Variant report

Variant	nsv538844
Chromosome Location	chr7:52963913-52989049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:195)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:195 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:52967496-52967799	HepG2	liver:	n/a	chr7:52967655-52967666 chr7:52967690-52967699 chr7:52967653-52967664 chr7:52967655-52967664
2	CTCF	chr7:52985720-52985870	Hela-S3	cervix:	n/a	n/a
3	CTCF	chr7:52985780-52985930	A549	lung:	n/a	n/a
4	CTCF	chr7:52985800-52985950	HL-60	blood:	n/a	n/a
5	CTCF	chr7:52985780-52985930	WERI-Rb-1	eye:	n/a	n/a
6	CTCF	chr7:52985800-52985950	GM12871	blood:	n/a	n/a
7	CTCF	chr7:52985760-52985910	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr7:52985800-52985950	SAEC	small airway:	n/a	n/a
9	CTCF	chr7:52988882-52988965	LNCaP	prostate:	n/a	chr7:52988900-52988907
10	CTCF	chr7:52985840-52985990	GM12873	blood:	n/a	n/a
11	CTCF	chr7:52985820-52985970	GM12866	blood:	n/a	n/a
12	CTCF	chr7:52981551-52981608	Fibrobl	skin:	n/a	n/a
13	CTCF	chr7:52985780-52985930	HRE	kidney:	n/a	n/a
14	CTCF	chr7:52985628-52986013	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr7:52985826-52985935	GM13976	blood:	n/a	n/a
16	CTCF	chr7:52985759-52985967	GM13977	blood:	n/a	n/a
17	CTCF	chr7:52988820-52988970	BE2_C	brain:	n/a	chr7:52988900-52988907
18	CTCF	chr7:52985760-52985910	NB4	blood:	n/a	n/a
19	CTCF	chr7:52985775-52985957	GM12891	blood:	n/a	n/a
20	CTCF	chr7:52985682-52986030	K562	blood:	n/a	n/a
21	CTCF	chr7:52988851-52988971	MCF-7	breast:	n/a	chr7:52988900-52988907
22	CTCF	chr7:52985827-52985922	GM10248	blood:	n/a	n/a
23	CTCF	chr7:52985840-52985990	HAc	cerebellar:	n/a	n/a
24	CTCF	chr7:52985780-52985930	SAEC	small airway:	n/a	n/a
25	CTCF	chr7:52985793-52985943	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr7:52985780-52985930	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr7:52985760-52985910	HCT-116	colon:	n/a	n/a
28	CTCF	chr7:52985760-52985910	K562	blood:	n/a	n/a
29	CTCF	chr7:52985760-52985910	NHEK	skin:	n/a	n/a
30	CTCF	chr7:52985800-52985950	Caco-2	colon:	n/a	n/a
31	CTCF	chr7:52985749-52985992	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:52985780-52985930	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr7:52985780-52985930	GM12878	blood:	n/a	n/a
34	CTCF	chr7:52985766-52985973	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr7:52985820-52985970	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr7:52985740-52985890	GM12872	blood:	n/a	n/a
37	CTCF	chr7:52975073-52975252	IMR90	lung:	n/a	n/a
38	CTCF	chr7:52985760-52985910	AG09309	skin:	n/a	n/a
39	CTCF	chr7:52988860-52989010	SK-N-SH_RA	brain:	n/a	chr7:52988900-52988907
40	CTCF	chr7:52985700-52985850	BE2_C	brain:	n/a	n/a
41	CTCF	chr7:52985820-52985970	NHEK	skin:	n/a	n/a
42	CTCF	chr7:52988894-52988933	Gliobla	brain:	n/a	chr7:52988900-52988907
43	CTCF	chr7:52985800-52985950	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr7:52985767-52985969	K562	blood:	n/a	n/a
45	CTCF	chr7:52988840-52988990	SK-N-SH_RA	brain:	n/a	chr7:52988900-52988907
46	CTCF	chr7:52985800-52985950	GM12875	blood:	n/a	n/a
47	CTCF	chr7:52985840-52985990	GM12874	blood:	n/a	n/a
48	CTCF	chr7:52985803-52985900	ProgFib	skin:	n/a	n/a
49	CTCF	chr7:52985740-52985890	GM12870	blood:	n/a	n/a
50	CTCF	chr7:52985688-52986048	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:52985263-52985313	AG04450	lung:	fetal
2	chr7:52985263-52985313	T-47D	breast:	n/a
3	chr7:52985263-52985313	HUVEC	blood vessel:	n/a
4	chr7:52985263-52985313	HCPEpiC	choroid plexus:	n/a
5	chr7:52985263-52985313	AG04449	skin:	fetal
6	chr7:52985263-52985313	RPTEC	kidney:	n/a
7	chr7:52985263-52985313	HCT-116	colon:	n/a
8	chr7:52985263-52985313	AG10803	skin:	n/a
9	chr7:52985263-52985313	MCF-7	breast:	n/a
10	chr7:52985263-52985313	SKMC	muscle:	n/a
11	chr7:52985263-52985313	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:52985263-52985313	GM12892	blood:	n/a
13	chr7:52985263-52985313	MCF10A-Er-Src	breast:	n/a
14	chr7:52985263-52985313	HIPEpiC	eye:	n/a
15	chr7:52985263-52985313	ProgFib	skin:	n/a
16	chr7:52985263-52985313	ECC-1	luminal epithelium:	n/a
17	chr7:52985263-52985313	Jurkat	blood:	n/a
18	chr7:52985263-52985313	Caco-2	colon:	n/a
19	chr7:52985263-52985313	HL-60	blood:	n/a
20	chr7:52985263-52985313	PrEC	prostate:	n/a
21	chr7:52985263-52985313	NHDF-neo	bronchial:	n/a
22	chr7:52985263-52985313	NT2-D1	testis:	n/a
23	chr7:52985263-52985313	HNPCEpiC	eye:	n/a
24	chr7:52985263-52985313	HCF	heart:	n/a
25	chr7:52985263-52985313	SK-N-SH_RA	brain:	n/a
26	chr7:52985263-52985313	HEK293	kidney:	embryo
27	chr7:52985263-52985313	Hepatocyte	liver:	n/a
28	chr7:52985263-52985313	HRCEpiC	kidney:	n/a
29	chr7:52985263-52985313	BE2_C	brain:	n/a
30	chr7:52985263-52985313	HAEpiC	amniotic membrane:	n/a
31	chr7:52985263-52985313	ovcar-3	ovarian:	n/a
32	chr7:52985263-52985313	GM06990	blood:	n/a
33	chr7:52985263-52985313	HRPEpiC	eye:	n/a
34	chr7:52985263-52985313	A549	lung:	n/a
35	chr7:52985263-52985313	HMEC	breast:	n/a
36	chr7:52985263-52985313	CMK	blood:	n/a
37	chr7:52985263-52985313	PANC-1	pancreas:	n/a
38	chr7:52985263-52985313	HRE	kidney:	n/a
39	chr7:52985263-52985313	GM12878	blood:	n/a
40	chr7:52985263-52985313	AG09309	skin:	n/a
41	chr7:52985263-52985313	SK-N-MC	brain:	n/a
42	chr7:52985263-52985313	HepG2	liver:	n/a
43	chr7:52985263-52985313	AoSMC	blood vessel:	n/a
44	chr7:52985263-52985313	U87	brain:	n/a
45	chr7:52985263-52985313	NB4	blood:	n/a
46	chr7:52985263-52985313	H1-hESC	embryonic stem cell:	embryo
47	chr7:52985263-52985313	NHBE	bronchial:	n/a
48	chr7:52985263-52985313	K562	blood:	n/a
49	chr7:52985263-52985313	Hela-S3	cervix:	n/a
50	chr7:52985263-52985313	GM12891	blood:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COBL-6	chr7:52964387-52965500	NONHSAT120623

No data

Variant related genes	Relation type
ENSG00000234304	TF binding region
ENSG00000234304	CpG island
ZNF148	miRNA target sites

Extended variants
information (count: 462 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189084465	chr7:52964397-52964398	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs552375353	chr7:52964405-52964406	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs565621735	chr7:52964433-52964434	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs528153499	chr7:52964457-52964458	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs117559264	chr7:52964478-52964479	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs548000201	chr7:52964492-52964493	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs35804710	chr7:52964496-52964497	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs567999526	chr7:52964514-52964515	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs59443321	chr7:52964518-52964519	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs556432172	chr7:52964525-52964526	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs560554112	chr7:52964553-52964554	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs76984210	chr7:52964563-52964564	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs193151640	chr7:52964564-52964565	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs116447962	chr7:52964633-52964634	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs184440189	chr7:52964642-52964643	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs188429444	chr7:52964658-52964659	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs112494490	chr7:52964693-52964694	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs191711632	chr7:52964723-52964724	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs554769682	chr7:52964762-52964763	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs144153311	chr7:52964794-52964795	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs543883990	chr7:52964843-52964844	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs563550870	chr7:52964856-52964857	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs532482381	chr7:52964887-52964888	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs545792448	chr7:52964936-52964937	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs61189367	chr7:52964949-52964950	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs567614435	chr7:52964969-52964970	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs151146010	chr7:52964986-52964987	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs184259889	chr7:52964999-52965000	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs370031811	chr7:52965029-52965030	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
30	rs530425416	chr7:52965040-52965041	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
31	rs139061321	chr7:52965058-52965059	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
32	rs75588705	chr7:52965063-52965064	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
33	rs566479063	chr7:52965081-52965082	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
34	rs539285993	chr7:52965110-52965111	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
35	rs369099807	chr7:52965127-52965128	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
36	rs538748812	chr7:52965134-52965135	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
37	rs559009782	chr7:52965147-52965148	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
38	rs10248339	chr7:52965158-52965159	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
39	rs149904195	chr7:52965177-52965178	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
40	rs555043611	chr7:52965182-52965183	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
41	rs201253734	chr7:52965188-52965189	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
42	rs73111897	chr7:52965189-52965190	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
43	rs571381095	chr7:52965191-52965192	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
44	rs367643961	chr7:52965192-52965193	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
45	rs61335520	chr7:52965205-52965206	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
46	rs111262389	chr7:52965208-52965209	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs537425435	chr7:52965210-52965211	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs557355411	chr7:52965212-52965213	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs77488045	chr7:52965248-52965249	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs368624790	chr7:52965249-52965250	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Gastrointestinal stromal cancer	20877625	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
Breast cancer	21990379	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:52965000-52965800	Active TSS	Stomach Smooth Muscle	stomach
2	chr7:52965200-52965600	Active TSS	Aorta	Aorta
3	chr7:52970800-52971800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr7:52971000-52971800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:52971200-52972000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:52971200-52972200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:52971400-52971800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:52971400-52972000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr7:52971400-52972400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr7:52971400-52972800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr7:52971800-52972200	Enhancers	Fetal Brain Female	brain
12	chr7:52979400-52979800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:52979400-52979800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr7:52979400-52979800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:52980800-52981000	Enhancers	Fetal Muscle Trunk	muscle
16	chr7:52983800-52984000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr7:52983800-52984400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr7:52983800-52985400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr7:52984000-52984600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:52984000-52985400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:52984000-52985600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:52984000-52985800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:52984400-52985200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:52984400-52985200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr7:52984400-52985400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:52984600-52985200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr7:52984600-52985400	Enhancers	Brain Substantia Nigra	brain
28	chr7:52984600-52985600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr7:52984800-52985200	Enhancers	H1 Cell Line	embryonic stem cell
30	chr7:52985200-52985400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr7:52985200-52988400	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr7:52988000-52988600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr7:52988400-52988800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr7:52988400-52989000	Enhancers	Brain Germinal Matrix	brain
35	chr7:52988600-52989000	Enhancers	Fetal Stomach	stomach
36	chr7:52988800-52989600	Enhancers	Placenta	Placenta

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