Variant report

Variant	nsv4900
Chromosome Location	chr5:81022018-81067365
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1419)
CpG islands
(count:915)
Chromatin interactive
region (count:58)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1419 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:81048263-81048618	K562	blood:	n/a	n/a
2	ARID3A	chr5:81057808-81058184	K562	blood:	n/a	n/a
3	ARID3A	chr5:81055533-81055748	K562	blood:	n/a	n/a
4	ARID3A	chr5:81056958-81057213	K562	blood:	n/a	n/a
5	ARID3A	chr5:81047100-81047417	K562	blood:	n/a	n/a
6	ARID3A	chr5:81054562-81054991	K562	blood:	n/a	n/a
7	ARID3A	chr5:81047152-81047393	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:81059998-81060002	K562	blood:	n/a	n/a
9	ARID3A	chr5:81049568-81051331	K562	blood:	n/a	n/a
10	ARID3A	chr5:81059347-81059740	K562	blood:	n/a	n/a
11	ATF1	chr5:81057199-81058024	K562	blood:	n/a	n/a
12	ATF1	chr5:81046732-81047309	K562	blood:	n/a	n/a
13	ATF2	chr5:81045187-81045739	GM12878	blood:	n/a	n/a
14	ATF2	chr5:81045141-81045881	GM12878	blood:	n/a	n/a
15	ATF2	chr5:81046961-81047462	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr5:81046629-81047509	GM12878	blood:	n/a	n/a
17	ATF2	chr5:81047037-81047445	GM12878	blood:	n/a	n/a
18	ATF2	chr5:81046902-81047549	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr5:81047029-81047461	A549	lung:	n/a	chr5:81047261-81047270
20	ATF3	chr5:81046976-81047516	A549	lung:	n/a	chr5:81047469-81047478 chr5:81047261-81047270
21	ATF3	chr5:81047089-81047411	K562	blood:	n/a	chr5:81047261-81047270
22	BACH1	chr5:81046703-81047547	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr5:81046756-81046995	K562	blood:	n/a	n/a
24	BACH1	chr5:81045559-81045802	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr5:81047249-81047453	K562	blood:	n/a	n/a
26	BATF	chr5:81045329-81045704	GM12878	blood:	n/a	n/a
27	BATF	chr5:81045268-81045772	GM12878	blood:	n/a	n/a
28	BCL11A	chr5:81047114-81047360	GM12878	blood:	n/a	n/a
29	BCL11A	chr5:81046689-81046983	GM12878	blood:	n/a	n/a
30	BCL11A	chr5:81047062-81047309	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL11A	chr5:81045363-81045810	GM12878	blood:	n/a	n/a
32	BCL3	chr5:81045244-81045847	GM12878	blood:	n/a	n/a
33	BCL3	chr5:81046691-81047677	GM12878	blood:	n/a	chr5:81046985-81046994
34	BCL3	chr5:81046899-81047536	A549	lung:	n/a	chr5:81046985-81046994
35	BCL3	chr5:81046876-81047552	A549	lung:	n/a	chr5:81046985-81046994
36	BCLAF1	chr5:81046616-81047549	GM12878	blood:	n/a	chr5:81046985-81046994
37	BCLAF1	chr5:81045100-81045822	GM12878	blood:	n/a	n/a
38	BCLAF1	chr5:81047006-81047548	K562	blood:	n/a	n/a
39	BCLAF1	chr5:81045131-81045806	GM12878	blood:	n/a	n/a
40	BCLAF1	chr5:81046631-81047845	GM12878	blood:	n/a	chr5:81046985-81046994 chr5:81047770-81047783
41	BHLHE40	chr5:81046674-81047690	K562	blood:	n/a	chr5:81047331-81047347
42	BHLHE40	chr5:81046589-81047662	GM12878	blood:	n/a	chr5:81047331-81047347
43	BHLHE40	chr5:81044987-81045795	GM12878	blood:	n/a	n/a
44	BHLHE40	chr5:81045521-81045682	K562	blood:	n/a	n/a
45	BHLHE40	chr5:81048138-81048344	K562	blood:	n/a	n/a
46	BHLHE40	chr5:81050505-81050773	K562	blood:	n/a	n/a
47	BHLHE40	chr5:81054571-81054850	K562	blood:	n/a	n/a
48	BHLHE40	chr5:81022463-81022471	GM12878	blood:	n/a	n/a
49	BHLHE40	chr5:81059587-81059667	K562	blood:	n/a	n/a
50	BHLHE40	chr5:81051162-81051484	K562	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:81046408-81046458	BE2_C	brain:	n/a
2	chr5:81047848-81047898	AG09309	skin:	n/a
3	chr5:81047246-81047296	Hepatocyte	liver:	n/a
4	chr5:81047188-81047238	HMEC	breast:	n/a
5	chr5:81046408-81046458	HCM	heart:	n/a
6	chr5:81051199-81051249	HCT-116	colon:	n/a
7	chr5:81048305-81048355	HCPEpiC	choroid plexus:	n/a
8	chr5:81048495-81048545	AG04450	lung:	fetal
9	chr5:81048495-81048545	GM12892	blood:	n/a
10	chr5:81047246-81047296	SKMC	muscle:	n/a
11	chr5:81046408-81046458	PFSK-1	brain:	n/a
12	chr5:81063103-81063153	HEK293	kidney:	embryo
13	chr5:81045418-81045468	HCT-116	colon:	n/a
14	chr5:81047188-81047238	BE2_C	brain:	n/a
15	chr5:81047486-81047536	K562	blood:	n/a
16	chr5:81051199-81051249	HCPEpiC	choroid plexus:	n/a
17	chr5:81043172-81043222	NB4	blood:	n/a
18	chr5:81051199-81051249	AG04450	lung:	fetal
19	chr5:81047246-81047296	HepG2	liver:	n/a
20	chr5:81048495-81048545	AG09309	skin:	n/a
21	chr5:81048495-81048545	PANC-1	pancreas:	n/a
22	chr5:81047184-81047234	NT2-D1	testis:	n/a
23	chr5:81048495-81048545	HNPCEpiC	eye:	n/a
24	chr5:81047486-81047536	HIPEpiC	eye:	n/a
25	chr5:81045966-81046016	SK-N-MC	brain:	n/a
26	chr5:81043172-81043222	HMEC	breast:	n/a
27	chr5:81063103-81063153	Caco-2	colon:	n/a
28	chr5:81046758-81046808	GM19239	blood:	n/a
29	chr5:81045966-81046016	Jurkat	blood:	n/a
30	chr5:81047249-81047299	SK-N-MC	brain:	n/a
31	chr5:81047188-81047238	RPTEC	kidney:	n/a
32	chr5:81047184-81047234	ProgFib	skin:	n/a
33	chr5:81048495-81048545	ovcar-3	ovarian:	n/a
34	chr5:81048305-81048355	HPAEpiC	pulmonary alveolar:	n/a
35	chr5:81045418-81045468	GM12892	blood:	n/a
36	chr5:81048305-81048355	HRPEpiC	eye:	n/a
37	chr5:81051199-81051249	SAEC	small airway:	n/a
38	chr5:81048495-81048545	BE2_C	brain:	n/a
39	chr5:81047246-81047296	HCPEpiC	choroid plexus:	n/a
40	chr5:81047184-81047234	AoSMC	blood vessel:	n/a
41	chr5:81045966-81046016	HEK293	kidney:	embryo
42	chr5:81063103-81063153	ProgFib	skin:	n/a
43	chr5:81047184-81047234	HRPEpiC	eye:	n/a
44	chr5:81047246-81047296	AG10803	skin:	n/a
45	chr5:81046408-81046458	H1-hESC	embryonic stem cell:	embryo
46	chr5:81047188-81047238	ovcar-3	ovarian:	n/a
47	chr5:81046758-81046808	A549	lung:	n/a
48	chr5:81047184-81047234	HCF	heart:	n/a
49	chr5:81047184-81047234	Jurkat	blood:	n/a
50	chr5:81046408-81046458	HPAEpiC	pulmonary alveolar:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:81041366..81043872-chr5:81148506..81150879,2	MCF-7	breast:
2	chr5:81046777..81047952-chr5:81146745..81148237,8	MCF-7	breast:
3	chr5:81011299..81014307-chr5:81021484..81024524,3	K562	blood:
4	chr5:81050581..81052753-chr5:81057564..81059448,2	MCF-7	breast:
5	chr5:81025124..81028928-chr5:81046978..81048834,3	K562	blood:
6	chr5:81047531..81050440-chr5:81268054..81269557,2	K562	blood:
7	chr5:81053903..81057293-chr5:81057315..81060035,4	K562	blood:
8	chr5:81045316..81049074-chr5:81266561..81269658,5	K562	blood:
9	chr5:80808501..80811000-chr5:81045914..81048051,2	MCF-7	breast:
10	chr5:80802774..80803458-chr5:81044304..81045045,2	MCF-7	breast:
11	chr5:81059460..81061720-chr5:81092374..81094863,2	K562	blood:
12	chr5:81034741..81036819-chr5:81039221..81041707,2	K562	blood:
13	chr5:81047832..81049783-chr5:81150744..81153734,2	MCF-7	breast:
14	chr5:81041105..81043899-chr5:81044992..81047327,2	MCF-7	breast:
15	chr5:81042198..81043973-chr5:81054034..81056633,2	K562	blood:
16	chr5:81033193..81036120-chr5:81145161..81147369,2	K562	blood:
17	chr5:81018633..81021063-chr5:81032875..81035374,3	K562	blood:
18	chr5:81020260..81022412-chr5:81045440..81047540,2	MCF-7	breast:
19	chr5:81037454..81039351-chr5:81039497..81041595,2	K562	blood:
20	chr5:81036698..81038199-chr5:81047468..81049173,2	K562	blood:
21	chr5:81059502..81061126-chr5:81067390..81068990,2	MCF-7	breast:
22	chr5:81054198..81057812-chr5:81146006..81150384,5	K562	blood:
23	chr5:81046805..81047696-chr5:81147370..81148097,5	MCF-7	breast:
24	chr5:81065434..81067134-chr5:81146311..81148855,2	K562	blood:
25	chr5:81034005..81036819-chr5:81039221..81041707,3	K562	blood:
26	chr5:81056056..81058943-chr5:81144399..81145914,2	K562	blood:
27	chr5:81029893..81032355-chr5:81038922..81041227,2	K562	blood:
28	chr5:81046053..81048819-chr5:81049705..81052088,6	MCF-7	breast:
29	chr5:81047664..81050586-chr5:81054821..81057159,3	MCF-7	breast:
30	chr5:81053903..81057293-chr5:81057315..81060035,4	K562	blood:
31	chr5:81004271..81006886-chr5:81025659..81027853,2	K562	blood:
32	chr5:81047664..81050586-chr5:81054821..81057159,3	MCF-7	breast:
33	chr5:81022356..81025954-chr5:81027509..81030484,4	K562	blood:
34	chr5:81037974..81042783-chr5:81043087..81048522,6	K562	blood:
35	chr5:81034741..81036819-chr5:81039221..81041707,2	K562	blood:
36	chr5:81051607..81053682-chr5:81571123..81573948,2	K562	blood:
37	chr5:81029893..81032355-chr5:81038922..81041227,2	K562	blood:
38	chr5:80940231..80942233-chr5:81040176..81042074,2	K562	blood:
39	chr5:81046850..81048241-chr5:81147402..81148427,4	Hela-S3	cervix:
40	chr5:81057535..81060032-chr5:81131821..81133349,2	K562	blood:
41	chr5:81042198..81043973-chr5:81054034..81056633,2	K562	blood:
42	chr5:81050581..81052753-chr5:81057564..81059448,2	MCF-7	breast:
43	chr5:81037454..81039351-chr5:81039497..81041595,2	K562	blood:
44	chr5:81012199..81014802-chr5:81035367..81038326,2	K562	blood:
45	chr5:81045698..81048740-chr5:81055494..81058903,3	MCF-7	breast:
46	chr5:81045980..81049009-chr5:81049247..81053935,6	MCF-7	breast:
47	chr5:81045699..81050245-chr5:81142897..81150556,22	MCF-7	breast:
48	chr5:81044752..81060050-chr5:81140268..81152732,43	K562	blood:
49	chr5:81043503..81052108-chr5:81144332..81149960,26	MCF-7	breast:
50	chr5:80809576..80810094-chr5:81044225..81044774,2	MCF-7	breast:

No data

Variant related genes	Relation type
SSBP2	TF binding region
SSBP2	CpG island
ENSG00000186468	chromatin interactions
ENSG00000152348	chromatin interactions
ENSG00000145687	chromatin interactions
ENSG00000249483	chromatin interactions

Extended variants
information (count: 1504 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1504 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538454206	chr5:81022036-81022037	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs547598716	chr5:81022044-81022045	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531670443	chr5:81022063-81022064	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs16899104	chr5:81022064-81022065	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs73137686	chr5:81022084-81022085	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs59001110	chr5:81022230-81022231	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs561914464	chr5:81022279-81022280	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142369650	chr5:81022301-81022302	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs576034177	chr5:81022303-81022304	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543377203	chr5:81022340-81022341	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200163169	chr5:81022341-81022342	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537514489	chr5:81022350-81022351	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs558778363	chr5:81022354-81022355	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs185883854	chr5:81022418-81022419	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541247935	chr5:81022420-81022421	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559910189	chr5:81022444-81022445	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527289791	chr5:81022477-81022478	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs10035917	chr5:81022494-81022495	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs78996891	chr5:81022503-81022504	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560826109	chr5:81022531-81022532	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75399664	chr5:81022597-81022598	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs74765865	chr5:81022608-81022609	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189959519	chr5:81022612-81022613	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35376767	chr5:81022662-81022663	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532268465	chr5:81022675-81022676	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs193035897	chr5:81022686-81022687	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565564013	chr5:81022724-81022725	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536097759	chr5:81022754-81022755	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146312999	chr5:81022805-81022806	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185184182	chr5:81022834-81022835	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537027584	chr5:81022889-81022890	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375259839	chr5:81022926-81022927	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558941679	chr5:81022932-81022933	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189736194	chr5:81022966-81022967	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535138875	chr5:81022972-81022973	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181252743	chr5:81022985-81022986	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs575094728	chr5:81023028-81023029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542481302	chr5:81023062-81023063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185024686	chr5:81023102-81023103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576037784	chr5:81023166-81023167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543036968	chr5:81023186-81023187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs608001	chr5:81023188-81023189	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs532081717	chr5:81023224-81023225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188257225	chr5:81023225-81023226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559084406	chr5:81023231-81023232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529831070	chr5:81023251-81023252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548007746	chr5:81023275-81023276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181860520	chr5:81023291-81023292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368855495	chr5:81023311-81023312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187641061	chr5:81023323-81023324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Tetralogy of Fallot	22912587	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1296 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80984200-81032000	Weak transcription	Esophagus	oesophagus
2	chr5:81008800-81044800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:81011600-81029800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:81014000-81022400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr5:81014400-81022800	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr5:81014600-81022800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr5:81015800-81023000	Weak transcription	Psoas Muscle	Psoas
8	chr5:81015800-81034600	Weak transcription	Left Ventricle	heart
9	chr5:81016000-81031800	Weak transcription	Ovary	ovary
10	chr5:81016000-81044800	Weak transcription	Fetal Stomach	stomach
11	chr5:81016200-81022200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr5:81018000-81031600	Weak transcription	Brain Angular Gyrus	brain
13	chr5:81018200-81022200	Enhancers	GM12878-XiMat	blood
14	chr5:81018400-81022400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr5:81018400-81023600	Weak transcription	Brain Substantia Nigra	brain
16	chr5:81018600-81022200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr5:81018600-81022400	Weak transcription	Fetal Heart	heart
18	chr5:81018600-81033800	Weak transcription	Thymus	Thymus
19	chr5:81018600-81038400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr5:81019400-81022400	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr5:81019800-81029000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr5:81020600-81022600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr5:81020600-81023000	Genic enhancers	Dnd41	blood
24	chr5:81020800-81039200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr5:81021000-81023400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr5:81021000-81023600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr5:81021000-81028200	Weak transcription	Primary B cells from cord blood	blood
28	chr5:81021000-81033600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr5:81021200-81022600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:81021200-81022800	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr5:81021200-81029800	Weak transcription	Primary T cells from cord blood	blood
32	chr5:81021400-81022200	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr5:81021400-81022200	Enhancers	Small Intestine	intestine
34	chr5:81021400-81022400	Genic enhancers	Fetal Thymus	thymus
35	chr5:81021400-81022800	Enhancers	Fetal Brain Female	brain
36	chr5:81021400-81022800	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr5:81021400-81023000	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr5:81021600-81022600	Enhancers	Brain Hippocampus Middle	brain
39	chr5:81021600-81023000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr5:81021600-81024400	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr5:81021600-81033600	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr5:81022000-81022400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr5:81022000-81022400	Enhancers	Primary B cells from peripheral blood	blood
44	chr5:81022000-81022400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr5:81022000-81022400	Enhancers	Brain Anterior Caudate	brain
46	chr5:81022000-81022400	Enhancers	Fetal Brain Male	brain
47	chr5:81022000-81022800	Enhancers	Adipose Nuclei	Adipose
48	chr5:81022000-81022800	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr5:81022000-81023000	Enhancers	Brain Germinal Matrix	brain
50	chr5:81022000-81023000	Enhancers	Colon Smooth Muscle	Colon

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