Variant report

Variant	esv2753501
Chromosome Location	chr7:83250118-83336854
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:772)
CpG islands
(count:857)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:772 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:83326054-83326296	HepG2	liver:	n/a	n/a
2	ATF2	chr7:83314148-83314718	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:83320387-83320709	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:83314164-83314746	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:83314089-83314752	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:83292858-83293028	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr7:83305055-83305388	GM12878	blood:	n/a	n/a
8	BATF	chr7:83305125-83305376	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:83324778-83325042	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr7:83314293-83314656	H1-hESC	embryonic stem cell:	n/a	chr7:83314584-83314593
11	BCL11A	chr7:83314331-83314638	H1-hESC	embryonic stem cell:	n/a	chr7:83314584-83314593
12	BHLHE40	chr7:83263042-83263059	K562	blood:	n/a	n/a
13	CBX3	chr7:83306261-83306956	HCT-116	colon:	n/a	n/a
14	CEBPB	chr7:83314678-83315048	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr7:83331695-83332003	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:83323482-83323812	A549	lung:	n/a	chr7:83323624-83323641
17	CEBPB	chr7:83323469-83323780	MCF-7	breast:	n/a	chr7:83323624-83323641
18	CEBPB	chr7:83323461-83323826	ECC-1	luminal epithelium:	n/a	chr7:83323624-83323641
19	CEBPB	chr7:83323473-83323810	IMR90	lung:	n/a	chr7:83323624-83323641
20	CEBPB	chr7:83319227-83319674	MCF-7	breast:	n/a	chr7:83319435-83319448 chr7:83319270-83319283 chr7:83319435-83319446
21	CEBPB	chr7:83314173-83315083	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr7:83284706-83284906	HepG2	liver:	n/a	chr7:83284806-83284817 chr7:83284807-83284818 chr7:83284808-83284817 chr7:83284806-83284819
23	CEBPB	chr7:83333903-83334169	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:83323457-83323812	A549	lung:	n/a	chr7:83323624-83323641
25	CEBPB	chr7:83323491-83323812	H1-hESC	embryonic stem cell:	n/a	chr7:83323624-83323641
26	CEBPB	chr7:83284706-83284956	A549	lung:	n/a	chr7:83284806-83284817 chr7:83284807-83284818 chr7:83284808-83284817 chr7:83284806-83284819
27	CEBPB	chr7:83306457-83306821	MCF-7	breast:	n/a	n/a
28	CEBPB	chr7:83306495-83307045	MCF-7	breast:	n/a	n/a
29	CEBPB	chr7:83314060-83314863	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:83333854-83334319	MCF-7	breast:	n/a	n/a
31	CEBPB	chr7:83328066-83328266	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:83272423-83272621	A549	lung:	n/a	n/a
33	CEBPB	chr7:83323453-83323818	HepG2	liver:	n/a	chr7:83323624-83323641
34	CEBPB	chr7:83323546-83323768	K562	blood:	n/a	chr7:83323624-83323641
35	CEBPB	chr7:83333874-83334298	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr7:83284737-83284879	H1-hESC	embryonic stem cell:	n/a	chr7:83284806-83284817 chr7:83284807-83284818 chr7:83284808-83284817 chr7:83284806-83284819
37	CEBPB	chr7:83333958-83334119	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr7:83323447-83323849	MCF-7	breast:	n/a	chr7:83323624-83323641
39	CEBPB	chr7:83315786-83316040	HepG2	liver:	n/a	chr7:83315925-83315936
40	CEBPB	chr7:83333882-83334242	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr7:83323461-83323756	ECC-1	luminal epithelium:	n/a	chr7:83323624-83323641
42	CEBPB	chr7:83306280-83307055	HCT-116	colon:	n/a	n/a
43	CEBPB	chr7:83306399-83306747	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr7:83323454-83323783	A549	lung:	n/a	chr7:83323624-83323641
45	CEBPB	chr7:83333910-83334171	MCF-7	breast:	n/a	n/a
46	CHD2	chr7:83258964-83258973	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr7:83306426-83306799	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr7:83314222-83314700	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr7:83277827-83278027	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTBP2	chr7:83277874-83278538	H1-hESC	embryonic stem cell:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:83277971-83278021	GM12878	blood:	n/a
2	chr7:83270795-83270845	RPTEC	kidney:	n/a
3	chr7:83302872-83302922	Caco-2	colon:	n/a
4	chr7:83277971-83278021	GM12878	blood:	n/a
5	chr7:83270795-83270845	RPTEC	kidney:	n/a
6	chr7:83302872-83302922	Caco-2	colon:	n/a
7	chr7:83325268-83325318	PANC-1	pancreas:	n/a
8	chr7:83277971-83278021	IMR90	lung:	fetal
9	chr7:83278594-83278644	H1-hESC	embryonic stem cell:	embryo
10	chr7:83319354-83319404	NHBE	bronchial:	n/a
11	chr7:83278462-83278512	GM19239	blood:	n/a
12	chr7:83278462-83278512	SK-N-MC	brain:	n/a
13	chr7:83278138-83278188	HCT-116	colon:	n/a
14	chr7:83277965-83278015	HepG2	liver:	n/a
15	chr7:83314331-83314381	HNPCEpiC	eye:	n/a
16	chr7:83278066-83278116	ovcar-3	ovarian:	n/a
17	chr7:83278462-83278512	LNCaP	prostate:	n/a
18	chr7:83302872-83302922	GM06990	blood:	n/a
19	chr7:83302872-83302922	HCT-116	colon:	n/a
20	chr7:83277965-83278015	AG09319	gingival:	n/a
21	chr7:83319354-83319404	T-47D	breast:	n/a
22	chr7:83304047-83304097	Jurkat	blood:	n/a
23	chr7:83314331-83314381	GM12892	blood:	n/a
24	chr7:83278504-83278554	SKMC	muscle:	n/a
25	chr7:83277971-83278021	HCM	heart:	n/a
26	chr7:83277971-83278021	HCT-116	colon:	n/a
27	chr7:83278138-83278188	AG04450	lung:	fetal
28	chr7:83278594-83278644	SAEC	small airway:	n/a
29	chr7:83319354-83319404	BE2_C	brain:	n/a
30	chr7:83278066-83278116	SK-N-SH	brain:	n/a
31	chr7:83278594-83278644	BJ	skin:	n/a
32	chr7:83304047-83304097	HCM	heart:	n/a
33	chr7:83304047-83304097	AG09309	skin:	n/a
34	chr7:83270795-83270845	AoSMC	blood vessel:	n/a
35	chr7:83325268-83325318	GM19239	blood:	n/a
36	chr7:83277965-83278015	CMK	blood:	n/a
37	chr7:83278462-83278512	SK-N-SH	brain:	n/a
38	chr7:83277941-83277991	LNCaP	prostate:	n/a
39	chr7:83325268-83325318	HNPCEpiC	eye:	n/a
40	chr7:83319354-83319404	HepG2	liver:	n/a
41	chr7:83278504-83278554	HNPCEpiC	eye:	n/a
42	chr7:83314331-83314381	HRCEpiC	kidney:	n/a
43	chr7:83325268-83325318	HAEpiC	amniotic membrane:	n/a
44	chr7:83277941-83277991	MCF10A-Er-Src	breast:	n/a
45	chr7:83314331-83314381	PFSK-1	brain:	n/a
46	chr7:83277965-83278015	PFSK-1	brain:	n/a
47	chr7:83270795-83270845	NHDF-neo	bronchial:	n/a
48	chr7:83277941-83277991	RPTEC	kidney:	n/a
49	chr7:83314331-83314381	HL-60	blood:	n/a
50	chr7:83278066-83278116	K562	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:83295134..83297291-chr7:83298108..83300813,3	MCF-7	breast:
2	chr7:83039933..83040950-chr7:83284946..83285918,7	MCF-7	breast:
3	chr7:83041300..83043900-chr7:83284952..83286608,2	MCF-7	breast:
4	chr7:83276388..83278355-chr7:83300202..83302453,2	MCF-7	breast:
5	chr7:83272057..83273573-chr7:83277268..83279945,2	MCF-7	breast:
6	chr7:83273917..83275585-chr7:83276258..83278022,2	MCF-7	breast:
7	chr7:83315115..83317340-chr7:83318179..83320541,2	MCF-7	breast:
8	chr7:83286638..83289416-chr7:83307592..83310241,2	MCF-7	breast:
9	chr7:83176039..83178817-chr7:83274663..83276467,2	MCF-7	breast:
10	chr7:83295134..83297291-chr7:83298108..83300813,3	MCF-7	breast:
11	chr7:83284977..83285856-chr9:77642295..77643232,2	MCF-7	breast:
12	chr7:83273917..83275585-chr7:83276258..83278022,2	MCF-7	breast:
13	chr7:83286638..83289416-chr7:83307592..83310241,2	MCF-7	breast:
14	chr7:82995345..82996578-chr7:83285135..83286120,3	MCF-7	breast:
15	chr7:83175225..83177446-chr7:83272648..83274551,2	MCF-7	breast:
16	chr7:83278470..83280493-chr7:83282066..83285729,4	K562	blood:
17	chr7:83176511..83177359-chr7:83306453..83306965,2	MCF-7	breast:
18	chr7:83315115..83317340-chr7:83318179..83320541,2	MCF-7	breast:
19	chr7:83042175..83042815-chr7:83285352..83285945,2	MCF-7	breast:
20	chr7:83040185..83040873-chr7:83285022..83285687,3	MCF-7	breast:
21	chr7:83278470..83280493-chr7:83282066..83285729,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC005008.2.1-6	chr7:83292735-83293941	NONHSAT121784

No data

Variant related genes	Relation type
RAD23BP2	TF binding region
SEMA3E	TF binding region
RAD23BP2	CpG island
SEMA3E	CpG island
ENSG00000170381	chromatin interactions
ENSG00000156017	chromatin interactions

Extended variants
information (count: 3034 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3034 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs42013	chr7:83250118-83250119	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369433330	chr7:83250135-83250136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76396710	chr7:83250141-83250142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74679578	chr7:83250155-83250156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552899734	chr7:83250164-83250165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78269493	chr7:83250181-83250182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77643509	chr7:83250185-83250186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75867317	chr7:83250192-83250193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557396583	chr7:83250228-83250229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577633814	chr7:83250253-83250254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181018548	chr7:83250254-83250255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138103018	chr7:83250280-83250281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528650327	chr7:83250309-83250310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186205190	chr7:83250399-83250400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149026008	chr7:83250417-83250418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530846256	chr7:83250482-83250483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189490394	chr7:83250489-83250490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111469832	chr7:83250493-83250494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181550261	chr7:83250494-83250495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185882886	chr7:83250530-83250531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546439584	chr7:83250531-83250532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566373891	chr7:83250548-83250549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572771694	chr7:83250565-83250566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535626723	chr7:83250690-83250691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191263552	chr7:83250785-83250786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372429869	chr7:83250832-83250833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568911517	chr7:83250833-83250834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537516069	chr7:83250835-83250836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183067620	chr7:83250841-83250842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577672526	chr7:83250846-83250847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545239858	chr7:83250854-83250855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377181393	chr7:83250876-83250877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200320678	chr7:83250900-83250901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113069667	chr7:83250969-83250970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186675779	chr7:83250970-83250971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553701145	chr7:83250972-83250973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529554487	chr7:83250994-83250995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573519669	chr7:83251052-83251053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549603595	chr7:83251066-83251067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190716175	chr7:83251073-83251074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562071150	chr7:83251086-83251087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138701523	chr7:83251127-83251128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561447783	chr7:83251172-83251173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370144637	chr7:83251181-83251182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377389731	chr7:83251195-83251196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182443387	chr7:83251215-83251216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546529113	chr7:83251245-83251246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187876862	chr7:83251290-83251291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538013092	chr7:83251307-83251308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559996424	chr7:83251353-83251354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
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
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:83246600-83252800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:83250400-83250600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:83254600-83255800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:83256600-83263400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:83257000-83269000	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr7:83258200-83258400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr7:83258400-83258800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr7:83258400-83258800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr7:83258400-83259200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:83258400-83259400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr7:83258400-83259400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:83258400-83259400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:83258400-83259400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:83258400-83259600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr7:83258400-83259600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr7:83258600-83259400	Enhancers	H9 Cell Line	embryonic stem cell
17	chr7:83258600-83259400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr7:83258600-83259400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr7:83258600-83259400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:83258800-83259000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr7:83258800-83259200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:83258800-83259200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
23	chr7:83258800-83259400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:83258800-83259400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr7:83259000-83259200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr7:83259000-83259400	Enhancers	Fetal Heart	heart
27	chr7:83259200-83259400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr7:83259200-83259600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr7:83263000-83263400	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr7:83263400-83263800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:83263800-83268000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:83268000-83269600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:83269000-83269800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr7:83269000-83271800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr7:83269200-83269400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr7:83269200-83269800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr7:83269200-83270600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr7:83269200-83271000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr7:83269200-83271000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:83269200-83271200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr7:83269200-83271600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr7:83269200-83271600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr7:83269400-83270000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr7:83269400-83270400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr7:83269400-83270800	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr7:83269400-83271600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr7:83269400-83271600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr7:83269600-83271000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:83269800-83273000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:83269800-83276200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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