Variant report

Variant	nsv526283
Chromosome Location	chr2:36851264-36880831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:511)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:36873379-36873727	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:36877205-36877537	HepG2	liver:	n/a	n/a
3	ATF1	chr2:36873395-36873735	K562	blood:	n/a	n/a
4	ATF2	chr2:36873300-36873758	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:36873285-36873766	GM12878	blood:	n/a	n/a
6	ATF2	chr2:36873297-36873747	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:36873274-36873760	GM12878	blood:	n/a	n/a
8	ATF3	chr2:36873306-36873764	K562	blood:	n/a	n/a
9	ATF3	chr2:36852487-36852779	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr2:36852471-36852899	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr2:36852467-36852862	A549	lung:	n/a	n/a
12	ATF3	chr2:36852490-36852747	K562	blood:	n/a	n/a
13	ATF3	chr2:36852451-36852883	HCT-116	colon:	n/a	n/a
14	ATF3	chr2:36877200-36877481	K562	blood:	n/a	n/a
15	BATF	chr2:36877282-36877486	GM12878	blood:	n/a	chr2:36877369-36877380
16	BHLHE40	chr2:36863498-36863643	K562	blood:	n/a	chr2:36863550-36863563
17	CBX3	chr2:36873308-36874078	HCT-116	colon:	n/a	n/a
18	CBX3	chr2:36873371-36873771	K562	blood:	n/a	n/a
19	CBX3	chr2:36852410-36852846	HCT-116	colon:	n/a	n/a
20	CBX3	chr2:36852533-36852784	K562	blood:	n/a	n/a
21	CBX3	chr2:36852419-36852820	K562	blood:	n/a	n/a
22	CBX3	chr2:36873286-36874221	HCT-116	colon:	n/a	n/a
23	CEBPB	chr2:36876898-36877516	A549	lung:	n/a	chr2:36877011-36877022
24	CEBPB	chr2:36852486-36852840	HCT-116	colon:	n/a	chr2:36852667-36852678
25	CEBPB	chr2:36852461-36852839	MCF-7	breast:	n/a	chr2:36852667-36852678
26	CEBPB	chr2:36852483-36852848	IMR90	lung:	n/a	chr2:36852667-36852678
27	CEBPB	chr2:36852494-36852847	H1-hESC	embryonic stem cell:	n/a	chr2:36852667-36852678
28	CEBPB	chr2:36852537-36852829	Hela-S3	cervix:	n/a	chr2:36852667-36852678
29	CEBPB	chr2:36852475-36852866	K562	blood:	n/a	chr2:36852667-36852678
30	CEBPB	chr2:36852468-36852799	K562	blood:	n/a	chr2:36852667-36852678
31	CEBPB	chr2:36852469-36852883	A549	lung:	n/a	chr2:36852667-36852678
32	CEBPB	chr2:36852517-36852703	K562	blood:	n/a	chr2:36852667-36852678
33	CEBPB	chr2:36876888-36877357	HepG2	liver:	n/a	chr2:36877011-36877022
34	CEBPB	chr2:36852361-36852948	A549	lung:	n/a	chr2:36852667-36852678
35	CEBPB	chr2:36852484-36852847	A549	lung:	n/a	chr2:36852667-36852678
36	CEBPB	chr2:36852450-36852854	ECC-1	luminal epithelium:	n/a	chr2:36852667-36852678
37	CEBPB	chr2:36876844-36877562	Hela-S3	cervix:	n/a	chr2:36877011-36877022
38	CEBPB	chr2:36852483-36852841	HepG2	liver:	n/a	chr2:36852667-36852678
39	CEBPB	chr2:36852534-36852832	ECC-1	luminal epithelium:	n/a	chr2:36852667-36852678
40	CEBPB	chr2:36852424-36852814	MCF-7	breast:	n/a	chr2:36852667-36852678
41	CHD2	chr2:36873152-36873155	HepG2	liver:	n/a	n/a
42	CHD2	chr2:36877185-36877570	Hela-S3	cervix:	n/a	n/a
43	CREB1	chr2:36877161-36877523	A549	lung:	n/a	n/a
44	CTCF	chr2:36873460-36873610	GM12867	blood:	n/a	n/a
45	CTCF	chr2:36873460-36873610	GM12873	blood:	n/a	n/a
46	CTCF	chr2:36873520-36873670	GM12874	blood:	n/a	n/a
47	CTCF	chr2:36873500-36873650	NB4	blood:	n/a	n/a
48	CTCF	chr2:36873540-36873690	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr2:36873520-36873670	GM12864	blood:	n/a	n/a
50	CTCF	chr2:36873520-36873670	HRE	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36877454-36877504	U87	brain:	n/a
2	chr2:36877454-36877504	AG10803	skin:	n/a
3	chr2:36877454-36877504	SK-N-SH_RA	brain:	n/a
4	chr2:36877454-36877504	HRPEpiC	eye:	n/a
5	chr2:36877454-36877504	H1-hESC	embryonic stem cell:	embryo
6	chr2:36877454-36877504	GM06990	blood:	n/a
7	chr2:36877454-36877504	Jurkat	blood:	n/a
8	chr2:36877454-36877504	HRE	kidney:	n/a
9	chr2:36877454-36877504	GM12878	blood:	n/a
10	chr2:36877454-36877504	PANC-1	pancreas:	n/a
11	chr2:36877454-36877504	ProgFib	skin:	n/a
12	chr2:36877454-36877504	HNPCEpiC	eye:	n/a
13	chr2:36877454-36877504	HCM	heart:	n/a
14	chr2:36877454-36877504	RPTEC	kidney:	n/a
15	chr2:36877454-36877504	SK-N-MC	brain:	n/a
16	chr2:36877454-36877504	T-47D	breast:	n/a
17	chr2:36877454-36877504	HCPEpiC	choroid plexus:	n/a
18	chr2:36877454-36877504	HEK293	kidney:	embryo
19	chr2:36877454-36877504	PrEC	prostate:	n/a
20	chr2:36877454-36877504	HMEC	breast:	n/a
21	chr2:36877454-36877504	AoSMC	blood vessel:	n/a
22	chr2:36877454-36877504	ovcar-3	ovarian:	n/a
23	chr2:36877454-36877504	LNCaP	prostate:	n/a
24	chr2:36877454-36877504	Caco-2	colon:	n/a
25	chr2:36877454-36877504	HUVEC	blood vessel:	n/a
26	chr2:36877454-36877504	NH-A	brain:	n/a
27	chr2:36877454-36877504	NHDF-neo	bronchial:	n/a
28	chr2:36877454-36877504	HCT-116	colon:	n/a
29	chr2:36877454-36877504	BJ	skin:	n/a
30	chr2:36877454-36877504	A549	lung:	n/a
31	chr2:36877454-36877504	Hepatocyte	liver:	n/a
32	chr2:36877454-36877504	HIPEpiC	eye:	n/a
33	chr2:36877454-36877504	PFSK-1	brain:	n/a
34	chr2:36877454-36877504	HAEpiC	amniotic membrane:	n/a
35	chr2:36877454-36877504	HepG2	liver:	n/a
36	chr2:36877454-36877504	HEEpiC	esophagus:	n/a
37	chr2:36877454-36877504	K562	blood:	n/a
38	chr2:36877454-36877504	GM12891	blood:	n/a
39	chr2:36877454-36877504	MCF-7	breast:	n/a
40	chr2:36877454-36877504	HCF	heart:	n/a
41	chr2:36877454-36877504	Hela-S3	cervix:	n/a
42	chr2:36877454-36877504	IMR90	lung:	fetal
43	chr2:36877454-36877504	ECC-1	luminal epithelium:	n/a
44	chr2:36877454-36877504	MCF10A-Er-Src	breast:	n/a
45	chr2:36877454-36877504	AG04449	skin:	fetal
46	chr2:36877454-36877504	CMK	blood:	n/a
47	chr2:36877454-36877504	NB4	blood:	n/a
48	chr2:36877454-36877504	AG09309	skin:	n/a
49	chr2:36877454-36877504	AG04450	lung:	fetal
50	chr2:36877454-36877504	SK-N-SH	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:36857170..36859524-chr2:36860213..36863125,2	K562	blood:
2	chr2:36578991..36579848-chr2:36873541..36874070,2	K562	blood:
3	chr2:36823336..36826112-chr2:36873879..36877943,4	MCF-7	breast:
4	chr2:36873347..36875175-chr2:36875195..36878718,3	MCF-7	breast:
5	chr2:36845094..36847827-chr2:36854780..36857434,2	K562	blood:
6	chr2:36823734..36826594-chr2:36851912..36854688,2	MCF-7	breast:
7	chr2:36823509..36825415-chr2:36873494..36875458,2	K562	blood:
8	chr2:36857170..36859524-chr2:36860213..36863125,2	K562	blood:
9	chr2:36846931..36849384-chr2:36851133..36853576,2	K562	blood:
10	chr2:36771862..36772834-chr2:36873432..36874042,2	MCF-7	breast:
11	chr2:36873347..36875175-chr2:36875195..36878718,3	MCF-7	breast:

No data

Variant related genes	Relation type
FEZ2	TF binding region
FEZ2	CpG island
ENSG00000171055	chromatin interactions

Extended variants
information (count: 1260 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1260 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11124523	chr2:36851264-36851265	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548103369	chr2:36851268-36851269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565608078	chr2:36851271-36851272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569596388	chr2:36851294-36851295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188972046	chr2:36851301-36851302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562901453	chr2:36851302-36851303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11124524	chr2:36851311-36851312	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs111667081	chr2:36851330-36851331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566939508	chr2:36851341-36851342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112442905	chr2:36851344-36851345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528110259	chr2:36851457-36851458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142325064	chr2:36851505-36851506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114867506	chr2:36851512-36851513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538546352	chr2:36851517-36851518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557127463	chr2:36851555-36851556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79907396	chr2:36851561-36851562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11678510	chr2:36851568-36851569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376959458	chr2:36851578-36851579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536772560	chr2:36851587-36851588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116591723	chr2:36851595-36851596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573355991	chr2:36851601-36851602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540679946	chr2:36851615-36851616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192658564	chr2:36851630-36851631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376056015	chr2:36851638-36851639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199629084	chr2:36851690-36851691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549322262	chr2:36851735-36851736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577476669	chr2:36851877-36851878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147944057	chr2:36851887-36851888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10174789	chr2:36851898-36851899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2372692	chr2:36851901-36851902	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs530200109	chr2:36851975-36851976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs116364148	chr2:36851994-36851995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs77446581	chr2:36852026-36852027	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs547812810	chr2:36852086-36852087	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs34780592	chr2:36852123-36852124	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs528169688	chr2:36852136-36852137	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs141853279	chr2:36852167-36852168	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566243464	chr2:36852198-36852199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs143786295	chr2:36852199-36852200	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs2005889	chr2:36852243-36852244	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs113047649	chr2:36852250-36852251	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs188752981	chr2:36852272-36852273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs554803054	chr2:36852276-36852277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs11900041	chr2:36852292-36852293	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs567013907	chr2:36852296-36852297	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192182707	chr2:36852297-36852298	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs558996802	chr2:36852347-36852348	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs577141629	chr2:36852350-36852351	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs370686648	chr2:36852354-36852355	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs570123970	chr2:36852355-36852356	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Breast cancer	21364760	CNVD
Wilms tumour	21544195	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
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36846600-36852400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:36852400-36852600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:36852400-36852800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:36852600-36852800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:36852600-36852800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
6	chr2:36853000-36866000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:36853200-36853400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr2:36854800-36855200	Enhancers	HepG2	liver
9	chr2:36858600-36859200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:36860800-36861000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr2:36861000-36862000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr2:36861600-36862600	Enhancers	NHDF-Ad	bronchial
13	chr2:36861800-36863000	Enhancers	Colon Smooth Muscle	Colon
14	chr2:36861800-36863000	Enhancers	HSMMtube	muscle
15	chr2:36862000-36862200	Enhancers	Brain Substantia Nigra	brain
16	chr2:36862000-36862200	Enhancers	Fetal Stomach	stomach
17	chr2:36862000-36862400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr2:36862000-36863000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:36862000-36863000	Enhancers	Muscle Satellite Cultured Cells	--
20	chr2:36862000-36863000	Enhancers	Osteobl	bone
21	chr2:36862000-36863200	Enhancers	Stomach Smooth Muscle	stomach
22	chr2:36862000-36864800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr2:36862200-36862600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr2:36862200-36862800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr2:36862200-36863000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:36862200-36863000	Enhancers	Aorta	Aorta
27	chr2:36862200-36863000	Enhancers	Brain Anterior Caudate	brain
28	chr2:36862200-36863000	Enhancers	Brain Cingulate Gyrus	brain
29	chr2:36862200-36863000	Enhancers	Brain Hippocampus Middle	brain
30	chr2:36862200-36863200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:36862400-36863000	Enhancers	Adipose Nuclei	Adipose
32	chr2:36862400-36869400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr2:36862600-36863000	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr2:36862600-36877000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr2:36862800-36863000	Enhancers	Brain Substantia Nigra	brain
36	chr2:36862800-36863000	Enhancers	Fetal Stomach	stomach
37	chr2:36863000-36864200	Weak transcription	Adipose Nuclei	Adipose
38	chr2:36864200-36864800	Enhancers	Adipose Nuclei	Adipose
39	chr2:36866000-36866600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:36870400-36877200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr2:36873200-36873600	Enhancers	Adipose Nuclei	Adipose
42	chr2:36873600-36873800	ZNF genes & repeats	Pancreas	Pancrea
43	chr2:36873800-36875200	Weak transcription	Pancreas	Pancrea
44	chr2:36874400-36877000	Weak transcription	NHLF	lung
45	chr2:36874600-36876600	Weak transcription	A549	lung
46	chr2:36875200-36875400	ZNF genes & repeats	Pancreas	Pancrea
47	chr2:36875200-36875600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr2:36875200-36875600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr2:36875200-36877400	Enhancers	Placenta	Placenta
50	chr2:36875400-36875600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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