Variant report

Variant	nsv900479
Chromosome Location	chr13:69824819-69984297
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	chr13:69905419-69905764	K562	blood:	n/a	n/a
2	ATF3	chr13:69905415-69905687	K562	blood:	n/a	n/a
3	BCL3	chr13:69893435-69893648	GM12878	blood:	n/a	n/a
4	BHLHE40	chr13:69839148-69839308	K562	blood:	n/a	n/a
5	BRCA1	chr13:69975267-69975337	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr13:69848362-69848728	K562	blood:	n/a	chr13:69848541-69848552
7	CEBPB	chr13:69848472-69848722	A549	lung:	n/a	chr13:69848541-69848552
8	CEBPB	chr13:69839218-69839553	K562	blood:	n/a	n/a
9	CEBPB	chr13:69848368-69848678	HCT-116	colon:	n/a	chr13:69848541-69848552
10	CEBPB	chr13:69963028-69963294	HepG2	liver:	n/a	n/a
11	CEBPB	chr13:69848366-69848618	K562	blood:	n/a	chr13:69848541-69848552
12	CEBPB	chr13:69964106-69964306	HepG2	liver:	n/a	chr13:69964268-69964281 chr13:69964268-69964281 chr13:69964267-69964284
13	CEBPB	chr13:69848369-69848743	Hela-S3	cervix:	n/a	chr13:69848541-69848552
14	CEBPB	chr13:69848404-69848697	A549	lung:	n/a	chr13:69848541-69848552
15	CEBPB	chr13:69848420-69848683	HepG2	liver:	n/a	chr13:69848541-69848552
16	CEBPB	chr13:69848265-69848814	HCT-116	colon:	n/a	chr13:69848541-69848552
17	CEBPB	chr13:69938542-69938717	HepG2	liver:	n/a	n/a
18	CHD2	chr13:69838411-69838604	Hela-S3	cervix:	n/a	n/a
19	CREB1	chr13:69898271-69898487	GM12878	blood:	n/a	n/a
20	CTCF	chr13:69832600-69832750	WI-38	lung:	n/a	n/a
21	CTCF	chr13:69898320-69898470	BE2_C	brain:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
22	CTCF	chr13:69898340-69898490	HRPEpiC	eye:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
23	CTCF	chr13:69898331-69898513	A549	lung:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
24	CTCF	chr13:69898420-69898570	HEEpiC	esophagus:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
25	CTCF	chr13:69898360-69898510	GM12865	blood:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
26	CTCF	chr13:69898280-69898430	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr13:69898357-69898536	Spleen_OC	spleen:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
28	CTCF	chr13:69898340-69898490	Caco-2	colon:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
29	CTCF	chr13:69836756-69836786	Lung_OC	lung:	n/a	n/a
30	CTCF	chr13:69898312-69898566	Medullo	brain:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
31	CTCF	chr13:69898360-69898510	HRPEpiC	eye:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
32	CTCF	chr13:69898379-69898460	GM10266	blood:	n/a	chr13:69898439-69898460
33	CTCF	chr13:69898387-69898512	LNCaP	prostate:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
34	CTCF	chr13:69898320-69898470	HRE	kidney:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
35	CTCF	chr13:69898380-69898530	HRE	kidney:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
36	CTCF	chr13:69898246-69898591	A549	lung:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
37	CTCF	chr13:69898380-69898493	Pancreas_OC	pancreas:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
38	CTCF	chr13:69881060-69881210	BE2_C	brain:	n/a	n/a
39	CTCF	chr13:69898251-69898512	H1-hESC	embryonic stem cell:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
40	CTCF	chr13:69898340-69898490	HMEC	breast:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
41	CTCF	chr13:69838641-69838695	MCF-7	breast:	n/a	n/a
42	CTCF	chr13:69891840-69891990	HAc	cerebellar:	n/a	n/a
43	CTCF	chr13:69898130-69898763	A549	lung:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
44	CTCF	chr13:69898349-69898490	LNCaP	prostate:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
45	CTCF	chr13:69881047-69881140	MCF-7	breast:	n/a	n/a
46	CTCF	chr13:69881000-69881150	Caco-2	colon:	n/a	n/a
47	CTCF	chr13:69898460-69898610	RPTEC	kidney:	n/a	n/a
48	CTCF	chr13:69898260-69898595	K562	blood:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
49	CTCF	chr13:69898334-69898508	HepG2	liver:	n/a	chr13:69898444-69898462 chr13:69898439-69898460
50	CTCF	chr13:69898320-69898470	RPTEC	kidney:	n/a	chr13:69898444-69898462 chr13:69898439-69898460

No.	Distal block	Cell Line	Cell type
1	chr13:69831283..69833346-chr13:69836562..69838763,2	MCF-7	breast:
2	chr13:69880056..69883403-chr13:69894393..69896223,3	K562	blood:
3	chr13:69880056..69883403-chr13:69894393..69896223,3	K562	blood:
4	chr13:69907576..69909388-chr13:69911366..69913093,2	K562	blood:
5	chr13:69882987..69885137-chr13:69885887..69888011,2	K562	blood:
6	chr13:69839216..69841490-chr13:69867661..69869798,2	K562	blood:
7	chr13:69795398..69798188-chr13:69884200..69887047,2	K562	blood:
8	chr13:69882987..69885137-chr13:69885887..69888011,2	K562	blood:
9	chr13:69907576..69909388-chr13:69911366..69913093,2	K562	blood:
10	chr13:69848018..69850252-chr13:69851858..69853538,2	K562	blood:
11	chr13:69873282..69873950-chr8:122455105..122456011,2	MCF-7	breast:
12	chr13:69911537..69914002-chr13:69917682..69920298,2	K562	blood:
13	chr13:69839216..69841490-chr13:69867661..69869798,2	K562	blood:
14	chr13:69911537..69914002-chr13:69917682..69920298,2	K562	blood:
15	chr13:69831283..69833346-chr13:69836562..69838763,2	MCF-7	breast:
16	chr13:69911537..69913957-chr13:69917587..69919398,3	K562	blood:
17	chr13:69848018..69850252-chr13:69851858..69853538,2	K562	blood:
18	chr12:90020572..90021493-chr13:69890906..69891812,2	MCF-7	breast:
19	chr13:69911537..69913957-chr13:69917587..69919398,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BORA-5	chr13:69885465-69885528	XLOC_010421
2	lnc-BORA-6	chr13:69865758-69866286	NONHSAT034241
3	lnc-BORA-5	chr13:69895477-69896233	XLOC_010421
4	lnc-BORA-24	chr13:69968333-69968468	NONHSAT034245
5	lnc-BORA-5	chr13:69885464-69885528	NONHSAT034243
6	lnc-BORA-6	chr13:69849271-69849396	NONHSAT034241
7	lnc-BORA-6	chr13:69849272-69849396	XLOC_010420
8	lnc-BORA-6	chr13:69844023-69844083	XLOC_010420
9	lnc-BORA-5	chr13:69895476-69896233	NONHSAT034243
10	lnc-BORA-6	chr13:69844022-69844083	NONHSAT034241
11	lnc-BORA-24	chr13:69980276-69980417	NONHSAT034245
12	lnc-BORA-6	chr13:69865759-69866286	XLOC_010420

Variant related genes	Relation type
SRSF1P1	TF binding region
LINC00401	TF binding region
ENSG00000237534	chromatin interactions
EIF5	miRNA target sites
EIF4G3	miRNA target sites

Extended variants
information (count: 1641 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1641 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544333229	chr13:69836807-69836808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181230691	chr13:69836820-69836821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530378991	chr13:69836841-69836842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112602873	chr13:69836847-69836848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540273246	chr13:69836858-69836859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115720860	chr13:69836864-69836865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530035812	chr13:69836883-69836884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185343072	chr13:69836953-69836954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188250046	chr13:69837009-69837010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374459717	chr13:69837010-69837011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs151161297	chr13:69837015-69837016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564732742	chr13:69837092-69837093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558018094	chr13:69837100-69837101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1596870	chr13:69837131-69837132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140297215	chr13:69837132-69837133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114103145	chr13:69837140-69837141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556952134	chr13:69837166-69837167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573967540	chr13:69837203-69837204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542943874	chr13:69837204-69837205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145409067	chr13:69837433-69837434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573404094	chr13:69837434-69837435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542023674	chr13:69837462-69837463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545585548	chr13:69837468-69837469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564786899	chr13:69837496-69837497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368760514	chr13:69837521-69837522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550485584	chr13:69837559-69837560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544196586	chr13:69837583-69837584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs180690190	chr13:69837599-69837600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562472595	chr13:69837634-69837635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560893456	chr13:69837658-69837659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373070202	chr13:69837665-69837666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151073631	chr13:69837669-69837670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71116905	chr13:69837686-69837687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141572721	chr13:69837687-69837688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9599444	chr13:69837688-69837689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs199638000	chr13:69837690-69837691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11841530	chr13:69837692-69837693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375320375	chr13:69837712-69837713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369311260	chr13:69837714-69837715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368937266	chr13:69837728-69837729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9572142	chr13:69837732-69837733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552358876	chr13:69837740-69837741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186305877	chr13:69837744-69837745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537173709	chr13:69837751-69837752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550542458	chr13:69837804-69837805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9564560	chr13:69837811-69837812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567359465	chr13:69837829-69837830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536543731	chr13:69837895-69837896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570984890	chr13:69837903-69837904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115744462	chr13:69837952-69837953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Myelofibrosis	22110671	CNVD
Esophageal cancer	21851588	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69836800-69837000	Enhancers	K562	blood
2	chr13:69837000-69838000	Weak transcription	K562	blood
3	chr13:69837600-69839600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr13:69838000-69839600	Enhancers	K562	blood
5	chr13:69838200-69839400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:69838400-69839000	Enhancers	Placenta Amnion	Placenta Amnion
7	chr13:69838400-69839200	Enhancers	Gastric	stomach
8	chr13:69838600-69839200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr13:69839400-69839800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr13:69839600-69839800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr13:69839600-69856400	Weak transcription	K562	blood
12	chr13:69853400-69853800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr13:69854000-69855000	Enhancers	Fetal Lung	lung
14	chr13:69855000-69857200	Weak transcription	Fetal Lung	lung
15	chr13:69857200-69858200	Enhancers	Fetal Lung	lung
16	chr13:69857400-69858600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr13:69858000-69858400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr13:69858200-69861200	Weak transcription	Fetal Lung	lung
19	chr13:69861200-69861600	Active TSS	Fetal Lung	lung
20	chr13:69861200-69862200	Active TSS	A549	lung
21	chr13:69861400-69862800	Active TSS	GM12878-XiMat	blood
22	chr13:69861600-69862000	Flanking Active TSS	Fetal Lung	lung
23	chr13:69862000-69862200	Active TSS	Fetal Lung	lung
24	chr13:69862800-69867000	Weak transcription	GM12878-XiMat	blood
25	chr13:69864600-69866800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr13:69865600-69865800	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr13:69865600-69866400	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr13:69865800-69870200	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr13:69866400-69866800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr13:69866800-69867200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr13:69866800-69867600	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr13:69867000-69867400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr13:69867000-69867400	Enhancers	GM12878-XiMat	blood
34	chr13:69867200-69868200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr13:69868200-69869000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr13:69869000-69870200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr13:69870000-69870800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr13:69870200-69870600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr13:69870400-69870600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr13:69873200-69873800	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr13:69873200-69874400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr13:69897200-69897800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr13:69918800-69919000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr13:69918800-69919000	ZNF genes & repeats	Esophagus	oesophagus
45	chr13:69923200-69923600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr13:69923600-69924600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr13:69923600-69924800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr13:69924800-69925600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr13:69925600-69925800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr13:69929000-69929600	Enhancers	Brain Germinal Matrix	brain

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