Variant report

Variant	nsv1002243
Chromosome Location	chr2:186692815-187150225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1570)
CpG islands
(count:367)
Chromatin interactive
region (count:64)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1570 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:186835223-186835544	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:186766781-186767039	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:187121356-187121642	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:186933182-186933390	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:187062701-187063034	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:186973201-186973628	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:187046339-187046834	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:186756102-186757040	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:186853506-186853842	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:186855637-186856004	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:186994689-186995458	HepG2	liver:	n/a	n/a
12	ATF1	chr2:186693024-186693115	K562	blood:	n/a	n/a
13	BACH1	chr2:186917756-186918018	H1-hESC	embryonic stem cell:	n/a	chr2:186917846-186917860
14	BACH1	chr2:186855743-186855846	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr2:186698786-186698866	H1-hESC	embryonic stem cell:	n/a	n/a
16	BHLHE40	chr2:186727838-186727908	K562	blood:	n/a	n/a
17	BHLHE40	chr2:186896017-186896505	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:186929279-186929572	GM12878	blood:	n/a	n/a
19	BRCA1	chr2:186775907-186775908	GM12878	blood:	n/a	n/a
20	CBX3	chr2:186700648-186700857	K562	blood:	n/a	n/a
21	CBX3	chr2:186836912-186837170	K562	blood:	n/a	n/a
22	CCNT2	chr2:186905250-186905377	K562	blood:	n/a	n/a
23	CCNT2	chr2:186966417-186966617	K562	blood:	n/a	n/a
24	CCNT2	chr2:186984780-186984935	K562	blood:	n/a	n/a
25	CCNT2	chr2:186798987-186799212	K562	blood:	n/a	n/a
26	CEBPB	chr2:186888229-186888431	HepG2	liver:	n/a	chr2:186888282-186888293 chr2:186888300-186888311
27	CEBPB	chr2:186756211-186756916	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:186994808-186995412	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:186995329-186995732	ECC-1	luminal epithelium:	n/a	chr2:186995442-186995455 chr2:186995444-186995455 chr2:186995444-186995455 chr2:186995442-186995455
30	CEBPB	chr2:186819149-186819471	A549	lung:	n/a	chr2:186819279-186819290
31	CEBPB	chr2:186863446-186863745	Hela-S3	cervix:	n/a	chr2:186863590-186863601
32	CEBPB	chr2:186853669-186853919	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:186881616-186881820	HepG2	liver:	n/a	chr2:186881764-186881775
34	CEBPB	chr2:186704316-186704484	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:186994724-186995491	HCT-116	colon:	n/a	chr2:186995442-186995455 chr2:186995444-186995455 chr2:186995444-186995455 chr2:186995442-186995455
36	CEBPB	chr2:186973209-186973488	HepG2	liver:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
37	CEBPB	chr2:186816833-186817243	Hela-S3	cervix:	n/a	chr2:186817033-186817046
38	CEBPB	chr2:186987162-186987415	HepG2	liver:	n/a	chr2:186987233-186987244
39	CEBPB	chr2:186888225-186888463	A549	lung:	n/a	chr2:186888282-186888293 chr2:186888300-186888311
40	CEBPB	chr2:186828874-186829177	A549	lung:	n/a	chr2:186829026-186829037
41	CEBPB	chr2:187047299-187047519	HepG2	liver:	n/a	chr2:187047425-187047436
42	CEBPB	chr2:186863427-186863776	IMR90	lung:	n/a	chr2:186863590-186863601
43	CEBPB	chr2:186881632-186881878	A549	lung:	n/a	chr2:186881764-186881775
44	CEBPB	chr2:186988737-186988903	A549	lung:	n/a	n/a
45	CEBPB	chr2:186843810-186844163	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr2:186994884-186995064	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:186719492-186720096	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr2:186918858-186919191	IMR90	lung:	n/a	chr2:186919035-186919044 chr2:186919033-186919044 chr2:186919034-186919045
49	CEBPB	chr2:186973165-186973556	HepG2	liver:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
50	CEBPB	chr2:186973194-186973541	IMR90	lung:	n/a	chr2:186973313-186973324 chr2:186973356-186973367

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:187120710-187120760	HIPEpiC	eye:	n/a
2	chr2:187120710-187120760	HIPEpiC	eye:	n/a
3	chr2:186924071-186924121	AG09309	skin:	n/a
4	chr2:186968467-186968517	HMEC	breast:	n/a
5	chr2:186968467-186968517	HEEpiC	esophagus:	n/a
6	chr2:186968467-186968517	ECC-1	luminal epithelium:	n/a
7	chr2:186988953-186989003	T-47D	breast:	n/a
8	chr2:186727863-186727913	NHBE	bronchial:	n/a
9	chr2:187120710-187120760	HEK293	kidney:	embryo
10	chr2:186924071-186924121	MCF-7	breast:	n/a
11	chr2:186924071-186924121	NHDF-neo	bronchial:	n/a
12	chr2:187081534-187081584	AG09309	skin:	n/a
13	chr2:186968467-186968517	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:186968467-186968517	SK-N-SH_RA	brain:	n/a
15	chr2:186988953-186989003	HCF	heart:	n/a
16	chr2:186924071-186924121	HEK293	kidney:	embryo
17	chr2:186968467-186968517	Hepatocyte	liver:	n/a
18	chr2:186924071-186924121	Caco-2	colon:	n/a
19	chr2:187120710-187120760	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:186988953-186989003	HMEC	breast:	n/a
21	chr2:186968467-186968517	HRE	kidney:	n/a
22	chr2:186727863-186727913	AG04449	skin:	fetal
23	chr2:186727863-186727913	HCT-116	colon:	n/a
24	chr2:186727863-186727913	GM12878	blood:	n/a
25	chr2:186968467-186968517	HEK293	kidney:	embryo
26	chr2:186924071-186924121	Hepatocyte	liver:	n/a
27	chr2:187081534-187081584	HCM	heart:	n/a
28	chr2:186968467-186968517	HCF	heart:	n/a
29	chr2:186924071-186924121	AG04449	skin:	fetal
30	chr2:186924071-186924121	HRCEpiC	kidney:	n/a
31	chr2:186727863-186727913	NB4	blood:	n/a
32	chr2:186924071-186924121	NHBE	bronchial:	n/a
33	chr2:186988953-186989003	HRPEpiC	eye:	n/a
34	chr2:186988953-186989003	HRE	kidney:	n/a
35	chr2:186988953-186989003	AG10803	skin:	n/a
36	chr2:187081534-187081584	AoSMC	blood vessel:	n/a
37	chr2:186988953-186989003	AG09319	gingival:	n/a
38	chr2:186924071-186924121	HUVEC	blood vessel:	n/a
39	chr2:186924071-186924121	HCM	heart:	n/a
40	chr2:186988953-186989003	PFSK-1	brain:	n/a
41	chr2:186968467-186968517	A549	lung:	n/a
42	chr2:186968467-186968517	ProgFib	skin:	n/a
43	chr2:186924071-186924121	AoSMC	blood vessel:	n/a
44	chr2:186968467-186968517	K562	blood:	n/a
45	chr2:186727863-186727913	SK-N-MC	brain:	n/a
46	chr2:186988953-186989003	RPTEC	kidney:	n/a
47	chr2:187120710-187120760	GM06990	blood:	n/a
48	chr2:186988953-186989003	AG04449	skin:	fetal
49	chr2:187120710-187120760	SK-N-MC	brain:	n/a
50	chr2:186988953-186989003	GM12891	blood:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:23092682..23094839-chr2:187127661..187130019,2	MCF-7	breast:
2	chr2:186882755..186884529-chr2:186886544..186888768,2	K562	blood:
3	chr2:186741175..186743547-chr2:186745596..186747466,2	K562	blood:
4	chr2:186734702..186736953-chr2:186739550..186741965,2	MCF-7	breast:
5	chr2:186948418..186950441-chr2:187047439..187049579,2	K562	blood:
6	chr2:186983605..186985165-chr2:186986733..186988771,2	MCF-7	breast:
7	chr2:187020003..187021879-chr2:187026559..187028779,2	MCF-7	breast:
8	chr2:187111432..187114258-chr2:187118686..187120723,2	MCF-7	breast:
9	chr2:186953883..186956490-chr2:186957329..186960004,2	K562	blood:
10	chr2:186948418..186950441-chr2:187047439..187049579,2	K562	blood:
11	chr2:186715733..186716239-chr20:13748197..13748697,2	MCF-7	breast:
12	chr2:186717272..186719201-chr2:186720753..186722385,2	K562	blood:
13	chr2:187121005..187121910-chr2:187323354..187324097,2	MCF-7	breast:
14	chr2:186717400..186719050-chr2:186723710..186725689,2	K562	blood:
15	chr2:186861297..186864828-chr2:186866334..186869154,3	K562	blood:
16	chr2:187080091..187081693-chr2:187086828..187089165,2	K562	blood:
17	chr2:186913950..186916894-chr2:186919637..186921761,2	K562	blood:
18	chr2:186851763..186854059-chr2:186854208..186855953,2	MCF-7	breast:
19	chr2:186905396..186906984-chr2:186927102..186929134,2	K562	blood:
20	chr2:186493563..186494107-chr2:187121512..187122407,2	MCF-7	breast:
21	chr2:187027645..187029211-chr2:187033628..187036309,2	MCF-7	breast:
22	chr2:186807275..186808106-chr7:110453455..110454048,2	HCT-116	colon:
23	chr2:186741094..186742675-chr2:186744709..186747466,2	K562	blood:
24	chr2:187080091..187081693-chr2:187086828..187089165,2	K562	blood:
25	chr2:186844422..186846233-chr2:187042627..187045441,2	K562	blood:
26	chr2:186760390..186763157-chr2:186764375..186766387,2	K562	blood:
27	chr2:186603700..186604546-chr2:187121410..187122246,2	MCF-7	breast:
28	chr2:186994332..186996558-chr2:186996994..186999214,2	MCF-7	breast:
29	chr2:186791324..186793332-chr2:186796322..186798371,2	K562	blood:
30	chr2:186603423..186604198-chr2:187120988..187121931,3	MCF-7	breast:
31	chr2:186953883..186956490-chr2:186957329..186960004,2	K562	blood:
32	chr2:43453747..43454591-chr2:186974749..186975692,2	HCT-116	colon:
33	chr2:186882755..186884529-chr2:186886544..186888768,2	K562	blood:
34	chr2:186717272..186719201-chr2:186720753..186722385,2	K562	blood:
35	chr2:186905396..186906984-chr2:186927102..186929134,2	K562	blood:
36	chr2:186994332..186996558-chr2:186996994..186999214,2	MCF-7	breast:
37	chr2:186791324..186793332-chr2:186796322..186798371,2	K562	blood:
38	chr2:186720960..186722500-chr2:186726629..186729211,2	K562	blood:
39	chr17:57913762..57915412-chr2:186861621..186864023,2	MCF-7	breast:
40	chr2:186898326..186901023-chr2:187349730..187351831,2	K562	blood:
41	chr2:187046232..187048383-chr2:187048758..187051703,2	MCF-7	breast:
42	chr2:186844422..186846233-chr2:187042627..187045441,2	K562	blood:
43	chr2:186778448..186780007-chr2:186782910..186785814,2	K562	blood:
44	chr2:186717400..186719050-chr2:186723710..186725689,2	K562	blood:
45	chr2:187144221..187146013-chr2:187148146..187151029,2	K562	blood:
46	chr2:187077199..187079062-chr2:187349198..187350991,2	K562	blood:
47	chr2:186741094..186742675-chr2:186744709..186747466,2	K562	blood:
48	chr2:186913950..186916894-chr2:186919637..186921761,2	K562	blood:
49	chr2:187046232..187048383-chr2:187048758..187051703,2	MCF-7	breast:
50	chr2:186966503..186967236-chr4:21954917..21955427,2	MCF-7	breast:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM2-3	chr2:187126284-187126336	NONHSAT075981
2	lnc-ZSWIM2-3	chr2:186947881-186947950	ENSG00000237877
3	lnc-FSIP2-4	chr2:186932840-186933840	NONHSAT075984
4	lnc-ZSWIM2-3	chr2:186898222-186898531	NONHSAT075981
5	lnc-ZSWIM2-3	chr2:187035921-187036575	NONHSAT075981
6	lnc-FSIP2-4	chr2:186964372-186965726	NONHSAT075984
7	lnc-ZSWIM2-3	chr2:186947881-186947960	ENSG00000237877.2
8	lnc-ZSWIM2-12	chr2:186800286-186800551	NONHSAT075977
9	lnc-FSIP2-2	chr2:186953806-186955337	NONHSAT075985
10	lnc-ZSWIM2-3	chr2:186898258-186898529	ENSG00000237877
11	lnc-FSIP2-4	chr2:186947780-186951158	NONHSAT075984
12	lnc-ZSWIM2-3	chr2:186897623-186897908	NONHSAT075981
13	lnc-FSIP2-3	chr2:186963163-186964146	NONHSAT075986
14	lnc-ZSWIM2-3	chr2:186946057-186946143	NONHSAT075981
15	lnc-ZSWIM2-3	chr2:186947881-186947960	ENSG00000237877
16	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877
17	lnc-ZSWIM2-3	chr2:186903058-186903159	ENSG00000237877
18	lnc-ZSWIM2-3	chr2:186947881-186947948	NR_110218
19	lnc-FSIP2-4	chr2:186923254-186923714	NONHSAT075984
20	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877
21	lnc-FSIP2-1	chr2:187001824-187002215	XLOC_001781
22	lnc-ZSWIM2-3	chr2:186951028-186951044	NR_110218
23	lnc-ZSWIM2-3	chr2:186897872-186898529	ENSG00000237877
24	lnc-ZSWIM2-3	chr2:186947881-186947951	NONHSAT075981
25	lnc-ZSWIM2-3	chr2:186897618-186898529	ENSG00000237877.2
26	lnc-ZSWIM2-13	chr2:186799635-186800049	NONHSAT075976
27	lnc-ZSWIM2-3	chr2:186904227-186904282	ENSG00000237877
28	lnc-ZSWIM2-3	chr2:186898261-186898529	NR_110218
29	lnc-ZSWIM2-4	chr2:186817485-186817647	XLOC_002427
30	lnc-FSIP2-4	chr2:186946053-186946143	NONHSAT075984
31	lnc-ZSWIM2-3	chr2:187006495-187007373	NONHSAT075981
32	lnc-ZSWIM2-3	chr2:186903058-186903162	NONHSAT075981
33	lnc-ZSWIM2-3	chr2:187079525-187079817	NONHSAT075981
34	lnc-ZSWIM2-3	chr2:186946057-186946143	NR_110218
35	lnc-ZSWIM2-10	chr2:187027676-187027972	NONHSAT075988
36	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877.2
37	lnc-ZSWIM2-3	chr2:187002952-187003542	NONHSAT075981
38	lnc-ZSWIM2-11	chr2:186821314-186821790	NONHSAT075979
39	lnc-ZSWIM2-4	chr2:186815194-186815488	XLOC_002427
40	lnc-ZSWIM2-3	chr2:186903058-186903162	NR_110218
41	lnc-FSIP2-1	chr2:186999554-187000911	XLOC_001781
42	lnc-ZSWIM2-3	chr2:186904227-186904282	NONHSAT075981
43	lnc-ZSWIM2-3	chr2:186904227-186904282	NR_110218

No data

Variant related genes	Relation type
RPL23AP35	TF binding region
ENSG00000237877	TF binding region
RPL21P32	TF binding region
ENSG00000226410	TF binding region
RPL23AP35	CpG island
ENSG00000237877	CpG island
RPL21P32	CpG island
ENSG00000226410	CpG island
ENSG00000188738	chromatin interactions
ENSG00000152518	chromatin interactions
ENSG00000237877	chromatin interactions
ENSG00000226747	chromatin interactions
ENSG00000226410	chromatin interactions
ENSG00000065548	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000075240	chromatin interactions
SNAI2	miRNA target sites

Extended variants
information (count: 13291 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:13291 , 50 per page) page: 1 2 3 4 5 6 7 ... 266

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578016105	chr2:186693202-186693203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545430043	chr2:186693217-186693218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560275001	chr2:186693277-186693278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192588795	chr2:186693291-186693292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs372039643	chr2:186693308-186693309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572291330	chr2:186693374-186693375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549289891	chr2:186693385-186693386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561213592	chr2:186693406-186693407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531823537	chr2:186693414-186693415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184110866	chr2:186693423-186693424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374856523	chr2:186693457-186693458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568982394	chr2:186693460-186693461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539151048	chr2:186693496-186693497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551415592	chr2:186693514-186693515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368449454	chr2:186693567-186693568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140316000	chr2:186693573-186693574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2193821	chr2:186693590-186693591	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs2193820	chr2:186693608-186693609	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs576040416	chr2:186693644-186693645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573966771	chr2:186693703-186693704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144234669	chr2:186693759-186693760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556387683	chr2:186693773-186693774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs578076714	chr2:186693777-186693778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545523274	chr2:186693852-186693853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545178204	chr2:186693864-186693865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554213397	chr2:186693871-186693872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543320901	chr2:186693907-186693908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111482517	chr2:186694009-186694010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs16827202	chr2:186694044-186694045	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs148914771	chr2:186694079-186694080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531880542	chr2:186694121-186694122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543650237	chr2:186694134-186694135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs368959629	chr2:186694206-186694207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114976534	chr2:186694207-186694208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142610679	chr2:186694221-186694222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551208585	chr2:186694257-186694258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17827241	chr2:186694258-186694259	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs562009649	chr2:186694267-186694268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527316838	chr2:186694287-186694288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150986069	chr2:186694302-186694303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547712824	chr2:186694414-186694415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188456399	chr2:186694571-186694572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188210368	chr2:186702082-186702083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536904936	chr2:186702094-186702095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375903886	chr2:186702101-186702102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200407483	chr2:186702103-186702104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560425480	chr2:186702117-186702118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192964656	chr2:186702128-186702129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373910367	chr2:186702176-186702177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs397713601	chr2:186702186-186702187	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186693200-186694600	Enhancers	Stomach Mucosa	stomach
2	chr2:186694200-186694600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:186702000-186702600	Enhancers	HepG2	liver
4	chr2:186712600-186713400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
5	chr2:186712800-186713400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr2:186715400-186716400	Weak transcription	Aorta	Aorta
7	chr2:186716000-186716400	Weak transcription	Ovary	ovary
8	chr2:186716200-186717000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
9	chr2:186716400-186716800	ZNF genes & repeats	Ovary	ovary
10	chr2:186716400-186717000	ZNF genes & repeats	Aorta	Aorta
11	chr2:186716600-186717000	ZNF genes & repeats	Left Ventricle	heart
12	chr2:186716800-186767200	Weak transcription	Ovary	ovary
13	chr2:186719400-186719800	ZNF genes & repeats	Aorta	Aorta
14	chr2:186719400-186719800	Enhancers	Stomach Mucosa	stomach
15	chr2:186719400-186720600	Enhancers	Hela-S3	cervix
16	chr2:186720200-186721800	Weak transcription	Pancreas	Pancrea
17	chr2:186721800-186728200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr2:186725200-186726000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr2:186726000-186727600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:186727400-186727600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr2:186727400-186728000	Enhancers	HepG2	liver
22	chr2:186727400-186729600	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr2:186727600-186727800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr2:186727600-186727800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:186727600-186729600	Active TSS	K562	blood
26	chr2:186727800-186728000	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr2:186727800-186728200	Enhancers	H9 Cell Line	embryonic stem cell
28	chr2:186727800-186730200	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr2:186728000-186728400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr2:186728000-186729000	Weak transcription	HepG2	liver
31	chr2:186728200-186729000	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr2:186728200-186729400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
33	chr2:186728400-186728600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr2:186728400-186729600	Active TSS	iPS-15b Cell Line	embryonic stem cell
35	chr2:186728600-186729600	Active TSS	HUES64 Cell Line	embryonic stem cell
36	chr2:186728800-186729600	Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr2:186728800-186729600	Active TSS	Placenta	Placenta
38	chr2:186729000-186729200	Enhancers	HepG2	liver
39	chr2:186729000-186729400	Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr2:186729000-186729600	Active TSS	H9 Cell Line	embryonic stem cell
41	chr2:186739800-186740200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:186740000-186740600	Enhancers	Fetal Brain Female	brain
43	chr2:186740200-186740600	Enhancers	Fetal Brain Male	brain
44	chr2:186742600-186743200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:186744800-186745200	Enhancers	HepG2	liver
46	chr2:186745600-186756600	Weak transcription	Left Ventricle	heart
47	chr2:186755200-186757800	Enhancers	HepG2	liver
48	chr2:186755400-186759600	Weak transcription	Fetal Intestine Small	intestine
49	chr2:186756200-186758600	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr2:186756600-186756800	Enhancers	Left Ventricle	heart

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