Variant report

Variant	nsv888044
Chromosome Location	chr7:53456941-53602556
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:53486223-53486324	K562	blood:	n/a	n/a
2	BRCA1	chr7:53587799-53587809	GM12878	blood:	n/a	n/a
3	CEBPB	chr7:53588410-53588727	HepG2	liver:	n/a	chr7:53588550-53588561 chr7:53588550-53588563 chr7:53588558-53588571 chr7:53588558-53588571 chr7:53588552-53588561 chr7:53588552-53588563
4	CEBPB	chr7:53505120-53505352	Hela-S3	cervix:	n/a	chr7:53505251-53505262
5	CEBPB	chr7:53587738-53588025	MCF-7	breast:	n/a	chr7:53587881-53587892
6	CEBPB	chr7:53530536-53530863	HepG2	liver:	n/a	chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530706 chr7:53530697-53530706
7	CEBPB	chr7:53587746-53588062	IMR90	lung:	n/a	chr7:53587881-53587892
8	CEBPB	chr7:53501280-53501444	K562	blood:	n/a	chr7:53501375-53501386
9	CEBPB	chr7:53572607-53572958	HepG2	liver:	n/a	chr7:53572763-53572774
10	CEBPB	chr7:53501358-53501394	H1-hESC	embryonic stem cell:	n/a	chr7:53501375-53501386
11	CEBPB	chr7:53587730-53588040	HepG2	liver:	n/a	chr7:53587881-53587892
12	CEBPB	chr7:53505078-53505387	HepG2	liver:	n/a	chr7:53505251-53505262
13	CEBPB	chr7:53530560-53530856	H1-hESC	embryonic stem cell:	n/a	chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530706 chr7:53530697-53530706
14	CEBPB	chr7:53588391-53589005	A549	lung:	n/a	chr7:53588550-53588561 chr7:53588550-53588563 chr7:53588558-53588571 chr7:53588558-53588571 chr7:53588552-53588561 chr7:53588552-53588563
15	CEBPB	chr7:53572631-53572945	IMR90	lung:	n/a	chr7:53572763-53572774
16	CEBPB	chr7:53572675-53572941	MCF-7	breast:	n/a	chr7:53572763-53572774
17	CEBPB	chr7:53530548-53530869	IMR90	lung:	n/a	chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530706 chr7:53530697-53530706
18	CEBPB	chr7:53587750-53588037	A549	lung:	n/a	chr7:53587881-53587892
19	CEBPB	chr7:53588393-53588685	Hela-S3	cervix:	n/a	chr7:53588550-53588561 chr7:53588550-53588563 chr7:53588558-53588571 chr7:53588558-53588571 chr7:53588552-53588561 chr7:53588552-53588563
20	CEBPB	chr7:53501208-53501545	HepG2	liver:	n/a	chr7:53501375-53501386
21	CEBPB	chr7:53530516-53530859	K562	blood:	n/a	chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530706 chr7:53530697-53530706
22	CEBPB	chr7:53502040-53502264	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr7:53501299-53501500	IMR90	lung:	n/a	chr7:53501375-53501386
24	CTCF	chr7:53497900-53498050	HPF	lung:	n/a	n/a
25	CTCF	chr7:53567900-53568050	HMEC	breast:	n/a	n/a
26	CTCF	chr7:53555705-53555765	GM20000	blood:	n/a	n/a
27	CTCF	chr7:53494120-53494270	GM12864	blood:	n/a	n/a
28	CTCF	chr7:53494200-53494350	HAc	cerebellar:	n/a	n/a
29	CTCF	chr7:53494260-53494410	RPTEC	kidney:	n/a	n/a
30	CTCF	chr7:53502289-53502325	Fibrobl	skin:	n/a	n/a
31	CTCF	chr7:53494180-53494330	RPTEC	kidney:	n/a	n/a
32	CTCF	chr7:53483246-53483300	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:53516240-53516390	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr7:53487840-53487990	RPTEC	kidney:	n/a	n/a
35	CTCF	chr7:53563059-53563122	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr7:53494172-53494333	Gliobla	brain:	n/a	n/a
37	CTCF	chr7:53572240-53572390	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr7:53563086-53563140	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr7:53488226-53488236	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr7:53488120-53488270	RPTEC	kidney:	n/a	n/a
41	CTCF	chr7:53527926-53528005	GM10248	blood:	n/a	n/a
42	CTCF	chr7:53535861-53535883	Medullo	brain:	n/a	n/a
43	CTCF	chr7:53494240-53494390	HRE	kidney:	n/a	n/a
44	CTCF	chr7:53557364-53557424	GM20000	blood:	n/a	n/a
45	CTCF	chr7:53473697-53473756	Medullo	brain:	n/a	n/a
46	CTCF	chr7:53498727-53498761	GM13977	blood:	n/a	n/a
47	CTCF	chr7:53494252-53494288	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr7:53494240-53494390	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:53494200-53494350	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr7:53488240-53488244	Kidney_OC	kidney:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:53480788..53483198-chr7:53496726..53498453,2	K562	blood:
2	chr7:53460851..53461831-chr9:14244620..14245120,2	MCF-7	breast:
3	chr7:53499272..53501434-chr7:53507043..53509851,2	K562	blood:
4	chr7:53581265..53583622-chr7:53585126..53587157,2	MCF-7	breast:
5	chr7:53588403..53590353-chr7:53592550..53594897,2	K562	blood:
6	chr20:52720034..52720613-chr7:53479832..53480332,2	MCF-7	breast:
7	chr7:53473728..53475869-chr7:53482133..53483752,2	K562	blood:
8	chr7:53473728..53475869-chr7:53482133..53483752,2	K562	blood:
9	chr7:53581265..53583622-chr7:53585126..53587157,2	MCF-7	breast:
10	chr7:53480788..53483198-chr7:53496726..53498453,2	K562	blood:
11	chr7:53499272..53501434-chr7:53507043..53509851,2	K562	blood:
12	chr7:53588403..53590353-chr7:53592550..53594897,2	K562	blood:
13	chr7:53263027..53265803-chr7:53508163..53510506,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEC61G-7	chr7:53466103-53466196	NONHSAT120634
2	lnc-SEC61G-7	chr7:53486490-53486578	NONHSAT120631
3	lnc-SEC61G-7	chr7:53486490-53486571	XLOC_006444
4	lnc-SEC61G-6	chr7:53582685-53582969	XLOC_006445
5	lnc-SEC61G-6	chr7:53584729-53584809	XLOC_006445
6	lnc-SEC61G-7	chr7:53466103-53466322	NONHSAT120630
7	lnc-SEC61G-7	chr7:53486490-53486585	NONHSAT120632
8	lnc-SEC61G-7	chr7:53484018-53484120	NONHSAT120626
9	lnc-SEC61G-7	chr7:53486490-53486506	NONHSAT120627
10	lnc-SEC61G-7	chr7:53466103-53466276	NONHSAT120628
11	lnc-SEC61G-12	chr7:53557841-53558132	NONHSAT120636
12	lnc-SEC61G-7	chr7:53466102-53466198	NONHSAT120635
13	lnc-SEC61G-7	chr7:53484018-53484072	NONHSAT120633
14	lnc-SEC61G-7	chr7:53466103-53466198	XLOC_006444

Variant related genes	Relation type
ENSG00000234105	TF binding region
RN7SKP218	TF binding region
DIEXF	miRNA target sites
CNOT6	miRNA target sites
MEIS1	miRNA target sites
DICER1	miRNA target sites

Extended variants
information (count: 2185 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:2185 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9642511	chr7:53456941-53456942	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11978823	chr7:53456959-53456960	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs147104610	chr7:53457019-53457020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534215141	chr7:53457044-53457045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529814501	chr7:53457116-53457117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548001591	chr7:53457123-53457124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566392492	chr7:53457137-53457138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186565917	chr7:53457199-53457200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138564280	chr7:53457264-53457265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552240607	chr7:53457265-53457266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570822121	chr7:53457284-53457285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192748881	chr7:53457299-53457300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369080960	chr7:53457355-53457356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374072031	chr7:53457400-53457401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528040682	chr7:53457401-53457402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539350036	chr7:53457405-53457406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543073312	chr7:53457434-53457435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548967666	chr7:53457444-53457445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144125193	chr7:53457450-53457451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11972381	chr7:53457480-53457481	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs536031274	chr7:53457523-53457524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554423995	chr7:53457531-53457532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572738652	chr7:53457536-53457537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540130600	chr7:53457543-53457544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113039524	chr7:53457553-53457554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371931715	chr7:53457555-53457556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576766559	chr7:53457560-53457561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370769137	chr7:53457587-53457588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543890824	chr7:53457598-53457599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562215197	chr7:53457624-53457625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149472001	chr7:53457679-53457680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541582453	chr7:53457705-53457706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554786218	chr7:53457714-53457715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559917128	chr7:53457721-53457722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577305909	chr7:53457736-53457737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527540328	chr7:53457764-53457765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573755759	chr7:53457765-53457766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564259204	chr7:53457794-53457795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139297892	chr7:53464211-53464212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76583021	chr7:53464212-53464213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145489701	chr7:53464240-53464241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182839926	chr7:53464246-53464247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543401329	chr7:53464263-53464264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527595980	chr7:53464338-53464339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs28667679	chr7:53464346-53464347	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs564463461	chr7:53464382-53464383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531785024	chr7:53464437-53464438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550275472	chr7:53464444-53464445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371500296	chr7:53464553-53464554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147718277	chr7:53464590-53464591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	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
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
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Cognitive impairment	21505072	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:53456800-53457200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr7:53457200-53457800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr7:53464200-53464400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:53464400-53465000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:53465000-53465800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:53465600-53466400	Active TSS	Fetal Kidney	kidney
7	chr7:53465800-53468000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:53468000-53468200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:53481600-53481800	Enhancers	Liver	Liver
10	chr7:53483200-53483400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:53483400-53485000	Enhancers	Liver	Liver
12	chr7:53483400-53485400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:53484800-53486600	Active TSS	Fetal Kidney	kidney
14	chr7:53485000-53486600	Flanking Active TSS	Liver	Liver
15	chr7:53485400-53486000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr7:53486000-53489400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:53486600-53487000	Enhancers	Liver	Liver
18	chr7:53486600-53489800	Weak transcription	Fetal Kidney	kidney
19	chr7:53487000-53487200	Flanking Active TSS	Liver	Liver
20	chr7:53487200-53489200	Enhancers	Liver	Liver
21	chr7:53488400-53489600	Enhancers	Placenta	Placenta
22	chr7:53489200-53493800	Weak transcription	Liver	Liver
23	chr7:53489400-53489600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr7:53489800-53490400	Enhancers	Fetal Kidney	kidney
25	chr7:53493800-53494400	Active TSS	Liver	Liver
26	chr7:53493800-53494400	Active TSS	Brain Cingulate Gyrus	brain
27	chr7:53493800-53494400	Active TSS	Hela-S3	cervix
28	chr7:53494000-53494400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr7:53494000-53494400	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr7:53494000-53494600	Active TSS	Brain Anterior Caudate	brain
31	chr7:53494000-53494600	Active TSS	Brain Hippocampus Middle	brain
32	chr7:53494200-53494600	Active TSS	Brain Angular Gyrus	brain
33	chr7:53494200-53494600	Enhancers	Placenta	Placenta
34	chr7:53494400-53494600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:53494400-53495000	Enhancers	Liver	Liver
36	chr7:53495000-53495400	Weak transcription	Liver	Liver
37	chr7:53495400-53496000	Enhancers	Liver	Liver
38	chr7:53504800-53505800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr7:53505000-53505400	Enhancers	Placenta	Placenta
40	chr7:53513600-53514000	Enhancers	Liver	Liver
41	chr7:53513800-53514600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr7:53513800-53514600	Enhancers	Ovary	ovary
43	chr7:53514000-53514400	Flanking Active TSS	Liver	Liver
44	chr7:53514400-53514600	Enhancers	Liver	Liver
45	chr7:53514400-53515200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:53514600-53517200	Weak transcription	Ovary	ovary
47	chr7:53517200-53517800	Enhancers	Ovary	ovary
48	chr7:53517800-53518800	Weak transcription	Ovary	ovary
49	chr7:53518800-53519600	Enhancers	Ovary	ovary
50	chr7:53536200-53536600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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