Variant report

Variant	nsv1014062
Chromosome Location	chr4:21270358-21479027
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	ARID3A	chr4:21409038-21409186	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:21409476-21409646	HepG2	liver:	n/a	n/a
3	BACH1	chr4:21340833-21340873	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:21386733-21386848	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr4:21471169-21471375	H1-hESC	embryonic stem cell:	n/a	n/a
6	CCNT2	chr4:21473772-21473970	K562	blood:	n/a	n/a
7	CEBPB	chr4:21362752-21363039	HepG2	liver:	n/a	chr4:21362916-21362927
8	CEBPB	chr4:21436283-21436393	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:21290177-21290449	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:21400056-21400228	A549	lung:	n/a	chr4:21400158-21400169
11	CEBPB	chr4:21400105-21400314	H1-hESC	embryonic stem cell:	n/a	chr4:21400158-21400169
12	CEBPB	chr4:21389302-21389614	HepG2	liver:	n/a	chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389457-21389470
13	CEBPB	chr4:21427707-21427907	K562	blood:	n/a	chr4:21427718-21427729
14	CEBPB	chr4:21331830-21332133	IMR90	lung:	n/a	chr4:21331975-21331986
15	CEBPB	chr4:21449350-21449652	H1-hESC	embryonic stem cell:	n/a	chr4:21449511-21449522
16	CEBPB	chr4:21416956-21417175	HepG2	liver:	n/a	chr4:21417025-21417036
17	CEBPB	chr4:21271650-21271791	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:21389323-21389632	H1-hESC	embryonic stem cell:	n/a	chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389457-21389470
19	CEBPB	chr4:21369419-21369766	HepG2	liver:	n/a	chr4:21369585-21369598 chr4:21369585-21369596 chr4:21369586-21369597
20	CEBPB	chr4:21399999-21400257	HepG2	liver:	n/a	chr4:21400158-21400169
21	CEBPB	chr4:21427556-21427932	HepG2	liver:	n/a	chr4:21427718-21427729
22	CEBPB	chr4:21346181-21346331	HepG2	liver:	n/a	chr4:21346213-21346224
23	CEBPB	chr4:21432334-21432679	IMR90	lung:	n/a	chr4:21432515-21432524 chr4:21432513-21432526 chr4:21432515-21432524 chr4:21432514-21432525 chr4:21432513-21432526 chr4:21432515-21432524
24	CEBPB	chr4:21369524-21369702	A549	lung:	n/a	chr4:21369585-21369598 chr4:21369585-21369596 chr4:21369586-21369597
25	CEBPB	chr4:21449344-21449649	HepG2	liver:	n/a	chr4:21449511-21449522
26	CEBPB	chr4:21283417-21283704	HepG2	liver:	n/a	chr4:21283560-21283571 chr4:21283560-21283573 chr4:21283557-21283574
27	CEBPB	chr4:21389446-21389557	K562	blood:	n/a	chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389457-21389470
28	CEBPB	chr4:21432340-21432662	HepG2	liver:	n/a	chr4:21432515-21432524 chr4:21432513-21432526 chr4:21432515-21432524 chr4:21432514-21432525 chr4:21432513-21432526 chr4:21432515-21432524
29	CEBPB	chr4:21400092-21400191	K562	blood:	n/a	chr4:21400158-21400169
30	CEBPB	chr4:21449371-21449658	Hela-S3	cervix:	n/a	chr4:21449511-21449522
31	CEBPB	chr4:21427566-21427787	A549	lung:	n/a	chr4:21427718-21427729
32	CEBPB	chr4:21331895-21332143	HepG2	liver:	n/a	chr4:21331975-21331986
33	CEBPB	chr4:21362771-21363035	A549	lung:	n/a	chr4:21362916-21362927
34	CEBPB	chr4:21290298-21290413	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:21432358-21432663	H1-hESC	embryonic stem cell:	n/a	chr4:21432515-21432524 chr4:21432513-21432526 chr4:21432515-21432524 chr4:21432514-21432525 chr4:21432513-21432526 chr4:21432515-21432524
36	CTCF	chr4:21471200-21471350	GM12870	blood:	n/a	n/a
37	CTCF	chr4:21471200-21471350	GM12871	blood:	n/a	n/a
38	CTCF	chr4:21471200-21471350	HCT-116	colon:	n/a	n/a
39	CTCF	chr4:21471166-21471363	GM12878	blood:	n/a	n/a
40	CTCF	chr4:21471200-21471350	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:21449120-21449270	BE2_C	brain:	n/a	n/a
42	CTCF	chr4:21471140-21471290	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr4:21471123-21471417	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:21471200-21471350	HPF	lung:	n/a	n/a
45	CTCF	chr4:21361598-21361642	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr4:21449080-21449230	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr4:21470909-21470945	GM10248	blood:	n/a	n/a
48	CTCF	chr4:21471172-21471392	Gliobla	brain:	n/a	n/a
49	CTCF	chr4:21471180-21471330	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr4:21412174-21412255	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:21470137-21470187	SK-N-SH	brain:	n/a
2	chr4:21470137-21470187	SK-N-SH	brain:	n/a
3	chr4:21306051-21306101	A549	lung:	n/a
4	chr4:21305805-21305855	GM19239	blood:	n/a
5	chr4:21306048-21306098	SKMC	muscle:	n/a
6	chr4:21305805-21305855	HCF	heart:	n/a
7	chr4:21306048-21306098	HAEpiC	amniotic membrane:	n/a
8	chr4:21305490-21305540	HNPCEpiC	eye:	n/a
9	chr4:21305941-21305991	HAEpiC	amniotic membrane:	n/a
10	chr4:21305549-21305599	AoSMC	blood vessel:	n/a
11	chr4:21306051-21306101	GM06990	blood:	n/a
12	chr4:21305805-21305855	HAEpiC	amniotic membrane:	n/a
13	chr4:21305549-21305599	AG04450	lung:	fetal
14	chr4:21305490-21305540	NB4	blood:	n/a
15	chr4:21306051-21306101	T-47D	breast:	n/a
16	chr4:21306048-21306098	T-47D	breast:	n/a
17	chr4:21305490-21305540	AG09309	skin:	n/a
18	chr4:21306048-21306098	A549	lung:	n/a
19	chr4:21305549-21305599	AG10803	skin:	n/a
20	chr4:21305941-21305991	SK-N-SH	brain:	n/a
21	chr4:21305805-21305855	U87	brain:	n/a
22	chr4:21305805-21305855	Caco-2	colon:	n/a
23	chr4:21305941-21305991	Jurkat	blood:	n/a
24	chr4:21305490-21305540	LNCaP	prostate:	n/a
25	chr4:21470137-21470187	RPTEC	kidney:	n/a
26	chr4:21305941-21305991	IMR90	lung:	fetal
27	chr4:21306051-21306101	HUVEC	blood vessel:	n/a
28	chr4:21306048-21306098	BJ	skin:	n/a
29	chr4:21305805-21305855	SK-N-MC	brain:	n/a
30	chr4:21305941-21305991	NHDF-neo	bronchial:	n/a
31	chr4:21305805-21305855	AG04450	lung:	fetal
32	chr4:21305490-21305540	ProgFib	skin:	n/a
33	chr4:21305490-21305540	T-47D	breast:	n/a
34	chr4:21305805-21305855	MCF10A-Er-Src	breast:	n/a
35	chr4:21305941-21305991	Hepatocyte	liver:	n/a
36	chr4:21305941-21305991	SKMC	muscle:	n/a
37	chr4:21305805-21305855	GM06990	blood:	n/a
38	chr4:21306048-21306098	GM12891	blood:	n/a
39	chr4:21470137-21470187	MCF10A-Er-Src	breast:	n/a
40	chr4:21305941-21305991	Caco-2	colon:	n/a
41	chr4:21470137-21470187	HEEpiC	esophagus:	n/a
42	chr4:21305941-21305991	GM12891	blood:	n/a
43	chr4:21305549-21305599	NHBE	bronchial:	n/a
44	chr4:21305941-21305991	HRPEpiC	eye:	n/a
45	chr4:21305549-21305599	HRCEpiC	kidney:	n/a
46	chr4:21470137-21470187	BJ	skin:	n/a
47	chr4:21470137-21470187	AG09319	gingival:	n/a
48	chr4:21306048-21306098	GM19239	blood:	n/a
49	chr4:21305805-21305855	HL-60	blood:	n/a
50	chr4:21306051-21306101	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr4:21373360..21375651-chr4:21376032..21378469,2	MCF-7	breast:
2	chr4:21373360..21375651-chr4:21376032..21378469,2	MCF-7	breast:
3	chr4:21186540..21187139-chr4:21470730..21471606,2	MCF-7	breast:
4	chr4:20774692..20775734-chr4:21470776..21471557,3	MCF-7	breast:
5	chr20:61279326..61279889-chr4:21329070..21329892,2	Hela-S3	cervix:
6	chr4:21372485..21375089-chr4:21376184..21378296,2	K562	blood:
7	chr4:21407818..21410530-chrX:40552943..40555484,2	MCF-7	breast:
8	chr4:21186139..21187069-chr4:21470759..21471732,3	MCF-7	breast:
9	chr4:21297051..21299486-chr4:21300587..21302226,2	MCF-7	breast:
10	chr4:21372485..21375089-chr4:21376184..21378296,2	K562	blood:
11	chr4:21297051..21299486-chr4:21300587..21302226,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACRGL-2	chr4:21317905-21318108	ENSG00000250243.2
2	lnc-PACRGL-2	chr4:21306165-21306236	ENSG00000250243.2
3	lnc-PACRGL-2	chr4:21316899-21316963	ENSG00000250243.2
4	lnc-GPR125-6	chr4:21454062-21463909	ucscGeneNc_uc003gqj_1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7978	chr4:21466361-21466381	MIMAT0031181

Variant related genes	Relation type
KCNIP4	TF binding region
ENSG00000250243	TF binding region
KCNIP4	CpG island
ENSG00000250243	CpG island

Extended variants
information (count: 2607 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2607 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556332726	chr4:21287845-21287846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs201289130	chr4:21287846-21287847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs202051908	chr4:21287847-21287848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535596619	chr4:21287848-21287849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554030206	chr4:21287857-21287858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572211686	chr4:21287874-21287875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546112418	chr4:21287876-21287877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558676998	chr4:21287884-21287885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181078689	chr4:21287894-21287895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs16870715	chr4:21287969-21287970	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs562597297	chr4:21287978-21287979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148028804	chr4:21287994-21287995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116149407	chr4:21288148-21288149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186326048	chr4:21288154-21288155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs34981272	chr4:21288164-21288165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114127276	chr4:21288182-21288183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552877399	chr4:21288184-21288185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570340824	chr4:21288236-21288237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77248544	chr4:21288245-21288246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549804262	chr4:21288254-21288255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568133615	chr4:21288296-21288297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535559899	chr4:21288361-21288362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552892535	chr4:21288366-21288367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553993499	chr4:21288371-21288372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541664835	chr4:21288387-21288388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527924172	chr4:21288652-21288653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112024528	chr4:21288674-21288675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186172012	chr4:21288849-21288850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs73249540	chr4:21288850-21288851	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs531932195	chr4:21288897-21288898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571290886	chr4:21288909-21288910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549761933	chr4:21288924-21288925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568096902	chr4:21288969-21288970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs138885302	chr4:21288993-21288994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528139562	chr4:21288995-21288996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547555489	chr4:21289008-21289009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542337055	chr4:21289066-21289067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565647957	chr4:21289141-21289142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76950743	chr4:21289194-21289195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs551310540	chr4:21289199-21289200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34746958	chr4:21291210-21291211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563876170	chr4:21291220-21291221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574370631	chr4:21291256-21291257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541387106	chr4:21291257-21291258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562770941	chr4:21291297-21291298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531484827	chr4:21291370-21291371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192263230	chr4:21291397-21291398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577604253	chr4:21291462-21291463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544995771	chr4:21291465-21291466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376982710	chr4:21291487-21291488	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21287800-21288400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:21288600-21289200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:21291200-21292800	Enhancers	Ovary	ovary
4	chr4:21291800-21292400	Enhancers	Fetal Lung	lung
5	chr4:21292200-21292600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr4:21292200-21293000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr4:21292400-21292600	Bivalent Enhancer	Fetal Lung	lung
8	chr4:21292400-21292800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:21301200-21301600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:21301600-21305200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:21303800-21304200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:21303800-21304200	Active TSS	Brain Germinal Matrix	brain
13	chr4:21303800-21304400	Enhancers	H1 Cell Line	embryonic stem cell
14	chr4:21304000-21304200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:21304000-21305200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr4:21304200-21304800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr4:21304200-21305400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr4:21304200-21305400	Weak transcription	Brain Germinal Matrix	brain
19	chr4:21304200-21305600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr4:21304400-21305000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr4:21304400-21305400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr4:21304600-21304800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr4:21304600-21305400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
24	chr4:21304600-21305400	Enhancers	Brain Hippocampus Middle	brain
25	chr4:21304800-21305000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr4:21304800-21305400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:21304800-21305400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
28	chr4:21305000-21305200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
29	chr4:21305000-21305200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
30	chr4:21305000-21305400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
31	chr4:21305000-21306400	Active TSS	Brain Anterior Caudate	brain
32	chr4:21305200-21305400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:21305200-21305400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
34	chr4:21305200-21305400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
35	chr4:21305200-21306000	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr4:21305200-21306400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
37	chr4:21305400-21305600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
38	chr4:21305400-21305600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
39	chr4:21305400-21305600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:21305400-21305600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:21305400-21305600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
42	chr4:21305400-21305600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
43	chr4:21305400-21305600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
44	chr4:21305400-21305600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
45	chr4:21305400-21305600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr4:21305400-21305600	Flanking Active TSS	Brain Hippocampus Middle	brain
47	chr4:21305400-21306200	Active TSS	Brain Substantia Nigra	brain
48	chr4:21305400-21306400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr4:21305400-21306400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:21305400-21306400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell

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