Variant report

Variant	esv2756077
Chromosome Location	chr2:37920941-37998864
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:720)
CpG islands
(count:550)
Chromatin interactive
region (count:23)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	chr2:37940290-37940750	K562	blood:	n/a	n/a
3	ARID3A	chr2:37945884-37946232	K562	blood:	n/a	n/a
4	ATF1	chr2:37940479-37940807	K562	blood:	n/a	n/a
5	ATF1	chr2:37938545-37938858	K562	blood:	n/a	n/a
6	ATF1	chr2:37945872-37946265	K562	blood:	n/a	n/a
7	ATF3	chr2:37995406-37996129	A549	lung:	n/a	n/a
8	ATF3	chr2:37995433-37996168	A549	lung:	n/a	n/a
9	BCL11A	chr2:37962705-37962895	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:37940546-37940813	GM12878	blood:	n/a	n/a
11	BCL3	chr2:37995243-37996336	A549	lung:	n/a	n/a
12	BCL3	chr2:37995811-37996081	GM12878	blood:	n/a	n/a
13	BCL3	chr2:37995167-37996320	A549	lung:	n/a	n/a
14	BCL3	chr2:37993027-37993826	A549	lung:	n/a	chr2:37993597-37993606
15	BCL3	chr2:37984248-37984605	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:37991364-37991559	K562	blood:	n/a	n/a
17	BHLHE40	chr2:37945886-37946387	K562	blood:	n/a	n/a
18	BHLHE40	chr2:37938610-37938663	K562	blood:	n/a	n/a
19	CBX3	chr2:37945729-37946316	K562	blood:	n/a	n/a
20	CCNT2	chr2:37945975-37946199	K562	blood:	n/a	n/a
21	CCNT2	chr2:37940581-37940741	K562	blood:	n/a	n/a
22	CEBPB	chr2:37980323-37980575	A549	lung:	n/a	n/a
23	CEBPB	chr2:37928487-37928584	K562	blood:	n/a	chr2:37928542-37928553
24	CEBPB	chr2:37993064-37993861	A549	lung:	n/a	n/a
25	CEBPB	chr2:37940527-37940702	K562	blood:	n/a	n/a
26	CEBPB	chr2:37977492-37977692	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:37958770-37959005	Hela-S3	cervix:	n/a	chr2:37958919-37958930
28	CEBPB	chr2:37948104-37948290	A549	lung:	n/a	n/a
29	CEBPB	chr2:37938535-37938821	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr2:37977395-37977710	MCF-7	breast:	n/a	n/a
31	CEBPB	chr2:37940453-37940854	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:37940535-37940788	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr2:37958765-37959048	A549	lung:	n/a	chr2:37958919-37958930
34	CEBPB	chr2:37945981-37946153	K562	blood:	n/a	n/a
35	CEBPB	chr2:37995096-37996236	A549	lung:	n/a	n/a
36	CEBPB	chr2:37979935-37980527	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:37938554-37939655	IMR90	lung:	n/a	chr2:37939317-37939329
38	CEBPB	chr2:37958749-37959043	HepG2	liver:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
39	CEBPB	chr2:37928474-37928610	HepG2	liver:	n/a	chr2:37928542-37928553
40	CEBPB	chr2:37928394-37928689	IMR90	lung:	n/a	chr2:37928542-37928553
41	CEBPB	chr2:37977474-37977568	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr2:37995121-37995973	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr2:37958826-37959080	K562	blood:	n/a	chr2:37958919-37958930
44	CEBPB	chr2:37940502-37940827	K562	blood:	n/a	n/a
45	CEBPB	chr2:37928502-37928667	Hela-S3	cervix:	n/a	chr2:37928542-37928553
46	CEBPB	chr2:37928450-37928683	A549	lung:	n/a	chr2:37928542-37928553
47	CEBPB	chr2:37995107-37996126	IMR90	lung:	n/a	n/a
48	CEBPB	chr2:37977457-37977649	K562	blood:	n/a	n/a
49	CEBPB	chr2:37995384-37995863	MCF-7	breast:	n/a	n/a
50	CEBPB	chr2:37958731-37959009	MCF-7	breast:	n/a	chr2:37958919-37958930 chr2:37958758-37958766

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37985316-37985366	Hela-S3	cervix:	n/a
2	chr2:37985316-37985366	Hela-S3	cervix:	n/a
3	chr2:37962248-37962298	Hepatocyte	liver:	n/a
4	chr2:37927157-37927207	A549	lung:	n/a
5	chr2:37997383-37997433	NHDF-neo	bronchial:	n/a
6	chr2:37962248-37962298	HIPEpiC	eye:	n/a
7	chr2:37927157-37927207	ovcar-3	ovarian:	n/a
8	chr2:37997383-37997433	HRPEpiC	eye:	n/a
9	chr2:37927157-37927207	MCF-7	breast:	n/a
10	chr2:37969786-37969836	SAEC	small airway:	n/a
11	chr2:37969786-37969836	NH-A	brain:	n/a
12	chr2:37997383-37997433	MCF-7	breast:	n/a
13	chr2:37927157-37927207	PANC-1	pancreas:	n/a
14	chr2:37948491-37948541	Hepatocyte	liver:	n/a
15	chr2:37938640-37938690	SKMC	muscle:	n/a
16	chr2:37985316-37985366	HCF	heart:	n/a
17	chr2:37997383-37997433	NHBE	bronchial:	n/a
18	chr2:37948491-37948541	MCF-7	breast:	n/a
19	chr2:37969786-37969836	A549	lung:	n/a
20	chr2:37997383-37997433	HCT-116	colon:	n/a
21	chr2:37962248-37962298	HMEC	breast:	n/a
22	chr2:37985316-37985366	Jurkat	blood:	n/a
23	chr2:37985316-37985366	ProgFib	skin:	n/a
24	chr2:37969786-37969836	GM06990	blood:	n/a
25	chr2:37962248-37962298	NB4	blood:	n/a
26	chr2:37948491-37948541	NT2-D1	testis:	n/a
27	chr2:37927157-37927207	T-47D	breast:	n/a
28	chr2:37993353-37993403	HCF	heart:	n/a
29	chr2:37927157-37927207	RPTEC	kidney:	n/a
30	chr2:37996000-37996050	PrEC	prostate:	n/a
31	chr2:37996000-37996050	GM06990	blood:	n/a
32	chr2:37962248-37962298	ProgFib	skin:	n/a
33	chr2:37993353-37993403	NT2-D1	testis:	n/a
34	chr2:37997383-37997433	HRE	kidney:	n/a
35	chr2:37997383-37997433	GM12892	blood:	n/a
36	chr2:37996000-37996050	HUVEC	blood vessel:	n/a
37	chr2:37948491-37948541	GM12892	blood:	n/a
38	chr2:37938640-37938690	SAEC	small airway:	n/a
39	chr2:37969786-37969836	GM19239	blood:	n/a
40	chr2:37948491-37948541	HCM	heart:	n/a
41	chr2:37997383-37997433	RPTEC	kidney:	n/a
42	chr2:37985316-37985366	HCT-116	colon:	n/a
43	chr2:37962248-37962298	HRE	kidney:	n/a
44	chr2:37948491-37948541	HRPEpiC	eye:	n/a
45	chr2:37996000-37996050	RPTEC	kidney:	n/a
46	chr2:37993353-37993403	SAEC	small airway:	n/a
47	chr2:37997383-37997433	HCF	heart:	n/a
48	chr2:37996000-37996050	K562	blood:	n/a
49	chr2:37985316-37985366	AG10803	skin:	n/a
50	chr2:37962248-37962298	HCT-116	colon:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:37993752..37996799-chr2:38014077..38017922,3	MCF-7	breast:
2	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
3	chr2:37896203..37899196-chr2:37994735..37996425,2	MCF-7	breast:
4	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
5	chr2:37919594..37922588-chr2:37925498..37927589,2	K562	blood:
6	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
7	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
8	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:
9	chr2:37897696..37900309-chr2:37936640..37940177,3	MCF-7	breast:
10	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
11	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:
12	chr2:37995679..37997775-chr2:38028677..38031407,2	MCF-7	breast:
13	chr2:37992694..37995245-chr2:38016725..38019213,2	MCF-7	breast:
14	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:
15	chr2:37965210..37967124-chr2:37973295..37975217,2	MCF-7	breast:
16	chr2:37992911..37994888-chr2:37999261..38002227,2	MCF-7	breast:
17	chr2:37958368..37961444-chr2:37963169..37965814,4	K562	blood:
18	chr2:37961835..37963512-chr2:37971098..37973001,2	MCF-7	breast:
19	chr2:37919594..37922588-chr2:37925498..37927589,2	K562	blood:
20	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
21	chr2:37903809..37907927-chr2:37994371..37997035,4	MCF-7	breast:
22	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:
23	chr2:37958368..37961673-chr2:37962589..37965814,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM82A1-3	chr2:37971476-37971786	XLOC_001431
2	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070138
3	lnc-PRKD3-1	chr2:37956758-37956921	NONHSAT070140
4	lnc-PRKD3-1	chr2:37956390-37956510	NONHSAT070138
5	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070140
6	lnc-FAM82A1-3	chr2:37974117-37974189	XLOC_001431

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: 4801 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:4801 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4993338	chr2:37920941-37920942	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76085276	chr2:37920957-37920958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539315159	chr2:37920958-37920959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185472839	chr2:37920989-37920990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188101058	chr2:37921005-37921006	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs182473267	chr2:37921028-37921029	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs139311965	chr2:37921035-37921036	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs555022869	chr2:37921047-37921048	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs573019413	chr2:37921062-37921063	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs375398133	chr2:37921093-37921094	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs567358734	chr2:37921097-37921098	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs187043559	chr2:37921154-37921155	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs530603358	chr2:37921227-37921228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552278589	chr2:37921228-37921229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370639672	chr2:37921302-37921303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576874137	chr2:37921312-37921313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150001305	chr2:37921338-37921339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12478461	chr2:37921341-37921342	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs376942102	chr2:37921365-37921366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530682174	chr2:37921384-37921385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12470514	chr2:37921394-37921395	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs192217381	chr2:37921395-37921396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528176696	chr2:37921406-37921407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532216817	chr2:37921408-37921409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547151158	chr2:37921414-37921415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546743720	chr2:37921438-37921439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571258108	chr2:37921483-37921484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs3731850	chr2:37921505-37921506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs551211055	chr2:37921506-37921507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569474526	chr2:37921521-37921522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536823360	chr2:37921545-37921546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183541094	chr2:37921566-37921567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554849435	chr2:37921587-37921588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12470584	chr2:37921604-37921605	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs77064111	chr2:37921608-37921609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78201790	chr2:37921609-37921610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371622325	chr2:37921629-37921630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540717256	chr2:37921644-37921645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541135656	chr2:37921647-37921648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34082461	chr2:37921651-37921652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147383521	chr2:37921688-37921689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149488821	chr2:37921689-37921690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185847284	chr2:37921701-37921702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576785464	chr2:37921741-37921742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190256107	chr2:37921800-37921801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11124599	chr2:37921801-37921802	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs11124600	chr2:37921829-37921830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11124601	chr2:37921831-37921832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77212458	chr2:37921832-37921833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376798763	chr2:37921861-37921862	Weak transcription	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:974 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37907000-37921000	Weak transcription	Stomach Mucosa	stomach
2	chr2:37916600-37922200	Weak transcription	Fetal Lung	lung
3	chr2:37916600-37926000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:37917200-37925600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr2:37917200-37938000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:37917200-37938800	Weak transcription	Aorta	Aorta
7	chr2:37918000-37922800	Weak transcription	Fetal Heart	heart
8	chr2:37920200-37921200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:37920400-37921000	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr2:37920400-37925800	Weak transcription	NHLF	lung
11	chr2:37920800-37925600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr2:37920800-37925600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:37921000-37921200	Active TSS	Stomach Mucosa	stomach
14	chr2:37921000-37922400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr2:37921200-37922200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:37922200-37922400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:37922200-37922600	Enhancers	Fetal Lung	lung
18	chr2:37922400-37922800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr2:37922800-37923000	Enhancers	Fetal Heart	heart
20	chr2:37924800-37927000	Enhancers	Placenta Amnion	Placenta Amnion
21	chr2:37925600-37926800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr2:37925600-37927000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:37925600-37927000	Enhancers	A549	lung
24	chr2:37925600-37927000	Enhancers	HUVEC	blood vessel
25	chr2:37925600-37927200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:37925600-37927200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr2:37925600-37927200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr2:37925600-37927400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:37925600-37927400	Enhancers	NH-A	brain
30	chr2:37925600-37927600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:37925800-37927000	Enhancers	Muscle Satellite Cultured Cells	--
32	chr2:37925800-37927000	Enhancers	Hela-S3	cervix
33	chr2:37925800-37927000	Enhancers	NHLF	lung
34	chr2:37925800-37927000	Enhancers	Osteobl	bone
35	chr2:37925800-37927400	Enhancers	HSMM	muscle
36	chr2:37926000-37926800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr2:37926000-37926800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr2:37926000-37926800	Enhancers	NHDF-Ad	bronchial
39	chr2:37926000-37927000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:37926000-37927000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr2:37926000-37927000	Enhancers	HMEC	breast
42	chr2:37926400-37926800	Enhancers	Fetal Muscle Leg	muscle
43	chr2:37926400-37927600	Enhancers	HSMMtube	muscle
44	chr2:37926600-37927000	Enhancers	Placenta	Placenta
45	chr2:37926600-37927600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr2:37926800-37932200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr2:37926800-37932200	Weak transcription	NHDF-Ad	bronchial
48	chr2:37927000-37932000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr2:37927000-37932200	Weak transcription	Osteobl	bone
50	chr2:37927000-37934200	Weak transcription	Placenta	Placenta

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