Variant report

Variant	esv2762642
Chromosome Location	chr7:4450968-4560220
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:612)
CpG islands
(count:427)
Chromatin interactive
region (count:14)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:4476207-4476541	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:4456113-4456402	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	BHLHE40	chr7:4456107-4456375	K562	blood:	n/a	n/a
6	BRCA1	chr7:4519369-4519376	HepG2	liver:	n/a	n/a
7	CBX3	chr7:4523514-4523852	K562	blood:	n/a	n/a
8	CBX3	chr7:4539559-4539829	K562	blood:	n/a	n/a
9	CBX3	chr7:4539569-4539857	K562	blood:	n/a	n/a
10	CBX3	chr7:4523526-4523869	K562	blood:	n/a	n/a
11	CCNT2	chr7:4456019-4456350	K562	blood:	n/a	n/a
12	CEBPB	chr7:4526879-4527083	K562	blood:	n/a	chr7:4527026-4527037
13	CEBPB	chr7:4526839-4527196	MCF-7	breast:	n/a	chr7:4527026-4527037
14	CEBPB	chr7:4526987-4527171	A549	lung:	n/a	chr7:4527026-4527037
15	CEBPB	chr7:4510874-4511113	K562	blood:	n/a	chr7:4511007-4511018
16	CEBPB	chr7:4526863-4527183	MCF-7	breast:	n/a	chr7:4527026-4527037
17	CEBPB	chr7:4526888-4527175	HepG2	liver:	n/a	chr7:4527026-4527037
18	CEBPB	chr7:4533851-4534051	A549	lung:	n/a	chr7:4533904-4533915
19	CEBPB	chr7:4510880-4511093	HepG2	liver:	n/a	chr7:4511007-4511018
20	CEBPB	chr7:4533878-4534018	HepG2	liver:	n/a	chr7:4533904-4533915
21	CEBPB	chr7:4533869-4534052	IMR90	lung:	n/a	chr7:4533904-4533915
22	CEBPB	chr7:4533824-4534026	K562	blood:	n/a	chr7:4533904-4533915
23	CEBPB	chr7:4510903-4511140	IMR90	lung:	n/a	chr7:4511007-4511018
24	CEBPB	chr7:4510906-4511100	A549	lung:	n/a	chr7:4511007-4511018
25	CEBPB	chr7:4526882-4527110	IMR90	lung:	n/a	chr7:4527026-4527037
26	CEBPB	chr7:4516153-4516177	HepG2	liver:	n/a	chr7:4516157-4516168
27	CEBPB	chr7:4543419-4543508	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:4526970-4527129	H1-hESC	embryonic stem cell:	n/a	chr7:4527026-4527037
29	CEBPD	chr7:4478262-4478862	K562	blood:	n/a	n/a
30	CEBPD	chr7:4478238-4478981	K562	blood:	n/a	n/a
31	CHD1	chr7:4519143-4519145	GM12878	blood:	n/a	n/a
32	CHD1	chr7:4541262-4541349	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr7:4540385-4540761	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:4512500-4512650	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr7:4543060-4543210	BE2_C	brain:	n/a	n/a
36	CTCF	chr7:4477142-4477216	H1-hESC	embryonic stem cell:	n/a	chr7:4477174-4477183
37	CTCF	chr7:4542900-4543050	HCT-116	colon:	n/a	n/a
38	CTCF	chr7:4519120-4519270	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr7:4519142-4519306	GM10248	blood:	n/a	n/a
40	CTCF	chr7:4543100-4543250	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr7:4519060-4519210	HCM	heart:	n/a	n/a
42	CTCF	chr7:4466136-4466292	LNCaP	prostate:	n/a	n/a
43	CTCF	chr7:4477040-4477190	K562	blood:	n/a	chr7:4477174-4477183
44	CTCF	chr7:4543026-4543227	K562	blood:	n/a	n/a
45	CTCF	chr7:4519140-4519290	GM12868	blood:	n/a	n/a
46	CTCF	chr7:4518966-4519575	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:4519180-4519330	GM12864	blood:	n/a	n/a
48	CTCF	chr7:4543040-4543190	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:4543032-4543168	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr7:4519140-4519290	NHDF-neo	bronchial:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4456403-4456453	HCT-116	colon:	n/a
2	chr7:4456403-4456453	SKMC	muscle:	n/a
3	chr7:4456119-4456169	ovcar-3	ovarian:	n/a
4	chr7:4456403-4456453	ECC-1	luminal epithelium:	n/a
5	chr7:4456341-4456391	GM12891	blood:	n/a
6	chr7:4456131-4456181	H1-hESC	embryonic stem cell:	embryo
7	chr7:4456403-4456453	T-47D	breast:	n/a
8	chr7:4456403-4456453	Hela-S3	cervix:	n/a
9	chr7:4456396-4456446	GM12892	blood:	n/a
10	chr7:4456396-4456446	BJ	skin:	n/a
11	chr7:4456396-4456446	MCF10A-Er-Src	breast:	n/a
12	chr7:4456119-4456169	Jurkat	blood:	n/a
13	chr7:4456341-4456391	SK-N-SH	brain:	n/a
14	chr7:4456119-4456169	AG09309	skin:	n/a
15	chr7:4456131-4456181	BE2_C	brain:	n/a
16	chr7:4456119-4456169	PrEC	prostate:	n/a
17	chr7:4456119-4456169	SK-N-SH_RA	brain:	n/a
18	chr7:4536838-4536888	Hela-S3	cervix:	n/a
19	chr7:4456403-4456453	HRPEpiC	eye:	n/a
20	chr7:4536864-4536914	HCM	heart:	n/a
21	chr7:4456403-4456453	MCF-7	breast:	n/a
22	chr7:4456341-4456391	HNPCEpiC	eye:	n/a
23	chr7:4456119-4456169	HRE	kidney:	n/a
24	chr7:4536864-4536914	AoSMC	blood vessel:	n/a
25	chr7:4456119-4456169	AoSMC	blood vessel:	n/a
26	chr7:4456119-4456169	PFSK-1	brain:	n/a
27	chr7:4536838-4536888	HepG2	liver:	n/a
28	chr7:4456341-4456391	HAEpiC	amniotic membrane:	n/a
29	chr7:4456341-4456391	GM12878	blood:	n/a
30	chr7:4456396-4456446	HRE	kidney:	n/a
31	chr7:4456131-4456181	Hela-S3	cervix:	n/a
32	chr7:4536838-4536888	NHBE	bronchial:	n/a
33	chr7:4456119-4456169	Caco-2	colon:	n/a
34	chr7:4536838-4536888	HEK293	kidney:	embryo
35	chr7:4456403-4456453	H1-hESC	embryonic stem cell:	embryo
36	chr7:4456396-4456446	AG09309	skin:	n/a
37	chr7:4456341-4456391	Hela-S3	cervix:	n/a
38	chr7:4456341-4456391	AG04449	skin:	fetal
39	chr7:4456341-4456391	HRPEpiC	eye:	n/a
40	chr7:4456396-4456446	AoSMC	blood vessel:	n/a
41	chr7:4456119-4456169	A549	lung:	n/a
42	chr7:4456341-4456391	BJ	skin:	n/a
43	chr7:4456131-4456181	HCPEpiC	choroid plexus:	n/a
44	chr7:4456341-4456391	A549	lung:	n/a
45	chr7:4456396-4456446	HEK293	kidney:	embryo
46	chr7:4456119-4456169	GM06990	blood:	n/a
47	chr7:4536864-4536914	Caco-2	colon:	n/a
48	chr7:4456341-4456391	HL-60	blood:	n/a
49	chr7:4536864-4536914	HMEC	breast:	n/a
50	chr7:4456131-4456181	HCT-116	colon:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
2	chr15:101629167..101629860-chr7:4485245..4486227,2	MCF-7	breast:
3	chr17:57920568..57922934-chr7:4466757..4469576,2	MCF-7	breast:
4	chr7:4551212..4552814-chr7:4554906..4557306,2	K562	blood:
5	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
6	chr7:4559356..4562288-chr7:4562408..4565136,2	MCF-7	breast:
7	chr7:4143002..4143685-chr7:4518859..4519662,3	MCF-7	breast:
8	chr7:4195210..4197944-chr7:4502921..4505536,2	MCF-7	breast:
9	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
10	chr7:4401235..4402088-chr7:4518606..4519411,2	MCF-7	breast:
11	chr7:4074370..4074950-chr7:4518765..4519624,3	MCF-7	breast:
12	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
13	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
14	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SDK1-1	chr7:4482317-4482707	l_3355_chr7:4440443-4482707_testes
2	lnc-RADIL-4	chr7:4513174-4513309	NONHSAT118863
3	lnc-FOXK1-1	chr7:4515791-4518319	XLOC_005972
4	lnc-RADIL-3	chr7:4455727-4456136	XLOC_006344
5	lnc-RADIL-4	chr7:4509330-4509430	NONHSAT118863
6	lnc-RADIL-3	chr7:4452562-4452778	XLOC_006344
7	lnc-RADIL-5	chr7:4472597-4475543	NONHSAT118861
8	lnc-FOXK1-1	chr7:4473994-4474153	XLOC_005972

No data

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

Extended variants
information (count: 3007 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3007 , 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	rs112668439	chr7:4452403-4452404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372787782	chr7:4452411-4452412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145812210	chr7:4452412-4452413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573660417	chr7:4452415-4452416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111428493	chr7:4452430-4452431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11980494	chr7:4452470-4452471	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs11982891	chr7:4452518-4452519	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs181015130	chr7:4452601-4452602	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs142485694	chr7:4452615-4452616	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs546664212	chr7:4452622-4452623	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs10951550	chr7:4452636-4452637	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs553885597	chr7:4452642-4452643	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs548874174	chr7:4452651-4452652	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs569084960	chr7:4452682-4452683	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs375028548	chr7:4452690-4452691	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs368795683	chr7:4452717-4452718	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs10266071	chr7:4452727-4452728	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs185038701	chr7:4452733-4452734	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs557973355	chr7:4452758-4452759	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs536736830	chr7:4452806-4452807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571338501	chr7:4452817-4452818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533903361	chr7:4452837-4452838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553877095	chr7:4452871-4452872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573697204	chr7:4452875-4452876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542606321	chr7:4452883-4452884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10248020	chr7:4452892-4452893	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs575932178	chr7:4452980-4452981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6951387	chr7:4452987-4452988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73671687	chr7:4452990-4452991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs533318884	chr7:4452994-4452995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs367544713	chr7:4452999-4453000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540345000	chr7:4453005-4453006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1009527	chr7:4453029-4453030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs191022365	chr7:4453048-4453049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73671688	chr7:4453113-4453114	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs543674383	chr7:4453217-4453218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569150526	chr7:4453227-4453228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545175351	chr7:4453232-4453233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565150048	chr7:4453234-4453235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183965461	chr7:4453264-4453265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571443788	chr7:4453266-4453267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545786863	chr7:4453312-4453313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367951882	chr7:4453325-4453326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567324501	chr7:4453329-4453330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536341950	chr7:4453333-4453334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556156828	chr7:4453341-4453342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575923540	chr7:4453349-4453350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544908006	chr7:4453352-4453353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558132671	chr7:4453379-4453380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs386709586	chr7:4453380-4453381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
early-passage human iPS cells	21368824	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

Chromatin state (count:186 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4452400-4452800	Enhancers	Fetal Brain Male	brain
2	chr7:4452800-4456000	Weak transcription	Fetal Brain Male	brain
3	chr7:4455000-4457600	Enhancers	Fetal Intestine Small	intestine
4	chr7:4455400-4455800	Enhancers	Duodenum Mucosa	Duodenum
5	chr7:4455600-4455800	Enhancers	Brain Substantia Nigra	brain
6	chr7:4455600-4455800	Enhancers	Duodenum Smooth Muscle	Duodenum
7	chr7:4455600-4455800	Enhancers	Fetal Intestine Large	intestine
8	chr7:4455600-4456600	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr7:4455800-4456000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:4455800-4456000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr7:4455800-4456000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr7:4455800-4456000	Active TSS	Adipose Nuclei	Adipose
13	chr7:4455800-4456000	Flanking Active TSS	Duodenum Mucosa	Duodenum
14	chr7:4455800-4456000	Active TSS	Fetal Brain Female	brain
15	chr7:4455800-4456000	Flanking Active TSS	Fetal Intestine Large	intestine
16	chr7:4455800-4456000	Enhancers	Fetal Stomach	stomach
17	chr7:4455800-4456000	Enhancers	HepG2	liver
18	chr7:4455800-4456200	Active TSS	Aorta	Aorta
19	chr7:4455800-4456200	Active TSS	Brain Germinal Matrix	brain
20	chr7:4455800-4456200	Flanking Active TSS	Brain Substantia Nigra	brain
21	chr7:4455800-4456200	Active TSS	Fetal Lung	lung
22	chr7:4455800-4456400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:4455800-4456400	Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr7:4455800-4456400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:4455800-4456400	Active TSS	Brain Hippocampus Middle	brain
26	chr7:4455800-4456400	Active TSS	Colon Smooth Muscle	Colon
27	chr7:4455800-4456400	Active TSS	Duodenum Smooth Muscle	Duodenum
28	chr7:4455800-4456400	Active TSS	A549	lung
29	chr7:4455800-4456600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr7:4455800-4456600	Active TSS	Brain Angular Gyrus	brain
31	chr7:4455800-4456600	Active TSS	Brain Anterior Caudate	brain
32	chr7:4455800-4456600	Active TSS	Brain Cingulate Gyrus	brain
33	chr7:4455800-4456600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr7:4455800-4456600	Active TSS	Stomach Mucosa	stomach
35	chr7:4455800-4456600	Active TSS	Stomach Smooth Muscle	stomach
36	chr7:4456000-4456200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr7:4456000-4456200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:4456000-4456200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr7:4456000-4456400	Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr7:4456000-4456400	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr7:4456000-4456400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr7:4456000-4456400	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr7:4456000-4456400	Flanking Active TSS	Fetal Brain Female	brain
44	chr7:4456000-4456400	Active TSS	Fetal Intestine Large	intestine
45	chr7:4456000-4456400	Enhancers	Fetal Muscle Trunk	muscle
46	chr7:4456000-4456400	Flanking Active TSS	Fetal Stomach	stomach
47	chr7:4456000-4456400	Enhancers	Ovary	ovary
48	chr7:4456000-4456400	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr7:4456000-4456400	Active TSS	Rectal Smooth Muscle	rectum
50	chr7:4456000-4456400	Active TSS	Skeletal Muscle Female	skeletal muscle

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