Variant report

Variant	nsv1013327
Chromosome Location	chr4:62989426-63149048
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:241)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:241 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:62989212-62989532	HepG2	liver:	n/a	chr4:62989381-62989392
2	CEBPB	chr4:62989244-62989506	A549	lung:	n/a	chr4:62989381-62989392
3	CEBPB	chr4:63117934-63118191	HepG2	liver:	n/a	chr4:63118060-63118071
4	CEBPB	chr4:63060156-63060317	K562	blood:	n/a	chr4:63060242-63060253
5	CEBPB	chr4:63060116-63060394	HepG2	liver:	n/a	chr4:63060242-63060253
6	CEBPB	chr4:62989222-62989522	IMR90	lung:	n/a	chr4:62989381-62989392
7	CEBPB	chr4:63060103-63060414	H1-hESC	embryonic stem cell:	n/a	chr4:63060242-63060253
8	CTCF	chr4:63084796-63084840	MCF-7	breast:	n/a	n/a
9	CTCF	chr4:63084729-63084856	ProgFib	skin:	n/a	n/a
10	CTCF	chr4:62996100-62996250	HPAF	blood vessel:	n/a	chr4:62996212-62996230 chr4:62996220-62996228
11	CTCF	chr4:63028360-63028510	BE2_C	brain:	n/a	n/a
12	CTCF	chr4:63028500-63028650	HEK293	kidney:	n/a	n/a
13	CTCF	chr4:63109700-63109850	HMEC	breast:	n/a	n/a
14	CTCF	chr4:63044133-63044167	GM13977	blood:	n/a	n/a
15	CTCF	chr4:63028620-63028770	BE2_C	brain:	n/a	n/a
16	CTCF	chr4:63044660-63044726	LNCaP	prostate:	n/a	n/a
17	CTCF	chr4:62996140-62996290	WERI-Rb-1	eye:	n/a	chr4:62996212-62996230 chr4:62996220-62996228
18	CTCF	chr4:63070536-63070605	LNCaP	prostate:	n/a	n/a
19	CTCF	chr4:63084801-63084838	Gliobla	brain:	n/a	n/a
20	CTCF	chr4:63109779-63109825	MCF-7	breast:	n/a	n/a
21	CTCF	chr4:63063060-63063210	NHLF	lung:	n/a	n/a
22	CTCF	chr4:63028320-63028470	GM12871	blood:	n/a	n/a
23	CTCF	chr4:63036040-63036190	GM12871	blood:	n/a	n/a
24	CTCF	chr4:63123905-63123970	Fibrobl	skin:	n/a	n/a
25	CTCF	chr4:63028340-63028490	HRE	kidney:	n/a	n/a
26	CTCF	chr4:63109796-63109852	GM13976	blood:	n/a	n/a
27	CTCF	chr4:63028390-63028735	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr4:63084773-63084831	Fibrobl	skin:	n/a	n/a
29	CTCF	chr4:63115860-63116010	GM12871	blood:	n/a	n/a
30	CTCF	chr4:62996140-62996290	HRE	kidney:	n/a	chr4:62996212-62996230 chr4:62996220-62996228
31	CTCF	chr4:63109678-63109982	GM12878	blood:	n/a	n/a
32	CTCF	chr4:63028460-63028610	NHEK	skin:	n/a	n/a
33	CTCF	chr4:62996072-62996377	GM12878	blood:	n/a	chr4:62996323-62996331 chr4:62996212-62996230 chr4:62996220-62996228
34	CTCF	chr4:62996120-62996270	HRPEpiC	eye:	n/a	chr4:62996212-62996230 chr4:62996220-62996228
35	CTCF	chr4:63109778-63109829	GM10248	blood:	n/a	n/a
36	CUX1	chr4:63113105-63113200	GM12878	blood:	n/a	n/a
37	E2F4	chr4:63001267-63001481	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr4:62998525-62998653	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr4:62996172-62996245	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr4:63067557-63067845	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr4:63132615-63133034	MCF10A-Er-Src	breast:	n/a	n/a
42	EP300	chr4:63057585-63057862	SK-N-SH_RA	brain:	n/a	chr4:63057706-63057720
43	EP300	chr4:63001109-63001726	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr4:63057008-63058185	SK-N-SH	brain:	n/a	chr4:63057856-63057866 chr4:63057706-63057720
45	EP300	chr4:63076479-63076580	GM12878	blood:	n/a	n/a
46	EP300	chr4:63001318-63001590	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr4:63057558-63057814	SK-N-SH_RA	brain:	n/a	chr4:63057706-63057720
48	EP300	chr4:63104940-63105795	SK-N-SH	brain:	n/a	n/a
49	EP300	chr4:63001053-63001756	SK-N-SH	brain:	n/a	n/a
50	ESR1	chr4:63011025-63011300	ECC-1	luminal epithelium:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:63075650-63075700	Jurkat	blood:	n/a
2	chr4:63075650-63075700	AoSMC	blood vessel:	n/a
3	chr4:63075650-63075700	ECC-1	luminal epithelium:	n/a
4	chr4:63075650-63075700	HUVEC	blood vessel:	n/a
5	chr4:63075650-63075700	HL-60	blood:	n/a
6	chr4:63075650-63075700	HCT-116	colon:	n/a
7	chr4:63075650-63075700	NH-A	brain:	n/a
8	chr4:63075650-63075700	NB4	blood:	n/a
9	chr4:63075650-63075700	GM12892	blood:	n/a
10	chr4:63075650-63075700	ovcar-3	ovarian:	n/a
11	chr4:63075650-63075700	AG09319	gingival:	n/a
12	chr4:63075650-63075700	NHBE	bronchial:	n/a
13	chr4:63075650-63075700	BJ	skin:	n/a
14	chr4:63075650-63075700	HAEpiC	amniotic membrane:	n/a
15	chr4:63075650-63075700	T-47D	breast:	n/a
16	chr4:63075650-63075700	LNCaP	prostate:	n/a
17	chr4:63075650-63075700	SK-N-MC	brain:	n/a
18	chr4:63075650-63075700	HNPCEpiC	eye:	n/a
19	chr4:63075650-63075700	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:63075650-63075700	PFSK-1	brain:	n/a
21	chr4:63075650-63075700	RPTEC	kidney:	n/a
22	chr4:63075650-63075700	CMK	blood:	n/a
23	chr4:63075650-63075700	H1-hESC	embryonic stem cell:	embryo
24	chr4:63075650-63075700	HRE	kidney:	n/a
25	chr4:63075650-63075700	PANC-1	pancreas:	n/a
26	chr4:63075650-63075700	NT2-D1	testis:	n/a
27	chr4:63075650-63075700	GM19239	blood:	n/a
28	chr4:63075650-63075700	Hepatocyte	liver:	n/a
29	chr4:63075650-63075700	HRCEpiC	kidney:	n/a
30	chr4:63075650-63075700	GM12878	blood:	n/a
31	chr4:63075650-63075700	HMEC	breast:	n/a
32	chr4:63075650-63075700	HIPEpiC	eye:	n/a
33	chr4:63075650-63075700	GM12891	blood:	n/a
34	chr4:63075650-63075700	HepG2	liver:	n/a
35	chr4:63075650-63075700	U87	brain:	n/a
36	chr4:63075650-63075700	K562	blood:	n/a
37	chr4:63075650-63075700	HRPEpiC	eye:	n/a
38	chr4:63075650-63075700	IMR90	lung:	fetal
39	chr4:63075650-63075700	HCM	heart:	n/a
40	chr4:63075650-63075700	SK-N-SH	brain:	n/a
41	chr4:63075650-63075700	HCPEpiC	choroid plexus:	n/a
42	chr4:63075650-63075700	AG10803	skin:	n/a
43	chr4:63075650-63075700	MCF-7	breast:	n/a
44	chr4:63075650-63075700	HCF	heart:	n/a
45	chr4:63075650-63075700	ProgFib	skin:	n/a
46	chr4:63075650-63075700	A549	lung:	n/a
47	chr4:63075650-63075700	SAEC	small airway:	n/a
48	chr4:63075650-63075700	HEEpiC	esophagus:	n/a
49	chr4:63075650-63075700	HEK293	kidney:	embryo
50	chr4:63075650-63075700	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:63129483..63131734-chr4:63132033..63135396,3	MCF-7	breast:
2	chr4:63083250..63085262-chr4:63091048..63093534,2	K562	blood:
3	chr4:63129483..63131734-chr4:63132033..63135396,3	MCF-7	breast:
4	chr4:63123536..63126256-chr4:63130076..63132728,2	K562	blood:
5	chr4:63123536..63126256-chr4:63130076..63132728,2	K562	blood:
6	chr4:63083250..63085262-chr4:63091048..63093534,2	K562	blood:
7	chr12:6147357..6147998-chr4:63072523..63073523,2	MCF-7	breast:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPHN3-2	chr4:63001669-63001972	XLOC_003555
2	lnc-TECRL-4	chr4:63002384-63002474	ENSG00000248692.1
3	lnc-TECRL-4	chr4:62992765-62992805	ENSG00000248692.1
4	lnc-LPHN3-2	chr4:63003454-63003541	NONHSAT096620
5	lnc-LPHN3-9	chr4:63114012-63114488	NONHSAT096627
6	lnc-LPHN3-2	chr4:63001669-63001972	XLOC_003555
7	lnc-TECRL-4	chr4:63002384-63002474	ENSG00000248692.1
8	lnc-LPHN3-2	chr4:63003455-63003541	XLOC_003555
9	lnc-LPHN3-2	chr4:63003455-63003541	XLOC_003555
10	lnc-TECRL-4	chr4:63023041-63023103	ENSG00000248692.1
11	lnc-TECRL-4	chr4:63031232-63031263	ENSG00000248692.1
12	lnc-TECRL-4	chr4:63021660-63021759	ENSG00000248692.1
13	lnc-TECRL-4	chr4:63023041-63023103	ENSG00000248692.1
14	lnc-TECRL-4	chr4:63002384-63002474	ENSG00000248692.1
15	lnc-TECRL-4	chr4:63031232-63031272	ENSG00000248692.1
16	lnc-TECRL-4	chr4:63023087-63023103	ENSG00000248692.1
17	lnc-LPHN3-2	chr4:63027477-63027983	XLOC_003555
18	lnc-TECRL-4	chr4:63027465-63027581	ENSG00000248692.1
19	lnc-TECRL-4	chr4:63002384-63002474	ENSG00000248692.1
20	lnc-TECRL-4	chr4:63031232-63031272	ENSG00000248692.1
21	lnc-LPHN3-3	chr4:63036128-63036192	XLOC_003556
22	lnc-LPHN3-2	chr4:63010854-63014062	XLOC_003555
23	lnc-LPHN3-2	chr4:63003455-63003541	XLOC_003555
24	lnc-LPHN3-2	chr4:63010851-63014062	NONHSAT096620
25	lnc-TECRL-4	chr4:62992765-62992805	ENSG00000248692.1
26	lnc-LPHN3-2	chr4:63001669-63001972	XLOC_003555
27	lnc-TECRL-4	chr4:63027465-63027581	ENSG00000248692.1
28	lnc-LPHN3-3	chr4:63031380-63031732	XLOC_003556
29	lnc-LPHN3-2	chr4:62999461-62999769	NONHSAT096620
30	lnc-LPHN3-2	chr4:63001668-63001972	NONHSAT096620
31	lnc-LPHN3-2	chr4:63010852-63014062	XLOC_003555
32	lnc-LPHN3-2	chr4:63027476-63027983	NONHSAT096620

No data

Variant related genes	Relation type
ENSG00000248692	TF binding region
RPL21P47	TF binding region
ENSG00000248692	CpG island
RPL21P47	CpG island
PSEN1	miRNA target sites
KIAA0368	miRNA target sites
ANTXR1	miRNA target sites

Extended variants
information (count: 4346 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:4346 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531219003	chr4:62989446-62989447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546107471	chr4:62989447-62989448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564334144	chr4:62989462-62989463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181898296	chr4:62989471-62989472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186069111	chr4:62989472-62989473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373432612	chr4:62989578-62989579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377395108	chr4:62989599-62989600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528853752	chr4:62989603-62989604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550866621	chr4:62989610-62989611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569091688	chr4:62989646-62989647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539700036	chr4:62989649-62989650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558031309	chr4:62989652-62989653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370746087	chr4:62989694-62989695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566662649	chr4:62989702-62989703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140631093	chr4:62989755-62989756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375203290	chr4:62989787-62989788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374998483	chr4:62989804-62989805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553459162	chr4:62989810-62989811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574800256	chr4:62989815-62989816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533830690	chr4:62989820-62989821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs367904031	chr4:62989821-62989822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189792378	chr4:62989839-62989840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144596129	chr4:62989867-62989868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546465262	chr4:62989871-62989872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs180737357	chr4:62989878-62989879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545256886	chr4:62989934-62989935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573054231	chr4:62989951-62989952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539960800	chr4:62989959-62989960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561410769	chr4:62989962-62989963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186018630	chr4:62989963-62989964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550334792	chr4:62989964-62989965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370879167	chr4:62989968-62989969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143092987	chr4:62989989-62989990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs55957725	chr4:62989997-62989998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138551952	chr4:62990004-62990005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552078347	chr4:62990082-62990083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7697748	chr4:62990100-62990101	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533948872	chr4:62990111-62990112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547134218	chr4:62990114-62990115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568487342	chr4:62990120-62990121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552259587	chr4:62990223-62990224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115324315	chr4:62990233-62990234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116235372	chr4:62990279-62990280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539746743	chr4:62990321-62990322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556090417	chr4:62990399-62990400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528945593	chr4:62990415-62990416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573115159	chr4:62990492-62990493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540458637	chr4:62990493-62990494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191371704	chr4:62990499-62990500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573703495	chr4:62990503-62990504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
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
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62985600-62991200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:62991200-62992400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:62991400-62992400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:62992400-62995800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:62995800-62996200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:62995800-62996800	Enhancers	Fetal Heart	heart
7	chr4:62996000-62996800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:62996200-62997200	Enhancers	Fetal Muscle Leg	muscle
9	chr4:62996400-62997000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:62996400-62997200	Enhancers	Fetal Muscle Trunk	muscle
11	chr4:62996600-62996800	Enhancers	Gastric	stomach
12	chr4:62996600-62997000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:62996600-62997000	Enhancers	Left Ventricle	heart
14	chr4:62996800-62998000	Weak transcription	Fetal Heart	heart
15	chr4:62998000-62998200	Enhancers	Fetal Heart	heart
16	chr4:62998200-62999000	Flanking Active TSS	Fetal Heart	heart
17	chr4:62999000-62999600	Enhancers	Fetal Heart	heart
18	chr4:62999000-63000400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr4:62999000-63001200	Enhancers	NH-A	brain
20	chr4:62999200-62999800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:62999200-63003400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr4:62999400-62999600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr4:62999400-62999800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr4:62999400-62999800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr4:62999400-63000800	Active TSS	Left Ventricle	heart
26	chr4:62999400-63001800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:62999400-63001800	Active TSS	Right Ventricle	heart
28	chr4:62999400-63002800	Active TSS	Right Atrium	heart
29	chr4:62999600-62999800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr4:62999600-63000200	Flanking Active TSS	Fetal Heart	heart
31	chr4:62999600-63000600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr4:62999800-63000600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr4:62999800-63000800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr4:62999800-63001800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:62999800-63002600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr4:63000000-63003000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr4:63000200-63001400	Active TSS	Fetal Heart	heart
38	chr4:63000600-63001400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr4:63000600-63001800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr4:63000800-63002200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:63000800-63002400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr4:63000800-63002800	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr4:63000800-63004000	Weak transcription	Left Ventricle	heart
44	chr4:63001000-63001800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:63001200-63001600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr4:63001400-63001600	Enhancers	H1 Cell Line	embryonic stem cell
47	chr4:63001400-63001800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr4:63001400-63002600	Weak transcription	Fetal Heart	heart
49	chr4:63001800-63003000	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr4:63001800-63004000	Weak transcription	Right Ventricle	heart

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