Variant report

Variant	nsv1027912
Chromosome Location	chr7:4462126-4575902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:627)
CpG islands
(count:244)
Chromatin interactive
region (count:15)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:627 , 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	chr7:4573177-4573308	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	chr7:4539569-4539857	K562	blood:	n/a	n/a
7	CBX3	chr7:4523526-4523869	K562	blood:	n/a	n/a
8	CBX3	chr7:4523514-4523852	K562	blood:	n/a	n/a
9	CBX3	chr7:4539559-4539829	K562	blood:	n/a	n/a
10	CEBPB	chr7:4526882-4527110	IMR90	lung:	n/a	chr7:4527026-4527037
11	CEBPB	chr7:4533824-4534026	K562	blood:	n/a	chr7:4533904-4533915
12	CEBPB	chr7:4533869-4534052	IMR90	lung:	n/a	chr7:4533904-4533915
13	CEBPB	chr7:4562197-4562343	HepG2	liver:	n/a	chr7:4562300-4562311
14	CEBPB	chr7:4533851-4534051	A549	lung:	n/a	chr7:4533904-4533915
15	CEBPB	chr7:4526970-4527129	H1-hESC	embryonic stem cell:	n/a	chr7:4527026-4527037
16	CEBPB	chr7:4533878-4534018	HepG2	liver:	n/a	chr7:4533904-4533915
17	CEBPB	chr7:4526879-4527083	K562	blood:	n/a	chr7:4527026-4527037
18	CEBPB	chr7:4510903-4511140	IMR90	lung:	n/a	chr7:4511007-4511018
19	CEBPB	chr7:4510874-4511113	K562	blood:	n/a	chr7:4511007-4511018
20	CEBPB	chr7:4526888-4527175	HepG2	liver:	n/a	chr7:4527026-4527037
21	CEBPB	chr7:4516153-4516177	HepG2	liver:	n/a	chr7:4516157-4516168
22	CEBPB	chr7:4510880-4511093	HepG2	liver:	n/a	chr7:4511007-4511018
23	CEBPB	chr7:4543419-4543508	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:4510906-4511100	A549	lung:	n/a	chr7:4511007-4511018
25	CEBPB	chr7:4526987-4527171	A549	lung:	n/a	chr7:4527026-4527037
26	CEBPB	chr7:4562189-4562372	K562	blood:	n/a	chr7:4562300-4562311
27	CEBPB	chr7:4526839-4527196	MCF-7	breast:	n/a	chr7:4527026-4527037
28	CEBPB	chr7:4526863-4527183	MCF-7	breast:	n/a	chr7:4527026-4527037
29	CEBPD	chr7:4572950-4573325	K562	blood:	n/a	n/a
30	CEBPD	chr7:4573063-4573272	K562	blood:	n/a	n/a
31	CEBPD	chr7:4478262-4478862	K562	blood:	n/a	n/a
32	CEBPD	chr7:4478238-4478981	K562	blood:	n/a	n/a
33	CHD1	chr7:4519143-4519145	GM12878	blood:	n/a	n/a
34	CHD1	chr7:4541262-4541349	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr7:4573126-4573556	K562	blood:	n/a	n/a
36	CHD2	chr7:4540385-4540761	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr7:4573233-4573376	HepG2	liver:	n/a	n/a
38	CTCF	chr7:4519100-4519250	HFF	foreskin:	n/a	n/a
39	CTCF	chr7:4543000-4543150	HepG2	liver:	n/a	n/a
40	CTCF	chr7:4519069-4519290	IMR90	lung:	n/a	n/a
41	CTCF	chr7:4519146-4519231	GM19238	blood:	n/a	n/a
42	CTCF	chr7:4519100-4519351	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr7:4512520-4512670	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr7:4519140-4519290	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr7:4519100-4519250	SAEC	small airway:	n/a	n/a
46	CTCF	chr7:4512479-4512710	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:4490280-4490430	NB4	blood:	n/a	n/a
48	CTCF	chr7:4512460-4512610	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:4490300-4490450	NHEK	skin:	n/a	n/a
50	CTCF	chr7:4519160-4519310	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4573716-4573766	HEEpiC	esophagus:	n/a
2	chr7:4536838-4536888	AG04449	skin:	fetal
3	chr7:4536864-4536914	PrEC	prostate:	n/a
4	chr7:4573716-4573766	MCF-7	breast:	n/a
5	chr7:4573716-4573766	SAEC	small airway:	n/a
6	chr7:4536864-4536914	HCF	heart:	n/a
7	chr7:4573716-4573766	AG04450	lung:	fetal
8	chr7:4573535-4573585	HepG2	liver:	n/a
9	chr7:4536838-4536888	HEK293	kidney:	embryo
10	chr7:4536838-4536888	AG09309	skin:	n/a
11	chr7:4536838-4536888	HCPEpiC	choroid plexus:	n/a
12	chr7:4536838-4536888	NH-A	brain:	n/a
13	chr7:4536864-4536914	SK-N-SH	brain:	n/a
14	chr7:4536838-4536888	CMK	blood:	n/a
15	chr7:4536864-4536914	MCF-7	breast:	n/a
16	chr7:4573535-4573585	Jurkat	blood:	n/a
17	chr7:4573716-4573766	PrEC	prostate:	n/a
18	chr7:4573716-4573766	HAEpiC	amniotic membrane:	n/a
19	chr7:4536838-4536888	NHDF-neo	bronchial:	n/a
20	chr7:4573716-4573766	AG04449	skin:	fetal
21	chr7:4573716-4573766	Hepatocyte	liver:	n/a
22	chr7:4536838-4536888	AoSMC	blood vessel:	n/a
23	chr7:4573535-4573585	Hela-S3	cervix:	n/a
24	chr7:4536864-4536914	PANC-1	pancreas:	n/a
25	chr7:4573535-4573585	AG04450	lung:	fetal
26	chr7:4536838-4536888	HRE	kidney:	n/a
27	chr7:4573535-4573585	ovcar-3	ovarian:	n/a
28	chr7:4573716-4573766	ECC-1	luminal epithelium:	n/a
29	chr7:4573716-4573766	HRE	kidney:	n/a
30	chr7:4573716-4573766	LNCaP	prostate:	n/a
31	chr7:4536864-4536914	HRE	kidney:	n/a
32	chr7:4573535-4573585	RPTEC	kidney:	n/a
33	chr7:4536838-4536888	Hela-S3	cervix:	n/a
34	chr7:4536838-4536888	GM12892	blood:	n/a
35	chr7:4536838-4536888	IMR90	lung:	fetal
36	chr7:4573535-4573585	GM12878	blood:	n/a
37	chr7:4536864-4536914	SKMC	muscle:	n/a
38	chr7:4573716-4573766	T-47D	breast:	n/a
39	chr7:4536838-4536888	GM12891	blood:	n/a
40	chr7:4573716-4573766	PANC-1	pancreas:	n/a
41	chr7:4573716-4573766	SK-N-MC	brain:	n/a
42	chr7:4573535-4573585	HPAEpiC	pulmonary alveolar:	n/a
43	chr7:4536864-4536914	SK-N-MC	brain:	n/a
44	chr7:4536864-4536914	GM19239	blood:	n/a
45	chr7:4573535-4573585	SK-N-SH_RA	brain:	n/a
46	chr7:4536864-4536914	HIPEpiC	eye:	n/a
47	chr7:4536864-4536914	IMR90	lung:	fetal
48	chr7:4536864-4536914	SK-N-SH_RA	brain:	n/a
49	chr7:4536838-4536888	HCF	heart:	n/a
50	chr7:4536864-4536914	AG09309	skin:	n/a

(count:15 , 50 per page) page: 1

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

(count:6 , 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	chr7:4509330-4509430	NONHSAT118863
3	lnc-RADIL-5	chr7:4472597-4475543	NONHSAT118861
4	lnc-RADIL-4	chr7:4513174-4513309	NONHSAT118863
5	lnc-FOXK1-1	chr7:4473994-4474153	XLOC_005972
6	lnc-FOXK1-1	chr7:4515791-4518319	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: 2707 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2707 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555572077	chr7:4462403-4462404	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs111981033	chr7:4462431-4462432	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs544305445	chr7:4462449-4462450	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs149847929	chr7:4462472-4462473	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs112521415	chr7:4462478-4462479	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs369089916	chr7:4462479-4462480	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs7807912	chr7:4462482-4462483	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs929347	chr7:4462496-4462497	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs58981239	chr7:4462512-4462513	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs13232858	chr7:4462595-4462596	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs550447907	chr7:4462621-4462622	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs551509943	chr7:4462670-4462671	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs111376620	chr7:4462671-4462672	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs527375154	chr7:4462676-4462677	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs113297450	chr7:4462698-4462699	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs576114263	chr7:4462716-4462717	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs6462821	chr7:4462717-4462718	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs10237068	chr7:4462735-4462736	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs555596556	chr7:4462751-4462752	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs371664213	chr7:4462764-4462765	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs533877190	chr7:4462786-4462787	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs375018956	chr7:4462796-4462797	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs543588191	chr7:4462814-4462815	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs538093011	chr7:4462840-4462841	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs575835163	chr7:4462871-4462872	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs578056042	chr7:4462879-4462880	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs143520965	chr7:4462882-4462883	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs374147625	chr7:4462883-4462884	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs553895270	chr7:4462938-4462939	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs542260144	chr7:4462962-4462963	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs573950125	chr7:4462995-4462996	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs560480242	chr7:4462997-4462998	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs542945622	chr7:4463005-4463006	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs7792641	chr7:4463032-4463033	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs531626810	chr7:4463051-4463052	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs147591938	chr7:4463061-4463062	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs112254944	chr7:4463091-4463092	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs552639556	chr7:4463103-4463104	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs527426649	chr7:4463106-4463107	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs115323280	chr7:4463199-4463200	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs567156345	chr7:4463206-4463207	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs564789955	chr7:4463209-4463210	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs189092837	chr7:4463225-4463226	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs75834904	chr7:4463238-4463239	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs7810278	chr7:4463248-4463249	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	mRNA abundance
46	rs182483773	chr7:4463264-4463265	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs186332293	chr7:4463297-4463298	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs189112681	chr7:4463302-4463303	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs181448794	chr7:4463305-4463306	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs115114083	chr7:4463318-4463319	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4462400-4463800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:4463000-4463200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:4464800-4465000	Enhancers	Gastric	stomach
4	chr7:4464800-4465200	Enhancers	Brain Substantia Nigra	brain
5	chr7:4465000-4467600	Weak transcription	Gastric	stomach
6	chr7:4465600-4468600	Enhancers	Fetal Brain Male	brain
7	chr7:4471600-4472000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
8	chr7:4472000-4473600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr7:4473200-4474000	Enhancers	Fetal Muscle Trunk	muscle
10	chr7:4473600-4473800	Enhancers	Fetal Stomach	stomach
11	chr7:4473600-4474000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr7:4473600-4474200	Enhancers	Fetal Kidney	kidney
13	chr7:4473800-4474000	Flanking Active TSS	Fetal Stomach	stomach
14	chr7:4473800-4475200	Active TSS	Skeletal Muscle Male	skeletal muscle
15	chr7:4474000-4474200	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
16	chr7:4474000-4476600	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr7:4474200-4474400	Active TSS	Fetal Stomach	stomach
18	chr7:4474200-4475200	Enhancers	Fetal Intestine Large	intestine
19	chr7:4474600-4478200	Enhancers	Fetal Intestine Small	intestine
20	chr7:4475000-4475200	Enhancers	Pancreas	Pancrea
21	chr7:4475000-4477400	Enhancers	Stomach Mucosa	stomach
22	chr7:4475200-4475400	Enhancers	A549	lung
23	chr7:4475200-4475600	Flanking Active TSS	Fetal Intestine Large	intestine
24	chr7:4475400-4476600	Weak transcription	Pancreas	Pancrea
25	chr7:4475400-4476600	Weak transcription	A549	lung
26	chr7:4475600-4478200	Enhancers	Fetal Intestine Large	intestine
27	chr7:4475800-4477200	Bivalent Enhancer	HepG2	liver
28	chr7:4476600-4477200	Enhancers	Pancreas	Pancrea
29	chr7:4476600-4477400	Enhancers	A549	lung
30	chr7:4476800-4477200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:4476800-4477200	Enhancers	Gastric	stomach
32	chr7:4477000-4477400	Enhancers	Fetal Muscle Trunk	muscle
33	chr7:4477000-4478200	Enhancers	Fetal Muscle Leg	muscle
34	chr7:4478000-4479400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr7:4478200-4483400	Weak transcription	Fetal Intestine Small	intestine
36	chr7:4482200-4486000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
37	chr7:4483000-4483200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr7:4483400-4485000	Enhancers	Fetal Intestine Large	intestine
39	chr7:4483400-4485000	Enhancers	Fetal Intestine Small	intestine
40	chr7:4483600-4483800	Enhancers	Fetal Kidney	kidney
41	chr7:4483800-4485400	Weak transcription	Fetal Kidney	kidney
42	chr7:4485000-4488600	Weak transcription	Fetal Intestine Large	intestine
43	chr7:4485000-4488600	Weak transcription	Fetal Intestine Small	intestine
44	chr7:4485400-4485800	ZNF genes & repeats	Fetal Kidney	kidney
45	chr7:4485600-4485800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr7:4485800-4491400	Weak transcription	Fetal Kidney	kidney
47	chr7:4488600-4489400	Enhancers	HepG2	liver
48	chr7:4488600-4489600	Enhancers	Fetal Intestine Large	intestine
49	chr7:4488600-4489600	Enhancers	Fetal Intestine Small	intestine
50	chr7:4489000-4489600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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