Variant report

Variant	nsv900486
Chromosome Location	chr13:70302991-70421896
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	BRCA1	chr13:70325178-70325338	GM12878	blood:	n/a	n/a
2	CBX3	chr13:70351107-70351445	K562	blood:	n/a	n/a
3	CEBPB	chr13:70328822-70329838	HepG2	liver:	n/a	chr13:70328921-70328934 chr13:70329806-70329823 chr13:70329607-70329616 chr13:70329605-70329618 chr13:70329607-70329616 chr13:70329605-70329618 chr13:70328859-70328868 chr13:70329607-70329618 chr13:70329607-70329616 chr13:70329605-70329618 chr13:70329607-70329616 chr13:70329607-70329618 chr13:70329605-70329616
4	CEBPB	chr13:70308944-70309274	HepG2	liver:	n/a	chr13:70309100-70309111 chr13:70309099-70309112
5	CEBPB	chr13:70329765-70329832	H1-hESC	embryonic stem cell:	n/a	chr13:70329806-70329823
6	CEBPB	chr13:70368078-70368276	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr13:70390969-70391070	GM10266	blood:	n/a	n/a
8	CTCF	chr13:70381758-70381815	Lung_OC	lung:	n/a	n/a
9	CTCF	chr13:70377800-70377950	GM12874	blood:	n/a	n/a
10	CTCF	chr13:70360719-70360758	Spleen_OC	spleen:	n/a	n/a
11	CTCF	chr13:70311760-70311910	BE2_C	brain:	n/a	n/a
12	CTCF	chr13:70356710-70356796	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr13:70341569-70341599	GM13977	blood:	n/a	n/a
14	E2F4	chr13:70329600-70329891	MCF10A-Er-Src	breast:	n/a	chr13:70329752-70329761
15	E2F4	chr13:70399699-70399899	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr13:70324263-70324404	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr13:70379717-70379799	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr13:70419540-70419740	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr13:70413194-70413388	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr13:70371208-70371402	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr13:70324917-70325034	MCF10A-Er-Src	breast:	n/a	n/a
22	EBF1	chr13:70402862-70403078	GM12878	blood:	n/a	n/a
23	EBF1	chr13:70402792-70403037	GM12878	blood:	n/a	n/a
24	EP300	chr13:70399669-70400085	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr13:70367798-70368912	SK-N-SH	brain:	n/a	n/a
26	EP300	chr13:70383172-70383738	ECC-1	luminal epithelium:	n/a	n/a
27	EP300	chr13:70349021-70349420	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr13:70368195-70368542	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr13:70393531-70395170	SK-N-SH	brain:	n/a	n/a
30	EP300	chr13:70394149-70394741	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr13:70394201-70394686	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr13:70399740-70399999	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr13:70368163-70368634	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr13:70399491-70400395	SK-N-SH	brain:	n/a	n/a
35	FAM48A	chr13:70413212-70413347	GM12878	blood:	n/a	n/a
36	FOS	chr13:70372956-70372997	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr13:70392060-70392202	MCF10A-Er-Src	breast:	n/a	chr13:70392167-70392177
38	FOXA2	chr13:70356498-70357123	A549	lung:	n/a	n/a
39	GABPA	chr13:70371816-70371946	GM12878	blood:	n/a	n/a
40	GATA2	chr13:70367882-70368691	SH-SY5Y	brain:	n/a	chr13:70368260-70368276 chr13:70368265-70368272 chr13:70368265-70368272 chr13:70368263-70368272 chr13:70368425-70368446 chr13:70368368-70368375 chr13:70368258-70368279 chr13:70368263-70368273 chr13:70368488-70368495 chr13:70368265-70368272
41	GATA2	chr13:70399732-70400068	SH-SY5Y	brain:	n/a	chr13:70399763-70399771 chr13:70399946-70399953
42	GATA2	chr13:70394080-70394977	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr13:70391575-70391825	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr13:70349010-70349478	SK-N-SH	brain:	n/a	chr13:70349263-70349270 chr13:70349263-70349270 chr13:70349263-70349270 chr13:70349154-70349175 chr13:70349256-70349277 chr13:70349183-70349193
45	GATA3	chr13:70368014-70368803	SK-N-SH	brain:	n/a	chr13:70368260-70368276 chr13:70368762-70368774 chr13:70368265-70368272 chr13:70368265-70368272 chr13:70368263-70368272 chr13:70368425-70368446 chr13:70368368-70368375 chr13:70368258-70368279 chr13:70368263-70368273 chr13:70368488-70368495 chr13:70368265-70368272
46	GATA3	chr13:70399795-70400073	SH-SY5Y	brain:	n/a	chr13:70399946-70399953
47	GATA3	chr13:70394206-70394748	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr13:70367968-70368859	SH-SY5Y	brain:	n/a	chr13:70368805-70368812 chr13:70368260-70368276 chr13:70368762-70368774 chr13:70368801-70368814 chr13:70368265-70368272 chr13:70368265-70368272 chr13:70368263-70368272 chr13:70368803-70368813 chr13:70368425-70368446 chr13:70368368-70368375 chr13:70368258-70368279 chr13:70368263-70368273 chr13:70368488-70368495 chr13:70368265-70368272 chr13:70368803-70368812
49	GATA3	chr13:70348940-70349273	SH-SY5Y	brain:	n/a	chr13:70349263-70349270 chr13:70349263-70349270 chr13:70348965-70348974 chr13:70349263-70349270 chr13:70349154-70349175 chr13:70348960-70348967 chr13:70349183-70349193
50	GATA3	chr13:70368154-70368633	SK-N-SH	brain:	n/a	chr13:70368260-70368276 chr13:70368265-70368272 chr13:70368265-70368272 chr13:70368263-70368272 chr13:70368425-70368446 chr13:70368368-70368375 chr13:70368258-70368279 chr13:70368263-70368273 chr13:70368488-70368495 chr13:70368265-70368272

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:70369137-70369187	NH-A	brain:	n/a
2	chr13:70369137-70369187	NHDF-neo	bronchial:	n/a
3	chr13:70369137-70369187	AG04449	skin:	fetal
4	chr13:70369137-70369187	AG09319	gingival:	n/a
5	chr13:70369137-70369187	AG09309	skin:	n/a
6	chr13:70369137-70369187	GM19239	blood:	n/a
7	chr13:70369137-70369187	SK-N-SH_RA	brain:	n/a
8	chr13:70369137-70369187	AG04450	lung:	fetal
9	chr13:70369137-70369187	H1-hESC	embryonic stem cell:	embryo
10	chr13:70369137-70369187	SAEC	small airway:	n/a
11	chr13:70369137-70369187	GM12892	blood:	n/a
12	chr13:70369137-70369187	SKMC	muscle:	n/a
13	chr13:70369137-70369187	HUVEC	blood vessel:	n/a
14	chr13:70369137-70369187	HL-60	blood:	n/a
15	chr13:70369137-70369187	ECC-1	luminal epithelium:	n/a
16	chr13:70369137-70369187	K562	blood:	n/a
17	chr13:70369137-70369187	SK-N-MC	brain:	n/a
18	chr13:70369137-70369187	BJ	skin:	n/a
19	chr13:70369137-70369187	HCM	heart:	n/a
20	chr13:70369137-70369187	Hela-S3	cervix:	n/a
21	chr13:70369137-70369187	ovcar-3	ovarian:	n/a
22	chr13:70369137-70369187	Jurkat	blood:	n/a
23	chr13:70369137-70369187	GM06990	blood:	n/a
24	chr13:70369137-70369187	NT2-D1	testis:	n/a
25	chr13:70369137-70369187	HEK293	kidney:	embryo
26	chr13:70369137-70369187	CMK	blood:	n/a
27	chr13:70369137-70369187	U87	brain:	n/a
28	chr13:70369137-70369187	GM12891	blood:	n/a
29	chr13:70369137-70369187	Caco-2	colon:	n/a
30	chr13:70369137-70369187	PFSK-1	brain:	n/a
31	chr13:70369137-70369187	HCPEpiC	choroid plexus:	n/a
32	chr13:70369137-70369187	ProgFib	skin:	n/a
33	chr13:70369137-70369187	BE2_C	brain:	n/a
34	chr13:70369137-70369187	PANC-1	pancreas:	n/a
35	chr13:70369137-70369187	LNCaP	prostate:	n/a
36	chr13:70369137-70369187	HNPCEpiC	eye:	n/a
37	chr13:70369137-70369187	T-47D	breast:	n/a
38	chr13:70369137-70369187	SK-N-SH	brain:	n/a
39	chr13:70369137-70369187	HEEpiC	esophagus:	n/a
40	chr13:70369137-70369187	GM12878	blood:	n/a
41	chr13:70369137-70369187	HCT-116	colon:	n/a
42	chr13:70369137-70369187	HepG2	liver:	n/a
43	chr13:70369137-70369187	HIPEpiC	eye:	n/a
44	chr13:70369137-70369187	HRCEpiC	kidney:	n/a
45	chr13:70369137-70369187	A549	lung:	n/a
46	chr13:70369137-70369187	MCF-7	breast:	n/a
47	chr13:70369137-70369187	AG10803	skin:	n/a
48	chr13:70369137-70369187	IMR90	lung:	fetal
49	chr13:70369137-70369187	HPAEpiC	pulmonary alveolar:	n/a
50	chr13:70369137-70369187	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
2	chr13:70343892..70346345-chr13:113863086..113865250,2	MCF-7	breast:
3	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
4	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
5	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:

Variant related genes	Relation type
RNY3P10	TF binding region
RNY3P10	CpG island
ENSG00000139842	chromatin interactions

Extended variants
information (count: 834 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:834 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75573984	chr13:70311241-70311242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527981417	chr13:70311257-70311258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186323250	chr13:70311263-70311264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577023248	chr13:70311288-70311289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533471692	chr13:70311337-70311338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs9529635	chr13:70311352-70311353	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs371210347	chr13:70311379-70311380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539485169	chr13:70311384-70311385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs78593347	chr13:70311398-70311399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147886766	chr13:70311399-70311400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141534115	chr13:70311427-70311428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34168639	chr13:70311434-70311435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76121261	chr13:70311451-70311452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572249066	chr13:70311469-70311470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150441953	chr13:70311483-70311484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533449412	chr13:70311539-70311540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577690893	chr13:70311542-70311543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543463405	chr13:70311630-70311631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563361860	chr13:70311663-70311664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573664750	chr13:70311699-70311700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111478710	chr13:70311702-70311703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190829385	chr13:70311703-70311704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182982901	chr13:70311707-70311708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551631280	chr13:70311728-70311729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541312770	chr13:70311784-70311785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569930764	chr13:70311785-70311786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533131715	chr13:70311814-70311815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549770094	chr13:70311823-70311824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149617449	chr13:70311871-70311872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372988031	chr13:70311914-70311915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529363333	chr13:70311915-70311916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549495215	chr13:70311923-70311924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565720724	chr13:70311924-70311925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534841247	chr13:70311972-70311973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs74090435	chr13:70311973-70311974	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs571580626	chr13:70311979-70311980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537005593	chr13:70312007-70312008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556687800	chr13:70312051-70312052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573629177	chr13:70312061-70312062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542351630	chr13:70312082-70312083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115834098	chr13:70312129-70312130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139027079	chr13:70312131-70312132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142274161	chr13:70312134-70312135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564396281	chr13:70312194-70312195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74090437	chr13:70312221-70312222	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs200313025	chr13:70312227-70312228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544140797	chr13:70312261-70312262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369392242	chr13:70312323-70312324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563521242	chr13:70312366-70312367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188647752	chr13:70312380-70312381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70311200-70312200	Enhancers	Pancreas	Pancrea
2	chr13:70311400-70311800	Enhancers	Gastric	stomach
3	chr13:70311600-70312200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:70312200-70313800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr13:70313800-70314200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr13:70333200-70333400	Enhancers	Esophagus	oesophagus
7	chr13:70343800-70344400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr13:70343800-70344600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr13:70343800-70344600	ZNF genes & repeats	Liver	Liver
10	chr13:70367600-70368200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr13:70367800-70368200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr13:70367800-70368600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr13:70367800-70368600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr13:70367800-70368600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr13:70367800-70368800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr13:70368000-70368200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr13:70368000-70368600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr13:70368000-70368600	Enhancers	H9 Cell Line	embryonic stem cell
19	chr13:70368000-70368600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr13:70368000-70368600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr13:70368000-70368600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr13:70368000-70368800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr13:70368200-70368600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr13:70368200-70368600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr13:70368200-70369000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr13:70368600-70368800	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr13:70368600-70369000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr13:70368600-70370400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr13:70370400-70371000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr13:70377400-70383200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr13:70383000-70383600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr13:70383200-70383600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr13:70383600-70383800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:70383800-70384000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr13:70393200-70395000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr13:70394200-70394600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr13:70399800-70400200	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr13:70399800-70400400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr13:70399800-70400600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr13:70400000-70400600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr13:70400000-70400800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr13:70400200-70402200	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr13:70402000-70403600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr13:70402200-70403200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr13:70402200-70403400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr13:70402600-70403200	Enhancers	Adipose Nuclei	Adipose
47	chr13:70402600-70403200	Enhancers	Placenta Amnion	Placenta Amnion
48	chr13:70402800-70403000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr13:70402800-70403200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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