Variant report

Variant	nsv999023
Chromosome Location	chr4:62739674-62784921
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	BCL11A	chr4:62784569-62784930	GM12878	blood:	n/a	n/a
2	BCL11A	chr4:62776961-62777222	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr4:62777008-62777401	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:62774642-62774878	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:62784716-62784950	GM12878	blood:	n/a	n/a
6	CHD2	chr4:62756329-62756347	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr4:62776912-62777363	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr4:62784676-62784919	GM12878	blood:	n/a	n/a
9	CTCF	chr4:62741653-62741674	GM10266	blood:	n/a	n/a
10	CTCF	chr4:62771442-62771497	GM10266	blood:	n/a	n/a
11	CTCF	chr4:62751440-62751590	BJ	skin:	n/a	n/a
12	EBF1	chr4:62777079-62777322	GM12878	blood:	n/a	n/a
13	EBF1	chr4:62774774-62775089	GM12878	blood:	n/a	n/a
14	EBF1	chr4:62784685-62785017	GM12878	blood:	n/a	n/a
15	EP300	chr4:62776920-62777241	H1-hESC	embryonic stem cell:	n/a	n/a
16	EP300	chr4:62761869-62762279	SK-N-SH_RA	brain:	n/a	n/a
17	EP300	chr4:62753992-62753998	K562	blood:	n/a	n/a
18	EP300	chr4:62762340-62762953	SK-N-SH_RA	brain:	n/a	chr4:62762790-62762804
19	EP300	chr4:62776881-62777350	H1-hESC	embryonic stem cell:	n/a	n/a
20	EP300	chr4:62784692-62784915	GM12878	blood:	n/a	n/a
21	EP300	chr4:62761371-62763174	SK-N-SH	brain:	n/a	chr4:62761414-62761428 chr4:62762790-62762804
22	EP300	chr4:62762389-62762796	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chr4:62774835-62774995	GM12878	blood:	n/a	n/a
24	EP300	chr4:62784591-62784998	GM12878	blood:	n/a	n/a
25	FAM48A	chr4:62746664-62746732	GM12878	blood:	n/a	n/a
26	FOS	chr4:62743720-62743869	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr4:62745870-62745981	MCF10A-Er-Src	breast:	n/a	chr4:62745945-62745955 chr4:62745945-62745955
28	FOS	chr4:62771133-62771140	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr4:62746299-62746395	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr4:62745852-62746004	MCF10A-Er-Src	breast:	n/a	chr4:62745945-62745955 chr4:62745945-62745955
31	FOS	chr4:62745788-62746076	MCF10A-Er-Src	breast:	n/a	chr4:62745945-62745955 chr4:62745945-62745955
32	FOS	chr4:62743713-62743893	MCF10A-Er-Src	breast:	n/a	n/a
33	FOXA1	chr4:62784735-62785123	ECC-1	luminal epithelium:	n/a	n/a
34	GABPA	chr4:62743549-62744291	HL-60	blood:	n/a	n/a
35	GATA2	chr4:62762354-62762985	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr4:62760076-62760183	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr4:62761924-62762835	SH-SY5Y	brain:	n/a	chr4:62761929-62761936
38	GATA3	chr4:62762462-62763023	SK-N-SH	brain:	n/a	n/a
39	GATA3	chr4:62762285-62762915	SK-N-SH	brain:	n/a	n/a
40	HDAC2	chr4:62776988-62777535	H1-hESC	embryonic stem cell:	n/a	n/a
41	IRF3	chr4:62777594-62777636	GM12878	blood:	n/a	n/a
42	JUN	chr4:62776929-62777256	H1-hESC	embryonic stem cell:	n/a	n/a
43	JUND	chr4:62748143-62748361	HepG2	liver:	n/a	n/a
44	MAFF	chr4:62757729-62758034	HepG2	liver:	n/a	n/a
45	MAFF	chr4:62784294-62784585	K562	blood:	n/a	chr4:62784423-62784437 chr4:62784417-62784435 chr4:62784398-62784416
46	MAFF	chr4:62757823-62758012	K562	blood:	n/a	n/a
47	MAFF	chr4:62784252-62784601	HepG2	liver:	n/a	chr4:62784423-62784437 chr4:62784417-62784435 chr4:62784398-62784416
48	MAFK	chr4:62784250-62784610	HepG2	liver:	n/a	chr4:62784419-62784435 chr4:62784420-62784431 chr4:62784422-62784438 chr4:62784420-62784440 chr4:62784419-62784434 chr4:62784423-62784437
49	MAFK	chr4:62784315-62784550	K562	blood:	n/a	chr4:62784419-62784435 chr4:62784420-62784431 chr4:62784422-62784438 chr4:62784420-62784440 chr4:62784419-62784434 chr4:62784423-62784437
50	MAFK	chr4:62757761-62757972	K562	blood:	n/a	chr4:62757875-62757889 chr4:62757876-62757887 chr4:62757877-62757888 chr4:62757876-62757887 chr4:62757872-62757888 chr4:62757872-62757887

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:62778452-62778502	SAEC	small airway:	n/a
2	chr4:62756100-62756150	GM06990	blood:	n/a
3	chr4:62774948-62774998	MCF-7	breast:	n/a
4	chr4:62774948-62774998	LNCaP	prostate:	n/a
5	chr4:62774948-62774998	HAEpiC	amniotic membrane:	n/a
6	chr4:62756100-62756150	CMK	blood:	n/a
7	chr4:62778452-62778502	HCM	heart:	n/a
8	chr4:62774948-62774998	HL-60	blood:	n/a
9	chr4:62778452-62778502	ProgFib	skin:	n/a
10	chr4:62756100-62756150	HCPEpiC	choroid plexus:	n/a
11	chr4:62756100-62756150	SKMC	muscle:	n/a
12	chr4:62774948-62774998	AG10803	skin:	n/a
13	chr4:62756100-62756150	HCM	heart:	n/a
14	chr4:62774948-62774998	GM06990	blood:	n/a
15	chr4:62756100-62756150	AG04449	skin:	fetal
16	chr4:62774948-62774998	HEEpiC	esophagus:	n/a
17	chr4:62756100-62756150	RPTEC	kidney:	n/a
18	chr4:62756100-62756150	GM19239	blood:	n/a
19	chr4:62778452-62778502	SK-N-MC	brain:	n/a
20	chr4:62778452-62778502	NHBE	bronchial:	n/a
21	chr4:62778452-62778502	AoSMC	blood vessel:	n/a
22	chr4:62774948-62774998	AoSMC	blood vessel:	n/a
23	chr4:62756100-62756150	A549	lung:	n/a
24	chr4:62756100-62756150	SAEC	small airway:	n/a
25	chr4:62756100-62756150	AG09319	gingival:	n/a
26	chr4:62778452-62778502	NB4	blood:	n/a
27	chr4:62778452-62778502	GM12878	blood:	n/a
28	chr4:62756100-62756150	HPAEpiC	pulmonary alveolar:	n/a
29	chr4:62778452-62778502	AG10803	skin:	n/a
30	chr4:62774948-62774998	NHBE	bronchial:	n/a
31	chr4:62778452-62778502	SK-N-SH_RA	brain:	n/a
32	chr4:62756100-62756150	NB4	blood:	n/a
33	chr4:62778452-62778502	NT2-D1	testis:	n/a
34	chr4:62756100-62756150	HNPCEpiC	eye:	n/a
35	chr4:62778452-62778502	HCPEpiC	choroid plexus:	n/a
36	chr4:62756100-62756150	MCF-7	breast:	n/a
37	chr4:62774948-62774998	Hepatocyte	liver:	n/a
38	chr4:62774948-62774998	NB4	blood:	n/a
39	chr4:62756100-62756150	NH-A	brain:	n/a
40	chr4:62774948-62774998	U87	brain:	n/a
41	chr4:62778452-62778502	HEK293	kidney:	embryo
42	chr4:62774948-62774998	HRCEpiC	kidney:	n/a
43	chr4:62774948-62774998	ECC-1	luminal epithelium:	n/a
44	chr4:62778452-62778502	Jurkat	blood:	n/a
45	chr4:62756100-62756150	HAEpiC	amniotic membrane:	n/a
46	chr4:62774948-62774998	Hela-S3	cervix:	n/a
47	chr4:62774948-62774998	T-47D	breast:	n/a
48	chr4:62778452-62778502	PFSK-1	brain:	n/a
49	chr4:62756100-62756150	MCF10A-Er-Src	breast:	n/a
50	chr4:62756100-62756150	GM12878	blood:	n/a

Variant related genes	Relation type
LPHN3	TF binding region
ENSG00000202169	TF binding region
LPHN3	CpG island
ENSG00000202169	CpG island

Extended variants
information (count: 1640 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1640 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6846033	chr4:62739674-62739675	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75356421	chr4:62739703-62739704	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs556249356	chr4:62739791-62739792	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs540482375	chr4:62739794-62739795	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs544372635	chr4:62739795-62739796	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs36008923	chr4:62739976-62739977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184346789	chr4:62739982-62739983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79148437	chr4:62740024-62740025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188600731	chr4:62740084-62740085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147628908	chr4:62740092-62740093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559892718	chr4:62740166-62740167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7688735	chr4:62740176-62740177	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs549007061	chr4:62740192-62740193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111867151	chr4:62740214-62740215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565456562	chr4:62740280-62740281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9312083	chr4:62740295-62740296	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs562477065	chr4:62740309-62740310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11335054	chr4:62740315-62740316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76731926	chr4:62740325-62740326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538158002	chr4:62740396-62740397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574417198	chr4:62740407-62740408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370596951	chr4:62740477-62740478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536250832	chr4:62740503-62740504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs199552447	chr4:62740505-62740506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369192329	chr4:62740506-62740507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371308217	chr4:62740507-62740508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11432355	chr4:62740508-62740509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs62304412	chr4:62740540-62740541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368265188	chr4:62740550-62740551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375175890	chr4:62740568-62740569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539525423	chr4:62740620-62740621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371067477	chr4:62740671-62740672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529673070	chr4:62740676-62740677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554342885	chr4:62740685-62740686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549226227	chr4:62740687-62740688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4860438	chr4:62740690-62740691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181712394	chr4:62740716-62740717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567623485	chr4:62740821-62740822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573961522	chr4:62740856-62740857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544540952	chr4:62740906-62740907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74491909	chr4:62740935-62740936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62304413	chr4:62740963-62740964	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs544770055	chr4:62740969-62740970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113692516	chr4:62741014-62741015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527395727	chr4:62741072-62741073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs193107790	chr4:62741073-62741074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542614586	chr4:62741096-62741097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560881170	chr4:62741097-62741098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531620783	chr4:62741117-62741118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189556364	chr4:62741193-62741194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Pancreatic cancer	17952125	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62724600-62742800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:62737800-62739800	Enhancers	Brain Germinal Matrix	brain
3	chr4:62737800-62740200	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr4:62738800-62739800	Enhancers	Brain Angular Gyrus	brain
5	chr4:62738800-62739800	Active TSS	Brain Anterior Caudate	brain
6	chr4:62739000-62740000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr4:62739000-62740200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:62739200-62739800	Enhancers	Brain Substantia Nigra	brain
9	chr4:62739200-62740000	Enhancers	Brain Hippocampus Middle	brain
10	chr4:62739200-62740200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr4:62739600-62740000	Enhancers	Brain Cingulate Gyrus	brain
12	chr4:62739600-62742600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr4:62739800-62740000	Enhancers	Brain Anterior Caudate	brain
14	chr4:62739800-62743800	Weak transcription	Brain Substantia Nigra	brain
15	chr4:62740200-62742000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr4:62740200-62763600	Weak transcription	Fetal Muscle Leg	muscle
17	chr4:62742000-62743600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:62742600-62744600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr4:62742800-62743400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:62743000-62745400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr4:62743400-62743600	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr4:62743600-62744400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:62743800-62744200	Enhancers	Primary hematopoietic stem cells	blood
24	chr4:62744400-62745400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:62746800-62775200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:62747800-62767800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:62748200-62748400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:62751200-62751400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr4:62751200-62751600	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr4:62751400-62751600	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr4:62751400-62751800	Enhancers	Fetal Intestine Small	intestine
32	chr4:62751400-62752200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr4:62751400-62752200	Enhancers	Fetal Kidney	kidney
34	chr4:62751400-62752400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr4:62751600-62751800	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr4:62751600-62752200	Active TSS	Duodenum Mucosa	Duodenum
37	chr4:62751600-62752200	Active TSS	Rectal Mucosa Donor 31	rectum
38	chr4:62751600-62752400	Active TSS	Rectal Mucosa Donor 29	rectum
39	chr4:62751600-62752800	Enhancers	Fetal Intestine Large	intestine
40	chr4:62751800-62752200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr4:62751800-62752200	Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr4:62751800-62752200	Active TSS	Fetal Intestine Small	intestine
43	chr4:62752000-62752200	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr4:62752200-62752600	Enhancers	Fetal Intestine Small	intestine
45	chr4:62754600-62755800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr4:62755000-62763600	Weak transcription	Fetal Stomach	stomach
47	chr4:62755600-62756400	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr4:62755600-62756600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr4:62755600-62767800	Weak transcription	Fetal Lung	lung
50	chr4:62755800-62757000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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