Variant report

Variant	nsv1005453
Chromosome Location	chr4:21295066-21454143
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	chr4:21409476-21409646	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:21409038-21409186	HepG2	liver:	n/a	n/a
3	BACH1	chr4:21386733-21386848	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:21340833-21340873	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr4:21427556-21427932	HepG2	liver:	n/a	chr4:21427718-21427729
6	CEBPB	chr4:21400092-21400191	K562	blood:	n/a	chr4:21400158-21400169
7	CEBPB	chr4:21389302-21389614	HepG2	liver:	n/a	chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389457-21389470
8	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
9	CEBPB	chr4:21449350-21449652	H1-hESC	embryonic stem cell:	n/a	chr4:21449511-21449522
10	CEBPB	chr4:21362752-21363039	HepG2	liver:	n/a	chr4:21362916-21362927
11	CEBPB	chr4:21389446-21389557	K562	blood:	n/a	chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389457-21389470
12	CEBPB	chr4:21449371-21449658	Hela-S3	cervix:	n/a	chr4:21449511-21449522
13	CEBPB	chr4:21346181-21346331	HepG2	liver:	n/a	chr4:21346213-21346224
14	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
15	CEBPB	chr4:21389323-21389632	H1-hESC	embryonic stem cell:	n/a	chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389457-21389470
16	CEBPB	chr4:21436283-21436393	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr4:21369419-21369766	HepG2	liver:	n/a	chr4:21369585-21369598 chr4:21369585-21369596 chr4:21369586-21369597
18	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
19	CEBPB	chr4:21416956-21417175	HepG2	liver:	n/a	chr4:21417025-21417036
20	CEBPB	chr4:21427707-21427907	K562	blood:	n/a	chr4:21427718-21427729
21	CEBPB	chr4:21400105-21400314	H1-hESC	embryonic stem cell:	n/a	chr4:21400158-21400169
22	CEBPB	chr4:21427566-21427787	A549	lung:	n/a	chr4:21427718-21427729
23	CEBPB	chr4:21331895-21332143	HepG2	liver:	n/a	chr4:21331975-21331986
24	CEBPB	chr4:21369524-21369702	A549	lung:	n/a	chr4:21369585-21369598 chr4:21369585-21369596 chr4:21369586-21369597
25	CEBPB	chr4:21400056-21400228	A549	lung:	n/a	chr4:21400158-21400169
26	CEBPB	chr4:21449344-21449649	HepG2	liver:	n/a	chr4:21449511-21449522
27	CEBPB	chr4:21399999-21400257	HepG2	liver:	n/a	chr4:21400158-21400169
28	CEBPB	chr4:21331830-21332133	IMR90	lung:	n/a	chr4:21331975-21331986
29	CEBPB	chr4:21362771-21363035	A549	lung:	n/a	chr4:21362916-21362927
30	CTCF	chr4:21449080-21449230	NB4	blood:	n/a	n/a
31	CTCF	chr4:21429040-21429190	Caco-2	colon:	n/a	n/a
32	CTCF	chr4:21310785-21310942	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr4:21449120-21449270	HMEC	breast:	n/a	n/a
34	CTCF	chr4:21361598-21361642	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr4:21328024-21328083	GM20000	blood:	n/a	n/a
36	CTCF	chr4:21412169-21412275	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:21449074-21449202	Medullo	brain:	n/a	n/a
38	CTCF	chr4:21449040-21449190	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr4:21412300-21412450	BE2_C	brain:	n/a	n/a
40	CTCF	chr4:21412140-21412290	NHEK	skin:	n/a	n/a
41	CTCF	chr4:21449040-21449190	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr4:21330160-21330310	NHEK	skin:	n/a	n/a
43	CTCF	chr4:21449060-21449210	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr4:21449140-21449290	HPF	lung:	n/a	n/a
45	CTCF	chr4:21412174-21412255	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:21449040-21449190	HepG2	liver:	n/a	n/a
47	CTCF	chr4:21449120-21449270	BE2_C	brain:	n/a	n/a
48	CTCF	chr4:21449040-21449190	RPTEC	kidney:	n/a	n/a
49	CTCF	chr4:21375949-21375989	GM10266	blood:	n/a	n/a
50	CTCF	chr4:21449080-21449230	HCPEpiC	choroid plexus:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:21305490-21305540	AG04449	skin:	fetal
2	chr4:21305490-21305540	AG04449	skin:	fetal
3	chr4:21305941-21305991	HRE	kidney:	n/a
4	chr4:21305941-21305991	ovcar-3	ovarian:	n/a
5	chr4:21305941-21305991	U87	brain:	n/a
6	chr4:21305490-21305540	HRCEpiC	kidney:	n/a
7	chr4:21305941-21305991	HEEpiC	esophagus:	n/a
8	chr4:21305490-21305540	Hepatocyte	liver:	n/a
9	chr4:21305805-21305855	SK-N-SH	brain:	n/a
10	chr4:21305805-21305855	SK-N-MC	brain:	n/a
11	chr4:21305549-21305599	SK-N-SH_RA	brain:	n/a
12	chr4:21306051-21306101	PFSK-1	brain:	n/a
13	chr4:21306048-21306098	HNPCEpiC	eye:	n/a
14	chr4:21306048-21306098	HEEpiC	esophagus:	n/a
15	chr4:21305805-21305855	PFSK-1	brain:	n/a
16	chr4:21305805-21305855	HCF	heart:	n/a
17	chr4:21306051-21306101	AG04449	skin:	fetal
18	chr4:21306051-21306101	ECC-1	luminal epithelium:	n/a
19	chr4:21305549-21305599	RPTEC	kidney:	n/a
20	chr4:21305805-21305855	GM06990	blood:	n/a
21	chr4:21305941-21305991	NHBE	bronchial:	n/a
22	chr4:21305805-21305855	SK-N-SH_RA	brain:	n/a
23	chr4:21305941-21305991	HNPCEpiC	eye:	n/a
24	chr4:21305941-21305991	T-47D	breast:	n/a
25	chr4:21306048-21306098	NHDF-neo	bronchial:	n/a
26	chr4:21306048-21306098	ovcar-3	ovarian:	n/a
27	chr4:21305941-21305991	IMR90	lung:	fetal
28	chr4:21305805-21305855	NHDF-neo	bronchial:	n/a
29	chr4:21305490-21305540	PANC-1	pancreas:	n/a
30	chr4:21306051-21306101	HMEC	breast:	n/a
31	chr4:21305805-21305855	AG09319	gingival:	n/a
32	chr4:21306048-21306098	HCM	heart:	n/a
33	chr4:21306051-21306101	MCF10A-Er-Src	breast:	n/a
34	chr4:21305941-21305991	HCT-116	colon:	n/a
35	chr4:21305490-21305540	HMEC	breast:	n/a
36	chr4:21305941-21305991	AG10803	skin:	n/a
37	chr4:21305941-21305991	SAEC	small airway:	n/a
38	chr4:21306048-21306098	BE2_C	brain:	n/a
39	chr4:21305549-21305599	Hela-S3	cervix:	n/a
40	chr4:21305941-21305991	ProgFib	skin:	n/a
41	chr4:21305490-21305540	GM06990	blood:	n/a
42	chr4:21305805-21305855	HRCEpiC	kidney:	n/a
43	chr4:21306048-21306098	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:21305549-21305599	PFSK-1	brain:	n/a
45	chr4:21306051-21306101	AG04450	lung:	fetal
46	chr4:21305490-21305540	ECC-1	luminal epithelium:	n/a
47	chr4:21305941-21305991	A549	lung:	n/a
48	chr4:21305490-21305540	AG04450	lung:	fetal
49	chr4:21305549-21305599	HIPEpiC	eye:	n/a
50	chr4:21306048-21306098	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:21297051..21299486-chr4:21300587..21302226,2	MCF-7	breast:
2	chr4:21297051..21299486-chr4:21300587..21302226,2	MCF-7	breast:
3	chr4:21407818..21410530-chrX:40552943..40555484,2	MCF-7	breast:
4	chr4:21372485..21375089-chr4:21376184..21378296,2	K562	blood:
5	chr4:21373360..21375651-chr4:21376032..21378469,2	MCF-7	breast:
6	chr20:61279326..61279889-chr4:21329070..21329892,2	Hela-S3	cervix:
7	chr4:21372485..21375089-chr4:21376184..21378296,2	K562	blood:
8	chr4:21373360..21375651-chr4:21376032..21378469,2	MCF-7	breast:

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

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

Extended variants
information (count: 1821 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1821 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116090729	chr4:21301183-21301184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs187717669	chr4:21301207-21301208	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs192566137	chr4:21301209-21301210	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs547334794	chr4:21301251-21301252	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs77014502	chr4:21301314-21301315	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs533897704	chr4:21301334-21301335	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs558562601	chr4:21301346-21301347	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs570588832	chr4:21301347-21301348	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs182162591	chr4:21301348-21301349	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs28735547	chr4:21301349-21301350	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs187549531	chr4:21301381-21301382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542410507	chr4:21301404-21301405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145687521	chr4:21301460-21301461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370250082	chr4:21301475-21301476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10516379	chr4:21301492-21301493	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs545801766	chr4:21301507-21301508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2007762	chr4:21301546-21301547	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs192796771	chr4:21301556-21301557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184754247	chr4:21301562-21301563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374189072	chr4:21301574-21301575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561830877	chr4:21301583-21301584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189859803	chr4:21301621-21301622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191926076	chr4:21301662-21301663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537340811	chr4:21301675-21301676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28433764	chr4:21301686-21301687	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs533083790	chr4:21301736-21301737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184395210	chr4:21301771-21301772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149588816	chr4:21301793-21301794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538247881	chr4:21301829-21301830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547141996	chr4:21301897-21301898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369718758	chr4:21301902-21301903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78670296	chr4:21301993-21301994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377325330	chr4:21301997-21301998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568561884	chr4:21302002-21302003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1038495	chr4:21302029-21302030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs560311068	chr4:21302085-21302086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554442457	chr4:21302108-21302109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189228086	chr4:21302183-21302184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201142965	chr4:21302208-21302209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs199767347	chr4:21302210-21302211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572756234	chr4:21302216-21302217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546566702	chr4:21302224-21302225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181820969	chr4:21302252-21302253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565296131	chr4:21302286-21302287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575909354	chr4:21302297-21302298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527347048	chr4:21302377-21302378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543410772	chr4:21302388-21302389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561602208	chr4:21302398-21302399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374540419	chr4:21302408-21302409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573712976	chr4:21302409-21302410	Weak transcription	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:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21301200-21301600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:21301600-21305200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:21303800-21304200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:21303800-21304200	Active TSS	Brain Germinal Matrix	brain
5	chr4:21303800-21304400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr4:21304000-21304200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:21304000-21305200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:21304200-21304800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr4:21304200-21305400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:21304200-21305400	Weak transcription	Brain Germinal Matrix	brain
11	chr4:21304200-21305600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:21304400-21305000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr4:21304400-21305400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr4:21304600-21304800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:21304600-21305400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
16	chr4:21304600-21305400	Enhancers	Brain Hippocampus Middle	brain
17	chr4:21304800-21305000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:21304800-21305400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:21304800-21305400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
20	chr4:21305000-21305200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
21	chr4:21305000-21305200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
22	chr4:21305000-21305400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
23	chr4:21305000-21306400	Active TSS	Brain Anterior Caudate	brain
24	chr4:21305200-21305400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:21305200-21305400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
26	chr4:21305200-21305400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
27	chr4:21305200-21306000	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr4:21305200-21306400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
29	chr4:21305400-21305600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
30	chr4:21305400-21305600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
31	chr4:21305400-21305600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:21305400-21305600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:21305400-21305600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
34	chr4:21305400-21305600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
35	chr4:21305400-21305600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
36	chr4:21305400-21305600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
37	chr4:21305400-21305600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr4:21305400-21305600	Flanking Active TSS	Brain Hippocampus Middle	brain
39	chr4:21305400-21306200	Active TSS	Brain Substantia Nigra	brain
40	chr4:21305400-21306400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:21305400-21306400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:21305400-21306400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
43	chr4:21305400-21306400	Active TSS	Brain Angular Gyrus	brain
44	chr4:21305400-21306400	Active TSS	Brain Cingulate Gyrus	brain
45	chr4:21305400-21306400	Active TSS	Brain Germinal Matrix	brain
46	chr4:21305400-21306400	Active TSS	Fetal Brain Female	brain
47	chr4:21305600-21305800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:21305600-21305800	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr4:21305600-21305800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:21305600-21305800	Enhancers	Gastric	stomach

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