205586	GM12878	blood:	n/a	n/a
22	ATF2	chr4:175204125-175205140	GM12878	blood:	n/a	n/a
23	ATF3	chr4:175040230-175040532	K562	blood:	n/a	n/a
24	ATF3	chr4:175204744-175205143	A549	lung:	n/a	n/a
25	ATF3	chr4:175181188-175181648	A549	lung:	n/a	n/a
26	ATF3	chr4:175204540-175204935	A549	lung:	n/a	n/a
27	ATF3	chr4:175075652-175076016	K562	blood:	n/a	n/a
28	BACH1	chr4:175133098-175133298	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr4:175112323-175112473	K562	blood:	n/a	n/a
30	BACH1	chr4:175114620-175114902	K562	blood:	n/a	chr4:175114824-175114838
31	BACH1	chr4:175205536-175205633	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr4:175041594-175041870	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr4:175135139-175136374	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr4:175119961-175120319	K562	blood:	n/a	n/a
35	BCL3	chr4:175204585-175205287	A549	lung:	n/a	chr4:175204819-175204828
36	BCL3	chr4:175114166-175114403	GM12878	blood:	n/a	n/a
37	BCL3	chr4:175181061-175181810	A549	lung:	n/a	n/a
38	BCL3	chr4:175181172-175181683	A549	lung:	n/a	n/a
39	BCLAF1	chr4:175204662-175205498	GM12878	blood:	n/a	chr4:175204819-175204828
40	BCLAF1	chr4:175204666-175205230	K562	blood:	n/a	chr4:175204819-175204828
41	BCLAF1	chr4:175203881-175204440	K562	blood:	n/a	n/a
42	BHLHE40	chr4:175202355-175202864	K562	blood:	n/a	n/a
43	BHLHE40	chr4:175177025-175177293	K562	blood:	n/a	n/a
44	BHLHE40	chr4:175204101-175205281	K562	blood:	n/a	n/a
45	BHLHE40	chr4:175132666-175133007	GM12878	blood:	n/a	n/a
46	BHLHE40	chr4:175112132-175112495	K562	blood:	n/a	n/a
47	BHLHE40	chr4:175041463-175041925	K562	blood:	n/a	n/a
48	BHLHE40	chr4:175117630-175117769	K562	blood:	n/a	n/a
49	BHLHE40	chr4:175199674-175200009	GM12878	blood:	n/a	n/a
50	BHLHE40	chr4:175119199-175119376	K562	blood:	n/a	n/a

(count:3237 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:175133151-175133201	LNCaP	prostate:	n/a
2	chr4:175205038-175205088	GM19239	blood:	n/a
3	chr4:175204714-175204764	SK-N-SH_RA	brain:	n/a
4	chr4:175206877-175206927	GM19239	blood:	n/a
5	chr4:175133151-175133201	LNCaP	prostate:	n/a
6	chr4:175205038-175205088	GM19239	blood:	n/a
7	chr4:175204714-175204764	SK-N-SH_RA	brain:	n/a
8	chr4:175206877-175206927	GM19239	blood:	n/a
9	chr4:175135604-175135654	U87	brain:	n/a
10	chr4:175133103-175133153	GM12891	blood:	n/a
11	chr4:175139081-175139131	NT2-D1	testis:	n/a
12	chr4:175224083-175224133	GM12878	blood:	n/a
13	chr4:175135997-175136047	GM12892	blood:	n/a
14	chr4:175134545-175134595	SAEC	small airway:	n/a
15	chr4:175204127-175204177	T-47D	breast:	n/a
16	chr4:175135997-175136047	SK-N-SH	brain:	n/a
17	chr4:175132871-175132921	SK-N-SH	brain:	n/a
18	chr4:175204712-175204762	HMEC	breast:	n/a
19	chr4:175216323-175216373	HCPEpiC	choroid plexus:	n/a
20	chr4:175206877-175206927	HUVEC	blood vessel:	n/a
21	chr4:175205098-175205148	BJ	skin:	n/a
22	chr4:175132871-175132921	GM06990	blood:	n/a
23	chr4:175205422-175205472	PrEC	prostate:	n/a
24	chr4:175140004-175140054	PrEC	prostate:	n/a
25	chr4:175204712-175204762	AoSMC	blood vessel:	n/a
26	chr4:175205820-175205870	ProgFib	skin:	n/a
27	chr4:175205159-175205209	HUVEC	blood vessel:	n/a
28	chr4:175135406-175135456	U87	brain:	n/a
29	chr4:175135937-175135987	NHDF-neo	bronchial:	n/a
30	chr4:175138488-175138538	HAEpiC	amniotic membrane:	n/a
31	chr4:175132871-175132921	HRCEpiC	kidney:	n/a
32	chr4:175204127-175204177	GM19239	blood:	n/a
33	chr4:175204418-175204468	PANC-1	pancreas:	n/a
34	chr4:175205422-175205472	AG10803	skin:	n/a
35	chr4:175205098-175205148	AG09319	gingival:	n/a
36	chr4:175205820-175205870	Caco-2	colon:	n/a
37	chr4:175204127-175204177	AG10803	skin:	n/a
38	chr4:175205489-175205539	AoSMC	blood vessel:	n/a
39	chr4:175205003-175205053	H1-hESC	embryonic stem cell:	embryo
40	chr4:175139165-175139215	HAEpiC	amniotic membrane:	n/a
41	chr4:175204879-175204929	NT2-D1	testis:	n/a
42	chr4:175205248-175205298	AG10803	skin:	n/a
43	chr4:175133151-175133201	SAEC	small airway:	n/a
44	chr4:175205044-175205094	HEEpiC	esophagus:	n/a
45	chr4:175205159-175205209	HRE	kidney:	n/a
46	chr4:175206877-175206927	U87	brain:	n/a
47	chr4:175139755-175139805	ProgFib	skin:	n/a
48	chr4:175204879-175204929	SK-N-SH_RA	brain:	n/a
49	chr4:175135997-175136047	AG04450	lung:	fetal
50	chr4:175204714-175204764	MCF-7	breast:	n/a

(count:165 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr4:175110555..175112491-chr4:175112693..175115212,2	K562	blood:
2	chr4:175082350..175084349-chr4:175086054..175089264,3	K562	blood:
3	chr4:175126822..175128871-chr4:175141864..175143664,2	K562	blood:
4	chr4:175164110..175166132-chr4:175169817..175172725,2	K562	blood:
5	chr4:175186610..175188170-chr4:175200585..175202935,2	K562	blood:
6	chr4:175220558..175223479-chr4:175227637..175230874,3	K562	blood:
7	chr4:175150650..175152595-chr4:175157441..175159670,2	K562	blood:
8	chr4:175117275..175119406-chr4:175125544..175127671,2	K562	blood:
9	chr4:175207634..175209393-chr4:175212176..175214357,2	MCF-7	breast:
10	chr1:144532740..144535674-chr4:175055478..175058497,9	K562	blood:
11	chr4:175162287..175164616-chr4:175167133..175169493,3	K562	blood:
12	chr4:175126822..175128871-chr4:175141864..175143664,2	K562	blood:
13	chr4:175168918..175171895-chr4:175175274..175177764,2	K562	blood:
14	chr4:175128539..175131146-chr4:175134712..175136684,2	K562	blood:
15	chr4:175180268..175182559-chr4:175204010..175205620,2	MCF-7	breast:
16	chr4:175117906..175119445-chr4:175125544..175128189,2	K562	blood:
17	chr4:175222302..175225291-chr4:175225581..175228426,3	K562	blood:
18	chr4:175171940..175174265-chr4:175174829..175177044,2	K562	blood:
19	chr4:175185339..175187975-chr4:175190769..175193376,4	K562	blood:
20	chr4:175203651..175207123-chr4:175224363..175226517,3	MCF-7	breast:
21	chr4:174996384..174998714-chr4:175000478..175003224,3	K562	blood:
22	chr4:175204822..175207502-chr4:175223831..175226122,2	K562	blood:
23	chr4:175132325..175134757-chr4:175137089..175139873,3	K562	blood:
24	chr4:175111911..175114409-chr4:175128663..175131764,4	K562	blood:
25	chr4:175143534..175144341-chr4:175180041..175181006,2	MCF-7	breast:
26	chr4:175179063..175181679-chr4:175196326..175198561,2	K562	blood:
27	chr4:175203968..175206484-chr4:175206530..175210065,3	MCF-7	breast:
28	chr4:175162287..175164616-chr4:175167133..175169493,3	K562	blood:
29	chr4:174424171..174426662-chr4:175151215..175153299,2	K562	blood:
30	chr4:175196583..175199350-chr4:175586239..175588239,2	K562	blood:
31	chr4:175130268..175132878-chr4:175141346..175143652,2	K562	blood:
32	chr4:175204473..175205373-chr9:130213191..130213790,2	Hela-S3	cervix:
33	chr4:175125538..175127533-chr4:175130389..175133008,2	K562	blood:
34	chr4:175112735..175115136-chr4:175124112..175126118,2	K562	blood:
35	chr4:175120452..175124043-chr4:175124423..175129022,4	K562	blood:
36	chr4:175172359..175176044-chr4:175180027..175182718,3	K562	blood:
37	chr4:175110555..175112491-chr4:175112693..175115212,2	K562	blood:
38	chr4:175091223..175092965-chr4:175135454..175137092,2	K562	blood:
39	chr4:175077638..175080510-chr4:175083476..175086344,3	K562	blood:
40	chr1:144533743..144534618-chr4:175056477..175057498,11	HCT-116	colon:
41	chr4:175132325..175134757-chr4:175137089..175139873,3	K562	blood:
42	chr4:175033636..175035417-chr4:175039229..175041008,2	K562	blood:
43	chr4:175224646..175226466-chr4:175228336..175231070,2	K562	blood:
44	chr4:175190016..175192606-chr4:175201922..175204827,4	K562	blood:
45	chr4:175111354..175114182-chr4:175118552..175121148,2	K562	blood:
46	chr4:175033636..175035417-chr4:175039229..175041008,2	K562	blood:
47	chr4:174996384..174998714-chr4:175000478..175003224,3	K562	blood:
48	chr4:175112074..175114182-chr4:175118552..175121515,3	K562	blood:
49	chr4:175160118..175162210-chr4:175163312..175164848,2	MCF-7	breast:
50	chr4:175111911..175114409-chr4:175128663..175131764,4	K562	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP44-7	chr4:175083604-175083683	l_2785_chr4:174856882-174860902_heart
2	lnc-CEP44-7	chr4:175086216-175086370	l_2785_chr4:174856882-174860902_heart
3	lnc-CEP44-7	chr4:175054945-175055046	l_2785_chr4:174856882-174860902_heart
4	lnc-FBXO8-4	chr4:175041570-175041668	ENSG00000248174
5	lnc-FBXO8-1	chr4:175090047-175090064	XLOC_004171
6	lnc-FBXO8-4	chr4:175017883-175017934	ENSG00000248174
7	lnc-CEP44-2	chr4:175008679-175008790	XLOC_003786
8	lnc-FBXO8-4	chr4:175018774-175018980	ENSG00000248174
9	lnc-CEP44-2	chr4:175101426-175101572	XLOC_003786
10	lnc-FBXO8-4	chr4:175018906-175018980	ENSG00000248174
11	lnc-FBXO8-1	chr4:175085593-175085716	ucscGeneNc_uc003itn_1
12	lnc-FBXO8-4	chr4:175141465-175141549	ENSG00000248174
13	lnc-FBXO8-1	chr4:175081933-175083487	ucscGeneNc_uc003itn_1
14	lnc-FBXO8-4	chr4:175041048-175041237	ENSG00000248174
15	lnc-CEP44-7	chr4:175086951-175087240	l_2785_chr4:174856882-174860902_heart
16	lnc-FBXO8-3	chr4:175056206-175057298	ENSG00000250957
17	lnc-FBXO8-7	chr4:175222085-175222665	l_2787_chr4:175222084-175233590_placenta
18	lnc-FBXO8-1	chr4:175148433-175148577	ucscGeneNc_uc003itn_1
19	lnc-FBXO8-4	chr4:175035192-175035423	ENSG00000248174
20	lnc-FBXO8-1	chr4:175085592-175085832	XLOC_004171
21	lnc-FBXO8-3	chr4:175075738-175075788	ENSG00000250957
22	lnc-FBXO8-4	chr4:175015811-175016604	ENSG00000248174
23	lnc-FBXO8-1	chr4:175089623-175089698	XLOC_004171
24	lnc-CEP44-7	chr4:175035942-175036006	l_2785_chr4:174856882-174860902_heart
25	lnc-HPGD-5	chr4:175169688-175171444	l_2786_chr4:175169687-175174274_placenta
26	lnc-HPGD-5	chr4:175174023-175174274	l_2786_chr4:175169687-175174274_placenta
27	lnc-FBXO8-4	chr4:175041048-175041237	ENSG00000248174
28	lnc-CEP44-7	chr4:175014010-175014192	l_2785_chr4:174856882-174860902_heart
29	lnc-CEP44-7	chr4:175083381-175083492	l_2785_chr4:174856882-174860902_heart

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	FBXO8	hsa-miR-19b-3p	chr4:175158339-175158360
2	FBXO8	hsa-miR-19b-3p	chr4:175158373-175158395
3	FBXO8	hsa-miR-19b-3p	chr4:175158345-175158338

Variant related genes	Relation type
ENSG00000248174	TF binding region
ENSG00000250957	TF binding region
CEP44	TF binding region
ENSG00000251213	TF binding region
FBXO8	TF binding region
ENSG00000248174	CpG island
ENSG00000250957	CpG island
CEP44	CpG island
ENSG00000251213	CpG island
FBXO8	CpG island
ENSG00000148356	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000153885	chromatin interactions
ENSG00000250957	chromatin interactions
ENSG00000197958	chromatin interactions
ENSG00000164118	chromatin interactions
ENSG00000119912	chromatin interactions
ENSG00000101447	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000164117	chromatin interactions
ENSG00000248174	chromatin interactions
BTAF1	miRNA target sites
ADAM9	miRNA target sites
C2orf69	miRNA target sites
COL4A1	miRNA target sites
MTMR3	miRNA target sites
PDCD6IP	miRNA target sites
SYNJ1	miRNA target sites

Extended variants
information (count: 7963 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:7963 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9996330	chr4:174984230-174984231	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77279238	chr4:174984237-174984238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532042319	chr4:174984263-174984264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77360170	chr4:174984283-174984284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575078648	chr4:174984525-174984526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181173436	chr4:174984561-174984562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183654301	chr4:174984566-174984567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372632582	chr4:174984572-174984573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544577039	chr4:174984621-174984622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570403653	chr4:174984622-174984623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10032108	chr4:174984633-174984634	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs550838219	chr4:174984642-174984643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533489457	chr4:174984656-174984657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550417041	chr4:174984668-174984669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577037247	chr4:174984693-174984694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545694055	chr4:174984710-174984711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148679097	chr4:174984758-174984759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569938944	chr4:174984759-174984760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528200070	chr4:174984764-174984765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs62336656	chr4:174984772-174984773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9999168	chr4:174984845-174984846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs561390132	chr4:174984874-174984875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530436024	chr4:174984898-174984899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555452582	chr4:174984906-174984907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369738354	chr4:174984909-174984910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142233155	chr4:174984937-174984938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182032723	chr4:174984941-174984942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs70947410	chr4:174984974-174984975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200552289	chr4:174984984-174984985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs397996307	chr4:174984985-174984986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567033544	chr4:174984995-174984996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113978853	chr4:174984999-174985000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535115200	chr4:174985037-174985038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186221396	chr4:174985058-174985059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114339261	chr4:174985063-174985064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113846768	chr4:174985104-174985105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113566419	chr4:174985128-174985129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144697793	chr4:174985145-174985146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558096370	chr4:174985189-174985190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs62336657	chr4:174985221-174985222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577094450	chr4:174985231-174985232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546054880	chr4:174985240-174985241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111580757	chr4:174985241-174985242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534429816	chr4:174985250-174985251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572987010	chr4:174985252-174985253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541586422	chr4:174985253-174985254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191737886	chr4:174985336-174985337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530495274	chr4:174985494-174985495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181754855	chr4:174985507-174985508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564095157	chr4:174985623-174985624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	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
Oral squamous cell carcinoma	17134496	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	22127048	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Gastric adenocarcinoma	19115996	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	18511947	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:3114 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:174983400-174984800	Enhancers	Fetal Lung	lung
2	chr4:174984600-174984800	Enhancers	Fetal Brain Male	brain
3	chr4:174984800-174988800	Weak transcription	Fetal Lung	lung
4	chr4:174986600-174986800	Enhancers	Fetal Brain Male	brain
5	chr4:174987800-174988600	Enhancers	Colon Smooth Muscle	Colon
6	chr4:174988000-174988800	Bivalent Enhancer	Fetal Brain Male	brain
7	chr4:174988200-174988400	Enhancers	Stomach Smooth Muscle	stomach
8	chr4:174988200-174988600	Enhancers	Left Ventricle	heart
9	chr4:174988200-174989800	Enhancers	Aorta	Aorta
10	chr4:174988400-174989000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr4:174988600-174991200	Weak transcription	Colon Smooth Muscle	Colon
12	chr4:174988800-174989800	Enhancers	Fetal Lung	lung
13	chr4:174989000-174989800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:174989000-174989800	Enhancers	Stomach Smooth Muscle	stomach
15	chr4:174989000-174990000	Enhancers	Fetal Heart	heart
16	chr4:174989400-174989800	Enhancers	Fetal Stomach	stomach
17	chr4:174989800-174990800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:174989800-174991000	Weak transcription	Fetal Lung	lung
19	chr4:174989800-174991000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr4:174990000-174991000	Weak transcription	Fetal Heart	heart
21	chr4:174990600-174991200	Enhancers	Brain Germinal Matrix	brain
22	chr4:174990800-174992200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:174991000-174991600	Enhancers	Fetal Lung	lung
24	chr4:174991000-174991600	Enhancers	Stomach Smooth Muscle	stomach
25	chr4:174991000-174991800	Enhancers	Fetal Heart	heart
26	chr4:174991200-174991600	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr4:174991200-174991800	Enhancers	Colon Smooth Muscle	Colon
28	chr4:174991600-174992400	Weak transcription	Stomach Smooth Muscle	stomach
29	chr4:174991600-174992600	Weak transcription	Fetal Lung	lung
30	chr4:174991800-174992200	Weak transcription	Fetal Heart	heart
31	chr4:174991800-174992400	Weak transcription	Colon Smooth Muscle	Colon
32	chr4:174992200-174992800	Enhancers	Fetal Heart	heart
33	chr4:174992200-174993000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr4:174992400-174992600	Enhancers	Colon Smooth Muscle	Colon
35	chr4:174992400-174993200	Enhancers	Stomach Smooth Muscle	stomach
36	chr4:174992800-174993000	Enhancers	Fetal Lung	lung
37	chr4:174993000-174993200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:174993800-174994800	Weak transcription	Ovary	ovary
39	chr4:174994400-174994600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr4:174994800-174995000	ZNF genes & repeats	Ovary	ovary
41	chr4:175000800-175002600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:175001000-175001400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:175001400-175006000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr4:175002600-175007200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr4:175005000-175006400	Enhancers	HUVEC	blood vessel
46	chr4:175005800-175006400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr4:175006000-175006200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:175006200-175006800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr4:175006400-175008400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr4:175007000-175007200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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