Variant report

Variant	nsv3723
Chromosome Location	chr3:20407711-20452881
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:82)
CpG islands
(count:185)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:82 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr3:20416798-20417091	GM12878	blood:	n/a	n/a
2	CEBPB	chr3:20421835-20421992	K562	blood:	n/a	n/a
3	CEBPB	chr3:20416950-20417260	K562	blood:	n/a	n/a
4	CEBPB	chr3:20439770-20440049	A549	lung:	n/a	n/a
5	CEBPB	chr3:20442866-20443121	HepG2	liver:	n/a	chr3:20442974-20442985
6	CEBPB	chr3:20447358-20447747	HepG2	liver:	n/a	chr3:20447481-20447492
7	CEBPB	chr3:20439832-20440032	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr3:20439795-20440063	K562	blood:	n/a	n/a
9	CEBPB	chr3:20421949-20421971	HepG2	liver:	n/a	n/a
10	CEBPB	chr3:20417034-20417209	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr3:20439757-20440083	IMR90	lung:	n/a	n/a
12	CEBPB	chr3:20439732-20440080	HepG2	liver:	n/a	n/a
13	CTCF	chr3:20414039-20414139	K562	blood:	n/a	n/a
14	CTCF	chr3:20413924-20414242	K562	blood:	n/a	n/a
15	CTCF	chr3:20440798-20440832	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr3:20423900-20424050	GM12866	blood:	n/a	n/a
17	CTCF	chr3:20425961-20426058	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr3:20413920-20414070	K562	blood:	n/a	n/a
19	CTCF	chr3:20448200-20448350	GM12871	blood:	n/a	n/a
20	CTCF	chr3:20411488-20411559	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr3:20421429-20421486	GM13976	blood:	n/a	n/a
22	CUX1	chr3:20419922-20420115	K562	blood:	n/a	n/a
23	E2F4	chr3:20419428-20419437	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr3:20447363-20447582	MCF10A-Er-Src	breast:	n/a	n/a
25	EBF1	chr3:20409792-20410035	GM12878	blood:	n/a	n/a
26	EBF1	chr3:20409751-20410037	GM12878	blood:	n/a	n/a
27	EBF1	chr3:20417008-20417208	GM12878	blood:	n/a	chr3:20417095-20417106
28	EP300	chr3:20424412-20424469	GM12878	blood:	n/a	n/a
29	EP300	chr3:20416888-20416962	GM12878	blood:	n/a	n/a
30	FOS	chr3:20447238-20447631	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr3:20447258-20447674	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr3:20427130-20427287	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr3:20442889-20443042	MCF10A-Er-Src	breast:	n/a	chr3:20443032-20443041
34	FOS	chr3:20447261-20447639	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr3:20447289-20447627	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr3:20447997-20448170	MCF10A-Er-Src	breast:	n/a	n/a
37	FOXA1	chr3:20435940-20436185	ECC-1	luminal epithelium:	n/a	n/a
38	GATA3	chr3:20449226-20449426	SH-SY5Y	brain:	n/a	chr3:20449296-20449303 chr3:20449292-20449305 chr3:20449373-20449384 chr3:20449273-20449290
39	GATA3	chr3:20445867-20445937	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr3:20439775-20439904	SH-SY5Y	brain:	n/a	n/a
41	IRF1	chr3:20419784-20419918	K562	blood:	n/a	n/a
42	IRF1	chr3:20412083-20412171	K562	blood:	n/a	n/a
43	MAFF	chr3:20443207-20443424	HepG2	liver:	n/a	n/a
44	MAFK	chr3:20443193-20443348	HepG2	liver:	n/a	chr3:20443285-20443300
45	MAFK	chr3:20443241-20443369	HepG2	liver:	n/a	chr3:20443285-20443300
46	MAX	chr3:20447442-20447474	NB4	blood:	n/a	n/a
47	MYC	chr3:20447315-20447607	MCF10A-Er-Src	breast:	n/a	chr3:20447508-20447517
48	MYC	chr3:20450555-20450606	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr3:20435951-20435969	MCF-7	breast:	n/a	n/a
50	POLR2A	chr3:20442793-20443110	U87	brain:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20448283-20448333	SK-N-SH	brain:	n/a
2	chr3:20448283-20448333	Jurkat	blood:	n/a
3	chr3:20448283-20448333	SK-N-SH	brain:	n/a
4	chr3:20448283-20448333	Jurkat	blood:	n/a
5	chr3:20412342-20412392	H1-hESC	embryonic stem cell:	embryo
6	chr3:20412342-20412392	LNCaP	prostate:	n/a
7	chr3:20412342-20412392	RPTEC	kidney:	n/a
8	chr3:20412342-20412392	U87	brain:	n/a
9	chr3:20448283-20448333	HL-60	blood:	n/a
10	chr3:20418856-20418906	SK-N-SH_RA	brain:	n/a
11	chr3:20412342-20412392	HRE	kidney:	n/a
12	chr3:20412342-20412392	HCT-116	colon:	n/a
13	chr3:20448283-20448333	AG09309	skin:	n/a
14	chr3:20418856-20418906	BE2_C	brain:	n/a
15	chr3:20418856-20418906	HCM	heart:	n/a
16	chr3:20418856-20418906	PANC-1	pancreas:	n/a
17	chr3:20448283-20448333	AG09319	gingival:	n/a
18	chr3:20418856-20418906	A549	lung:	n/a
19	chr3:20448283-20448333	NT2-D1	testis:	n/a
20	chr3:20418856-20418906	HRE	kidney:	n/a
21	chr3:20448283-20448333	HAEpiC	amniotic membrane:	n/a
22	chr3:20448283-20448333	HPAEpiC	pulmonary alveolar:	n/a
23	chr3:20448283-20448333	NHBE	bronchial:	n/a
24	chr3:20418856-20418906	HepG2	liver:	n/a
25	chr3:20418856-20418906	NH-A	brain:	n/a
26	chr3:20418856-20418906	HAEpiC	amniotic membrane:	n/a
27	chr3:20412342-20412392	PFSK-1	brain:	n/a
28	chr3:20448283-20448333	HRCEpiC	kidney:	n/a
29	chr3:20448283-20448333	PFSK-1	brain:	n/a
30	chr3:20448283-20448333	HepG2	liver:	n/a
31	chr3:20418856-20418906	GM12892	blood:	n/a
32	chr3:20418856-20418906	Hela-S3	cervix:	n/a
33	chr3:20418856-20418906	HMEC	breast:	n/a
34	chr3:20448283-20448333	IMR90	lung:	fetal
35	chr3:20412342-20412392	Caco-2	colon:	n/a
36	chr3:20448283-20448333	PANC-1	pancreas:	n/a
37	chr3:20418856-20418906	HIPEpiC	eye:	n/a
38	chr3:20412342-20412392	NH-A	brain:	n/a
39	chr3:20448283-20448333	AoSMC	blood vessel:	n/a
40	chr3:20448283-20448333	GM12891	blood:	n/a
41	chr3:20418856-20418906	PrEC	prostate:	n/a
42	chr3:20418856-20418906	AG09319	gingival:	n/a
43	chr3:20448283-20448333	Caco-2	colon:	n/a
44	chr3:20412342-20412392	GM12878	blood:	n/a
45	chr3:20412342-20412392	SK-N-MC	brain:	n/a
46	chr3:20418856-20418906	NT2-D1	testis:	n/a
47	chr3:20448283-20448333	PrEC	prostate:	n/a
48	chr3:20412342-20412392	AoSMC	blood vessel:	n/a
49	chr3:20448283-20448333	MCF-7	breast:	n/a
50	chr3:20418856-20418906	Caco-2	colon:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
2	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
3	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:
4	chr3:20413525..20416049-chr3:20420124..20421856,2	K562	blood:
5	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:
6	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
7	chr3:20413525..20416049-chr3:20420124..20421856,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-3	chr3:20429741-20432054	ENSG00000261734.1

No data

Variant related genes	Relation type
ENSG00000261734	TF binding region
ENSG00000261734	CpG island

Extended variants
information (count: 1778 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1778 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs193276308	chr3:20407712-20407713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543581672	chr3:20407717-20407718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12488347	chr3:20407777-20407778	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs577282696	chr3:20407795-20407796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564460061	chr3:20407804-20407805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2139521	chr3:20407825-20407826	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs540511673	chr3:20407829-20407830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561975674	chr3:20407844-20407845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529464326	chr3:20407856-20407857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182363233	chr3:20407873-20407874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143712811	chr3:20407879-20407880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12488414	chr3:20407880-20407881	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs139271656	chr3:20407887-20407888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149980820	chr3:20407897-20407898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35672995	chr3:20407929-20407930	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs74966893	chr3:20407936-20407937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568285307	chr3:20407960-20407961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535255876	chr3:20407972-20407973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149112283	chr3:20408001-20408002	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs113898451	chr3:20408026-20408027	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs539460839	chr3:20408047-20408048	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs550890918	chr3:20408052-20408053	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs572881674	chr3:20408102-20408103	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs540573274	chr3:20408147-20408148	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs142197001	chr3:20408162-20408163	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs147827664	chr3:20408192-20408193	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs116068668	chr3:20408203-20408204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563420655	chr3:20408215-20408216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187904209	chr3:20408221-20408222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552278965	chr3:20408245-20408246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116253560	chr3:20408261-20408262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192679492	chr3:20408280-20408281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs62241779	chr3:20408308-20408309	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs568213719	chr3:20408462-20408463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554592459	chr3:20408465-20408466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535658251	chr3:20408498-20408499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550465644	chr3:20408506-20408507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569015569	chr3:20408511-20408512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567065676	chr3:20408560-20408561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539575506	chr3:20408580-20408581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557829113	chr3:20408582-20408583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375052536	chr3:20408589-20408590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566612335	chr3:20408603-20408604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568365756	chr3:20408625-20408626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572944904	chr3:20408627-20408628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533895647	chr3:20408637-20408638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536913232	chr3:20408643-20408644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375125839	chr3:20408662-20408663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556029554	chr3:20408663-20408664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs137999349	chr3:20408683-20408684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20405400-20408000	Weak transcription	Fetal Intestine Small	intestine
2	chr3:20408000-20408200	ZNF genes & repeats	Fetal Intestine Small	intestine
3	chr3:20408200-20415600	Weak transcription	Fetal Intestine Small	intestine
4	chr3:20410800-20411000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:20411600-20411800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:20415600-20415800	Enhancers	Fetal Intestine Large	intestine
7	chr3:20415600-20417200	Enhancers	Fetal Intestine Small	intestine
8	chr3:20415800-20416000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr3:20415800-20417000	Weak transcription	Fetal Intestine Large	intestine
10	chr3:20416000-20418400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr3:20417000-20420000	Enhancers	Fetal Intestine Large	intestine
12	chr3:20417200-20418200	Weak transcription	Fetal Intestine Small	intestine
13	chr3:20418200-20419400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr3:20418200-20420200	Enhancers	Fetal Intestine Small	intestine
15	chr3:20418400-20419000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:20418400-20419200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:20418400-20419600	Enhancers	H9 Cell Line	embryonic stem cell
18	chr3:20418400-20420000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr3:20418400-20420000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr3:20418400-20420400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr3:20418600-20420200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr3:20418600-20420200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr3:20419000-20419800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr3:20419200-20419400	Enhancers	Small Intestine	intestine
25	chr3:20419200-20419800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:20419200-20420400	Enhancers	Duodenum Mucosa	Duodenum
27	chr3:20419400-20420000	Enhancers	Duodenum Smooth Muscle	Duodenum
28	chr3:20419800-20420000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:20419800-20420200	Enhancers	Fetal Stomach	stomach
30	chr3:20419800-20420600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr3:20420000-20420200	Enhancers	Small Intestine	intestine
32	chr3:20420000-20420400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:20420000-20421800	Weak transcription	Fetal Intestine Large	intestine
34	chr3:20420200-20421800	Weak transcription	Fetal Intestine Small	intestine
35	chr3:20420400-20421800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:20421800-20422000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:20421800-20422200	Enhancers	Aorta	Aorta
38	chr3:20421800-20422200	Enhancers	Fetal Intestine Large	intestine
39	chr3:20421800-20422200	Enhancers	Fetal Intestine Small	intestine
40	chr3:20422000-20422200	Enhancers	Fetal Stomach	stomach
41	chr3:20422200-20423400	Weak transcription	Fetal Intestine Large	intestine
42	chr3:20422200-20423400	Weak transcription	Fetal Intestine Small	intestine
43	chr3:20423400-20424800	Enhancers	Fetal Intestine Large	intestine
44	chr3:20423400-20425000	Enhancers	Fetal Intestine Small	intestine
45	chr3:20426800-20427600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
46	chr3:20427600-20433200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr3:20433000-20433400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr3:20433000-20433600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr3:20433200-20433400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr3:20433200-20433600	Enhancers	HUES6 Cell Line	embryonic stem cell

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