Variant report

Variant	nsv900372
Chromosome Location	chr13:65449535-65577032
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	BATF	chr13:65503121-65503331	GM12878	blood:	n/a	n/a
2	BCL11A	chr13:65512859-65513178	GM12878	blood:	n/a	n/a
3	BCL11A	chr13:65512818-65513084	GM12878	blood:	n/a	n/a
4	BHLHE40	chr13:65512810-65513130	GM12878	blood:	n/a	n/a
5	CEBPB	chr13:65503142-65503716	IMR90	lung:	n/a	n/a
6	CEBPB	chr13:65503090-65503733	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr13:65449988-65450076	H1-hESC	embryonic stem cell:	n/a	chr13:65450034-65450043 chr13:65450033-65450044 chr13:65450032-65450045 chr13:65450032-65450045 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450032-65450043 chr13:65450032-65450045 chr13:65450032-65450043
8	CEBPB	chr13:65549489-65549824	HepG2	liver:	n/a	chr13:65549674-65549685 chr13:65549616-65549627
9	CEBPB	chr13:65449866-65450161	HepG2	liver:	n/a	chr13:65450034-65450043 chr13:65450033-65450044 chr13:65450032-65450045 chr13:65450032-65450045 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450032-65450043 chr13:65450032-65450045 chr13:65450032-65450043
10	CEBPB	chr13:65530999-65531037	HepG2	liver:	n/a	chr13:65531013-65531026 chr13:65531015-65531026 chr13:65531010-65531027 chr13:65531013-65531024 chr13:65531013-65531026
11	CEBPB	chr13:65486134-65486601	A549	lung:	n/a	n/a
12	CEBPB	chr13:65449858-65450171	IMR90	lung:	n/a	chr13:65450034-65450043 chr13:65450033-65450044 chr13:65450032-65450045 chr13:65450032-65450045 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450032-65450043 chr13:65450032-65450045 chr13:65450032-65450043
13	CEBPB	chr13:65463368-65463605	IMR90	lung:	n/a	n/a
14	CEBPB	chr13:65499086-65499360	HepG2	liver:	n/a	chr13:65499202-65499213
15	CEBPB	chr13:65549486-65549834	IMR90	lung:	n/a	chr13:65549674-65549685 chr13:65549616-65549627
16	CEBPB	chr13:65499086-65499312	A549	lung:	n/a	chr13:65499202-65499213
17	CHD1	chr13:65568223-65568415	GM12878	blood:	n/a	n/a
18	CHD2	chr13:65567966-65568470	GM12878	blood:	n/a	n/a
19	CHD2	chr13:65499635-65499713	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr13:65499005-65499076	GM19238	blood:	n/a	n/a
21	CTCF	chr13:65551897-65551982	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr13:65571720-65571870	BE2_C	brain:	n/a	n/a
23	CTCF	chr13:65502073-65502093	Fibrobl	skin:	n/a	n/a
24	CTCF	chr13:65571780-65571930	AG10803	skin:	n/a	n/a
25	CTCF	chr13:65502048-65502064	Fibrobl	skin:	n/a	n/a
26	CTCF	chr13:65519280-65519430	HPAF	blood vessel:	n/a	chr13:65519402-65519423
27	CTCF	chr13:65571760-65571910	Caco-2	colon:	n/a	n/a
28	CTCF	chr13:65519389-65519419	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr13:65460240-65460390	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr13:65571680-65571830	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr13:65519389-65519432	ProgFib	skin:	n/a	chr13:65519402-65519423
32	CTCF	chr13:65571794-65571840	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr13:65571700-65571850	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr13:65571720-65571870	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr13:65480102-65480131	GM13976	blood:	n/a	n/a
36	CTCF	chr13:65515436-65515516	GM10248	blood:	n/a	n/a
37	CTCF	chr13:65571700-65571850	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr13:65519300-65519450	AG10803	skin:	n/a	chr13:65519402-65519423
39	CTCF	chr13:65532360-65532510	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr13:65571760-65571910	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr13:65503954-65504015	GM10248	blood:	n/a	n/a
42	CTCF	chr13:65530122-65530177	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr13:65559841-65559911	Lung_OC	lung:	n/a	n/a
44	CTCF	chr13:65519390-65519427	Gliobla	brain:	n/a	chr13:65519402-65519423
45	CTCF	chr13:65571760-65571910	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr13:65571800-65571950	HepG2	liver:	n/a	n/a
47	CTCF	chr13:65475340-65475433	NHEK	skin:	n/a	n/a
48	CTCF	chr13:65519300-65519450	HMEC	breast:	n/a	chr13:65519402-65519423
49	CTCF	chr13:65571780-65571930	AG04450	lung:	n/a	n/a
50	CTCF	chr13:65571680-65571830	AG04450	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:65532878-65532928	BE2_C	brain:	n/a
2	chr13:65532878-65532928	BE2_C	brain:	n/a
3	chr13:65533500-65533550	HIPEpiC	eye:	n/a
4	chr13:65532796-65532846	Hela-S3	cervix:	n/a
5	chr13:65532273-65532323	Jurkat	blood:	n/a
6	chr13:65533139-65533189	ECC-1	luminal epithelium:	n/a
7	chr13:65532408-65532458	Hela-S3	cervix:	n/a
8	chr13:65500124-65500174	HRPEpiC	eye:	n/a
9	chr13:65500124-65500174	HAEpiC	amniotic membrane:	n/a
10	chr13:65500141-65500191	GM19239	blood:	n/a
11	chr13:65532878-65532928	NHDF-neo	bronchial:	n/a
12	chr13:65500124-65500174	HCF	heart:	n/a
13	chr13:65532820-65532870	SK-N-SH_RA	brain:	n/a
14	chr13:65500072-65500122	HPAEpiC	pulmonary alveolar:	n/a
15	chr13:65500141-65500191	NB4	blood:	n/a
16	chr13:65533139-65533189	HPAEpiC	pulmonary alveolar:	n/a
17	chr13:65532581-65532631	AG09309	skin:	n/a
18	chr13:65500072-65500122	LNCaP	prostate:	n/a
19	chr13:65500072-65500122	HUVEC	blood vessel:	n/a
20	chr13:65532820-65532870	HEK293	kidney:	embryo
21	chr13:65532878-65532928	HEK293	kidney:	embryo
22	chr13:65532796-65532846	ECC-1	luminal epithelium:	n/a
23	chr13:65532581-65532631	SK-N-SH_RA	brain:	n/a
24	chr13:65532820-65532870	K562	blood:	n/a
25	chr13:65532820-65532870	NT2-D1	testis:	n/a
26	chr13:65532581-65532631	HCT-116	colon:	n/a
27	chr13:65532273-65532323	HRE	kidney:	n/a
28	chr13:65500124-65500174	ECC-1	luminal epithelium:	n/a
29	chr13:65533139-65533189	GM19239	blood:	n/a
30	chr13:65532796-65532846	Hepatocyte	liver:	n/a
31	chr13:65500124-65500174	Jurkat	blood:	n/a
32	chr13:65532581-65532631	GM12892	blood:	n/a
33	chr13:65532878-65532928	Jurkat	blood:	n/a
34	chr13:65500141-65500191	Jurkat	blood:	n/a
35	chr13:65532408-65532458	K562	blood:	n/a
36	chr13:65500072-65500122	U87	brain:	n/a
37	chr13:65532408-65532458	HNPCEpiC	eye:	n/a
38	chr13:65532878-65532928	K562	blood:	n/a
39	chr13:65532408-65532458	GM19239	blood:	n/a
40	chr13:65533500-65533550	RPTEC	kidney:	n/a
41	chr13:65532581-65532631	AG04450	lung:	fetal
42	chr13:65500141-65500191	SK-N-MC	brain:	n/a
43	chr13:65532273-65532323	HPAEpiC	pulmonary alveolar:	n/a
44	chr13:65533139-65533189	SK-N-SH	brain:	n/a
45	chr13:65532878-65532928	MCF10A-Er-Src	breast:	n/a
46	chr13:65500141-65500191	PrEC	prostate:	n/a
47	chr13:65500124-65500174	AG09319	gingival:	n/a
48	chr13:65532820-65532870	PANC-1	pancreas:	n/a
49	chr13:65500124-65500174	NHBE	bronchial:	n/a
50	chr13:65532820-65532870	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:65501243..65504224-chr17:41399641..41402005,2	K562	blood:
2	chr13:65512386..65514959-chr13:65519104..65520898,2	K562	blood:
3	chr13:65512386..65514959-chr13:65519104..65520898,2	K562	blood:
4	chr13:65452228..65453752-chr13:65456863..65459026,2	MCF-7	breast:
5	chr13:65452228..65453752-chr13:65456863..65459026,2	MCF-7	breast:
6	chr13:65501223..65502743-chr17:41399641..41401888,2	K562	blood:
7	chr13:65490694..65491214-chr8:101576105..101576870,2	K562	blood:
8	chr13:65502724..65504224-chr17:41400395..41402648,2	MCF-7	breast:

Variant related genes	Relation type
LGMNP1	TF binding region
LGMNP1	CpG island

Extended variants
information (count: 1238 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1238 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12430200	chr13:65449535-65449536	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184641997	chr13:65449561-65449562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545286222	chr13:65449563-65449564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558910309	chr13:65449577-65449578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575475043	chr13:65449596-65449597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544576730	chr13:65449619-65449620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561165314	chr13:65449654-65449655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571784719	chr13:65449675-65449676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144706849	chr13:65449722-65449723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540372996	chr13:65449726-65449727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560272513	chr13:65449739-65449740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372826436	chr13:65449746-65449747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9540253	chr13:65449762-65449763	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs552382217	chr13:65449763-65449764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200159367	chr13:65449781-65449782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371994675	chr13:65449782-65449783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569193601	chr13:65449789-65449790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531953533	chr13:65449853-65449854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12430231	chr13:65449887-65449888	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs567156108	chr13:65449889-65449890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369393332	chr13:65449922-65449923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536308069	chr13:65449937-65449938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75828091	chr13:65450040-65450041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9540254	chr13:65450077-65450078	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs190341105	chr13:65450100-65450101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558820199	chr13:65450111-65450112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140273236	chr13:65450113-65450114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181669313	chr13:65450114-65450115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76948906	chr13:65450168-65450169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145260452	chr13:65450170-65450171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574750547	chr13:65450184-65450185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540302218	chr13:65450199-65450200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560193180	chr13:65450204-65450205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114406840	chr13:65450258-65450259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187631475	chr13:65450274-65450275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534679213	chr13:65450295-65450296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9528841	chr13:65450328-65450329	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs147970417	chr13:65450338-65450339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115898189	chr13:65450398-65450399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560906479	chr13:65450544-65450545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529676880	chr13:65450653-65450654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112936801	chr13:65450655-65450656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142011058	chr13:65450657-65450658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375280603	chr13:65450660-65450661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544881775	chr13:65450694-65450695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191012830	chr13:65450749-65450750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114283728	chr13:65450764-65450765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538103727	chr13:65450784-65450785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs57458844	chr13:65450808-65450809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs150692402	chr13:65450863-65450864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Multiple myeloma	17550852	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65446600-65451400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:65451400-65451600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:65470000-65470400	Active TSS	Gastric	stomach
4	chr13:65474200-65474400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr13:65482800-65483800	Enhancers	HUVEC	blood vessel
6	chr13:65483000-65483400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr13:65483000-65483400	Enhancers	HMEC	breast
8	chr13:65483000-65483600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr13:65483400-65484400	Weak transcription	HMEC	breast
10	chr13:65483400-65485600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr13:65483600-65485600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr13:65483800-65485600	Weak transcription	HUVEC	blood vessel
13	chr13:65484400-65485000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr13:65484400-65487000	Enhancers	HMEC	breast
15	chr13:65485000-65485400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr13:65485400-65486200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr13:65485600-65485800	Enhancers	A549	lung
18	chr13:65485600-65486200	Enhancers	NHEK	skin
19	chr13:65485600-65487000	Enhancers	Muscle Satellite Cultured Cells	--
20	chr13:65485600-65487000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr13:65485600-65487000	Enhancers	HUVEC	blood vessel
22	chr13:65485600-65487200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr13:65485600-65487200	Enhancers	NH-A	brain
24	chr13:65485800-65486000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr13:65485800-65486000	Flanking Active TSS	A549	lung
26	chr13:65486000-65486400	Active TSS	A549	lung
27	chr13:65486200-65489000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr13:65486400-65486800	Enhancers	A549	lung
29	chr13:65486600-65486800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr13:65486800-65487000	Active TSS	A549	lung
31	chr13:65487000-65487600	Weak transcription	HUVEC	blood vessel
32	chr13:65487600-65487800	ZNF genes & repeats	HUVEC	blood vessel
33	chr13:65487800-65488000	Weak transcription	HUVEC	blood vessel
34	chr13:65498600-65499000	Active TSS	Gastric	stomach
35	chr13:65499400-65499600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr13:65499400-65499800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr13:65499600-65502800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr13:65499800-65500000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr13:65500000-65500200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr13:65502400-65503400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr13:65502400-65503800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr13:65502400-65504400	Enhancers	Placenta Amnion	Placenta Amnion
43	chr13:65502600-65503800	Enhancers	Muscle Satellite Cultured Cells	--
44	chr13:65502800-65503000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr13:65502800-65503000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr13:65502800-65503000	Enhancers	Hela-S3	cervix
47	chr13:65502800-65503200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr13:65502800-65503200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr13:65502800-65503200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr13:65502800-65503200	Enhancers	HMEC	breast

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