Variant report

Variant	nsv900271
Chromosome Location	chr13:63254200-63347522
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	BACH1	chr13:63295336-63295437	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr13:63269331-63269362	GM12878	blood:	n/a	n/a
3	BHLHE40	chr13:63321881-63322081	HepG2	liver:	n/a	n/a
4	CBX3	chr13:63280130-63280699	HCT-116	colon:	n/a	n/a
5	CEBPB	chr13:63284596-63284820	HepG2	liver:	n/a	chr13:63284686-63284697 chr13:63284686-63284699 chr13:63284683-63284700
6	CEBPB	chr13:63293850-63294143	IMR90	lung:	n/a	n/a
7	CEBPB	chr13:63345098-63345406	Hela-S3	cervix:	n/a	chr13:63345274-63345285
8	CEBPB	chr13:63322255-63322610	IMR90	lung:	n/a	chr13:63322373-63322382 chr13:63322371-63322382
9	CEBPB	chr13:63322272-63322576	HepG2	liver:	n/a	chr13:63322373-63322382 chr13:63322371-63322382
10	CEBPB	chr13:63345122-63345399	IMR90	lung:	n/a	chr13:63345274-63345285
11	CEBPB	chr13:63345104-63345397	HepG2	liver:	n/a	chr13:63345274-63345285
12	CEBPB	chr13:63345100-63345369	A549	lung:	n/a	chr13:63345274-63345285
13	CEBPB	chr13:63342444-63342551	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr13:63301684-63301705	Medullo	brain:	n/a	n/a
15	CTCF	chr13:63304305-63304364	MCF-7	breast:	n/a	n/a
16	CTCF	chr13:63346020-63346170	HCT-116	colon:	n/a	n/a
17	CTCF	chr13:63345920-63346070	HPF	lung:	n/a	n/a
18	CTCF	chr13:63346020-63346170	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr13:63346020-63346170	BE2_C	brain:	n/a	n/a
20	CTCF	chr13:63346000-63346150	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr13:63318470-63318588	LNCaP	prostate:	n/a	n/a
22	E2F4	chr13:63346267-63346524	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr13:63343401-63343836	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr13:63256760-63257044	MCF10A-Er-Src	breast:	n/a	n/a
25	EP300	chr13:63276194-63278176	SK-N-SH	brain:	n/a	chr13:63277679-63277687 chr13:63277158-63277166
26	EP300	chr13:63271554-63272626	SK-N-SH	brain:	n/a	chr13:63272327-63272337 chr13:63272076-63272083
27	EP300	chr13:63276624-63277207	SK-N-SH_RA	brain:	n/a	chr13:63277158-63277166
28	EP300	chr13:63278850-63279679	SK-N-SH	brain:	n/a	chr13:63278942-63278950 chr13:63278881-63278890
29	EP300	chr13:63276685-63276979	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr13:63277011-63277196	SK-N-SH_RA	brain:	n/a	chr13:63277158-63277166
31	FOS	chr13:63278854-63279054	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr13:63280104-63280615	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr13:63321759-63322070	MCF10A-Er-Src	breast:	n/a	chr13:63321943-63321955 chr13:63321943-63321954 chr13:63321946-63321953 chr13:63321944-63321953
34	FOS	chr13:63321793-63322109	MCF10A-Er-Src	breast:	n/a	chr13:63321943-63321955 chr13:63321943-63321954 chr13:63321946-63321953 chr13:63321944-63321953
35	FOS	chr13:63280157-63280597	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr13:63280078-63280607	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr13:63321798-63322067	MCF10A-Er-Src	breast:	n/a	chr13:63321943-63321955 chr13:63321943-63321954 chr13:63321946-63321953 chr13:63321944-63321953
38	FOS	chr13:63280190-63280619	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr13:63257112-63257312	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr13:63321885-63322089	MCF10A-Er-Src	breast:	n/a	chr13:63321943-63321955 chr13:63321943-63321954 chr13:63321946-63321953 chr13:63321944-63321953
41	FOS	chr13:63257040-63257247	MCF10A-Er-Src	breast:	n/a	n/a
42	FOSL1	chr13:63321820-63322195	HCT-116	colon:	n/a	chr13:63321943-63321955 chr13:63321943-63321954 chr13:63321946-63321953 chr13:63321944-63321953
43	FOSL1	chr13:63280129-63280681	HCT-116	colon:	n/a	n/a
44	FOSL1	chr13:63280094-63280759	HCT-116	colon:	n/a	n/a
45	GATA1	chr13:63262967-63263833	PBDE	blood:	n/a	chr13:63263085-63263106
46	GATA2	chr13:63276545-63277335	SH-SY5Y	brain:	n/a	chr13:63276768-63276775
47	GATA3	chr13:63276508-63277161	SH-SY5Y	brain:	n/a	chr13:63276768-63276775
48	GATA3	chr13:63279012-63279426	SK-N-SH	brain:	n/a	n/a
49	GATA3	chr13:63279041-63279502	SK-N-SH	brain:	n/a	n/a
50	GATA3	chr13:63322487-63322570	SH-SY5Y	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:63264349-63264399	HCM	heart:	n/a
2	chr13:63264349-63264399	GM06990	blood:	n/a
3	chr13:63264349-63264399	AG10803	skin:	n/a
4	chr13:63264349-63264399	NH-A	brain:	n/a
5	chr13:63264349-63264399	T-47D	breast:	n/a
6	chr13:63264349-63264399	HEK293	kidney:	embryo
7	chr13:63264349-63264399	LNCaP	prostate:	n/a
8	chr13:63264349-63264399	SKMC	muscle:	n/a
9	chr13:63264349-63264399	SK-N-MC	brain:	n/a
10	chr13:63264349-63264399	HL-60	blood:	n/a
11	chr13:63264349-63264399	NHDF-neo	bronchial:	n/a
12	chr13:63264349-63264399	HCT-116	colon:	n/a
13	chr13:63264349-63264399	SK-N-SH_RA	brain:	n/a
14	chr13:63264349-63264399	PANC-1	pancreas:	n/a
15	chr13:63264349-63264399	Hepatocyte	liver:	n/a
16	chr13:63264349-63264399	Caco-2	colon:	n/a
17	chr13:63264349-63264399	HMEC	breast:	n/a
18	chr13:63264349-63264399	GM12892	blood:	n/a
19	chr13:63264349-63264399	NHBE	bronchial:	n/a
20	chr13:63264349-63264399	HRPEpiC	eye:	n/a
21	chr13:63264349-63264399	PFSK-1	brain:	n/a
22	chr13:63264349-63264399	BJ	skin:	n/a
23	chr13:63264349-63264399	HCF	heart:	n/a
24	chr13:63264349-63264399	SK-N-SH	brain:	n/a
25	chr13:63264349-63264399	IMR90	lung:	fetal
26	chr13:63264349-63264399	RPTEC	kidney:	n/a
27	chr13:63264349-63264399	AG09319	gingival:	n/a
28	chr13:63264349-63264399	PrEC	prostate:	n/a
29	chr13:63264349-63264399	ECC-1	luminal epithelium:	n/a
30	chr13:63264349-63264399	Hela-S3	cervix:	n/a
31	chr13:63264349-63264399	AG04450	lung:	fetal
32	chr13:63264349-63264399	ovcar-3	ovarian:	n/a
33	chr13:63264349-63264399	AoSMC	blood vessel:	n/a
34	chr13:63264349-63264399	H1-hESC	embryonic stem cell:	embryo
35	chr13:63264349-63264399	K562	blood:	n/a
36	chr13:63264349-63264399	Jurkat	blood:	n/a
37	chr13:63264349-63264399	HPAEpiC	pulmonary alveolar:	n/a
38	chr13:63264349-63264399	HEEpiC	esophagus:	n/a
39	chr13:63264349-63264399	AG04449	skin:	fetal
40	chr13:63264349-63264399	HCPEpiC	choroid plexus:	n/a
41	chr13:63264349-63264399	GM12878	blood:	n/a
42	chr13:63264349-63264399	BE2_C	brain:	n/a
43	chr13:63264349-63264399	A549	lung:	n/a
44	chr13:63264349-63264399	CMK	blood:	n/a
45	chr13:63264349-63264399	GM19239	blood:	n/a
46	chr13:63264349-63264399	HRCEpiC	kidney:	n/a
47	chr13:63264349-63264399	ProgFib	skin:	n/a
48	chr13:63264349-63264399	MCF10A-Er-Src	breast:	n/a
49	chr13:63264349-63264399	AG09309	skin:	n/a
50	chr13:63264349-63264399	HNPCEpiC	eye:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH20-18	chr13:63311883-63313757	ucscGeneNc_uc010aeh_1
2	lnc-PCDH20-18	chr13:63311204-63311359	ucscGeneNc_uc010aeh_1
3	lnc-PCDH20-18	chr13:63300981-63301286	ucscGeneNc_uc010aeh_1
4	lnc-PCDH20-18	chr13:63315448-63316259	ucscGeneNc_uc010aeh_1
5	lnc-PCDH20-3	chr13:63306427-63306492	ENSG00000228669
6	lnc-PCDH20-18	chr13:63303588-63303661	ucscGeneNc_uc010aeh_1
7	lnc-PCDH20-4	chr13:63321841-63322054	NONHSAT034155
8	lnc-PCDH20-3	chr13:63274749-63274830	ENSG00000228669
9	lnc-PCDH20-18	chr13:63303588-63303986	NONHSAT034152
10	lnc-PCDH20-3	chr13:63306227-63306313	ENSG00000228669
11	lnc-PCDH20-18	chr13:63300903-63301293	NONHSAT034152
12	lnc-PCDH20-4	chr13:63321740-63322054	XLOC_010638
13	lnc-PCDH20-3	chr13:63260138-63260227	ENSG00000228669
14	lnc-PCDH20-3	chr13:63305993-63306328	ENSG00000228669

Variant related genes	Relation type
LINC00448	TF binding region
LINC00448	CpG island

Extended variants
information (count: 764 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574858447	chr13:63260149-63260150	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs527508518	chr13:63263039-63263040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530169011	chr13:63263045-63263046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189816628	chr13:63263056-63263057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376786660	chr13:63263107-63263108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200450914	chr13:63263108-63263109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140468358	chr13:63263109-63263110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116778831	chr13:63263110-63263111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114475342	chr13:63263112-63263113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181837998	chr13:63263118-63263119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551078954	chr13:63263127-63263128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569188810	chr13:63263154-63263155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs59198117	chr13:63263157-63263158	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs546680471	chr13:63263226-63263227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185065079	chr13:63263246-63263247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555565050	chr13:63263261-63263262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566800392	chr13:63263262-63263263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534127314	chr13:63263307-63263308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558770901	chr13:63263309-63263310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577010884	chr13:63263315-63263316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543934145	chr13:63263333-63263334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574002399	chr13:63263388-63263389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574371476	chr13:63263426-63263427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541773830	chr13:63263432-63263433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560195974	chr13:63263437-63263438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189396793	chr13:63263445-63263446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs180966177	chr13:63263455-63263456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564307199	chr13:63263469-63263470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531515033	chr13:63263471-63263472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113387411	chr13:63263515-63263516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs71098966	chr13:63263516-63263517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551119666	chr13:63263523-63263524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74085307	chr13:63263598-63263599	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs530051751	chr13:63263609-63263610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570812364	chr13:63263634-63263635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185197652	chr13:63263734-63263735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs35351023	chr13:63263802-63263803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189902829	chr13:63263830-63263831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558806500	chr13:63263884-63263885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570738509	chr13:63263887-63263888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs9630341	chr13:63263914-63263915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555998783	chr13:63263916-63263917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs3924162	chr13:63263920-63263921	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs541558644	chr13:63263943-63263944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553772186	chr13:63263952-63263953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572055271	chr13:63263953-63263954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546147584	chr13:63263983-63263984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573077088	chr13:63264000-63264001	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs564347818	chr13:63264024-63264025	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs541680871	chr13:63264036-63264037	Enhancers Flanking Active TSS	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
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
Myelofibrosis	22110671	CNVD
Anaplastic thyroid cancer	18753363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	21346763	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:63263000-63265000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr13:63263200-63264400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr13:63263200-63266000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr13:63263400-63264000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr13:63263600-63264400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr13:63263600-63265200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr13:63264000-63264200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr13:63264000-63265800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr13:63264200-63264600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr13:63264200-63264600	Enhancers	H9 Cell Line	embryonic stem cell
11	chr13:63264200-63264600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr13:63264200-63265200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr13:63264400-63264600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr13:63264600-63264800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr13:63264800-63265000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr13:63265000-63266000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr13:63266000-63266400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr13:63270800-63271000	Enhancers	Pancreas	Pancrea
19	chr13:63279000-63279200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr13:63279000-63280000	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr13:63279800-63280000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr13:63280000-63284800	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr13:63284600-63285200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr13:63284800-63285400	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr13:63289200-63290800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr13:63289800-63290200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr13:63296000-63296600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr13:63304000-63304400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr13:63304000-63304400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr13:63321200-63321600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr13:63341800-63342000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr13:63341800-63342000	Enhancers	Gastric	stomach

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