Variant report

Variant	nsv464287
Chromosome Location	chr7:4495001-4646250
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:747)
CpG islands
(count:305)
Chromatin interactive
region (count:17)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:747 , 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	chr7:4601500-4601710	K562	blood:	n/a	n/a
2	ARID3A	chr7:4573177-4573308	K562	blood:	n/a	n/a
3	ATF2	chr7:4540407-4540709	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr7:4539804-4540066	HepG2	liver:	n/a	n/a
5	BRCA1	chr7:4519369-4519376	HepG2	liver:	n/a	n/a
6	CBX3	chr7:4523526-4523869	K562	blood:	n/a	n/a
7	CBX3	chr7:4539559-4539829	K562	blood:	n/a	n/a
8	CBX3	chr7:4523514-4523852	K562	blood:	n/a	n/a
9	CBX3	chr7:4539569-4539857	K562	blood:	n/a	n/a
10	CBX3	chr7:4592673-4592898	K562	blood:	n/a	n/a
11	CEBPB	chr7:4606356-4606718	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:4526839-4527196	MCF-7	breast:	n/a	chr7:4527026-4527037
13	CEBPB	chr7:4526863-4527183	MCF-7	breast:	n/a	chr7:4527026-4527037
14	CEBPB	chr7:4606363-4606718	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:4606342-4606723	K562	blood:	n/a	n/a
16	CEBPB	chr7:4606287-4606701	A549	lung:	n/a	n/a
17	CEBPB	chr7:4606348-4606704	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:4510874-4511113	K562	blood:	n/a	chr7:4511007-4511018
19	CEBPB	chr7:4516153-4516177	HepG2	liver:	n/a	chr7:4516157-4516168
20	CEBPB	chr7:4606355-4606641	K562	blood:	n/a	n/a
21	CEBPB	chr7:4562189-4562372	K562	blood:	n/a	chr7:4562300-4562311
22	CEBPB	chr7:4510880-4511093	HepG2	liver:	n/a	chr7:4511007-4511018
23	CEBPB	chr7:4606462-4606612	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:4585045-4585090	A549	lung:	n/a	n/a
25	CEBPB	chr7:4526879-4527083	K562	blood:	n/a	chr7:4527026-4527037
26	CEBPB	chr7:4606368-4606733	MCF-7	breast:	n/a	n/a
27	CEBPB	chr7:4526987-4527171	A549	lung:	n/a	chr7:4527026-4527037
28	CEBPB	chr7:4510906-4511100	A549	lung:	n/a	chr7:4511007-4511018
29	CEBPB	chr7:4533824-4534026	K562	blood:	n/a	chr7:4533904-4533915
30	CEBPB	chr7:4606920-4607086	HepG2	liver:	n/a	chr7:4606937-4606948
31	CEBPB	chr7:4606335-4606705	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr7:4606356-4606720	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:4526970-4527129	H1-hESC	embryonic stem cell:	n/a	chr7:4527026-4527037
34	CEBPB	chr7:4606331-4606697	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr7:4526882-4527110	IMR90	lung:	n/a	chr7:4527026-4527037
36	CEBPB	chr7:4606437-4606623	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:4533878-4534018	HepG2	liver:	n/a	chr7:4533904-4533915
38	CEBPB	chr7:4562197-4562343	HepG2	liver:	n/a	chr7:4562300-4562311
39	CEBPB	chr7:4606357-4606697	A549	lung:	n/a	n/a
40	CEBPB	chr7:4533869-4534052	IMR90	lung:	n/a	chr7:4533904-4533915
41	CEBPB	chr7:4510903-4511140	IMR90	lung:	n/a	chr7:4511007-4511018
42	CEBPB	chr7:4584957-4585000	HepG2	liver:	n/a	chr7:4584972-4584983
43	CEBPB	chr7:4526888-4527175	HepG2	liver:	n/a	chr7:4527026-4527037
44	CEBPB	chr7:4533851-4534051	A549	lung:	n/a	chr7:4533904-4533915
45	CEBPB	chr7:4543419-4543508	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:4606365-4606717	A549	lung:	n/a	n/a
47	CEBPD	chr7:4572950-4573325	K562	blood:	n/a	n/a
48	CEBPD	chr7:4573063-4573272	K562	blood:	n/a	n/a
49	CHD1	chr7:4541262-4541349	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr7:4519143-4519145	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4536864-4536914	SK-N-SH	brain:	n/a
2	chr7:4536838-4536888	AG10803	skin:	n/a
3	chr7:4630518-4630568	NHDF-neo	bronchial:	n/a
4	chr7:4536838-4536888	HCF	heart:	n/a
5	chr7:4573716-4573766	HCF	heart:	n/a
6	chr7:4630518-4630568	HL-60	blood:	n/a
7	chr7:4536838-4536888	AG04450	lung:	fetal
8	chr7:4573535-4573585	Hela-S3	cervix:	n/a
9	chr7:4573535-4573585	HCM	heart:	n/a
10	chr7:4536864-4536914	AG09319	gingival:	n/a
11	chr7:4630518-4630568	HAEpiC	amniotic membrane:	n/a
12	chr7:4573535-4573585	HL-60	blood:	n/a
13	chr7:4630518-4630568	HPAEpiC	pulmonary alveolar:	n/a
14	chr7:4536864-4536914	BE2_C	brain:	n/a
15	chr7:4536838-4536888	LNCaP	prostate:	n/a
16	chr7:4573716-4573766	HUVEC	blood vessel:	n/a
17	chr7:4573535-4573585	NB4	blood:	n/a
18	chr7:4536864-4536914	AG04450	lung:	fetal
19	chr7:4536838-4536888	NB4	blood:	n/a
20	chr7:4536838-4536888	PrEC	prostate:	n/a
21	chr7:4536838-4536888	MCF10A-Er-Src	breast:	n/a
22	chr7:4630518-4630568	U87	brain:	n/a
23	chr7:4630518-4630568	HRPEpiC	eye:	n/a
24	chr7:4630518-4630568	HCPEpiC	choroid plexus:	n/a
25	chr7:4573716-4573766	ProgFib	skin:	n/a
26	chr7:4573716-4573766	ECC-1	luminal epithelium:	n/a
27	chr7:4536864-4536914	PFSK-1	brain:	n/a
28	chr7:4536838-4536888	GM19239	blood:	n/a
29	chr7:4536838-4536888	HRCEpiC	kidney:	n/a
30	chr7:4536864-4536914	BJ	skin:	n/a
31	chr7:4536838-4536888	HMEC	breast:	n/a
32	chr7:4573716-4573766	Jurkat	blood:	n/a
33	chr7:4630518-4630568	HCM	heart:	n/a
34	chr7:4630518-4630568	ProgFib	skin:	n/a
35	chr7:4536838-4536888	HUVEC	blood vessel:	n/a
36	chr7:4536838-4536888	MCF-7	breast:	n/a
37	chr7:4536864-4536914	GM06990	blood:	n/a
38	chr7:4573535-4573585	AG09309	skin:	n/a
39	chr7:4630518-4630568	HEEpiC	esophagus:	n/a
40	chr7:4630518-4630568	AG04449	skin:	fetal
41	chr7:4536864-4536914	LNCaP	prostate:	n/a
42	chr7:4536838-4536888	Caco-2	colon:	n/a
43	chr7:4536864-4536914	RPTEC	kidney:	n/a
44	chr7:4536864-4536914	HNPCEpiC	eye:	n/a
45	chr7:4573535-4573585	HEK293	kidney:	embryo
46	chr7:4536864-4536914	HEEpiC	esophagus:	n/a
47	chr7:4573716-4573766	HCPEpiC	choroid plexus:	n/a
48	chr7:4536864-4536914	U87	brain:	n/a
49	chr7:4573716-4573766	Caco-2	colon:	n/a
50	chr7:4573535-4573585	NHBE	bronchial:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4143002..4143685-chr7:4518859..4519662,3	MCF-7	breast:
2	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
3	chr7:4601107..4601677-chr7:4670928..4671456,2	MCF-7	breast:
4	chr7:4401235..4402088-chr7:4518606..4519411,2	MCF-7	breast:
5	chr7:4195210..4197944-chr7:4502921..4505536,2	MCF-7	breast:
6	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
7	chr7:4613003..4615813-chr7:4681464..4683495,2	MCF-7	breast:
8	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
9	chr7:4074370..4074950-chr7:4518765..4519624,3	MCF-7	breast:
10	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
11	chr20:52556259..52556926-chr7:4599215..4599761,2	MCF-7	breast:
12	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
13	chr7:4551212..4552814-chr7:4554906..4557306,2	K562	blood:
14	chr7:4559356..4562288-chr7:4562408..4565136,2	MCF-7	breast:
15	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
16	chr7:4642981..4645443-chr7:4649025..4651972,2	K562	blood:
17	chr7:4559356..4562288-chr7:4562408..4565136,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXK1-1	chr7:4515791-4518319	XLOC_005972
2	lnc-RADIL-2	chr7:4645445-4645678	NONHSAT118868
3	lnc-RADIL-2	chr7:4645446-4645678	XLOC_006345
4	lnc-RADIL-4	chr7:4509330-4509430	NONHSAT118863
5	lnc-RADIL-2	chr7:4645445-4645678	FPKM1_group_29021_transcript_1
6	lnc-RADIL-4	chr7:4513174-4513309	NONHSAT118863

No data

Variant related genes	Relation type
CYP3A54P	TF binding region
CYP3A54P	CpG island
ENSG00000164916	chromatin interactions
ENSG00000261809	chromatin interactions
ENSG00000236352	chromatin interactions
VEGFA	miRNA target sites
TTC30A	miRNA target sites

Extended variants
information (count: 2291 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2291 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377236195	chr7:4497207-4497208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs36017293	chr7:4497235-4497236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs71032965	chr7:4497236-4497237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs398003477	chr7:4497253-4497254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148948174	chr7:4497265-4497266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557238357	chr7:4497275-4497276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571031817	chr7:4497276-4497277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186864425	chr7:4497287-4497288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368549007	chr7:4497289-4497290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553327916	chr7:4497334-4497335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573365062	chr7:4497335-4497336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191276990	chr7:4497338-4497339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs555889697	chr7:4497344-4497345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78712446	chr7:4497371-4497372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376752455	chr7:4497372-4497373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547866046	chr7:4497373-4497374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369368875	chr7:4497381-4497382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544571079	chr7:4497397-4497398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7806129	chr7:4497398-4497399	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs138282024	chr7:4497406-4497407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539431763	chr7:4497438-4497439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540504189	chr7:4497442-4497443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549682193	chr7:4497466-4497467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565003682	chr7:4497472-4497473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560116608	chr7:4497537-4497538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74797028	chr7:4497566-4497567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548707930	chr7:4497603-4497604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111380571	chr7:4497618-4497619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531207413	chr7:4497631-4497632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188970342	chr7:4497662-4497663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs895710	chr7:4497688-4497689	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs895711	chr7:4497691-4497692	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs74771684	chr7:4497702-4497703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs193236085	chr7:4497703-4497704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185273139	chr7:4497705-4497706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373845842	chr7:4497752-4497753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540811202	chr7:4497795-4497796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536016589	chr7:4497824-4497825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144139621	chr7:4497830-4497831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575780800	chr7:4497884-4497885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544632444	chr7:4497902-4497903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557899131	chr7:4497907-4497908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577946558	chr7:4497933-4497934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190119269	chr7:4497944-4497945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146903600	chr7:4497947-4497948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10266265	chr7:4497968-4497969	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs529060784	chr7:4497977-4497978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542363340	chr7:4497988-4497989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562261498	chr7:4498008-4498009	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs567531906	chr7:4498022-4498023	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4497200-4498000	Enhancers	Fetal Muscle Trunk	muscle
2	chr7:4497400-4498200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr7:4497400-4498200	Enhancers	Adipose Nuclei	Adipose
4	chr7:4497400-4498600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr7:4497400-4498600	Enhancers	Fetal Muscle Leg	muscle
6	chr7:4497400-4498600	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr7:4497400-4498800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr7:4497400-4498800	Enhancers	Ovary	ovary
9	chr7:4497600-4498200	Enhancers	Brain Germinal Matrix	brain
10	chr7:4497600-4498200	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr7:4497600-4498400	Enhancers	Colon Smooth Muscle	Colon
12	chr7:4497600-4498400	Enhancers	Fetal Brain Male	brain
13	chr7:4497600-4498600	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr7:4497800-4498200	Enhancers	Fetal Brain Female	brain
15	chr7:4498000-4498600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
16	chr7:4498200-4498600	Enhancers	Brain Hippocampus Middle	brain
17	chr7:4498600-4500200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr7:4498600-4500200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr7:4499600-4499800	Enhancers	Aorta	Aorta
20	chr7:4499800-4500600	Enhancers	Fetal Intestine Large	intestine
21	chr7:4499800-4502600	Weak transcription	Aorta	Aorta
22	chr7:4500200-4500600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:4500200-4500600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:4500200-4501200	Enhancers	Fetal Intestine Small	intestine
25	chr7:4500200-4502600	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr7:4500800-4501400	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr7:4501400-4501600	Active TSS	Monocytes-CD14+_RO01746	blood
28	chr7:4501600-4501800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr7:4509000-4510000	Enhancers	H9 Cell Line	embryonic stem cell
30	chr7:4509000-4510000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr7:4509200-4509600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr7:4509200-4509800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr7:4509400-4509800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr7:4509400-4510000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:4509600-4510000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr7:4509600-4510000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr7:4509600-4510200	Enhancers	Aorta	Aorta
38	chr7:4509800-4513200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:4510000-4511200	Enhancers	Brain Germinal Matrix	brain
40	chr7:4510000-4512200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr7:4510000-4512200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr7:4510000-4512400	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr7:4512200-4512400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:4512200-4513000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr7:4512200-4513000	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr7:4512400-4512600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
47	chr7:4512400-4513000	Enhancers	H9 Cell Line	embryonic stem cell
48	chr7:4512600-4512800	Enhancers	Adipose Nuclei	Adipose
49	chr7:4512600-4512800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
50	chr7:4513000-4513200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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