Variant report

Variant	nsv882363
Chromosome Location	chr5:89643399-89725515
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1346)
CpG islands
(count:980)
Chromatin interactive
region (count:121)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:89704636-89706774	K562	blood:	n/a	n/a
2	ARID3A	chr5:89704880-89706162	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:89717184-89717335	K562	blood:	n/a	n/a
4	ATF1	chr5:89655329-89655438	K562	blood:	n/a	n/a
5	ATF1	chr5:89704808-89706340	K562	blood:	n/a	n/a
6	ATF2	chr5:89704762-89705527	GM12878	blood:	n/a	n/a
7	ATF2	chr5:89643241-89643686	GM12878	blood:	n/a	n/a
8	ATF2	chr5:89704856-89705330	GM12878	blood:	n/a	n/a
9	ATF2	chr5:89664592-89665096	GM12878	blood:	n/a	n/a
10	ATF2	chr5:89705752-89706245	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:89705961-89706480	K562	blood:	n/a	n/a
12	BACH1	chr5:89694822-89694861	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:89705147-89706238	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr5:89664725-89665020	GM12878	blood:	n/a	n/a
15	BATF	chr5:89664645-89665014	GM12878	blood:	n/a	n/a
16	BATF	chr5:89720144-89720415	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:89664612-89665096	GM12878	blood:	n/a	n/a
18	BCL11A	chr5:89664712-89664971	GM12878	blood:	n/a	n/a
19	BCL3	chr5:89705728-89706097	GM12878	blood:	n/a	chr5:89705755-89705764 chr5:89705753-89705766
20	BCL3	chr5:89704727-89705331	A549	lung:	n/a	chr5:89704915-89704924
21	BCLAF1	chr5:89704762-89705654	GM12878	blood:	n/a	chr5:89704915-89704924
22	BCLAF1	chr5:89704829-89705608	GM12878	blood:	n/a	chr5:89704915-89704924
23	BCLAF1	chr5:89705736-89706370	GM12878	blood:	n/a	chr5:89705755-89705764 chr5:89705753-89705766
24	BCLAF1	chr5:89705739-89706436	GM12878	blood:	n/a	chr5:89705755-89705764 chr5:89705753-89705766
25	BHLHE40	chr5:89643386-89643445	GM12878	blood:	n/a	n/a
26	BHLHE40	chr5:89704883-89706217	GM12878	blood:	n/a	n/a
27	BHLHE40	chr5:89677436-89677519	K562	blood:	n/a	n/a
28	BHLHE40	chr5:89664735-89665031	GM12878	blood:	n/a	n/a
29	BHLHE40	chr5:89698628-89698665	K562	blood:	n/a	n/a
30	BHLHE40	chr5:89717217-89717233	K562	blood:	n/a	n/a
31	BHLHE40	chr5:89682067-89682386	GM12878	blood:	n/a	n/a
32	BHLHE40	chr5:89704941-89706347	K562	blood:	n/a	n/a
33	BRCA1	chr5:89704982-89705562	GM12878	blood:	n/a	n/a
34	BRCA1	chr5:89704946-89706133	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr5:89704767-89706606	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr5:89717176-89717181	HepG2	liver:	n/a	n/a
37	BRCA1	chr5:89704853-89705415	HepG2	liver:	n/a	n/a
38	BRCA1	chr5:89705843-89706096	HepG2	liver:	n/a	n/a
39	CBX3	chr5:89704814-89706268	K562	blood:	n/a	n/a
40	CBX3	chr5:89688150-89688640	K562	blood:	n/a	n/a
41	CCNT2	chr5:89704927-89706118	K562	blood:	n/a	chr5:89705756-89705765
42	CCNT2	chr5:89704307-89704506	K562	blood:	n/a	n/a
43	CEBPB	chr5:89704937-89705277	K562	blood:	n/a	n/a
44	CEBPB	chr5:89704651-89706050	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr5:89710637-89710673	K562	blood:	n/a	n/a
46	CEBPB	chr5:89671978-89672262	A549	lung:	n/a	chr5:89672113-89672124
47	CEBPB	chr5:89690842-89691254	K562	blood:	n/a	chr5:89691057-89691066 chr5:89691057-89691066 chr5:89691057-89691066 chr5:89691055-89691066
48	CEBPB	chr5:89703376-89703734	K562	blood:	n/a	n/a
49	CEBPB	chr5:89681931-89682274	K562	blood:	n/a	n/a
50	CEBPB	chr5:89671958-89672300	HepG2	liver:	n/a	chr5:89672113-89672124

(count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:89705938-89705988	NHDF-neo	bronchial:	n/a
2	chr5:89705801-89705851	T-47D	breast:	n/a
3	chr5:89705910-89705960	HUVEC	blood vessel:	n/a
4	chr5:89687197-89687247	NH-A	brain:	n/a
5	chr5:89705938-89705988	NHDF-neo	bronchial:	n/a
6	chr5:89705801-89705851	T-47D	breast:	n/a
7	chr5:89705910-89705960	HUVEC	blood vessel:	n/a
8	chr5:89687197-89687247	NH-A	brain:	n/a
9	chr5:89706015-89706065	HRPEpiC	eye:	n/a
10	chr5:89705579-89705629	SK-N-MC	brain:	n/a
11	chr5:89663024-89663074	HEEpiC	esophagus:	n/a
12	chr5:89706015-89706065	GM12878	blood:	n/a
13	chr5:89705938-89705988	HEK293	kidney:	embryo
14	chr5:89705806-89705856	HCM	heart:	n/a
15	chr5:89705894-89705944	MCF10A-Er-Src	breast:	n/a
16	chr5:89706015-89706065	HRCEpiC	kidney:	n/a
17	chr5:89706015-89706065	ECC-1	luminal epithelium:	n/a
18	chr5:89705346-89705396	HAEpiC	amniotic membrane:	n/a
19	chr5:89705497-89705547	HUVEC	blood vessel:	n/a
20	chr5:89705635-89705685	HCF	heart:	n/a
21	chr5:89705806-89705856	NT2-D1	testis:	n/a
22	chr5:89705938-89705988	AG04449	skin:	fetal
23	chr5:89705894-89705944	GM12891	blood:	n/a
24	chr5:89705801-89705851	AG09319	gingival:	n/a
25	chr5:89705938-89705988	GM12892	blood:	n/a
26	chr5:89706015-89706065	Hepatocyte	liver:	n/a
27	chr5:89687197-89687247	BE2_C	brain:	n/a
28	chr5:89705759-89705809	ProgFib	skin:	n/a
29	chr5:89705234-89705284	HRPEpiC	eye:	n/a
30	chr5:89705346-89705396	HUVEC	blood vessel:	n/a
31	chr5:89705938-89705988	SKMC	muscle:	n/a
32	chr5:89706015-89706065	AG09319	gingival:	n/a
33	chr5:89705910-89705960	SK-N-MC	brain:	n/a
34	chr5:89663024-89663074	PrEC	prostate:	n/a
35	chr5:89705801-89705851	HUVEC	blood vessel:	n/a
36	chr5:89705806-89705856	SAEC	small airway:	n/a
37	chr5:89705346-89705396	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:89705635-89705685	Jurkat	blood:	n/a
39	chr5:89705894-89705944	ProgFib	skin:	n/a
40	chr5:89705579-89705629	HepG2	liver:	n/a
41	chr5:89706015-89706065	HMEC	breast:	n/a
42	chr5:89705635-89705685	Hepatocyte	liver:	n/a
43	chr5:89705497-89705547	HRCEpiC	kidney:	n/a
44	chr5:89705234-89705284	PANC-1	pancreas:	n/a
45	chr5:89663024-89663074	HEK293	kidney:	embryo
46	chr5:89709157-89709207	HCM	heart:	n/a
47	chr5:89709157-89709207	NB4	blood:	n/a
48	chr5:89706015-89706065	HAEpiC	amniotic membrane:	n/a
49	chr5:89705801-89705851	GM12892	blood:	n/a
50	chr5:89705894-89705944	AG04449	skin:	fetal

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:89705231..89707575-chr5:89854422..89857316,5	K562	blood:
2	chr5:89701553..89708894-chr5:89768084..89771807,14	K562	blood:
3	chr5:89660556..89663088-chr5:89667143..89669250,2	K562	blood:
4	chr5:89655874..89657982-chr5:89662995..89664774,3	K562	blood:
5	chr5:89652468..89654381-chr5:89703919..89706192,2	MCF-7	breast:
6	chr5:89643789..89646702-chr5:89648704..89650360,2	K562	blood:
7	chr5:89695237..89698064-chr5:89699685..89702781,3	K562	blood:
8	chr5:89680611..89687152-chr5:89704124..89707534,9	K562	blood:
9	chr5:68530475..68532147-chr5:89705204..89707833,2	MCF-7	breast:
10	chr5:89705809..89706309-chr7:44837083..44837652,2	NB4	blood:
11	chr5:89582967..89585771-chr5:89708218..89710360,2	K562	blood:
12	chr5:89688512..89690490-chr5:89692215..89693760,2	K562	blood:
13	chr5:89705042..89707173-chr5:90677000..90680355,4	K562	blood:
14	chr5:89688086..89690325-chr5:89696489..89699229,2	MCF-7	breast:
15	chr5:89713487..89716183-chr5:89718029..89719658,2	K562	blood:
16	chr5:89704649..89705392-chr9:123604695..123605609,2	HCT-116	colon:
17	chr5:89703907..89705481-chr5:89717381..89719278,2	MCF-7	breast:
18	chr5:89665829..89668334-chr5:89692394..89695020,2	K562	blood:
19	chr5:89689507..89693206-chr5:89701477..89705408,4	K562	blood:
20	chr5:89716690..89717570-chr5:89825587..89826330,4	MCF-7	breast:
21	chr5:89704759..89705573-chr7:21466952..21467883,2	Hela-S3	cervix:
22	chr5:14664623..14665342-chr5:89705556..89706261,2	HCT-116	colon:
23	chr5:89701624..89708275-chr5:89936212..89939090,6	K562	blood:
24	chr5:89478032..89480920-chr5:89706398..89708148,2	K562	blood:
25	chr5:89675039..89677573-chr5:89683021..89684602,2	K562	blood:
26	chr5:89711869..89714412-chr5:89724479..89727359,2	MCF-7	breast:
27	chr5:89713487..89716183-chr5:89718029..89719658,2	K562	blood:
28	chr5:89708357..89712406-chr5:89768883..89772493,4	K562	blood:
29	chr14:64009982..64010703-chr5:89705356..89706024,2	HCT-116	colon:
30	chr5:89705215..89707531-chr5:90675292..90676863,2	K562	blood:
31	chr15:62682227..62682755-chr5:89705071..89706015,2	Hela-S3	cervix:
32	chr5:89688086..89690325-chr5:89696489..89699229,2	MCF-7	breast:
33	chr5:88178723..88181688-chr5:89702719..89707070,5	K562	blood:
34	chr5:89718278..89720087-chr5:89828600..89831257,2	K562	blood:
35	chr5:89643789..89646702-chr5:89647757..89650360,3	K562	blood:
36	chr5:89703250..89710229-chr5:89936398..89944611,13	K562	blood:
37	chr5:89694031..89696960-chr5:89697104..89699987,2	MCF-7	breast:
38	chr5:89700626..89703101-chr5:108745991..108748143,2	K562	blood:
39	chr5:89703358..89707086-chr5:89823955..89827154,6	MCF-7	breast:
40	chr5:89705209..89706757-chr5:89853526..89855162,2	MCF-7	breast:
41	chr5:89706309..89708086-chr5:89715390..89717566,2	MCF-7	breast:
42	chr5:89684756..89687141-chr5:89703504..89706860,3	MCF-7	breast:
43	chr5:89714823..89717429-chr5:89724054..89725966,2	K562	blood:
44	chr5:89691057..89693186-chr5:90677649..90680418,2	K562	blood:
45	chr5:89660556..89663088-chr5:89667143..89669250,2	K562	blood:
46	chr5:89700975..89703312-chr5:89824839..89827243,2	K562	blood:
47	chr5:89703591..89705335-chr6:26204580..26206448,2	K562	blood:
48	chr5:89602779..89605252-chr5:89706386..89708061,2	MCF-7	breast:
49	chr5:89643789..89646702-chr5:89648704..89650360,2	K562	blood:
50	chr5:89694031..89696960-chr5:89697104..89699987,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CETN3-1	chr5:89684285-89685180	ENSG00000260871.1
2	lnc-POLR3G-1	chr5:89709154-89712311	XLOC_004467
3	lnc-POLR3G-1	chr5:89705933-89706121	XLOC_004467
4	lnc-POLR3G-1	chr5:89705817-89706179	NONHSAT102730
5	lnc-CETN3-1	chr5:89684285-89684930	NONHSAT102727
6	lnc-POLR3G-1	chr5:89705872-89706121	XLOC_004467
7	lnc-POLR3G-1	chr5:89706317-89706486	NR_105024
8	lnc-CETN3-2	chr5:89648854-89649347	ENSG00000253321
9	lnc-CETN3-2	chr5:89652349-89652426	ENSG00000253321
10	lnc-POLR3G-1	chr5:89706317-89706495	XLOC_004467
11	lnc-POLR3G-1	chr5:89705817-89706121	NR_105024
12	lnc-POLR3G-1	chr5:89706185-89706485	NONHSAT102730

No data

Variant related genes	Relation type
CETN3	TF binding region
ENSG00000255647	TF binding region
ENSG00000253321	TF binding region
ENSG00000260871	TF binding region
CETN3	CpG island
ENSG00000255647	CpG island
ENSG00000253321	CpG island
ENSG00000260871	CpG island
ENSG00000237886	chromatin interactions
ENSG00000248555	chromatin interactions
ENSG00000082898	chromatin interactions
ENSG00000113369	chromatin interactions
ENSG00000260871	chromatin interactions
ENSG00000171522	chromatin interactions
ENSG00000198518	chromatin interactions
ENSG00000153140	chromatin interactions
ENSG00000154124	chromatin interactions
ENSG00000176018	chromatin interactions
ENSG00000148400	chromatin interactions
ENSG00000095261	chromatin interactions
ENSG00000113356	chromatin interactions
ENSG00000255647	chromatin interactions
ENSG00000134058	chromatin interactions
ENSG00000176055	chromatin interactions
ENSG00000226752	chromatin interactions
ENSG00000261360	chromatin interactions
ENSG00000248309	chromatin interactions
ENSG00000154001	chromatin interactions
ENSG00000106077	chromatin interactions
ENSG00000171914	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000261242	chromatin interactions
ENSG00000120254	chromatin interactions
ENSG00000105866	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000164199	chromatin interactions
ENSG00000081189	chromatin interactions
ENSG00000196262	chromatin interactions
ENSG00000122034	chromatin interactions
ENSG00000265181	chromatin interactions
VEGFA	miRNA target sites

Extended variants
information (count: 1831 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139306328	chr5:89648841-89648842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141005892	chr5:89648879-89648880	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs568233022	chr5:89648931-89648932	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs537558154	chr5:89648941-89648942	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs557447032	chr5:89648966-89648967	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs570758414	chr5:89649022-89649023	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs539815372	chr5:89649037-89649038	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs143332179	chr5:89649044-89649045	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs573463059	chr5:89649113-89649114	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs1897833	chr5:89649118-89649119	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs555559598	chr5:89649167-89649168	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs575392704	chr5:89649211-89649212	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs543117728	chr5:89649215-89649216	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs113197409	chr5:89649266-89649267	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs79545430	chr5:89649295-89649296	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs545767221	chr5:89649330-89649331	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs186292565	chr5:89649333-89649334	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs138684944	chr5:89649335-89649336	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs141195802	chr5:89649406-89649407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560701960	chr5:89649419-89649420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574289785	chr5:89649436-89649437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548467146	chr5:89649471-89649472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs13155242	chr5:89649538-89649539	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs74534530	chr5:89649557-89649558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535456143	chr5:89650629-89650630	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs549309920	chr5:89650634-89650635	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs569193700	chr5:89650636-89650637	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565588116	chr5:89650645-89650646	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs182601080	chr5:89650651-89650652	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs186806514	chr5:89650670-89650671	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs10514324	chr5:89650677-89650678	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs146003487	chr5:89650709-89650710	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539526604	chr5:89650720-89650721	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs552745839	chr5:89650731-89650732	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs3114648	chr5:89650757-89650758	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs192491832	chr5:89650758-89650759	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs184806942	chr5:89650779-89650780	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs551232914	chr5:89650784-89650785	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs575632941	chr5:89650901-89650902	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs187320841	chr5:89650952-89650953	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs114908647	chr5:89650974-89650975	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs113821248	chr5:89651068-89651069	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs3097989	chr5:89651076-89651077	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs560206969	chr5:89651150-89651151	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs139955509	chr5:89651163-89651164	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs548946218	chr5:89651238-89651239	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs568882842	chr5:89651274-89651275	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs377555841	chr5:89651350-89651351	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs143510425	chr5:89651360-89651361	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs546700613	chr5:89651385-89651386	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	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
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1068 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89648800-89649600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr5:89651400-89651800	Enhancers	Fetal Lung	lung
3	chr5:89651600-89652000	Enhancers	Fetal Brain Male	brain
4	chr5:89651800-89652000	Enhancers	Brain Germinal Matrix	brain
5	chr5:89651800-89652200	Weak transcription	Fetal Lung	lung
6	chr5:89652000-89652200	Flanking Active TSS	Fetal Brain Male	brain
7	chr5:89652000-89653000	Weak transcription	Brain Germinal Matrix	brain
8	chr5:89652200-89652400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr5:89652200-89652400	Enhancers	Fetal Brain Female	brain
10	chr5:89652200-89653600	Enhancers	Fetal Lung	lung
11	chr5:89652200-89656400	Enhancers	Fetal Brain Male	brain
12	chr5:89652400-89652600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr5:89652400-89652800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr5:89652400-89652800	Flanking Active TSS	Fetal Brain Female	brain
15	chr5:89652400-89652800	Enhancers	Stomach Smooth Muscle	stomach
16	chr5:89652400-89653400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr5:89652600-89653400	Enhancers	Brain Substantia Nigra	brain
18	chr5:89652800-89653000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr5:89652800-89653200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:89652800-89653800	Enhancers	Fetal Brain Female	brain
21	chr5:89653000-89654000	Enhancers	Brain Germinal Matrix	brain
22	chr5:89653400-89654800	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr5:89654000-89655000	Weak transcription	Brain Germinal Matrix	brain
24	chr5:89654600-89655200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr5:89654800-89655400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr5:89654800-89655600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr5:89654800-89655600	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr5:89655000-89655200	Enhancers	Brain Germinal Matrix	brain
29	chr5:89655000-89655400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr5:89655200-89655600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr5:89662400-89662600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr5:89662400-89663400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr5:89662400-89663400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr5:89662400-89663400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr5:89662600-89663200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr5:89662600-89663400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:89662600-89663400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr5:89662600-89663400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr5:89662800-89663200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr5:89662800-89663200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr5:89662800-89663200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr5:89662800-89663200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr5:89664000-89665200	Enhancers	GM12878-XiMat	blood
44	chr5:89664800-89665200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:89666800-89668800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
46	chr5:89667000-89667200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr5:89668800-89669200	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr5:89668800-89669600	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr5:89669200-89669600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr5:89669200-89669600	Enhancers	H9 Cell Line	embryonic stem cell

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