Variant report

Variant	nsv535929
Chromosome Location	chr2:133930876-134055434
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:832)
CpG islands
(count:856)
Chromatin interactive
region (count:38)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:832 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr2:133958614-133959030	HCT-116	colon:	n/a	n/a
2	BACH1	chr2:134022701-134024075	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr2:134005181-134005429	GM12878	blood:	n/a	n/a
4	BCL3	chr2:134023525-134024142	A549	lung:	n/a	n/a
5	BCL3	chr2:134023499-134024135	A549	lung:	n/a	n/a
6	BRCA1	chr2:134004476-134004492	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr2:133958587-133958930	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr2:134022507-134023986	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr2:133958628-133959001	HCT-116	colon:	n/a	n/a
10	CBX3	chr2:133958614-133959033	HCT-116	colon:	n/a	n/a
11	CEBPB	chr2:134011419-134011757	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:134022735-134025209	Hela-S3	cervix:	n/a	chr2:134024205-134024216
13	CEBPB	chr2:134053980-134054421	Hela-S3	cervix:	n/a	chr2:134054150-134054163 chr2:134054152-134054163 chr2:134054150-134054163
14	CEBPB	chr2:133958646-133959106	HCT-116	colon:	n/a	chr2:133958814-133958825
15	CEBPB	chr2:133958590-133959360	Hela-S3	cervix:	n/a	chr2:133958814-133958825
16	CEBPB	chr2:133958461-133959335	A549	lung:	n/a	chr2:133958814-133958825
17	CEBPB	chr2:134051161-134051752	IMR90	lung:	n/a	chr2:134051271-134051288
18	CEBPB	chr2:133958611-133959057	A549	lung:	n/a	chr2:133958814-133958825
19	CEBPB	chr2:134028771-134028886	A549	lung:	n/a	n/a
20	CEBPB	chr2:133951692-133952052	IMR90	lung:	n/a	chr2:133951845-133951856
21	CEBPB	chr2:134054015-134054327	IMR90	lung:	n/a	chr2:134054150-134054163 chr2:134054152-134054163 chr2:134054150-134054163
22	CEBPB	chr2:134043952-134044155	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:133998771-133999171	IMR90	lung:	n/a	chr2:133999017-133999028
24	CEBPB	chr2:133951727-133952071	A549	lung:	n/a	chr2:133951845-133951856
25	CEBPB	chr2:134043848-134044248	MCF-7	breast:	n/a	n/a
26	CEBPB	chr2:133958623-133959309	IMR90	lung:	n/a	chr2:133958814-133958825
27	CEBPB	chr2:133951704-133952046	HepG2	liver:	n/a	chr2:133951845-133951856
28	CEBPB	chr2:133956313-133956548	HepG2	liver:	n/a	chr2:133956438-133956449
29	CEBPB	chr2:134003450-134003684	A549	lung:	n/a	chr2:134003550-134003561
30	CEBPB	chr2:134043975-134044199	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:133956284-133956587	A549	lung:	n/a	chr2:133956438-133956449
32	CEBPB	chr2:133958819-133958836	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:134043852-134044617	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:134043932-134044239	A549	lung:	n/a	n/a
35	CEBPB	chr2:133964466-133964533	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr2:134003410-134003684	IMR90	lung:	n/a	chr2:134003550-134003561
37	CEBPB	chr2:134043906-134044270	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:134003426-134003717	HepG2	liver:	n/a	chr2:134003550-134003561
39	CEBPB	chr2:134000488-134000570	A549	lung:	n/a	n/a
40	CEBPB	chr2:133951548-133952193	A549	lung:	n/a	chr2:133951845-133951856
41	CEBPB	chr2:133958624-133959238	A549	lung:	n/a	chr2:133958814-133958825
42	CEBPB	chr2:134043877-134044226	MCF-7	breast:	n/a	n/a
43	CEBPB	chr2:133956290-133956581	Hela-S3	cervix:	n/a	chr2:133956438-133956449
44	CEBPB	chr2:133951683-133952095	A549	lung:	n/a	chr2:133951845-133951856
45	CEBPB	chr2:134045260-134045655	IMR90	lung:	n/a	n/a
46	CEBPB	chr2:134044066-134044190	K562	blood:	n/a	n/a
47	CEBPB	chr2:134043889-134044238	A549	lung:	n/a	n/a
48	CEBPB	chr2:134000355-134000651	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:134024047-134024339	IMR90	lung:	n/a	chr2:134024205-134024216
50	CEBPB	chr2:133958606-133959047	HCT-116	colon:	n/a	chr2:133958814-133958825

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:134024266-134024316	GM12878	blood:	n/a
2	chr2:134004614-134004664	CMK	blood:	n/a
3	chr2:134024266-134024316	GM12878	blood:	n/a
4	chr2:134004614-134004664	CMK	blood:	n/a
5	chr2:134024266-134024316	HEK293	kidney:	embryo
6	chr2:133934804-133934854	AG04450	lung:	fetal
7	chr2:134024266-134024316	ProgFib	skin:	n/a
8	chr2:134020041-134020091	SK-N-MC	brain:	n/a
9	chr2:134028440-134028490	IMR90	lung:	fetal
10	chr2:134020041-134020091	SAEC	small airway:	n/a
11	chr2:134010875-134010925	PrEC	prostate:	n/a
12	chr2:134024266-134024316	BJ	skin:	n/a
13	chr2:134023210-134023260	HAEpiC	amniotic membrane:	n/a
14	chr2:133998732-133998782	SKMC	muscle:	n/a
15	chr2:134024459-134024509	GM19239	blood:	n/a
16	chr2:134023210-134023260	BE2_C	brain:	n/a
17	chr2:133934804-133934854	ProgFib	skin:	n/a
18	chr2:134024418-134024468	HCM	heart:	n/a
19	chr2:134010875-134010925	AG09319	gingival:	n/a
20	chr2:133934804-133934854	HRCEpiC	kidney:	n/a
21	chr2:134028440-134028490	LNCaP	prostate:	n/a
22	chr2:134010875-134010925	HRE	kidney:	n/a
23	chr2:134028440-134028490	NHBE	bronchial:	n/a
24	chr2:134028440-134028490	NH-A	brain:	n/a
25	chr2:134024418-134024468	T-47D	breast:	n/a
26	chr2:134024266-134024316	Hela-S3	cervix:	n/a
27	chr2:134004614-134004664	SK-N-SH_RA	brain:	n/a
28	chr2:134024093-134024143	HEEpiC	esophagus:	n/a
29	chr2:133998732-133998782	Hepatocyte	liver:	n/a
30	chr2:134024093-134024143	SK-N-SH_RA	brain:	n/a
31	chr2:134024459-134024509	PFSK-1	brain:	n/a
32	chr2:134023210-134023260	SAEC	small airway:	n/a
33	chr2:134010875-134010925	K562	blood:	n/a
34	chr2:134024459-134024509	SK-N-MC	brain:	n/a
35	chr2:134024266-134024316	GM19239	blood:	n/a
36	chr2:134024459-134024509	K562	blood:	n/a
37	chr2:134023662-134023712	SKMC	muscle:	n/a
38	chr2:134023662-134023712	PANC-1	pancreas:	n/a
39	chr2:134024266-134024316	AG09309	skin:	n/a
40	chr2:134024459-134024509	AG04449	skin:	fetal
41	chr2:134023662-134023712	SAEC	small airway:	n/a
42	chr2:134028440-134028490	T-47D	breast:	n/a
43	chr2:134023662-134023712	SK-N-SH	brain:	n/a
44	chr2:134052012-134052062	AG04449	skin:	fetal
45	chr2:133998732-133998782	ProgFib	skin:	n/a
46	chr2:134024093-134024143	T-47D	breast:	n/a
47	chr2:134020041-134020091	RPTEC	kidney:	n/a
48	chr2:134024266-134024316	SK-N-SH	brain:	n/a
49	chr2:133998732-133998782	GM06990	blood:	n/a
50	chr2:134024093-134024143	AG10803	skin:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:134035082..134037430-chr2:134042512..134044195,2	MCF-7	breast:
2	chr2:133999579..134001370-chr2:134029081..134031077,2	K562	blood:
3	chr2:133953064..133954873-chr2:134023809..134025378,2	MCF-7	breast:
4	chr16:30709997..30710818-chr2:134023319..134023932,2	Hela-S3	cervix:
5	chr2:134020179..134020906-chr2:134601878..134602419,2	MCF-7	breast:
6	chr2:134019393..134021124-chr2:134030265..134032879,2	K562	blood:
7	chr2:133980114..133981949-chr2:133983146..133984842,2	MCF-7	breast:
8	chr2:134003474..134006247-chr2:134007339..134011249,3	MCF-7	breast:
9	chr2:133978989..133981496-chr2:133987532..133990158,2	MCF-7	breast:
10	chr2:134038890..134041623-chr2:134041735..134044144,2	MCF-7	breast:
11	chr2:133978989..133981496-chr2:133987532..133990158,2	MCF-7	breast:
12	chr2:133999579..134001370-chr2:134029081..134031077,2	K562	blood:
13	chr16:64509112..64511965-chr2:133985884..133987569,2	MCF-7	breast:
14	chr19:18793804..18794673-chr2:134023005..134023895,2	Hela-S3	cervix:
15	chr2:134003474..134006247-chr2:134007339..134011249,3	MCF-7	breast:
16	chr2:133932748..133934866-chr2:133936195..133938875,2	MCF-7	breast:
17	chr2:133932748..133934866-chr2:133936195..133938875,2	MCF-7	breast:
18	chr2:134019393..134021124-chr2:134030265..134032879,2	K562	blood:
19	chr2:134019056..134021492-chr2:134262374..134264487,2	MCF-7	breast:
20	chr2:134020528..134022424-chr2:134324632..134327514,2	MCF-7	breast:
21	chr2:134028269..134031265-chr2:134033002..134035310,2	MCF-7	breast:
22	chr2:134028269..134031265-chr2:134033002..134035310,2	MCF-7	breast:
23	chr2:134020255..134021142-chr2:134318343..134319277,2	MCF-7	breast:
24	chr2:134033733..134036491-chr2:134192911..134194605,2	MCF-7	breast:
25	chr2:134015404..134018015-chr2:134019119..134021924,2	MCF-7	breast:
26	chr2:133426638..133429342-chr2:133954852..133957761,2	MCF-7	breast:
27	chr1:154946346..154946996-chr2:134023337..134024323,2	Hela-S3	cervix:
28	chr2:134035082..134037430-chr2:134042512..134044195,2	MCF-7	breast:
29	chr2:134031322..134033202-chr2:134041949..134044223,2	MCF-7	breast:
30	chr2:134031322..134033202-chr2:134041949..134044223,2	MCF-7	breast:
31	chr2:134015404..134018015-chr2:134019119..134021924,2	MCF-7	breast:
32	chr2:133980114..133981949-chr2:133983146..133984842,2	MCF-7	breast:
33	chr2:133969380..133971037-chr2:133972484..133974149,2	MCF-7	breast:
34	chr2:133969380..133971037-chr2:133972484..133974149,2	MCF-7	breast:
35	chr2:134020208..134021163-chr2:134537454..134538295,5	MCF-7	breast:
36	chr2:134020041..134020759-chr2:134398921..134399467,2	MCF-7	breast:
37	chr2:134020760..134021325-chr2:134537400..134538161,2	K562	blood:
38	chr2:134038890..134041623-chr2:134041735..134044144,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 4351 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4351 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539800958	chr2:133930878-133930879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs138622718	chr2:133930901-133930902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573256438	chr2:133930916-133930917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557735591	chr2:133930947-133930948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114197540	chr2:133930960-133930961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555909231	chr2:133930972-133930973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs111695454	chr2:133931003-133931004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181617321	chr2:133931164-133931165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs9287424	chr2:133931214-133931215	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs184689750	chr2:133931219-133931220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141651266	chr2:133931341-133931342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146199999	chr2:133931357-133931358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540334671	chr2:133931385-133931386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147987164	chr2:133931387-133931388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563039646	chr2:133931394-133931395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550182233	chr2:133931462-133931463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548933119	chr2:133931473-133931474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201748223	chr2:133931527-133931528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561133642	chr2:133931543-133931544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189475690	chr2:133931546-133931547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573909092	chr2:133931548-133931549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533750937	chr2:133931549-133931550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550105909	chr2:133931599-133931600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571518579	chr2:133931609-133931610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10206887	chr2:133931611-133931612	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs551785892	chr2:133931637-133931638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562809431	chr2:133931650-133931651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542235046	chr2:133931656-133931657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34651882	chr2:133931678-133931679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375305604	chr2:133931711-133931712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369368592	chr2:133931771-133931772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566882886	chr2:133931793-133931794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141611434	chr2:133931802-133931803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6722535	chr2:133931881-133931882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs6750290	chr2:133931956-133931957	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs73000868	chr2:133931992-133931993	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs62180668	chr2:133932011-133932012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs6722768	chr2:133932031-133932032	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs549089607	chr2:133932115-133932116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150914290	chr2:133932198-133932199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553706550	chr2:133932228-133932229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572092841	chr2:133932251-133932252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542697426	chr2:133932259-133932260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560778116	chr2:133932273-133932274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs71909848	chr2:133932274-133932275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs398060551	chr2:133932286-133932287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35751471	chr2:133932287-133932288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546498041	chr2:133932288-133932289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369457535	chr2:133932289-133932290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34523356	chr2:133932290-133932291	Weak transcription	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:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133923600-133937000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:133924800-133932400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr2:133925600-133932400	Weak transcription	Osteobl	bone
4	chr2:133927200-133931000	Weak transcription	Fetal Brain Male	brain
5	chr2:133928200-133931200	Weak transcription	A549	lung
6	chr2:133929000-133931800	Weak transcription	Brain Anterior Caudate	brain
7	chr2:133929400-133934800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:133930600-133931400	Enhancers	Liver	Liver
9	chr2:133931000-133931200	Enhancers	Fetal Brain Male	brain
10	chr2:133931200-133931400	Enhancers	A549	lung
11	chr2:133931400-133935000	Weak transcription	Liver	Liver
12	chr2:133932400-133933400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr2:133932400-133933600	Enhancers	Osteobl	bone
14	chr2:133932400-133933800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr2:133932800-133933200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr2:133933200-133934800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:133933400-133933800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr2:133933400-133935000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr2:133933600-133934800	Weak transcription	Osteobl	bone
20	chr2:133934200-133935200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:133934800-133935200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:133934800-133935200	Enhancers	Osteobl	bone
23	chr2:133934800-133935400	Enhancers	NHLF	lung
24	chr2:133934800-133935600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:133934800-133935600	Enhancers	Gastric	stomach
26	chr2:133934800-133935600	Enhancers	Ovary	ovary
27	chr2:133935000-133935400	Enhancers	Liver	Liver
28	chr2:133935000-133935600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr2:133935200-133935400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:133935400-133935600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr2:133935600-133935800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr2:133935600-133937600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:133935800-133938600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr2:133937000-133937400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:133937200-133937800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:133937400-133937600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:133937600-133938200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:133937600-133938400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:133943600-133946000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:133946000-133949000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:133949600-133951000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:133950200-133950800	Enhancers	Liver	Liver
43	chr2:133950800-133951000	Flanking Active TSS	A549	lung
44	chr2:133950800-133952600	Flanking Active TSS	Liver	Liver
45	chr2:133951000-133951600	Enhancers	A549	lung
46	chr2:133951000-133954000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr2:133951600-133951800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr2:133951600-133952200	Flanking Active TSS	A549	lung
49	chr2:133951800-133952000	Enhancers	NHLF	lung
50	chr2:133951800-133952200	Enhancers	HUVEC	blood vessel

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