Variant report

Variant	nsv1030062
Chromosome Location	chr7:18915874-18943409
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:211)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:211 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr7:18934946-18935470	HCT-116	colon:	n/a	n/a
2	CEBPB	chr7:18934830-18935687	HCT-116	colon:	n/a	chr7:18935614-18935626
3	CEBPB	chr7:18940561-18940789	IMR90	lung:	n/a	chr7:18940689-18940702 chr7:18940622-18940635
4	CTCF	chr7:18933937-18933971	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr7:18933905-18934018	GM12878	blood:	n/a	n/a
6	CTCF	chr7:18933896-18934040	SK-N-SH_RA	brain:	n/a	n/a
7	CTCF	chr7:18933871-18934041	Gliobla	brain:	n/a	n/a
8	CTCF	chr7:18930846-18930895	LNCaP	prostate:	n/a	n/a
9	CTCF	chr7:18933820-18933970	BE2_C	brain:	n/a	n/a
10	CTCF	chr7:18930800-18930950	SK-N-SH_RA	brain:	n/a	chr7:18930887-18930908 chr7:18930885-18930903
11	CTCF	chr7:18932860-18933010	HUVEC	blood vessel:	n/a	n/a
12	CTCF	chr7:18933976-18933987	MCF-7	breast:	n/a	n/a
13	CTCF	chr7:18933860-18934010	GM12872	blood:	n/a	n/a
14	CTCF	chr7:18933840-18933990	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr7:18933980-18934130	Caco-2	colon:	n/a	n/a
16	CTCF	chr7:18933988-18934004	MCF-7	breast:	n/a	n/a
17	CTCF	chr7:18933860-18934010	HPF	lung:	n/a	n/a
18	CTCF	chr7:18933880-18934030	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr7:18933820-18933970	GM12871	blood:	n/a	n/a
20	CTCF	chr7:18932820-18932970	BE2_C	brain:	n/a	n/a
21	CTCF	chr7:18933880-18934030	BE2_C	brain:	n/a	n/a
22	CTCF	chr7:18933880-18934030	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr7:18931060-18931210	A549	lung:	n/a	n/a
24	CTCF	chr7:18933860-18934010	HMEC	breast:	n/a	n/a
25	CTCF	chr7:18933340-18933490	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr7:18941580-18941730	NB4	blood:	n/a	n/a
27	CTCF	chr7:18933853-18934067	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:18933880-18934030	HCT-116	colon:	n/a	n/a
29	CTCF	chr7:18933860-18934010	HEK293	kidney:	n/a	n/a
30	CTCF	chr7:18933820-18933970	HMEC	breast:	n/a	n/a
31	CTCF	chr7:18921940-18922170	GM06990	blood:	n/a	n/a
32	CTCF	chr7:18933683-18934245	HCT-116	colon:	n/a	n/a
33	CTCF	chr7:18932780-18932930	HEK293	kidney:	n/a	n/a
34	CTCF	chr7:18933910-18933982	ProgFib	skin:	n/a	n/a
35	CTCF	chr7:18916820-18916970	Caco-2	colon:	n/a	n/a
36	CTCF	chr7:18930720-18930870	BE2_C	brain:	n/a	n/a
37	CTCF	chr7:18933900-18934050	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr7:18933943-18934073	NHEK	skin:	n/a	n/a
39	CTCF	chr7:18933840-18933990	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr7:18933966-18933968	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:18932760-18932910	BE2_C	brain:	n/a	n/a
42	CTCF	chr7:18933839-18934134	GM12878	blood:	n/a	n/a
43	CTCF	chr7:18930780-18930930	BE2_C	brain:	n/a	chr7:18930887-18930908 chr7:18930885-18930903
44	CTCF	chr7:18933956-18933988	Medullo	brain:	n/a	n/a
45	E2F4	chr7:18940557-18940687	MCF10A-Er-Src	breast:	n/a	n/a
46	EBF1	chr7:18928938-18928965	GM12878	blood:	n/a	n/a
47	EP300	chr7:18929424-18930310	SK-N-SH	brain:	n/a	n/a
48	EP300	chr7:18935916-18936372	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr7:18934863-18935640	SK-N-SH	brain:	n/a	n/a
50	EP300	chr7:18928046-18935809	SK-N-SH	brain:	n/a	chr7:18930351-18930360 chr7:18929205-18929219 chr7:18928386-18928400 chr7:18930389-18930399

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:18929612-18929662	A549	lung:	n/a
2	chr7:18929612-18929662	GM12878	blood:	n/a
3	chr7:18929612-18929662	HEEpiC	esophagus:	n/a
4	chr7:18929612-18929662	BE2_C	brain:	n/a
5	chr7:18929612-18929662	U87	brain:	n/a
6	chr7:18929612-18929662	SK-N-SH_RA	brain:	n/a
7	chr7:18929612-18929662	NHDF-neo	bronchial:	n/a
8	chr7:18929612-18929662	GM12892	blood:	n/a
9	chr7:18929612-18929662	HAEpiC	amniotic membrane:	n/a
10	chr7:18929612-18929662	HRCEpiC	kidney:	n/a
11	chr7:18929612-18929662	NT2-D1	testis:	n/a
12	chr7:18929612-18929662	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:18929612-18929662	SK-N-MC	brain:	n/a
14	chr7:18929612-18929662	SK-N-SH	brain:	n/a
15	chr7:18929612-18929662	ECC-1	luminal epithelium:	n/a
16	chr7:18929612-18929662	H1-hESC	embryonic stem cell:	embryo
17	chr7:18929612-18929662	HIPEpiC	eye:	n/a
18	chr7:18929612-18929662	GM06990	blood:	n/a
19	chr7:18929612-18929662	PFSK-1	brain:	n/a
20	chr7:18929612-18929662	AoSMC	blood vessel:	n/a
21	chr7:18929612-18929662	GM12891	blood:	n/a
22	chr7:18929612-18929662	RPTEC	kidney:	n/a
23	chr7:18929612-18929662	NH-A	brain:	n/a
24	chr7:18929612-18929662	AG09309	skin:	n/a
25	chr7:18929612-18929662	HCT-116	colon:	n/a
26	chr7:18929612-18929662	NHBE	bronchial:	n/a
27	chr7:18929612-18929662	AG10803	skin:	n/a
28	chr7:18929612-18929662	HCF	heart:	n/a
29	chr7:18929612-18929662	IMR90	lung:	fetal
30	chr7:18929612-18929662	BJ	skin:	n/a
31	chr7:18929612-18929662	ovcar-3	ovarian:	n/a
32	chr7:18929612-18929662	HRPEpiC	eye:	n/a
33	chr7:18929612-18929662	NB4	blood:	n/a
34	chr7:18929612-18929662	AG04450	lung:	fetal
35	chr7:18929612-18929662	HL-60	blood:	n/a
36	chr7:18929612-18929662	T-47D	breast:	n/a
37	chr7:18929612-18929662	PrEC	prostate:	n/a
38	chr7:18929612-18929662	MCF10A-Er-Src	breast:	n/a
39	chr7:18929612-18929662	CMK	blood:	n/a
40	chr7:18929612-18929662	Caco-2	colon:	n/a
41	chr7:18929612-18929662	PANC-1	pancreas:	n/a
42	chr7:18929612-18929662	HNPCEpiC	eye:	n/a
43	chr7:18929612-18929662	HCPEpiC	choroid plexus:	n/a
44	chr7:18929612-18929662	Hela-S3	cervix:	n/a
45	chr7:18929612-18929662	SAEC	small airway:	n/a
46	chr7:18929612-18929662	HUVEC	blood vessel:	n/a
47	chr7:18929612-18929662	AG04449	skin:	fetal
48	chr7:18929612-18929662	ProgFib	skin:	n/a
49	chr7:18929612-18929662	AG09319	gingival:	n/a
50	chr7:18929612-18929662	HCM	heart:	n/a

No data

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TWIST1-2	chr7:18932183-18932263	ENSG00000226522.1
2	lnc-TWIST1-2	chr7:18938932-18939056	ENSG00000226522.1
3	lnc-TWIST1-2	chr7:18931719-18931825	ENSG00000226522.1

No data

Variant related genes	Relation type
ENSG00000226522	TF binding region
ENSG00000226522	CpG island

Extended variants
information (count: 1250 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1250 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10486314	chr7:18915874-18915875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141630668	chr7:18915897-18915898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575018545	chr7:18915902-18915903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572881271	chr7:18915972-18915973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540187456	chr7:18915987-18915988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561647343	chr7:18916005-18916006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184083504	chr7:18916059-18916060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544106450	chr7:18916062-18916063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560519174	chr7:18916084-18916085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562688726	chr7:18916092-18916093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577321637	chr7:18916109-18916110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533099546	chr7:18916150-18916151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551264617	chr7:18916156-18916157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559974231	chr7:18916158-18916159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13221164	chr7:18916168-18916169	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs562937108	chr7:18916272-18916273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546944769	chr7:18916287-18916288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71017009	chr7:18916326-18916327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553888457	chr7:18916327-18916328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs398066667	chr7:18916342-18916343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531865933	chr7:18916399-18916400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535925595	chr7:18916422-18916423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550932335	chr7:18916460-18916461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569468289	chr7:18916461-18916462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539993703	chr7:18916530-18916531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558498651	chr7:18916531-18916532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573546241	chr7:18916563-18916564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35024729	chr7:18916602-18916603	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs555321822	chr7:18916607-18916608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62448079	chr7:18916609-18916610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573689461	chr7:18916640-18916641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10486315	chr7:18916641-18916642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs571562568	chr7:18916649-18916650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73684307	chr7:18916672-18916673	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs188808223	chr7:18916673-18916674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs180734396	chr7:18916733-18916734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73320062	chr7:18916788-18916789	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs527561726	chr7:18916859-18916860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546710054	chr7:18916877-18916878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529943097	chr7:18916886-18916887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11531457	chr7:18916974-18916975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562102892	chr7:18917011-18917012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117091173	chr7:18917018-18917019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546826139	chr7:18917020-18917021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11543622	chr7:18917060-18917061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs79803519	chr7:18917092-18917093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540056885	chr7:18917104-18917105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13224833	chr7:18917133-18917134	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs538410452	chr7:18917245-18917246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144516402	chr7:18917250-18917251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18903000-18940000	Weak transcription	Aorta	Aorta
2	chr7:18906200-18929200	Weak transcription	Left Ventricle	heart
3	chr7:18928800-18929400	Enhancers	Adipose Nuclei	Adipose
4	chr7:18928800-18930000	Enhancers	HUVEC	blood vessel
5	chr7:18928800-18931200	Enhancers	Fetal Heart	heart
6	chr7:18929200-18929400	Enhancers	Right Atrium	heart
7	chr7:18929200-18929800	Enhancers	Left Ventricle	heart
8	chr7:18929200-18930000	Enhancers	HMEC	breast
9	chr7:18929200-18930200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr7:18929200-18931400	Enhancers	NHDF-Ad	bronchial
11	chr7:18929200-18931600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:18929400-18929600	Enhancers	Fetal Stomach	stomach
13	chr7:18929400-18930000	Enhancers	Dnd41	blood
14	chr7:18929400-18930000	Enhancers	Osteobl	bone
15	chr7:18929400-18930200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:18929400-18930800	Weak transcription	Adipose Nuclei	Adipose
17	chr7:18929400-18931000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr7:18929400-18931200	Enhancers	NHLF	lung
19	chr7:18929600-18929800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr7:18929800-18930800	Weak transcription	Fetal Stomach	stomach
21	chr7:18929800-18931000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr7:18929800-18931000	Enhancers	Stomach Smooth Muscle	stomach
23	chr7:18930000-18931200	Enhancers	Colon Smooth Muscle	Colon
24	chr7:18930000-18932800	Weak transcription	HMEC	breast
25	chr7:18930000-18934400	Weak transcription	Osteobl	bone
26	chr7:18930000-18934800	Weak transcription	HUVEC	blood vessel
27	chr7:18930200-18930600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr7:18930200-18934800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr7:18930400-18931200	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr7:18930400-18931200	Enhancers	Fetal Lung	lung
31	chr7:18930400-18931400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:18930600-18930800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr7:18930800-18931200	Enhancers	Adipose Nuclei	Adipose
34	chr7:18930800-18931400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr7:18930800-18931400	Enhancers	Fetal Stomach	stomach
36	chr7:18930800-18934600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr7:18931000-18931200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr7:18931000-18931400	Enhancers	Right Atrium	heart
39	chr7:18931000-18934600	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr7:18931200-18933400	Weak transcription	Fetal Heart	heart
41	chr7:18931200-18934400	Weak transcription	NHLF	lung
42	chr7:18931200-18943400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr7:18931400-18934200	Weak transcription	NHDF-Ad	bronchial
44	chr7:18931400-18934600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:18931400-18940000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr7:18931600-18934400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr7:18932600-18935200	Enhancers	NHEK	skin
48	chr7:18932800-18935200	Enhancers	HMEC	breast
49	chr7:18933400-18933800	Enhancers	Fetal Heart	heart
50	chr7:18934000-18934200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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