Variant report

Variant	nsv876859
Chromosome Location	chr3:60519576-60558331
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:157)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:157 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr3:60541358-60541754	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr3:60538939-60539154	GM12878	blood:	n/a	n/a
3	BATF	chr3:60541502-60541804	GM12878	blood:	n/a	chr3:60541671-60541682
4	BATF	chr3:60541461-60541885	GM12878	blood:	n/a	chr3:60541671-60541682
5	BATF	chr3:60522246-60522459	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:60541504-60541905	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:60541461-60541764	GM12878	blood:	n/a	n/a
8	BCL3	chr3:60541457-60541820	GM12878	blood:	n/a	n/a
9	BCLAF1	chr3:60541470-60541822	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:60541385-60541970	GM12878	blood:	n/a	n/a
11	CEBPB	chr3:60556976-60557552	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr3:60541559-60541835	GM12878	blood:	n/a	n/a
13	CEBPB	chr3:60528680-60529009	K562	blood:	n/a	n/a
14	CHD1	chr3:60541274-60541431	GM12878	blood:	n/a	n/a
15	CREB1	chr3:60538902-60539194	GM12878	blood:	n/a	n/a
16	CTBP2	chr3:60541259-60542058	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr3:60542685-60542751	GM13976	blood:	n/a	n/a
18	CTCF	chr3:60522294-60522513	LNCaP	prostate:	n/a	n/a
19	CTCF	chr3:60529465-60529510	GM10266	blood:	n/a	n/a
20	CTCF	chr3:60538760-60538803	ProgFib	skin:	n/a	n/a
21	CTCF	chr3:60522216-60522593	GM12878	blood:	n/a	n/a
22	CTCF	chr3:60522322-60522498	LNCaP	prostate:	n/a	n/a
23	E2F4	chr3:60541587-60541787	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F6	chr3:60541294-60541973	H1-hESC	embryonic stem cell:	n/a	n/a
25	E2F6	chr3:60541455-60541753	H1-hESC	embryonic stem cell:	n/a	n/a
26	EBF1	chr3:60522186-60522458	GM12878	blood:	n/a	n/a
27	EBF1	chr3:60538986-60539146	GM12878	blood:	n/a	n/a
28	ELK1	chr3:60520533-60520646	K562	blood:	n/a	n/a
29	EP300	chr3:60541150-60541877	GM12878	blood:	n/a	chr3:60541334-60541348
30	EP300	chr3:60541529-60541829	GM12878	blood:	n/a	n/a
31	EP300	chr3:60538947-60539177	GM12878	blood:	n/a	n/a
32	EP300	chr3:60538179-60538345	K562	blood:	n/a	n/a
33	EP300	chr3:60522141-60522486	GM12878	blood:	n/a	n/a
34	EP300	chr3:60541239-60541802	ECC-1	luminal epithelium:	n/a	chr3:60541334-60541348
35	EP300	chr3:60538967-60539167	GM12878	blood:	n/a	n/a
36	EP300	chr3:60532015-60532049	GM12878	blood:	n/a	n/a
37	EP300	chr3:60541489-60541858	GM12878	blood:	n/a	n/a
38	ESR1	chr3:60522223-60522721	ECC-1	luminal epithelium:	n/a	n/a
39	FOS	chr3:60541512-60541851	MCF10A-Er-Src	breast:	n/a	chr3:60541828-60541837
40	FOS	chr3:60547468-60547524	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr3:60542086-60542097	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr3:60541472-60541936	MCF10A-Er-Src	breast:	n/a	chr3:60541828-60541837
43	FOS	chr3:60541509-60541836	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr3:60539030-60539077	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr3:60541440-60541862	MCF10A-Er-Src	breast:	n/a	chr3:60541828-60541837
46	FOXA1	chr3:60525705-60525938	HepG2	liver:	n/a	n/a
47	FOXA1	chr3:60525709-60525909	T-47D	breast:	n/a	n/a
48	FOXM1	chr3:60541409-60541792	GM12878	blood:	n/a	n/a
49	GATA3	chr3:60538348-60538757	SK-N-SH	brain:	n/a	chr3:60538496-60538503
50	GATA3	chr3:60545824-60545984	SH-SY5Y	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:60534659-60534709	GM19239	blood:	n/a
2	chr3:60541935-60541985	HepG2	liver:	n/a
3	chr3:60541935-60541985	HCM	heart:	n/a
4	chr3:60534659-60534709	AoSMC	blood vessel:	n/a
5	chr3:60541935-60541985	SKMC	muscle:	n/a
6	chr3:60534659-60534709	AG09309	skin:	n/a
7	chr3:60541935-60541985	HAEpiC	amniotic membrane:	n/a
8	chr3:60534659-60534709	ECC-1	luminal epithelium:	n/a
9	chr3:60534659-60534709	SAEC	small airway:	n/a
10	chr3:60541935-60541985	GM06990	blood:	n/a
11	chr3:60541935-60541985	GM12878	blood:	n/a
12	chr3:60541935-60541985	NHDF-neo	bronchial:	n/a
13	chr3:60541935-60541985	MCF-7	breast:	n/a
14	chr3:60534659-60534709	GM06990	blood:	n/a
15	chr3:60541935-60541985	HCF	heart:	n/a
16	chr3:60541935-60541985	AoSMC	blood vessel:	n/a
17	chr3:60541935-60541985	RPTEC	kidney:	n/a
18	chr3:60541935-60541985	HRE	kidney:	n/a
19	chr3:60541935-60541985	AG09309	skin:	n/a
20	chr3:60541935-60541985	HRPEpiC	eye:	n/a
21	chr3:60534659-60534709	PANC-1	pancreas:	n/a
22	chr3:60541935-60541985	ProgFib	skin:	n/a
23	chr3:60534659-60534709	AG04449	skin:	fetal
24	chr3:60541935-60541985	HL-60	blood:	n/a
25	chr3:60541935-60541985	AG04450	lung:	fetal
26	chr3:60534659-60534709	LNCaP	prostate:	n/a
27	chr3:60541935-60541985	HCPEpiC	choroid plexus:	n/a
28	chr3:60541935-60541985	HNPCEpiC	eye:	n/a
29	chr3:60534659-60534709	Hepatocyte	liver:	n/a
30	chr3:60534659-60534709	HPAEpiC	pulmonary alveolar:	n/a
31	chr3:60534659-60534709	HNPCEpiC	eye:	n/a
32	chr3:60541935-60541985	Hela-S3	cervix:	n/a
33	chr3:60541935-60541985	A549	lung:	n/a
34	chr3:60534659-60534709	NH-A	brain:	n/a
35	chr3:60534659-60534709	PrEC	prostate:	n/a
36	chr3:60541935-60541985	PANC-1	pancreas:	n/a
37	chr3:60541935-60541985	Jurkat	blood:	n/a
38	chr3:60534659-60534709	HRE	kidney:	n/a
39	chr3:60541935-60541985	ovcar-3	ovarian:	n/a
40	chr3:60534659-60534709	NB4	blood:	n/a
41	chr3:60541935-60541985	NHBE	bronchial:	n/a
42	chr3:60534659-60534709	GM12892	blood:	n/a
43	chr3:60541935-60541985	GM12892	blood:	n/a
44	chr3:60534659-60534709	HepG2	liver:	n/a
45	chr3:60541935-60541985	BJ	skin:	n/a
46	chr3:60541935-60541985	SK-N-SH_RA	brain:	n/a
47	chr3:60534659-60534709	HEEpiC	esophagus:	n/a
48	chr3:60541935-60541985	K562	blood:	n/a
49	chr3:60534659-60534709	HCT-116	colon:	n/a
50	chr3:60534659-60534709	NHBE	bronchial:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:60540686..60542357-chr3:60544396..60547360,2	MCF-7	breast:
2	chr3:60532780..60534867-chr3:60539940..60541452,2	K562	blood:
3	chr3:60540686..60542357-chr3:60544396..60547360,2	MCF-7	breast:
4	chr3:60532780..60534867-chr3:60539940..60541452,2	K562	blood:
5	chr3:60500352..60502884-chr3:60536251..60537952,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FEZF2-9	chr3:60521543-60522712	NONHSAT090160

No data

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

Extended variants
information (count: 2152 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2152 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs241698	chr3:60519576-60519577	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139835434	chr3:60519620-60519621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538618923	chr3:60519634-60519635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556728754	chr3:60519671-60519672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75162716	chr3:60519697-60519698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs9868436	chr3:60519703-60519704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535925997	chr3:60519718-60519719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554719047	chr3:60519754-60519755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs193254872	chr3:60519774-60519775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573446021	chr3:60519776-60519777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540854987	chr3:60519781-60519782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559276124	chr3:60519832-60519833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376002750	chr3:60519854-60519855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145351258	chr3:60519870-60519871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576114614	chr3:60519876-60519877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544594917	chr3:60519882-60519883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562694772	chr3:60519883-60519884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530118041	chr3:60519926-60519927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541887768	chr3:60519927-60519928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560236044	chr3:60519931-60519932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528249758	chr3:60519956-60519957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377213293	chr3:60519967-60519968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546424870	chr3:60519970-60519971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139378064	chr3:60519992-60519993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34837102	chr3:60520005-60520006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs242240	chr3:60520020-60520021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543244320	chr3:60520023-60520024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369307496	chr3:60520027-60520028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs242241	chr3:60520029-60520030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532259239	chr3:60520038-60520039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550860405	chr3:60520045-60520046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574881193	chr3:60520095-60520096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568725349	chr3:60520119-60520120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113100186	chr3:60520146-60520147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529217023	chr3:60520156-60520157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536265139	chr3:60520160-60520161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78775671	chr3:60520171-60520172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563992117	chr3:60520172-60520173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs367668966	chr3:60520173-60520174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201649221	chr3:60520191-60520192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200149923	chr3:60520192-60520193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201016576	chr3:60520193-60520194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58578826	chr3:60520194-60520195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71092610	chr3:60520196-60520197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73103788	chr3:60520197-60520198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184780173	chr3:60520236-60520237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs17063482	chr3:60520257-60520258	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs375598336	chr3:60520271-60520272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559089749	chr3:60520276-60520277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12486187	chr3:60520279-60520280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Urothelial cell carcinoma	18451213	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Mental retardation	17847001	CNVD
Neuroticism	17667963	CNVD
Squamous cell cancer	19047905	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Autism	22102821	CNVD
Prostate cancer	19363497	CNVD
Malaria	21533027	CNVD
Colorectal cancer	21518781	CNVD
Esophageal cancer	21518781	CNVD
Cancer	20164919	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD

Chromatin state (count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60509400-60523400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr3:60519200-60522200	Weak transcription	Fetal Kidney	kidney
3	chr3:60521600-60522200	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr3:60521800-60522800	Enhancers	GM12878-XiMat	blood
5	chr3:60522000-60523400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr3:60522200-60522600	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr3:60522200-60522800	Enhancers	Fetal Kidney	kidney
8	chr3:60522200-60523800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr3:60523400-60523600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr3:60523400-60528600	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr3:60525800-60526400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr3:60526400-60529400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr3:60528600-60529000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr3:60528800-60529200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr3:60528800-60529200	Enhancers	Rectal Smooth Muscle	rectum
16	chr3:60528800-60529600	Enhancers	Fetal Stomach	stomach
17	chr3:60529000-60531000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr3:60529200-60531200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr3:60529400-60529600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:60530800-60531000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr3:60531000-60531600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr3:60531000-60534400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr3:60531200-60531600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr3:60531200-60532200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr3:60531200-60533800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr3:60531200-60536200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr3:60531400-60531600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr3:60531400-60533800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:60531600-60531800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr3:60531600-60533400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr3:60531600-60533600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr3:60531800-60532200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr3:60532000-60532200	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr3:60532200-60532600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:60532200-60532600	Enhancers	Primary B cells from peripheral blood	blood
36	chr3:60532200-60532600	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr3:60532200-60533000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr3:60532600-60533800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr3:60533000-60536200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr3:60533400-60534000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr3:60533400-60534200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr3:60533400-60534400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr3:60533400-60536000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr3:60533600-60533800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr3:60533600-60536800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr3:60533800-60534000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr3:60533800-60534000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr3:60533800-60541200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:60533800-60541200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr3:60533800-60541400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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