Variant report

Variant	esv32731
Chromosome Location	chr2:37949762-38014411
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:651)
CpG islands
(count:733)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37991365-37991558	K562	blood:	n/a	n/a
2	ARID3A	chr2:38008255-38008449	K562	blood:	n/a	n/a
3	ARID3A	chr2:38008289-38008447	HepG2	liver:	n/a	n/a
4	ATF1	chr2:38008194-38008403	K562	blood:	n/a	n/a
5	ATF3	chr2:37995433-37996168	A549	lung:	n/a	n/a
6	ATF3	chr2:37995406-37996129	A549	lung:	n/a	n/a
7	BCL11A	chr2:37962705-37962895	GM12878	blood:	n/a	n/a
8	BCL3	chr2:37984248-37984605	GM12878	blood:	n/a	n/a
9	BCL3	chr2:37995243-37996336	A549	lung:	n/a	n/a
10	BCL3	chr2:37995167-37996320	A549	lung:	n/a	n/a
11	BCL3	chr2:37995811-37996081	GM12878	blood:	n/a	n/a
12	BCL3	chr2:37993027-37993826	A549	lung:	n/a	chr2:37993597-37993606
13	BHLHE40	chr2:37991364-37991559	K562	blood:	n/a	n/a
14	CEBPB	chr2:37995121-37995973	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:37958826-37959080	K562	blood:	n/a	chr2:37958919-37958930
16	CEBPB	chr2:37962124-37962469	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:38010242-38010354	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:37979966-37980544	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:37977457-37977649	K562	blood:	n/a	n/a
20	CEBPB	chr2:37995096-37996236	A549	lung:	n/a	n/a
21	CEBPB	chr2:37980380-37980532	K562	blood:	n/a	n/a
22	CEBPB	chr2:37980323-37980575	A549	lung:	n/a	n/a
23	CEBPB	chr2:37995107-37996126	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:38009717-38009981	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:37993064-37993861	A549	lung:	n/a	n/a
26	CEBPB	chr2:38003700-38004019	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:37979935-37980527	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:37958770-37959005	Hela-S3	cervix:	n/a	chr2:37958919-37958930
29	CEBPB	chr2:37958768-37959040	IMR90	lung:	n/a	chr2:37958919-37958930
30	CEBPB	chr2:37977395-37977710	MCF-7	breast:	n/a	n/a
31	CEBPB	chr2:37977492-37977692	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr2:38014155-38014275	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:37958765-37959048	A549	lung:	n/a	chr2:37958919-37958930
34	CEBPB	chr2:37977474-37977568	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:37980414-37980446	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr2:37995384-37995863	MCF-7	breast:	n/a	n/a
37	CEBPB	chr2:37995436-37996046	A549	lung:	n/a	n/a
38	CEBPB	chr2:37958749-37959043	HepG2	liver:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
39	CEBPB	chr2:37958731-37959009	MCF-7	breast:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
40	CHD2	chr2:37965707-37965907	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr2:37995538-37996021	A549	lung:	n/a	n/a
42	CREB1	chr2:37995443-37995913	A549	lung:	n/a	n/a
43	CTCF	chr2:37959340-37959490	GM12873	blood:	n/a	n/a
44	CTCF	chr2:38005280-38005430	GM12871	blood:	n/a	n/a
45	CTCF	chr2:37974527-37974579	MCF-7	breast:	n/a	n/a
46	CTCF	chr2:37965360-37965510	Caco-2	colon:	n/a	n/a
47	CTCF	chr2:37959400-37959550	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr2:37974260-37974410	GM12873	blood:	n/a	n/a
49	CTCF	chr2:37998740-37998890	AG10803	skin:	n/a	n/a
50	CTCF	chr2:37995800-37995950	SK-N-SH_RA	brain:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:38003689-38003739	Jurkat	blood:	n/a
2	chr2:38003689-38003739	Jurkat	blood:	n/a
3	chr2:37969786-37969836	HEEpiC	esophagus:	n/a
4	chr2:37996000-37996050	ProgFib	skin:	n/a
5	chr2:37996000-37996050	T-47D	breast:	n/a
6	chr2:37993353-37993403	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:37985316-37985366	AG09319	gingival:	n/a
8	chr2:38001560-38001610	NHBE	bronchial:	n/a
9	chr2:38009031-38009081	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:37997383-37997433	U87	brain:	n/a
11	chr2:38001560-38001610	PANC-1	pancreas:	n/a
12	chr2:38001560-38001610	GM19239	blood:	n/a
13	chr2:37969786-37969836	ovcar-3	ovarian:	n/a
14	chr2:38006837-38006887	Hepatocyte	liver:	n/a
15	chr2:37985316-37985366	HCT-116	colon:	n/a
16	chr2:37962248-37962298	U87	brain:	n/a
17	chr2:38004845-38004895	HNPCEpiC	eye:	n/a
18	chr2:38011852-38011902	AG04450	lung:	fetal
19	chr2:38004845-38004895	HIPEpiC	eye:	n/a
20	chr2:37985316-37985366	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:37997383-37997433	AG09319	gingival:	n/a
22	chr2:38006837-38006887	SK-N-SH	brain:	n/a
23	chr2:37962248-37962298	NHDF-neo	bronchial:	n/a
24	chr2:38003689-38003739	PFSK-1	brain:	n/a
25	chr2:37985316-37985366	HCPEpiC	choroid plexus:	n/a
26	chr2:37985316-37985366	ECC-1	luminal epithelium:	n/a
27	chr2:37996000-37996050	GM12891	blood:	n/a
28	chr2:38003689-38003739	HCT-116	colon:	n/a
29	chr2:37993353-37993403	PFSK-1	brain:	n/a
30	chr2:38001560-38001610	Caco-2	colon:	n/a
31	chr2:38006837-38006887	SKMC	muscle:	n/a
32	chr2:38009031-38009081	A549	lung:	n/a
33	chr2:37962248-37962298	SK-N-SH_RA	brain:	n/a
34	chr2:37997383-37997433	PrEC	prostate:	n/a
35	chr2:37962248-37962298	ovcar-3	ovarian:	n/a
36	chr2:38006837-38006887	HCPEpiC	choroid plexus:	n/a
37	chr2:38011852-38011902	NT2-D1	testis:	n/a
38	chr2:37997383-37997433	BE2_C	brain:	n/a
39	chr2:38001560-38001610	HL-60	blood:	n/a
40	chr2:38009031-38009081	K562	blood:	n/a
41	chr2:37962248-37962298	HL-60	blood:	n/a
42	chr2:37962248-37962298	NT2-D1	testis:	n/a
43	chr2:37997383-37997433	AoSMC	blood vessel:	n/a
44	chr2:38004845-38004895	HMEC	breast:	n/a
45	chr2:38001560-38001610	U87	brain:	n/a
46	chr2:37993353-37993403	ECC-1	luminal epithelium:	n/a
47	chr2:38001560-38001610	GM12891	blood:	n/a
48	chr2:38001560-38001610	Hepatocyte	liver:	n/a
49	chr2:38011852-38011902	SK-N-SH	brain:	n/a
50	chr2:38009031-38009081	HRCEpiC	kidney:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:38014081..38015700-chr2:38016379..38018909,2	K562	blood:
2	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:
3	chr2:38009523..38011432-chr2:38018601..38021487,2	MCF-7	breast:
4	chr2:38008016..38010858-chr2:38012069..38014697,2	MCF-7	breast:
5	chr2:37993752..37996799-chr2:38014077..38017922,3	MCF-7	breast:
6	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:
7	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:
8	chr2:37887391..37889613-chr2:38000617..38003018,2	K562	blood:
9	chr2:38000546..38002739-chr2:38022244..38024636,2	MCF-7	breast:
10	chr2:38008016..38010858-chr2:38012069..38014697,2	MCF-7	breast:
11	chr2:37992911..37994888-chr2:37999261..38002227,2	MCF-7	breast:
12	chr2:37958368..37961444-chr2:37963169..37965814,4	K562	blood:
13	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
14	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:
15	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
16	chr2:37992911..37994888-chr2:37999261..38002227,2	MCF-7	breast:
17	chr2:37958368..37961673-chr2:37962589..37965814,3	K562	blood:
18	chr2:37961835..37963512-chr2:37971098..37973001,2	MCF-7	breast:
19	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
20	chr2:37992694..37995245-chr2:38016725..38019213,2	MCF-7	breast:
21	chr2:37896203..37899196-chr2:37994735..37996425,2	MCF-7	breast:
22	chr2:37903809..37907927-chr2:37994371..37997035,4	MCF-7	breast:
23	chr2:37995679..37997775-chr2:38028677..38031407,2	MCF-7	breast:
24	chr2:37993752..37996799-chr2:38014077..38017922,3	MCF-7	breast:
25	chr2:37965210..37967124-chr2:37973295..37975217,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKD3-1	chr2:37956758-37956921	NONHSAT070140
2	lnc-FAM82A1-3	chr2:37971476-37971786	XLOC_001431
3	lnc-FAM82A1-3	chr2:37974117-37974189	XLOC_001431
4	lnc-PRKD3-1	chr2:37956390-37956510	NONHSAT070138

No data

Variant related genes	Relation type
ENSG00000236572	TF binding region
CDC42EP3	TF binding region
ENSG00000236572	CpG island
CDC42EP3	CpG island
ENSG00000236572	chromatin interactions
ENSG00000163171	chromatin interactions
ACVR2B	miRNA target sites

Extended variants
information (count: 4480 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:4480 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543545464	chr2:37949762-37949763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs369338260	chr2:37949776-37949777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577700507	chr2:37949796-37949797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534613785	chr2:37956444-37956445	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs367599170	chr2:37956449-37956450	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs533157301	chr2:37956450-37956451	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs2373296	chr2:37956452-37956453	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs543925938	chr2:37956458-37956459	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs562112583	chr2:37956460-37956461	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs140115041	chr2:37956462-37956463	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs67715405	chr2:37956469-37956470	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs529679927	chr2:37956484-37956485	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs181011265	chr2:37956804-37956805	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs571076642	chr2:37956818-37956819	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs72880736	chr2:37956841-37956842	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs556679038	chr2:37956843-37956844	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs144559132	chr2:37956903-37956904	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs74613555	chr2:37957804-37957805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182333403	chr2:37957809-37957810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186509603	chr2:37957830-37957831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571131634	chr2:37957834-37957835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140190509	chr2:37957856-37957857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77340358	chr2:37957919-37957920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556292608	chr2:37957953-37957954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574559740	chr2:37957958-37957959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534319512	chr2:37957965-37957966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535673403	chr2:37958012-37958013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116352358	chr2:37958044-37958045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572216794	chr2:37958066-37958067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs199659849	chr2:37958083-37958084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374024249	chr2:37958100-37958101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115124959	chr2:37958112-37958113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192519306	chr2:37958140-37958141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs79345540	chr2:37958155-37958156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77893629	chr2:37958159-37958160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78657079	chr2:37958161-37958162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79685244	chr2:37958165-37958166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145856398	chr2:37958185-37958186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184608584	chr2:37958195-37958196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75470065	chr2:37958213-37958214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75025392	chr2:37958217-37958218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76377072	chr2:37958220-37958221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568465259	chr2:37958229-37958230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75941057	chr2:37958256-37958257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs80252098	chr2:37958259-37958260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs75382848	chr2:37958269-37958270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs75957030	chr2:37958271-37958272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529451251	chr2:37958286-37958287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79198444	chr2:37958288-37958289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72795780	chr2:37958299-37958300	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37947200-37949800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:37957800-37959000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:37958400-37959800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:37958800-37959000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr2:37958800-37959000	Enhancers	Stomach Smooth Muscle	stomach
6	chr2:37958800-37963600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr2:37959000-37959600	Enhancers	Fetal Muscle Leg	muscle
8	chr2:37959000-37960000	Enhancers	NHDF-Ad	bronchial
9	chr2:37959000-37960800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr2:37959000-37961200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:37959000-37961600	Enhancers	Fetal Heart	heart
12	chr2:37959000-37965000	Enhancers	Fetal Kidney	kidney
13	chr2:37959200-37959400	Enhancers	Colon Smooth Muscle	Colon
14	chr2:37959200-37959400	Enhancers	Osteobl	bone
15	chr2:37959200-37959800	Enhancers	Fetal Stomach	stomach
16	chr2:37959200-37961000	Weak transcription	Stomach Smooth Muscle	stomach
17	chr2:37959400-37959600	Enhancers	Rectal Smooth Muscle	rectum
18	chr2:37959400-37959800	Enhancers	Aorta	Aorta
19	chr2:37959400-37960400	Weak transcription	Colon Smooth Muscle	Colon
20	chr2:37959400-37961200	Weak transcription	Osteobl	bone
21	chr2:37959600-37962000	Weak transcription	Fetal Muscle Leg	muscle
22	chr2:37959800-37960000	Enhancers	Right Ventricle	heart
23	chr2:37959800-37960800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr2:37959800-37961000	Weak transcription	Fetal Stomach	stomach
25	chr2:37959800-37961000	Weak transcription	Rectal Smooth Muscle	rectum
26	chr2:37959800-37962000	Weak transcription	Aorta	Aorta
27	chr2:37960000-37960400	Weak transcription	NHDF-Ad	bronchial
28	chr2:37960000-37961200	Weak transcription	Right Ventricle	heart
29	chr2:37960000-37962000	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr2:37960400-37961600	Enhancers	NHDF-Ad	bronchial
31	chr2:37960400-37963400	Enhancers	Colon Smooth Muscle	Colon
32	chr2:37960800-37961400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr2:37960800-37961600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:37960800-37965800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr2:37961000-37961400	Enhancers	Fetal Stomach	stomach
36	chr2:37961000-37962000	Enhancers	Stomach Smooth Muscle	stomach
37	chr2:37961000-37963000	Enhancers	Rectal Smooth Muscle	rectum
38	chr2:37961200-37961400	Enhancers	H9 Cell Line	embryonic stem cell
39	chr2:37961200-37961400	Enhancers	Left Ventricle	heart
40	chr2:37961200-37961400	Enhancers	Right Ventricle	heart
41	chr2:37961200-37961600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr2:37961200-37962000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr2:37961200-37962000	Enhancers	Osteobl	bone
44	chr2:37961200-37962200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:37961200-37962600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr2:37961200-37963000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr2:37961200-37963400	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr2:37961200-37963600	Enhancers	Muscle Satellite Cultured Cells	--
49	chr2:37961400-37961600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:37961400-37962600	Weak transcription	Fetal Stomach	stomach

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