Variant report

Variant	esv3375790
Chromosome Location	chr2:133906915-134222833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2092)
CpG islands
(count:1955)
Chromatin interactive
region (count:82)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2092 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:133929022-133929350	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:133915573-133916005	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:134175247-134175333	HepG2	liver:	n/a	n/a
4	ATF3	chr2:133958614-133959030	HCT-116	colon:	n/a	n/a
5	BACH1	chr2:134097037-134097041	K562	blood:	n/a	n/a
6	BACH1	chr2:134022701-134024075	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr2:134005181-134005429	GM12878	blood:	n/a	n/a
8	BCL3	chr2:134023525-134024142	A549	lung:	n/a	n/a
9	BCL3	chr2:134104177-134104553	GM12878	blood:	n/a	n/a
10	BCL3	chr2:134182427-134182865	A549	lung:	n/a	chr2:134182682-134182691
11	BCL3	chr2:134023499-134024135	A549	lung:	n/a	n/a
12	BCL3	chr2:134084062-134084604	A549	lung:	n/a	chr2:134084326-134084335 chr2:134084327-134084336
13	BHLHE40	chr2:134173057-134173395	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:134210183-134210251	A549	lung:	n/a	n/a
15	BHLHE40	chr2:134119719-134119882	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:134069959-134070256	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:134178421-134178431	GM12878	blood:	n/a	n/a
18	BRCA1	chr2:134004476-134004492	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr2:134081191-134081206	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr2:134084130-134084724	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr2:134102290-134102899	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr2:134022507-134023986	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr2:134103274-134103787	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr2:134192464-134193282	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr2:133958587-133958930	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr2:134191027-134191600	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr2:134119678-134120195	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr2:133958614-133959033	HCT-116	colon:	n/a	n/a
29	CBX3	chr2:133958628-133959001	HCT-116	colon:	n/a	n/a
30	CEBPB	chr2:134215824-134216231	Hela-S3	cervix:	n/a	chr2:134216036-134216053
31	CEBPB	chr2:134064374-134064789	A549	lung:	n/a	chr2:134064375-134064388
32	CEBPB	chr2:133998771-133999171	IMR90	lung:	n/a	chr2:133999017-133999028
33	CEBPB	chr2:134081659-134082211	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:134134628-134134894	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:133927773-133927830	H1-hESC	embryonic stem cell:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
36	CEBPB	chr2:134119668-134119880	A549	lung:	n/a	n/a
37	CEBPB	chr2:134180449-134180667	H1-hESC	embryonic stem cell:	n/a	chr2:134180572-134180583
38	CEBPB	chr2:134170046-134171171	Hela-S3	cervix:	n/a	chr2:134170438-134170451
39	CEBPB	chr2:134053980-134054421	Hela-S3	cervix:	n/a	chr2:134054150-134054163 chr2:134054152-134054163 chr2:134054150-134054163
40	CEBPB	chr2:133956292-133956570	IMR90	lung:	n/a	chr2:133956438-133956449
41	CEBPB	chr2:134180445-134180899	A549	lung:	n/a	chr2:134180572-134180583
42	CEBPB	chr2:133924821-133925142	HepG2	liver:	n/a	chr2:133924973-133924984
43	CEBPB	chr2:134180439-134180906	IMR90	lung:	n/a	chr2:134180572-134180583
44	CEBPB	chr2:133964466-133964533	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr2:133958623-133959309	IMR90	lung:	n/a	chr2:133958814-133958825
46	CEBPB	chr2:134215934-134216227	MCF-7	breast:	n/a	chr2:134216036-134216053
47	CEBPB	chr2:134179214-134179774	A549	lung:	n/a	chr2:134179420-134179433
48	CEBPB	chr2:133911686-133911964	MCF-7	breast:	n/a	chr2:133911792-133911803
49	CEBPB	chr2:134074709-134075358	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr2:133927644-133927947	MCF-7	breast:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797

(count:1955 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:134135267-134135317	GM12878	blood:	n/a
2	chr2:134163531-134163581	AG09309	skin:	n/a
3	chr2:133934804-133934854	IMR90	lung:	fetal
4	chr2:134135267-134135317	GM12878	blood:	n/a
5	chr2:134163531-134163581	AG09309	skin:	n/a
6	chr2:133934804-133934854	IMR90	lung:	fetal
7	chr2:134024418-134024468	RPTEC	kidney:	n/a
8	chr2:134028440-134028490	PANC-1	pancreas:	n/a
9	chr2:134180560-134180610	AG09319	gingival:	n/a
10	chr2:134169851-134169901	GM12878	blood:	n/a
11	chr2:134163531-134163581	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:133998732-133998782	HCPEpiC	choroid plexus:	n/a
13	chr2:134163531-134163581	HCPEpiC	choroid plexus:	n/a
14	chr2:134024459-134024509	HRPEpiC	eye:	n/a
15	chr2:134180028-134180078	CMK	blood:	n/a
16	chr2:134020041-134020091	HepG2	liver:	n/a
17	chr2:134099762-134099812	HepG2	liver:	n/a
18	chr2:134180028-134180078	AG04450	lung:	fetal
19	chr2:134119805-134119855	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:134068922-134068972	HIPEpiC	eye:	n/a
21	chr2:134052012-134052062	U87	brain:	n/a
22	chr2:134010875-134010925	AG09309	skin:	n/a
23	chr2:134119805-134119855	PFSK-1	brain:	n/a
24	chr2:134052012-134052062	AG04449	skin:	fetal
25	chr2:134068922-134068972	HCT-116	colon:	n/a
26	chr2:134169851-134169901	LNCaP	prostate:	n/a
27	chr2:134119805-134119855	Caco-2	colon:	n/a
28	chr2:134024459-134024509	AG10803	skin:	n/a
29	chr2:134191960-134192010	HRCEpiC	kidney:	n/a
30	chr2:133927261-133927311	SK-N-SH	brain:	n/a
31	chr2:134024459-134024509	HRE	kidney:	n/a
32	chr2:134004614-134004664	NT2-D1	testis:	n/a
33	chr2:134004614-134004664	Hela-S3	cervix:	n/a
34	chr2:133927261-133927311	PrEC	prostate:	n/a
35	chr2:134169851-134169901	AG04449	skin:	fetal
36	chr2:134023662-134023712	SK-N-SH_RA	brain:	n/a
37	chr2:133927261-133927311	PFSK-1	brain:	n/a
38	chr2:134191960-134192010	RPTEC	kidney:	n/a
39	chr2:134182001-134182051	HepG2	liver:	n/a
40	chr2:134180560-134180610	HUVEC	blood vessel:	n/a
41	chr2:134023210-134023260	HIPEpiC	eye:	n/a
42	chr2:134169851-134169901	ProgFib	skin:	n/a
43	chr2:134024618-134024668	Jurkat	blood:	n/a
44	chr2:134147854-134147904	HL-60	blood:	n/a
45	chr2:134024266-134024316	AoSMC	blood vessel:	n/a
46	chr2:134024418-134024468	NH-A	brain:	n/a
47	chr2:134127568-134127618	LNCaP	prostate:	n/a
48	chr2:134147854-134147904	HRPEpiC	eye:	n/a
49	chr2:134068922-134068972	CMK	blood:	n/a
50	chr2:134127568-134127618	Caco-2	colon:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:134033733..134036491-chr2:134192911..134194605,2	MCF-7	breast:
2	chr2:134179232..134182620-chr2:134183188..134186859,3	MCF-7	breast:
3	chr2:134031322..134033202-chr2:134041949..134044223,2	MCF-7	breast:
4	chr2:134020528..134022424-chr2:134324632..134327514,2	MCF-7	breast:
5	chr2:134154022..134156001-chr2:134158455..134161393,2	MCF-7	breast:
6	chr2:133106208..133106974-chr2:133928762..133929385,2	MCF-7	breast:
7	chr2:134213310..134215966-chr2:134217222..134219588,2	MCF-7	breast:
8	chr2:134179093..134179648-chr2:134601629..134602249,2	MCF-7	breast:
9	chr1:154946346..154946996-chr2:134023337..134024323,2	Hela-S3	cervix:
10	chr16:30709997..30710818-chr2:134023319..134023932,2	Hela-S3	cervix:
11	chr2:134038890..134041623-chr2:134041735..134044144,2	MCF-7	breast:
12	chr2:134031322..134033202-chr2:134041949..134044223,2	MCF-7	breast:
13	chr2:134213310..134215966-chr2:134217222..134219588,2	MCF-7	breast:
14	chr2:134088192..134090911-chr2:134099454..134100959,2	MCF-7	breast:
15	chr2:134089345..134089856-chr2:134262223..134263005,2	MCF-7	breast:
16	chr2:134168124..134170815-chr2:134171824..134174647,2	K562	blood:
17	chr2:134084453..134086561-chr2:134089070..134091697,3	MCF-7	breast:
18	chr2:134035082..134037430-chr2:134042512..134044195,2	MCF-7	breast:
19	chr2:134019393..134021124-chr2:134030265..134032879,2	K562	blood:
20	chr2:134088192..134090911-chr2:134099454..134100959,2	MCF-7	breast:
21	chr2:134101590..134103181-chr2:134107237..134110074,2	K562	blood:
22	chr2:133999579..134001370-chr2:134029081..134031077,2	K562	blood:
23	chr2:134147354..134149666-chr2:134150601..134153236,2	K562	blood:
24	chr2:133980114..133981949-chr2:133983146..133984842,2	MCF-7	breast:
25	chr2:134179232..134182620-chr2:134183188..134186859,3	MCF-7	breast:
26	chr2:133434344..133435258-chr2:133928761..133929306,2	MCF-7	breast:
27	chr2:133999579..134001370-chr2:134029081..134031077,2	K562	blood:
28	chr2:133978989..133981496-chr2:133987532..133990158,2	MCF-7	breast:
29	chr2:133969380..133971037-chr2:133972484..133974149,2	MCF-7	breast:
30	chr2:133978989..133981496-chr2:133987532..133990158,2	MCF-7	breast:
31	chr2:134073505..134075455-chr2:134080739..134083280,2	MCF-7	breast:
32	chr2:133907650..133909821-chr2:133911613..133914505,3	MCF-7	breast:
33	chr2:134154022..134156001-chr2:134158455..134161393,2	MCF-7	breast:
34	chr2:134083491..134086031-chr2:134262913..134265457,2	MCF-7	breast:
35	chr2:134088967..134089889-chr2:134250249..134251166,2	MCF-7	breast:
36	chr2:134200313..134200915-chr2:134250302..134251048,2	MCF-7	breast:
37	chr2:133408307..133409298-chr2:133928740..133929575,3	MCF-7	breast:
38	chr2:134028269..134031265-chr2:134033002..134035310,2	MCF-7	breast:
39	chr2:134020179..134020906-chr2:134601878..134602419,2	MCF-7	breast:
40	chr2:134015404..134018015-chr2:134019119..134021924,2	MCF-7	breast:
41	chr2:133969380..133971037-chr2:133972484..133974149,2	MCF-7	breast:
42	chr2:134035082..134037430-chr2:134042512..134044195,2	MCF-7	breast:
43	chr2:134073505..134075455-chr2:134080739..134083280,2	MCF-7	breast:
44	chr2:133922662..133923182-chr20:49410946..49412118,12	MCF-7	breast:
45	chr2:133427423..133430466-chr2:133927227..133930556,4	MCF-7	breast:
46	chr19:18793804..18794673-chr2:134023005..134023895,2	Hela-S3	cervix:
47	chr2:134019393..134021124-chr2:134030265..134032879,2	K562	blood:
48	chr2:133304031..133305145-chr2:133928594..133929580,6	MCF-7	breast:
49	chr2:134033733..134036491-chr2:134192911..134194605,2	MCF-7	breast:
50	chr2:134089010..134089877-chr2:134262426..134263057,3	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR39-4	chr2:134023767-134023868	NR_110294
2	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953
3	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953
4	lnc-GPR39-4	chr2:134026488-134026613	NR_110294
5	lnc-GPR39-4	chr2:134023814-134024008	ENSG00000226953.3
6	lnc-GPR39-4	chr2:134026488-134026613	ENSG00000226953.3
7	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953.3
8	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953.3
9	lnc-LYPD1-4	chr2:134148681-134148970	NONHSAT074547
10	lnc-GPR39-4	chr2:134026488-134026582	ENSG00000226953
11	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953
12	lnc-GPR39-4	chr2:134023767-134023868	ENSG00000226953
13	lnc-GPR39-4	chr2:134026488-134026613	ENSG00000226953
14	lnc-GPR39-4	chr2:134024845-134024996	NR_110294
15	lnc-GPR39-4	chr2:134042267-134042330	NR_110294
16	lnc-GPR39-4	chr2:134025928-134026014	NR_110294
17	lnc-GPR39-4	chr2:134022540-134022674	ENSG00000226953
18	lnc-GPR39-4	chr2:134042267-134042334	ENSG00000226953
19	lnc-LYPD1-1	chr2:134191067-134191468	ENSG00000232474.1
20	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953
21	lnc-LYPD1-1	chr2:134189237-134189388	ENSG00000232474.1

No data

Variant related genes	Relation type
NCKAP5-IT1	TF binding region
RNU6-579P	TF binding region
RN7SKP154	TF binding region
ENSG00000226953	TF binding region
NCKAP5-IT1	CpG island
RNU6-579P	CpG island
RN7SKP154	CpG island
ENSG00000226953	CpG island
ENSG00000150551	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000124243	chromatin interactions
ENSG00000080603	chromatin interactions
ENSG00000105662	chromatin interactions
ENSG00000222068	chromatin interactions
ENSG00000252688	chromatin interactions
ENSG00000176771	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000226953	chromatin interactions
IQCB1	miRNA target sites
CALU	miRNA target sites
ATOX1	miRNA target sites
LRIG1	miRNA target sites
TNFSF10	miRNA target sites
NFKB1	miRNA target sites
KIF23	miRNA target sites
SMCR7L	miRNA target sites
FNTA	miRNA target sites

Extended variants
information (count: 11324 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:11324 , 50 per page) page: 1 2 3 4 5 6 7 ... 227

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570145603	chr2:133906931-133906932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs16857341	chr2:133906942-133906943	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs142220886	chr2:133906996-133906997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533185639	chr2:133907003-133907004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538392153	chr2:133907004-133907005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs7605672	chr2:133907022-133907023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75781506	chr2:133907043-133907044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150790057	chr2:133907072-133907073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536459510	chr2:133907081-133907082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186393096	chr2:133907085-133907086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554437033	chr2:133907096-133907097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs13395452	chr2:133907137-133907138	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs12468373	chr2:133907141-133907142	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs17793177	chr2:133907151-133907152	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs370602835	chr2:133907152-133907153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549155549	chr2:133907163-133907164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs578069505	chr2:133907175-133907176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545550047	chr2:133907185-133907186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190189881	chr2:133907186-133907187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560147924	chr2:133907236-133907237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181850156	chr2:133907257-133907258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561279723	chr2:133907285-133907286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187382006	chr2:133907368-133907369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553781043	chr2:133907369-133907370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550057678	chr2:133907424-133907425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377407706	chr2:133907432-133907433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564565758	chr2:133907485-133907486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570497659	chr2:133907493-133907494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531965277	chr2:133907530-133907531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139156583	chr2:133907551-133907552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565786468	chr2:133907563-133907564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs16857345	chr2:133907588-133907589	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs548371608	chr2:133907622-133907623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76353891	chr2:133907638-133907639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537391743	chr2:133907680-133907681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558871677	chr2:133907731-133907732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145221314	chr2:133907744-133907745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73000829	chr2:133907856-133907857	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs73000831	chr2:133907863-133907864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572506162	chr2:133907864-133907865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114708331	chr2:133907866-133907867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561573791	chr2:133907918-133907919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576207512	chr2:133907933-133907934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543741072	chr2:133907961-133907962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79063840	chr2:133907980-133907981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147596833	chr2:133908000-133908001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191055063	chr2:133908101-133908102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547369578	chr2:133908176-133908177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35141307	chr2:133908177-133908178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183279157	chr2:133908209-133908210	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2285 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133887800-133912600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:133900200-133908200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:133904400-133913600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:133906800-133907400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:133908200-133909200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:133909200-133910600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:133910200-133911400	Enhancers	Liver	Liver
8	chr2:133910600-133911800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:133910600-133923000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:133911400-133914800	Weak transcription	Liver	Liver
11	chr2:133911800-133920600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:133912000-133913000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr2:133912600-133912800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:133912800-133917000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr2:133912800-133922600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:133914800-133915200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:133914800-133917400	Enhancers	Liver	Liver
18	chr2:133915200-133916400	Enhancers	HepG2	liver
19	chr2:133917000-133917200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr2:133917200-133919200	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr2:133920600-133921600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr2:133921600-133923600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:133922000-133923200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr2:133922600-133924800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:133923000-133924600	Enhancers	Osteobl	bone
26	chr2:133923000-133924800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:133923200-133923400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr2:133923400-133923800	Enhancers	NHDF-Ad	bronchial
29	chr2:133923600-133924200	Enhancers	Muscle Satellite Cultured Cells	--
30	chr2:133923600-133924400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr2:133923600-133937000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:133923800-133924400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:133923800-133924600	Weak transcription	NHDF-Ad	bronchial
34	chr2:133924600-133924800	Enhancers	NHDF-Ad	bronchial
35	chr2:133924600-133925400	Weak transcription	Osteobl	bone
36	chr2:133924800-133926000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:133924800-133932400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr2:133925400-133925600	Enhancers	Osteobl	bone
39	chr2:133925600-133932400	Weak transcription	Osteobl	bone
40	chr2:133926000-133928000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr2:133926400-133927200	Enhancers	Fetal Brain Male	brain
42	chr2:133927200-133928000	Enhancers	Pancreas	Pancrea
43	chr2:133927200-133931000	Weak transcription	Fetal Brain Male	brain
44	chr2:133927800-133928000	Enhancers	A549	lung
45	chr2:133927800-133928400	Enhancers	Brain Substantia Nigra	brain
46	chr2:133927800-133929000	Enhancers	Brain Anterior Caudate	brain
47	chr2:133928000-133929000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:133928200-133931200	Weak transcription	A549	lung
49	chr2:133929000-133929400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:133929000-133931800	Weak transcription	Brain Anterior Caudate	brain

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