Variant report

Variant	nsv537426
Chromosome Location	chr4:186929542-187130319
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3525)
CpG islands
(count:5133)
Chromatin interactive
region (count:76)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3525 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187123009-187123375	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:187058552-187058902	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:187112517-187112766	K562	blood:	n/a	n/a
4	ARID3A	chr4:186942758-186943110	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:187058644-187058864	K562	blood:	n/a	n/a
6	ARID3A	chr4:187124713-187124813	K562	blood:	n/a	n/a
7	ARID3A	chr4:187112910-187112928	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:186989219-186989538	HepG2	liver:	n/a	n/a
9	ATF1	chr4:187125220-187125793	K562	blood:	n/a	n/a
10	ATF1	chr4:187027151-187027480	K562	blood:	n/a	n/a
11	ATF1	chr4:186932010-186932347	K562	blood:	n/a	n/a
12	ATF2	chr4:187111626-187112084	GM12878	blood:	n/a	n/a
13	ATF2	chr4:187071057-187071421	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr4:187112363-187112834	GM12878	blood:	n/a	n/a
15	ATF2	chr4:187027166-187027483	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr4:187112340-187112962	GM12878	blood:	n/a	n/a
17	ATF2	chr4:186979842-186980247	GM12878	blood:	n/a	n/a
18	ATF2	chr4:187055315-187055866	GM12878	blood:	n/a	n/a
19	ATF3	chr4:187123084-187123309	K562	blood:	n/a	n/a
20	ATF3	chr4:186932095-186932280	K562	blood:	n/a	n/a
21	ATF3	chr4:187112294-187112519	K562	blood:	n/a	n/a
22	BACH1	chr4:187112705-187112885	K562	blood:	n/a	n/a
23	BACH1	chr4:187025719-187026243	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr4:187082521-187082663	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr4:187111645-187113416	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr4:187066156-187066584	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr4:187026701-187026862	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr4:187055418-187055866	GM12878	blood:	n/a	n/a
29	BATF	chr4:187058420-187058694	GM12878	blood:	n/a	n/a
30	BATF	chr4:187058431-187058728	GM12878	blood:	n/a	n/a
31	BATF	chr4:186979789-186980186	GM12878	blood:	n/a	n/a
32	BATF	chr4:187055371-187055785	GM12878	blood:	n/a	n/a
33	BATF	chr4:186954961-186955292	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:187112453-187112795	GM12878	blood:	n/a	chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
35	BCL11A	chr4:187055420-187055843	GM12878	blood:	n/a	n/a
36	BCL11A	chr4:186979854-186980169	GM12878	blood:	n/a	n/a
37	BCL11A	chr4:186979842-186980224	GM12878	blood:	n/a	n/a
38	BCL3	chr4:186979865-186980155	GM12878	blood:	n/a	n/a
39	BCL3	chr4:187112454-187113086	GM12878	blood:	n/a	chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
40	BCL3	chr4:187112551-187113002	GM12878	blood:	n/a	chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
41	BCL3	chr4:187055433-187055716	GM12878	blood:	n/a	n/a
42	BCL3	chr4:186979857-186980236	GM12878	blood:	n/a	n/a
43	BCL3	chr4:187123689-187124048	GM12878	blood:	n/a	n/a
44	BCL3	chr4:187059720-187060074	GM12878	blood:	n/a	n/a
45	BCLAF1	chr4:187055428-187055813	GM12878	blood:	n/a	n/a
46	BCLAF1	chr4:187112309-187112982	K562	blood:	n/a	chr4:187112372-187112380 chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
47	BCLAF1	chr4:187112386-187113126	GM12878	blood:	n/a	chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
48	BCLAF1	chr4:187055345-187055835	GM12878	blood:	n/a	n/a
49	BCLAF1	chr4:187112247-187113106	GM12878	blood:	n/a	chr4:187112372-187112380 chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
50	BCLAF1	chr4:187112371-187112924	K562	blood:	n/a	chr4:187112372-187112380 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582

(count:5133 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187078771-187078821	HRPEpiC	eye:	n/a
2	chr4:187109237-187109287	NT2-D1	testis:	n/a
3	chr4:187065940-187065990	HRE	kidney:	n/a
4	chr4:187112763-187112813	SAEC	small airway:	n/a
5	chr4:187025420-187025470	HL-60	blood:	n/a
6	chr4:186933893-186933943	K562	blood:	n/a
7	chr4:187013645-187013695	GM12878	blood:	n/a
8	chr4:186933893-186933943	HL-60	blood:	n/a
9	chr4:187065417-187065467	SK-N-MC	brain:	n/a
10	chr4:187078771-187078821	HRPEpiC	eye:	n/a
11	chr4:187109237-187109287	NT2-D1	testis:	n/a
12	chr4:187065940-187065990	HRE	kidney:	n/a
13	chr4:187112763-187112813	SAEC	small airway:	n/a
14	chr4:187025420-187025470	HL-60	blood:	n/a
15	chr4:186933893-186933943	K562	blood:	n/a
16	chr4:187013645-187013695	GM12878	blood:	n/a
17	chr4:186933893-186933943	HL-60	blood:	n/a
18	chr4:187065417-187065467	SK-N-MC	brain:	n/a
19	chr4:187065831-187065881	LNCaP	prostate:	n/a
20	chr4:186990315-186990365	Jurkat	blood:	n/a
21	chr4:187090481-187090531	NB4	blood:	n/a
22	chr4:186934295-186934345	HRCEpiC	kidney:	n/a
23	chr4:187126073-187126123	HAEpiC	amniotic membrane:	n/a
24	chr4:187025897-187025947	HCT-116	colon:	n/a
25	chr4:186933511-186933561	K562	blood:	n/a
26	chr4:187063756-187063806	HEEpiC	esophagus:	n/a
27	chr4:187066279-187066329	NB4	blood:	n/a
28	chr4:186990324-186990374	Hepatocyte	liver:	n/a
29	chr4:187003000-187003050	HIPEpiC	eye:	n/a
30	chr4:187109237-187109287	AG10803	skin:	n/a
31	chr4:187065516-187065566	K562	blood:	n/a
32	chr4:187026225-187026275	HAEpiC	amniotic membrane:	n/a
33	chr4:187088169-187088219	HEEpiC	esophagus:	n/a
34	chr4:186933456-186933506	Hepatocyte	liver:	n/a
35	chr4:187070357-187070407	ovcar-3	ovarian:	n/a
36	chr4:187125413-187125463	AG09319	gingival:	n/a
37	chr4:186933511-186933561	HEEpiC	esophagus:	n/a
38	chr4:187039516-187039566	AoSMC	blood vessel:	n/a
39	chr4:187078828-187078878	HIPEpiC	eye:	n/a
40	chr4:187025420-187025470	Hela-S3	cervix:	n/a
41	chr4:186944909-186944959	SK-N-SH	brain:	n/a
42	chr4:186960904-186960954	HEEpiC	esophagus:	n/a
43	chr4:186960991-186961041	CMK	blood:	n/a
44	chr4:187126073-187126123	AG09309	skin:	n/a
45	chr4:187066430-187066480	GM12878	blood:	n/a
46	chr4:187070357-187070407	AG09319	gingival:	n/a
47	chr4:187065516-187065566	NHDF-neo	bronchial:	n/a
48	chr4:187113578-187113628	Jurkat	blood:	n/a
49	chr4:187037318-187037368	PrEC	prostate:	n/a
50	chr4:187078771-187078821	HMEC	breast:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:187106828..187109765-chr4:187110186..187112854,4	K562	blood:
2	chr12:52452615..52453609-chr4:187112686..187113538,2	Hela-S3	cervix:
3	chr4:187118539..187120138-chr4:187121607..187123644,3	MCF-7	breast:
4	chr4:186988828..186989568-chr4:187053779..187054412,2	MCF-7	breast:
5	chr4:187062784..187065890-chr4:187111242..187113420,3	MCF-7	breast:
6	chr4:187092198..187094078-chr4:187111646..187113279,2	MCF-7	breast:
7	chr4:187065362..187066941-chr4:187069127..187071220,2	K562	blood:
8	chr4:187092687..187094578-chr4:187097251..187099352,2	MCF-7	breast:
9	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
10	chr4:186985477..186986987-chr4:187047828..187050010,2	K562	blood:
11	chr4:186988895..186989419-chr4:187058283..187058978,2	K562	blood:
12	chr4:187116069..187118838-chr4:187120195..187124189,4	MCF-7	breast:
13	chr4:187083351..187085783-chr4:187086821..187088983,2	K562	blood:
14	chr4:187061612..187063617-chr4:187065011..187066705,2	K562	blood:
15	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
16	chr16:17073810..17074454-chr4:186958456..186959434,2	MCF-7	breast:
17	chr4:186988828..186989568-chr4:187053779..187054412,2	MCF-7	breast:
18	chr4:186985477..186986987-chr4:187047828..187050010,2	K562	blood:
19	chr4:186988859..186989716-chr4:187058329..187059203,5	MCF-7	breast:
20	chr4:187053677..187057505-chr4:187060435..187064236,4	K562	blood:
21	chr4:187021448..187022968-chr6:31674535..31677393,2	K562	blood:
22	chr4:187036166..187038039-chr4:187110587..187113537,2	K562	blood:
23	chr4:186988972..186989928-chr4:187122701..187123491,2	MCF-7	breast:
24	chr4:186988972..186989928-chr4:187122701..187123491,2	MCF-7	breast:
25	chr4:187111353..187115983-chr4:187119045..187124895,10	MCF-7	breast:
26	chr4:187091730..187094624-chr4:187097179..187100415,3	MCF-7	breast:
27	chr22:41487362..41488310-chr4:187112180..187112692,2	Hela-S3	cervix:
28	chr4:187122087..187123852-chr4:187421026..187423788,3	K562	blood:
29	chr4:187065362..187066941-chr4:187069127..187071220,2	K562	blood:
30	chr4:186988895..186989419-chr4:187058283..187058978,2	K562	blood:
31	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
32	chr4:186953201..186953720-chr4:187058277..187058867,2	MCF-7	breast:
33	chr4:186981542..186984257-chr4:186986669..186988190,2	MCF-7	breast:
34	chr4:186543758..186545756-chr4:186936731..186939343,2	K562	blood:
35	chr4:187121686..187123375-chr4:187456206..187458817,2	K562	blood:
36	chr4:187125089..187127684-chr4:187129515..187131962,3	K562	blood:
37	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
38	chr4:186933593..186936469-chr4:186945344..186948028,2	K562	blood:
39	chr4:186561687..186562665-chr4:186959039..186959962,3	MCF-7	breast:
40	chr4:187117801..187120230-chr4:187120810..187122503,2	K562	blood:
41	chr4:187053677..187057505-chr4:187060435..187064236,4	K562	blood:
42	chr4:187117801..187120230-chr4:187120810..187122503,2	K562	blood:
43	chr4:187125089..187127684-chr4:187129515..187131962,3	K562	blood:
44	chr4:187109253..187118277-chr4:187122555..187126883,14	K562	blood:
45	chr4:187106383..187110529-chr4:187110531..187113610,6	K562	blood:
46	chr4:187000465..187002106-chr4:187010501..187012706,2	MCF-7	breast:
47	chr4:187000465..187002106-chr4:187010501..187012706,2	MCF-7	breast:
48	chr4:187111874..187113781-chr4:187171263..187172793,2	MCF-7	breast:
49	chr4:187083351..187085783-chr4:187086821..187088983,2	K562	blood:
50	chr4:187053833..187057505-chr4:187060435..187064133,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TLR3-1	chr4:186936734-186936900	XLOC_003820
2	lnc-KLKB1-1	chr4:187125593-187125738	NONHSAT099647
3	lnc-SORBS2-4	chr4:187110186-187112644	NONHSAT099644
4	lnc-KLKB1-1	chr4:187125555-187125774	NONHSAT099646
5	lnc-KLKB1-1	chr4:187125257-187125426	NONHSAT099646
6	lnc-TLR3-1	chr4:186939607-186940103	XLOC_003820
7	lnc-KLKB1-1	chr4:187125389-187125458	NONHSAT099648
8	lnc-SORBS2-2	chr4:186937392-186938595	XLOC_004212
9	lnc-KLKB1-1	chr4:187125555-187125762	NONHSAT099648
10	lnc-KLKB1-1	chr4:187125266-187125400	NONHSAT099647
11	lnc-SORBS2-2	chr4:186940952-186941235	XLOC_004212
12	lnc-TLR3-1	chr4:186938433-186938541	XLOC_003820

No data

Variant related genes	Relation type
CYP4V2	TF binding region
ENSG00000253013	TF binding region
ENSG00000250327	TF binding region
FAM149A	TF binding region
RNU4-64P	TF binding region
ENSG00000269302	TF binding region
TLR3	TF binding region
KLKB1	TF binding region
ORAOV1P1	TF binding region
CYP4V2	CpG island
ENSG00000253013	CpG island
ENSG00000250327	CpG island
FAM149A	CpG island
RNU4-64P	CpG island
ENSG00000269302	CpG island
TLR3	CpG island
KLKB1	CpG island
ORAOV1P1	CpG island
ENSG00000100393	chromatin interactions
ENSG00000212387	chromatin interactions
ENSG00000269302	chromatin interactions
ENSG00000251165	chromatin interactions
ENSG00000172059	chromatin interactions
ENSG00000251008	chromatin interactions
ENSG00000259884	chromatin interactions
ENSG00000164344	chromatin interactions
ENSG00000145476	chromatin interactions
ENSG00000204424	chromatin interactions
ENSG00000222727	chromatin interactions
ENSG00000250641	chromatin interactions
ENSG00000109794	chromatin interactions
EIF3J	miRNA target sites
DOK3	miRNA target sites

Extended variants
information (count: 8541 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:8541 , 50 per page) page: 1 2 3 4 5 6 7 ... 171

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188917285	chr4:186929548-186929549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563646968	chr4:186929568-186929569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529259613	chr4:186929574-186929575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573337384	chr4:186929605-186929606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549138877	chr4:186929617-186929618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568329807	chr4:186929618-186929619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527368345	chr4:186929623-186929624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2008461	chr4:186929646-186929647	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs547291398	chr4:186929670-186929671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570271732	chr4:186929714-186929715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539261416	chr4:186929786-186929787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75456846	chr4:186929934-186929935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556193735	chr4:186930010-186930011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77842933	chr4:186930013-186930014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535413082	chr4:186930018-186930019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537348101	chr4:186930046-186930047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555111073	chr4:186930067-186930068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377325309	chr4:186930072-186930073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572776569	chr4:186930073-186930074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200149986	chr4:186930076-186930077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541700952	chr4:186930084-186930085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558500355	chr4:186930087-186930088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192363635	chr4:186930096-186930097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75973985	chr4:186930106-186930107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143088488	chr4:186930128-186930129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574086395	chr4:186930129-186930130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564765525	chr4:186930130-186930131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs543003821	chr4:186930150-186930151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148210133	chr4:186930167-186930168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528474051	chr4:186930168-186930169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76967554	chr4:186930190-186930191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141047254	chr4:186930191-186930192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532939165	chr4:186930192-186930193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549743806	chr4:186930216-186930217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535463981	chr4:186930268-186930269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs116676798	chr4:186930277-186930278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553510658	chr4:186930288-186930289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182458153	chr4:186930292-186930293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150245203	chr4:186930315-186930316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565640422	chr4:186930325-186930326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572074571	chr4:186930339-186930340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139393061	chr4:186930403-186930404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77948837	chr4:186930437-186930438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114374192	chr4:186930495-186930496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537638702	chr4:186930496-186930497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143300591	chr4:186930514-186930515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574178142	chr4:186930564-186930565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187879677	chr4:186930567-186930568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559433206	chr4:186930568-186930569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191650607	chr4:186930629-186930630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
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
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17086460	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD

Chromatin state (count:4016 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:186919800-186936400	Weak transcription	Right Atrium	heart
2	chr4:186924200-186932800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:186928200-186930000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:186928600-186934200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:186929200-186929600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr4:186929600-186937400	Weak transcription	Spleen	Spleen
7	chr4:186929800-186933000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:186930000-186930200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:186930200-186933000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:186932800-186933000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:186933000-186933200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:186933000-186933200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:186933000-186933600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:186933200-186934000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:186933200-186934200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:186933200-186935000	Enhancers	Fetal Heart	heart
17	chr4:186933400-186934200	Enhancers	Right Ventricle	heart
18	chr4:186933600-186934800	Enhancers	Left Ventricle	heart
19	chr4:186933800-186935400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr4:186933800-186935800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr4:186934000-186934800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr4:186934000-186935400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr4:186934200-186934800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:186934200-186935000	Enhancers	H9 Cell Line	embryonic stem cell
25	chr4:186934200-186935000	Enhancers	Fetal Lung	lung
26	chr4:186934200-186935400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr4:186934200-186935800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr4:186934200-186936400	Weak transcription	Right Ventricle	heart
29	chr4:186934200-186936600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr4:186934400-186934600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr4:186934600-186934800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr4:186934600-186935000	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr4:186934600-186935000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr4:186934600-186935400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr4:186934800-186935000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr4:186934800-186935200	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr4:186934800-186936400	Weak transcription	Left Ventricle	heart
38	chr4:186934800-186946400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:186934800-186950400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr4:186935000-186936400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr4:186935000-186936400	Weak transcription	Fetal Heart	heart
42	chr4:186935000-186939000	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr4:186935000-186942000	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr4:186935200-186935400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr4:186935400-186936400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr4:186935400-186936400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr4:186935400-186936600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr4:186935400-186938600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr4:186935400-186939000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:186935800-186936200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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