Variant report

Variant	nsv1011100
Chromosome Location	chr2:133900062-134046163
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1149)
CpG islands
(count:920)
Chromatin interactive
region (count:50)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1149 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:133915573-133916005	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:133929022-133929350	HepG2	liver:	n/a	n/a
3	ATF3	chr2:133958614-133959030	HCT-116	colon:	n/a	n/a
4	BACH1	chr2:134022701-134024075	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr2:134005181-134005429	GM12878	blood:	n/a	n/a
6	BCL3	chr2:134023499-134024135	A549	lung:	n/a	n/a
7	BCL3	chr2:134023525-134024142	A549	lung:	n/a	n/a
8	BRCA1	chr2:134022507-134023986	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr2:134004476-134004492	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr2:133958587-133958930	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr2:133958628-133959001	HCT-116	colon:	n/a	n/a
12	CBX3	chr2:133958614-133959033	HCT-116	colon:	n/a	n/a
13	CEBPB	chr2:133923387-133923427	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:134024047-134024339	IMR90	lung:	n/a	chr2:134024205-134024216
15	CEBPB	chr2:134045260-134045655	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:133958624-133959238	A549	lung:	n/a	chr2:133958814-133958825
17	CEBPB	chr2:134000488-134000570	A549	lung:	n/a	n/a
18	CEBPB	chr2:134028771-134028886	A549	lung:	n/a	n/a
19	CEBPB	chr2:134043906-134044270	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:133927367-133927908	Hela-S3	cervix:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
21	CEBPB	chr2:133911620-133911962	HepG2	liver:	n/a	chr2:133911792-133911803
22	CEBPB	chr2:133956290-133956581	Hela-S3	cervix:	n/a	chr2:133956438-133956449
23	CEBPB	chr2:134043952-134044155	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:133927649-133927954	IMR90	lung:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
25	CEBPB	chr2:134043852-134044617	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:133956284-133956587	A549	lung:	n/a	chr2:133956438-133956449
27	CEBPB	chr2:134003410-134003684	IMR90	lung:	n/a	chr2:134003550-134003561
28	CEBPB	chr2:133911651-133911930	IMR90	lung:	n/a	chr2:133911792-133911803
29	CEBPB	chr2:134000355-134000651	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:134044066-134044190	K562	blood:	n/a	n/a
31	CEBPB	chr2:134003450-134003684	A549	lung:	n/a	chr2:134003550-134003561
32	CEBPB	chr2:133911686-133911964	MCF-7	breast:	n/a	chr2:133911792-133911803
33	CEBPB	chr2:133958606-133959047	HCT-116	colon:	n/a	chr2:133958814-133958825
34	CEBPB	chr2:133927773-133927830	H1-hESC	embryonic stem cell:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
35	CEBPB	chr2:133951692-133952052	IMR90	lung:	n/a	chr2:133951845-133951856
36	CEBPB	chr2:133964466-133964533	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr2:133958461-133959335	A549	lung:	n/a	chr2:133958814-133958825
38	CEBPB	chr2:133958646-133959106	HCT-116	colon:	n/a	chr2:133958814-133958825
39	CEBPB	chr2:134043975-134044199	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr2:133924811-133925135	IMR90	lung:	n/a	chr2:133924973-133924984
41	CEBPB	chr2:133924821-133925142	HepG2	liver:	n/a	chr2:133924973-133924984
42	CEBPB	chr2:133927441-133927955	HepG2	liver:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
43	CEBPB	chr2:134043877-134044226	MCF-7	breast:	n/a	n/a
44	CEBPB	chr2:134043932-134044239	A549	lung:	n/a	n/a
45	CEBPB	chr2:134022735-134025209	Hela-S3	cervix:	n/a	chr2:134024205-134024216
46	CEBPB	chr2:133958623-133959309	IMR90	lung:	n/a	chr2:133958814-133958825
47	CEBPB	chr2:133951548-133952193	A549	lung:	n/a	chr2:133951845-133951856
48	CEBPB	chr2:133956292-133956570	IMR90	lung:	n/a	chr2:133956438-133956449
49	CEBPB	chr2:133924899-133925138	A549	lung:	n/a	chr2:133924973-133924984
50	CEBPB	chr2:133927438-133927952	A549	lung:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797

(count:920 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:134024093-134024143	BJ	skin:	n/a
2	chr2:133998732-133998782	NHDF-neo	bronchial:	n/a
3	chr2:133923604-133923654	HPAEpiC	pulmonary alveolar:	n/a
4	chr2:134024459-134024509	HCF	heart:	n/a
5	chr2:133927261-133927311	HCT-116	colon:	n/a
6	chr2:134024093-134024143	BJ	skin:	n/a
7	chr2:133998732-133998782	NHDF-neo	bronchial:	n/a
8	chr2:133923604-133923654	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:134024459-134024509	HCF	heart:	n/a
10	chr2:133927261-133927311	HCT-116	colon:	n/a
11	chr2:134010875-134010925	Hela-S3	cervix:	n/a
12	chr2:133934804-133934854	Caco-2	colon:	n/a
13	chr2:134024418-134024468	GM06990	blood:	n/a
14	chr2:133934804-133934854	HCPEpiC	choroid plexus:	n/a
15	chr2:134024459-134024509	T-47D	breast:	n/a
16	chr2:134023662-134023712	H1-hESC	embryonic stem cell:	embryo
17	chr2:133998732-133998782	GM19239	blood:	n/a
18	chr2:134024266-134024316	GM12878	blood:	n/a
19	chr2:134028440-134028490	A549	lung:	n/a
20	chr2:134024618-134024668	ECC-1	luminal epithelium:	n/a
21	chr2:133998732-133998782	HRE	kidney:	n/a
22	chr2:134023210-134023260	K562	blood:	n/a
23	chr2:133998732-133998782	MCF10A-Er-Src	breast:	n/a
24	chr2:134010875-134010925	IMR90	lung:	fetal
25	chr2:134020041-134020091	PrEC	prostate:	n/a
26	chr2:134010875-134010925	HCM	heart:	n/a
27	chr2:133998732-133998782	AG04450	lung:	fetal
28	chr2:134023662-134023712	HL-60	blood:	n/a
29	chr2:134023662-134023712	HepG2	liver:	n/a
30	chr2:133927261-133927311	ovcar-3	ovarian:	n/a
31	chr2:134010875-134010925	HCT-116	colon:	n/a
32	chr2:134023210-134023260	ovcar-3	ovarian:	n/a
33	chr2:134028440-134028490	GM12891	blood:	n/a
34	chr2:134024418-134024468	BJ	skin:	n/a
35	chr2:133934804-133934854	GM12891	blood:	n/a
36	chr2:133934804-133934854	SK-N-SH_RA	brain:	n/a
37	chr2:133927261-133927311	Jurkat	blood:	n/a
38	chr2:134024093-134024143	SK-N-SH_RA	brain:	n/a
39	chr2:134024618-134024668	GM12891	blood:	n/a
40	chr2:134024618-134024668	HCPEpiC	choroid plexus:	n/a
41	chr2:133998732-133998782	HMEC	breast:	n/a
42	chr2:133998732-133998782	HEEpiC	esophagus:	n/a
43	chr2:134010875-134010925	BE2_C	brain:	n/a
44	chr2:134023210-134023260	SAEC	small airway:	n/a
45	chr2:134024418-134024468	HCM	heart:	n/a
46	chr2:134024459-134024509	HRE	kidney:	n/a
47	chr2:134024266-134024316	HEEpiC	esophagus:	n/a
48	chr2:134023662-134023712	T-47D	breast:	n/a
49	chr2:133998732-133998782	CMK	blood:	n/a
50	chr2:134020041-134020091	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:133304640..133305382-chr2:133928983..133929651,2	MCF-7	breast:
2	chr2:134019056..134021492-chr2:134262374..134264487,2	MCF-7	breast:
3	chr2:133428080..133428797-chr2:133928852..133929367,2	MCF-7	breast:
4	chr2:134019393..134021124-chr2:134030265..134032879,2	K562	blood:
5	chr2:133106208..133106974-chr2:133928762..133929385,2	MCF-7	breast:
6	chr2:134031322..134033202-chr2:134041949..134044223,2	MCF-7	breast:
7	chr2:134020041..134020759-chr2:134398921..134399467,2	MCF-7	breast:
8	chr2:133978989..133981496-chr2:133987532..133990158,2	MCF-7	breast:
9	chr2:133922662..133923182-chr20:49410946..49412118,12	MCF-7	breast:
10	chr1:154946346..154946996-chr2:134023337..134024323,2	Hela-S3	cervix:
11	chr2:133932748..133934866-chr2:133936195..133938875,2	MCF-7	breast:
12	chr2:133953064..133954873-chr2:134023809..134025378,2	MCF-7	breast:
13	chr2:133426257..133428194-chr2:133927974..133930516,2	MCF-7	breast:
14	chr2:134035082..134037430-chr2:134042512..134044195,2	MCF-7	breast:
15	chr2:134015404..134018015-chr2:134019119..134021924,2	MCF-7	breast:
16	chr2:133969380..133971037-chr2:133972484..133974149,2	MCF-7	breast:
17	chr2:134003474..134006247-chr2:134007339..134011249,3	MCF-7	breast:
18	chr2:134020255..134021142-chr2:134318343..134319277,2	MCF-7	breast:
19	chr2:133304031..133305145-chr2:133928594..133929580,6	MCF-7	breast:
20	chr2:134003474..134006247-chr2:134007339..134011249,3	MCF-7	breast:
21	chr2:133922662..133923182-chr20:49410992..49411888,4	MCF-7	breast:
22	chr2:134028269..134031265-chr2:134033002..134035310,2	MCF-7	breast:
23	chr16:30709997..30710818-chr2:134023319..134023932,2	Hela-S3	cervix:
24	chr2:133969380..133971037-chr2:133972484..133974149,2	MCF-7	breast:
25	chr2:134033733..134036491-chr2:134192911..134194605,2	MCF-7	breast:
26	chr2:134020528..134022424-chr2:134324632..134327514,2	MCF-7	breast:
27	chr2:133907650..133909821-chr2:133911613..133914505,3	MCF-7	breast:
28	chr2:134020179..134020906-chr2:134601878..134602419,2	MCF-7	breast:
29	chr2:134015404..134018015-chr2:134019119..134021924,2	MCF-7	breast:
30	chr2:134038890..134041623-chr2:134041735..134044144,2	MCF-7	breast:
31	chr2:133932748..133934866-chr2:133936195..133938875,2	MCF-7	breast:
32	chr2:134019393..134021124-chr2:134030265..134032879,2	K562	blood:
33	chr2:133434344..133435258-chr2:133928761..133929306,2	MCF-7	breast:
34	chr2:133999579..134001370-chr2:134029081..134031077,2	K562	blood:
35	chr2:133980114..133981949-chr2:133983146..133984842,2	MCF-7	breast:
36	chr2:134020760..134021325-chr2:134537400..134538161,2	K562	blood:
37	chr2:133427423..133430466-chr2:133927227..133930556,4	MCF-7	breast:
38	chr2:133978989..133981496-chr2:133987532..133990158,2	MCF-7	breast:
39	chr19:18793804..18794673-chr2:134023005..134023895,2	Hela-S3	cervix:
40	chr2:134031322..134033202-chr2:134041949..134044223,2	MCF-7	breast:
41	chr2:133980114..133981949-chr2:133983146..133984842,2	MCF-7	breast:
42	chr2:133408307..133409298-chr2:133928740..133929575,3	MCF-7	breast:
43	chr2:134020208..134021163-chr2:134537454..134538295,5	MCF-7	breast:
44	chr2:133907650..133909821-chr2:133911613..133914505,3	MCF-7	breast:
45	chr16:64509112..64511965-chr2:133985884..133987569,2	MCF-7	breast:
46	chr2:134038890..134041623-chr2:134041735..134044144,2	MCF-7	breast:
47	chr2:134028269..134031265-chr2:134033002..134035310,2	MCF-7	breast:
48	chr2:133426638..133429342-chr2:133954852..133957761,2	MCF-7	breast:
49	chr2:134035082..134037430-chr2:134042512..134044195,2	MCF-7	breast:
50	chr2:133999579..134001370-chr2:134029081..134031077,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953
2	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953.3
3	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953
4	lnc-GPR39-4	chr2:134026488-134026613	ENSG00000226953.3
5	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953
6	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953.3
7	lnc-GPR39-4	chr2:134023814-134024008	ENSG00000226953.3
8	lnc-GPR39-4	chr2:134026488-134026582	ENSG00000226953
9	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953
10	lnc-GPR39-4	chr2:134042267-134042330	NR_110294
11	lnc-GPR39-4	chr2:134024845-134024996	NR_110294
12	lnc-GPR39-4	chr2:134025928-134026014	NR_110294
13	lnc-GPR39-4	chr2:134042267-134042334	ENSG00000226953
14	lnc-GPR39-4	chr2:134022540-134022674	ENSG00000226953
15	lnc-GPR39-4	chr2:134023767-134023868	ENSG00000226953
16	lnc-GPR39-4	chr2:134026488-134026613	NR_110294
17	lnc-GPR39-4	chr2:134023767-134023868	NR_110294
18	lnc-GPR39-4	chr2:134026488-134026613	ENSG00000226953

No data

Variant related genes	Relation type
ENSG00000226953	TF binding region
ENSG00000226953	CpG island
ENSG00000080603	chromatin interactions
ENSG00000150551	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000176771	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000105662	chromatin interactions
ENSG00000124243	chromatin interactions
ENSG00000226953	chromatin interactions
KIF23	miRNA target sites
NFKB1	miRNA target sites
LRIG1	miRNA target sites
CALU	miRNA target sites
ATOX1	miRNA target sites
FNTA	miRNA target sites
IQCB1	miRNA target sites
SMCR7L	miRNA target sites
TNFSF10	miRNA target sites

Extended variants
information (count: 5186 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:5186 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192090462	chr2:133900093-133900094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7558369	chr2:133900095-133900096	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs7561032	chr2:133900128-133900129	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs111267834	chr2:133900149-133900150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368292480	chr2:133900153-133900154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113735819	chr2:133900156-133900157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558434721	chr2:133900177-133900178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75443573	chr2:133900196-133900197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184481546	chr2:133900206-133900207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190030105	chr2:133900295-133900296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372245877	chr2:133900313-133900314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572462087	chr2:133900343-133900344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201522708	chr2:133900374-133900375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542801961	chr2:133900432-133900433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76233614	chr2:133900538-133900539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35657153	chr2:133900552-133900553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576425217	chr2:133900565-133900566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544015621	chr2:133900596-133900597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199704985	chr2:133900659-133900660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565088885	chr2:133900663-133900664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371809661	chr2:133900666-133900667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528617210	chr2:133900667-133900668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532673574	chr2:133900670-133900671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs397802499	chr2:133900676-133900677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547672658	chr2:133900698-133900699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368502097	chr2:133900744-133900745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372121666	chr2:133900774-133900775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558967183	chr2:133900793-133900794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555890637	chr2:133900842-133900843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574171107	chr2:133900886-133900887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555135190	chr2:133900887-133900888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144193282	chr2:133900909-133900910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569749309	chr2:133900914-133900915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182210854	chr2:133900946-133900947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185641969	chr2:133900960-133900961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146525262	chr2:133900964-133900965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534956816	chr2:133900978-133900979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs16857210	chr2:133900979-133900980	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs139619714	chr2:133901016-133901017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189393477	chr2:133901045-133901046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554636893	chr2:133901063-133901064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576483199	chr2:133901093-133901094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543508890	chr2:133901095-133901096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114822503	chr2:133901144-133901145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573634292	chr2:133901151-133901152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115769524	chr2:133901186-133901187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559604990	chr2:133901256-133901257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71413539	chr2:133901351-133901352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113585449	chr2:133901365-133901366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548262354	chr2:133901374-133901375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1120 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133887800-133912600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:133897000-133900200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:133898000-133900400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:133898000-133901400	Weak transcription	Brain Substantia Nigra	brain
5	chr2:133898200-133901000	Weak transcription	Brain Cingulate Gyrus	brain
6	chr2:133898800-133901000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr2:133899000-133901000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:133899600-133902200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr2:133899600-133902200	Weak transcription	Brain Anterior Caudate	brain
10	chr2:133900000-133900200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr2:133900000-133900200	Enhancers	Brain Hippocampus Middle	brain
12	chr2:133900200-133900600	Weak transcription	Brain Hippocampus Middle	brain
13	chr2:133900200-133908200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:133900600-133901800	Enhancers	Brain Hippocampus Middle	brain
15	chr2:133901000-133901400	Enhancers	Brain Cingulate Gyrus	brain
16	chr2:133901000-133901600	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr2:133901000-133901600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr2:133901400-133901800	Enhancers	Brain Substantia Nigra	brain
19	chr2:133901800-133904200	Weak transcription	Brain Substantia Nigra	brain
20	chr2:133901800-133904400	Weak transcription	Brain Hippocampus Middle	brain
21	chr2:133902200-133902400	Enhancers	Brain Anterior Caudate	brain
22	chr2:133904200-133904400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:133904200-133905000	Enhancers	Brain Substantia Nigra	brain
24	chr2:133904400-133905200	Enhancers	Brain Hippocampus Middle	brain
25	chr2:133904400-133913600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:133906800-133907400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:133908200-133909200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:133909200-133910600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:133910200-133911400	Enhancers	Liver	Liver
30	chr2:133910600-133911800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:133910600-133923000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr2:133911400-133914800	Weak transcription	Liver	Liver
33	chr2:133911800-133920600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:133912000-133913000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr2:133912600-133912800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr2:133912800-133917000	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr2:133912800-133922600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:133914800-133915200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:133914800-133917400	Enhancers	Liver	Liver
40	chr2:133915200-133916400	Enhancers	HepG2	liver
41	chr2:133917000-133917200	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr2:133917200-133919200	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr2:133920600-133921600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:133921600-133923600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:133922000-133923200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr2:133922600-133924800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:133923000-133924600	Enhancers	Osteobl	bone
48	chr2:133923000-133924800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr2:133923200-133923400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr2:133923400-133923800	Enhancers	NHDF-Ad	bronchial

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