Variant report

Variant	nsv888523
Chromosome Location	chr7:80088592-80142217
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:471)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:80117772-80117988	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:80128367-80129128	HepG2	liver:	n/a	n/a
3	BACH1	chr7:80110643-80110676	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:80107995-80108383	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:80104300-80104503	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:80128743-80128980	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr7:80127785-80128117	GM12878	blood:	n/a	n/a
8	BCL3	chr7:80112328-80112532	GM12878	blood:	n/a	n/a
9	BRCA1	chr7:80110448-80110844	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr7:80096014-80096932	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr7:80108002-80108365	HCT-116	colon:	n/a	n/a
12	CCNT2	chr7:80097910-80098110	K562	blood:	n/a	n/a
13	CCNT2	chr7:80127711-80127911	K562	blood:	n/a	n/a
14	CEBPB	chr7:80128270-80128909	A549	lung:	n/a	n/a
15	CEBPB	chr7:80108091-80108406	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr7:80128218-80128933	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:80112355-80112659	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:80110488-80110956	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr7:80102216-80102549	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr7:80128302-80128946	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:80112396-80112598	A549	lung:	n/a	n/a
22	CEBPB	chr7:80117784-80118057	A549	lung:	n/a	chr7:80117893-80117904
23	CEBPB	chr7:80110550-80110853	MCF-7	breast:	n/a	n/a
24	CEBPB	chr7:80112308-80112686	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:80128659-80128970	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:80117713-80118094	Hela-S3	cervix:	n/a	chr7:80117893-80117904
27	CEBPB	chr7:80110545-80110722	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr7:80135250-80135976	MCF-7	breast:	n/a	chr7:80135843-80135854
29	CEBPB	chr7:80099344-80099951	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:80128357-80128974	MCF-7	breast:	n/a	n/a
31	CEBPB	chr7:80117764-80118029	H1-hESC	embryonic stem cell:	n/a	chr7:80117893-80117904
32	CEBPB	chr7:80095945-80096970	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:80115162-80115578	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:80117734-80118078	IMR90	lung:	n/a	chr7:80117893-80117904
35	CEBPB	chr7:80128375-80128965	A549	lung:	n/a	n/a
36	CEBPB	chr7:80112375-80112643	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:80117713-80118087	HepG2	liver:	n/a	chr7:80117893-80117904
38	CEBPB	chr7:80127695-80128252	GM12878	blood:	n/a	n/a
39	CHD2	chr7:80110525-80110863	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr7:80096480-80096775	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr7:80099399-80099702	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr7:80128466-80128949	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr7:80107180-80107330	RPTEC	kidney:	n/a	n/a
44	CTCF	chr7:80114480-80114520	GM13976	blood:	n/a	n/a
45	CTCF	chr7:80133369-80133438	Lung_OC	lung:	n/a	n/a
46	CTCF	chr7:80120160-80120310	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:80120140-80120290	GM06990	blood:	n/a	n/a
48	E2F4	chr7:80138764-80138896	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr7:80107993-80108240	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr7:80128353-80128879	MCF10A-Er-Src	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80142060-80142110	SAEC	small airway:	n/a
2	chr7:80142060-80142110	MCF-7	breast:	n/a
3	chr7:80142060-80142110	HRPEpiC	eye:	n/a
4	chr7:80142060-80142110	SK-N-SH	brain:	n/a
5	chr7:80142060-80142110	T-47D	breast:	n/a
6	chr7:80096608-80096658	CMK	blood:	n/a
7	chr7:80142060-80142110	BE2_C	brain:	n/a
8	chr7:80142060-80142110	CMK	blood:	n/a
9	chr7:80142060-80142110	GM12878	blood:	n/a
10	chr7:80142060-80142110	SKMC	muscle:	n/a
11	chr7:80096608-80096658	U87	brain:	n/a
12	chr7:80096608-80096658	HRE	kidney:	n/a
13	chr7:80096608-80096658	T-47D	breast:	n/a
14	chr7:80142060-80142110	AG04450	lung:	fetal
15	chr7:80142060-80142110	GM19239	blood:	n/a
16	chr7:80096608-80096658	HepG2	liver:	n/a
17	chr7:80096608-80096658	SK-N-SH_RA	brain:	n/a
18	chr7:80142060-80142110	HepG2	liver:	n/a
19	chr7:80096608-80096658	SK-N-MC	brain:	n/a
20	chr7:80142060-80142110	MCF10A-Er-Src	breast:	n/a
21	chr7:80096608-80096658	MCF10A-Er-Src	breast:	n/a
22	chr7:80142060-80142110	ECC-1	luminal epithelium:	n/a
23	chr7:80096608-80096658	HAEpiC	amniotic membrane:	n/a
24	chr7:80142060-80142110	SK-N-MC	brain:	n/a
25	chr7:80096608-80096658	A549	lung:	n/a
26	chr7:80142060-80142110	PrEC	prostate:	n/a
27	chr7:80096608-80096658	AG04449	skin:	fetal
28	chr7:80142060-80142110	HRE	kidney:	n/a
29	chr7:80142060-80142110	HMEC	breast:	n/a
30	chr7:80142060-80142110	Hela-S3	cervix:	n/a
31	chr7:80142060-80142110	GM06990	blood:	n/a
32	chr7:80096608-80096658	GM12892	blood:	n/a
33	chr7:80096608-80096658	Hepatocyte	liver:	n/a
34	chr7:80142060-80142110	HEEpiC	esophagus:	n/a
35	chr7:80096608-80096658	GM19239	blood:	n/a
36	chr7:80142060-80142110	HCF	heart:	n/a
37	chr7:80142060-80142110	HRCEpiC	kidney:	n/a
38	chr7:80096608-80096658	HEEpiC	esophagus:	n/a
39	chr7:80096608-80096658	ProgFib	skin:	n/a
40	chr7:80096608-80096658	GM12891	blood:	n/a
41	chr7:80096608-80096658	NB4	blood:	n/a
42	chr7:80142060-80142110	NB4	blood:	n/a
43	chr7:80096608-80096658	NHBE	bronchial:	n/a
44	chr7:80142060-80142110	U87	brain:	n/a
45	chr7:80096608-80096658	AoSMC	blood vessel:	n/a
46	chr7:80096608-80096658	NT2-D1	testis:	n/a
47	chr7:80142060-80142110	HNPCEpiC	eye:	n/a
48	chr7:80096608-80096658	HNPCEpiC	eye:	n/a
49	chr7:80142060-80142110	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:80096608-80096658	SKMC	muscle:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:80096464..80097970-chr7:80098984..80101525,2	K562	blood:
2	chr7:80096594..80099585-chr7:80101660..80104577,2	MCF-7	breast:
3	chr7:80125854..80128249-chr7:80143744..80146199,2	MCF-7	breast:
4	chr7:80102854..80105069-chr7:80112565..80115333,2	K562	blood:
5	chr7:80096464..80097970-chr7:80098984..80101525,2	K562	blood:
6	chr7:80096594..80099585-chr7:80101660..80104577,2	MCF-7	breast:
7	chr7:80130973..80133838-chr7:80134281..80135849,2	MCF-7	breast:
8	chr7:80130973..80133838-chr7:80134281..80135849,2	MCF-7	breast:
9	chr7:80102854..80105069-chr7:80112565..80115333,2	K562	blood:

No data

Variant related genes	Relation type
GNAT3	TF binding region
GNAT3	CpG island

Extended variants
information (count: 2017 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2017 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17147968	chr7:80088592-80088593	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140834641	chr7:80088635-80088636	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs190840698	chr7:80088661-80088662	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs182271505	chr7:80088671-80088672	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs557178158	chr7:80088694-80088695	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs552123289	chr7:80088760-80088761	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs568969621	chr7:80088800-80088801	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs144678729	chr7:80088839-80088840	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539468181	chr7:80088846-80088847	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71555068	chr7:80088904-80088905	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187346480	chr7:80088983-80088984	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79917558	chr7:80088995-80088996	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78238372	chr7:80088996-80088997	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs80109471	chr7:80088997-80088998	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs80303750	chr7:80089000-80089001	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572400484	chr7:80089007-80089008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541321990	chr7:80089049-80089050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191711538	chr7:80089052-80089053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147877600	chr7:80089082-80089083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543561152	chr7:80089107-80089108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563252892	chr7:80089121-80089122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537954618	chr7:80089140-80089141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551913601	chr7:80089224-80089225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558909589	chr7:80089266-80089267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528801257	chr7:80089289-80089290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73386744	chr7:80089325-80089326	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs560566572	chr7:80089430-80089431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73159414	chr7:80089464-80089465	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs75576557	chr7:80089515-80089516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78792156	chr7:80089516-80089517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377261436	chr7:80089517-80089518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537260154	chr7:80089535-80089536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140470452	chr7:80089536-80089537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149980768	chr7:80089549-80089550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539902199	chr7:80089566-80089567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568948148	chr7:80089599-80089600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553131695	chr7:80089641-80089642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74708934	chr7:80089656-80089657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547691602	chr7:80089662-80089663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73386746	chr7:80089680-80089681	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs554910151	chr7:80089681-80089682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574749845	chr7:80089736-80089737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs799934	chr7:80089790-80089791	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs557094909	chr7:80089791-80089792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576898141	chr7:80089796-80089797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545875505	chr7:80089809-80089810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571538535	chr7:80089811-80089812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558971200	chr7:80089835-80089836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534096060	chr7:80089841-80089842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528079471	chr7:80089873-80089874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Cancer	20164919	CNVD
Breast cancer	21611746	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80081200-80092800	Weak transcription	Fetal Intestine Small	intestine
2	chr7:80084600-80088800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:80088200-80088600	Enhancers	Liver	Liver
4	chr7:80088400-80089000	Active TSS	Adipose Nuclei	Adipose
5	chr7:80088400-80089000	Active TSS	Osteobl	bone
6	chr7:80088600-80089000	Active TSS	Liver	Liver
7	chr7:80088800-80089200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:80089000-80089200	Enhancers	Liver	Liver
9	chr7:80089200-80092200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:80092200-80093800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:80092600-80093000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr7:80092600-80093000	Enhancers	HUVEC	blood vessel
13	chr7:80092800-80093200	Enhancers	A549	lung
14	chr7:80092800-80093200	Enhancers	Hela-S3	cervix
15	chr7:80092800-80097400	Enhancers	Fetal Intestine Small	intestine
16	chr7:80093000-80096000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr7:80093200-80094600	Weak transcription	Hela-S3	cervix
18	chr7:80093200-80095000	Weak transcription	A549	lung
19	chr7:80093400-80093600	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr7:80093600-80094600	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr7:80093800-80094000	Enhancers	Fetal Heart	heart
22	chr7:80093800-80095600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:80094000-80095400	Weak transcription	Fetal Heart	heart
24	chr7:80094600-80096400	Enhancers	Hela-S3	cervix
25	chr7:80094600-80098400	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr7:80094800-80095000	Enhancers	Small Intestine	intestine
27	chr7:80094800-80095600	Enhancers	Left Ventricle	heart
28	chr7:80095000-80096200	Enhancers	A549	lung
29	chr7:80095000-80096600	Weak transcription	Small Intestine	intestine
30	chr7:80095200-80095600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr7:80095200-80095600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:80095400-80095600	Enhancers	Right Atrium	heart
33	chr7:80095400-80097000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr7:80095400-80097200	Enhancers	Fetal Heart	heart
35	chr7:80095400-80097200	Enhancers	Fetal Intestine Large	intestine
36	chr7:80095600-80097200	Enhancers	Duodenum Mucosa	Duodenum
37	chr7:80095600-80097800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr7:80095600-80106800	Weak transcription	Right Atrium	heart
39	chr7:80096000-80096200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:80096000-80096200	Enhancers	Adipose Nuclei	Adipose
41	chr7:80096000-80096600	Enhancers	NHLF	lung
42	chr7:80096000-80096800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr7:80096000-80096800	Enhancers	Fetal Lung	lung
44	chr7:80096000-80096800	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr7:80096000-80097000	Enhancers	Muscle Satellite Cultured Cells	--
46	chr7:80096000-80097000	Enhancers	Osteobl	bone
47	chr7:80096000-80097200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr7:80096200-80096400	Enhancers	Liver	Liver
49	chr7:80096200-80096600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:80096200-80096600	Enhancers	Duodenum Smooth Muscle	Duodenum

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