Variant report

Variant	nsv464452
Chromosome Location	chr7:53454892-53590250
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	chr7:53587746-53588062	IMR90	lung:	n/a	chr7:53587881-53587892
4	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
5	CEBPB	chr7:53505078-53505387	HepG2	liver:	n/a	chr7:53505251-53505262
6	CEBPB	chr7:53501358-53501394	H1-hESC	embryonic stem cell:	n/a	chr7:53501375-53501386
7	CEBPB	chr7:53501299-53501500	IMR90	lung:	n/a	chr7:53501375-53501386
8	CEBPB	chr7:53572675-53572941	MCF-7	breast:	n/a	chr7:53572763-53572774
9	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
10	CEBPB	chr7:53587750-53588037	A549	lung:	n/a	chr7:53587881-53587892
11	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
12	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
13	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
14	CEBPB	chr7:53502040-53502264	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr7:53501208-53501545	HepG2	liver:	n/a	chr7:53501375-53501386
16	CEBPB	chr7:53587738-53588025	MCF-7	breast:	n/a	chr7:53587881-53587892
17	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
18	CEBPB	chr7:53505120-53505352	Hela-S3	cervix:	n/a	chr7:53505251-53505262
19	CEBPB	chr7:53572607-53572958	HepG2	liver:	n/a	chr7:53572763-53572774
20	CEBPB	chr7:53501280-53501444	K562	blood:	n/a	chr7:53501375-53501386
21	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
22	CEBPB	chr7:53587730-53588040	HepG2	liver:	n/a	chr7:53587881-53587892
23	CEBPB	chr7:53572631-53572945	IMR90	lung:	n/a	chr7:53572763-53572774
24	CTCF	chr7:53475374-53475388	GM13976	blood:	n/a	n/a
25	CTCF	chr7:53516240-53516390	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr7:53494120-53494270	BE2_C	brain:	n/a	n/a
27	CTCF	chr7:53563086-53563140	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:53488226-53488236	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr7:53488240-53488244	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr7:53473697-53473756	Medullo	brain:	n/a	n/a
31	CTCF	chr7:53494180-53494330	RPTEC	kidney:	n/a	n/a
32	CTCF	chr7:53567900-53568050	HMEC	breast:	n/a	n/a
33	CTCF	chr7:53572240-53572390	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr7:53494240-53494390	HRE	kidney:	n/a	n/a
35	CTCF	chr7:53498727-53498761	GM13977	blood:	n/a	n/a
36	CTCF	chr7:53494252-53494288	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr7:53494200-53494350	HAc	cerebellar:	n/a	n/a
38	CTCF	chr7:53487840-53487990	RPTEC	kidney:	n/a	n/a
39	CTCF	chr7:53557364-53557424	GM20000	blood:	n/a	n/a
40	CTCF	chr7:53497900-53498050	HPF	lung:	n/a	n/a
41	CTCF	chr7:53494240-53494390	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr7:53567920-53568070	HMEC	breast:	n/a	n/a
43	CTCF	chr7:53535861-53535883	Medullo	brain:	n/a	n/a
44	CTCF	chr7:53488151-53488225	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr7:53483246-53483300	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:53494240-53494390	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:53488120-53488270	RPTEC	kidney:	n/a	n/a
48	CTCF	chr7:53527926-53528005	GM10248	blood:	n/a	n/a
49	CTCF	chr7:53494172-53494333	Gliobla	brain:	n/a	n/a
50	CTCF	chr7:53528060-53528210	AG10803	skin:	n/a	n/a

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

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

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

Extended variants
information (count: 2091 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:2091 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11983950	chr7:53454892-53454893	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73127379	chr7:53454897-53454898	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs538560717	chr7:53454903-53454904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117492067	chr7:53454916-53454917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs17833062	chr7:53454919-53454920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539794714	chr7:53454920-53454921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561027736	chr7:53454922-53454923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551531264	chr7:53454932-53454933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62451905	chr7:53454940-53454941	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs540394802	chr7:53455014-53455015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372639783	chr7:53455041-53455042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182049164	chr7:53455055-53455056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146558229	chr7:53455072-53455073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs17135704	chr7:53455110-53455111	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs563228618	chr7:53455112-53455113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370062773	chr7:53455150-53455151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75617366	chr7:53455155-53455156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537660369	chr7:53455212-53455213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185145972	chr7:53455259-53455260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567334778	chr7:53455296-53455297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534715163	chr7:53455302-53455303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs56085967	chr7:53455340-53455341	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs149162896	chr7:53455344-53455345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189852273	chr7:53455361-53455362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556960030	chr7:53455373-53455374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182845233	chr7:53455426-53455427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536220819	chr7:53455432-53455433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554562266	chr7:53455443-53455444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572963268	chr7:53455467-53455468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143313224	chr7:53455482-53455483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565417202	chr7:53455499-53455500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577347335	chr7:53455523-53455524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs151287655	chr7:53455543-53455544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367858925	chr7:53455566-53455567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373343249	chr7:53455590-53455591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563012001	chr7:53455600-53455601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2877132	chr7:53455603-53455604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548957874	chr7:53455614-53455615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77722655	chr7:53455619-53455620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs62451906	chr7:53455640-53455641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186611482	chr7:53455656-53455657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546709580	chr7:53455683-53455684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571161722	chr7:53455753-53455754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571355218	chr7:53455754-53455755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538434183	chr7:53455787-53455788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550776121	chr7:53455788-53455789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140554654	chr7:53455815-53455816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79647747	chr7:53455833-53455834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371029628	chr7:53455844-53455845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566515731	chr7:53455861-53455862	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:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:53448000-53456600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr7:53456600-53456800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr7:53456800-53457200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr7:53457200-53457800	Enhancers	Placenta Amnion	Placenta Amnion
5	chr7:53464200-53464400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:53464400-53465000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr7:53465000-53465800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:53465600-53466400	Active TSS	Fetal Kidney	kidney
9	chr7:53465800-53468000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr7:53468000-53468200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:53481600-53481800	Enhancers	Liver	Liver
12	chr7:53483200-53483400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:53483400-53485000	Enhancers	Liver	Liver
14	chr7:53483400-53485400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:53484800-53486600	Active TSS	Fetal Kidney	kidney
16	chr7:53485000-53486600	Flanking Active TSS	Liver	Liver
17	chr7:53485400-53486000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:53486000-53489400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:53486600-53487000	Enhancers	Liver	Liver
20	chr7:53486600-53489800	Weak transcription	Fetal Kidney	kidney
21	chr7:53487000-53487200	Flanking Active TSS	Liver	Liver
22	chr7:53487200-53489200	Enhancers	Liver	Liver
23	chr7:53488400-53489600	Enhancers	Placenta	Placenta
24	chr7:53489200-53493800	Weak transcription	Liver	Liver
25	chr7:53489400-53489600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:53489800-53490400	Enhancers	Fetal Kidney	kidney
27	chr7:53493800-53494400	Active TSS	Liver	Liver
28	chr7:53493800-53494400	Active TSS	Brain Cingulate Gyrus	brain
29	chr7:53493800-53494400	Active TSS	Hela-S3	cervix
30	chr7:53494000-53494400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr7:53494000-53494400	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr7:53494000-53494600	Active TSS	Brain Anterior Caudate	brain
33	chr7:53494000-53494600	Active TSS	Brain Hippocampus Middle	brain
34	chr7:53494200-53494600	Active TSS	Brain Angular Gyrus	brain
35	chr7:53494200-53494600	Enhancers	Placenta	Placenta
36	chr7:53494400-53494600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:53494400-53495000	Enhancers	Liver	Liver
38	chr7:53495000-53495400	Weak transcription	Liver	Liver
39	chr7:53495400-53496000	Enhancers	Liver	Liver
40	chr7:53504800-53505800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr7:53505000-53505400	Enhancers	Placenta	Placenta
42	chr7:53513600-53514000	Enhancers	Liver	Liver
43	chr7:53513800-53514600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr7:53513800-53514600	Enhancers	Ovary	ovary
45	chr7:53514000-53514400	Flanking Active TSS	Liver	Liver
46	chr7:53514400-53514600	Enhancers	Liver	Liver
47	chr7:53514400-53515200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:53514600-53517200	Weak transcription	Ovary	ovary
49	chr7:53517200-53517800	Enhancers	Ovary	ovary
50	chr7:53517800-53518800	Weak transcription	Ovary	ovary

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