Variant report

Variant	nsv997743
Chromosome Location	chr4:78126462-78217004
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	ATF1	chr4:78153907-78154134	K562	blood:	n/a	n/a
2	BATF	chr4:78140257-78140528	GM12878	blood:	n/a	chr4:78140400-78140410 chr4:78140399-78140410
3	BHLHE40	chr4:78161829-78161910	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:78169965-78170247	HepG2	liver:	n/a	n/a
5	BHLHE40	chr4:78161695-78162114	K562	blood:	n/a	n/a
6	BRCA1	chr4:78161761-78161808	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:78161727-78161966	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr4:78142599-78142677	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:78136969-78137231	HepG2	liver:	n/a	chr4:78137093-78137104
10	CEBPB	chr4:78215423-78215638	IMR90	lung:	n/a	chr4:78215544-78215555
11	CEBPB	chr4:78215400-78215689	HepG2	liver:	n/a	chr4:78215544-78215555
12	CEBPB	chr4:78169257-78169440	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:78142460-78142826	IMR90	lung:	n/a	n/a
14	CEBPB	chr4:78136939-78137228	A549	lung:	n/a	chr4:78137093-78137104
15	CEBPB	chr4:78142464-78142815	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr4:78171884-78171912	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:78215392-78215580	K562	blood:	n/a	chr4:78215544-78215555
18	CTCF	chr4:78161655-78161983	GM19238	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
19	CTCF	chr4:78161740-78161890	GM12864	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
20	CTCF	chr4:78161730-78161954	GM20000	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
21	CTCF	chr4:78161760-78161910	HPF	lung:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
22	CTCF	chr4:78149327-78149409	K562	blood:	n/a	chr4:78149335-78149353
23	CTCF	chr4:78161760-78161910	GM12866	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
24	CTCF	chr4:78170660-78170810	HEEpiC	esophagus:	n/a	chr4:78170664-78170685 chr4:78170669-78170687 chr4:78170675-78170684
25	CTCF	chr4:78170620-78170770	HAc	cerebellar:	n/a	chr4:78170664-78170685 chr4:78170669-78170687 chr4:78170675-78170684
26	CTCF	chr4:78161740-78161890	NHLF	lung:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
27	CTCF	chr4:78156460-78156610	HEK293	kidney:	n/a	n/a
28	CTCF	chr4:78162140-78162290	NHLF	lung:	n/a	n/a
29	CTCF	chr4:78161940-78162090	A549	lung:	n/a	n/a
30	CTCF	chr4:78188204-78188241	GM19239	blood:	n/a	n/a
31	CTCF	chr4:78161740-78161890	GM06990	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
32	CTCF	chr4:78149280-78149430	MCF-7	breast:	n/a	chr4:78149335-78149353
33	CTCF	chr4:78149230-78149445	K562	blood:	n/a	chr4:78149335-78149353
34	CTCF	chr4:78161700-78161850	HCT-116	colon:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
35	CTCF	chr4:78161678-78161978	LNCaP	prostate:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
36	CTCF	chr4:78161080-78161230	GM12873	blood:	n/a	n/a
37	CTCF	chr4:78161610-78161992	T-47D	breast:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
38	CTCF	chr4:78161666-78161954	MCF-7	breast:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
39	CTCF	chr4:78161547-78162124	MCF-7	breast:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
40	CTCF	chr4:78161659-78161989	GM12878	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
41	CTCF	chr4:78161555-78162030	MCF-7	breast:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
42	CTCF	chr4:78161740-78161890	MCF-7	breast:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
43	CTCF	chr4:78197280-78197430	GM12873	blood:	n/a	n/a
44	CTCF	chr4:78197286-78197491	K562	blood:	n/a	n/a
45	CTCF	chr4:78170560-78170710	NHEK	skin:	n/a	chr4:78170664-78170685 chr4:78170669-78170687 chr4:78170675-78170684
46	CTCF	chr4:78161704-78162008	ECC-1	luminal epithelium:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
47	CTCF	chr4:78161820-78161970	WI-38	lung:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
48	CTCF	chr4:78154046-78154095	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr4:78188194-78188260	NHEK	skin:	n/a	n/a
50	CTCF	chr4:78170540-78170690	HCT-116	colon:	n/a	chr4:78170664-78170685 chr4:78170669-78170687 chr4:78170675-78170684

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78156196-78156246	HCM	heart:	n/a
2	chr4:78156196-78156246	HL-60	blood:	n/a
3	chr4:78156196-78156246	ECC-1	luminal epithelium:	n/a
4	chr4:78156196-78156246	SAEC	small airway:	n/a
5	chr4:78156196-78156246	GM06990	blood:	n/a
6	chr4:78156196-78156246	Caco-2	colon:	n/a
7	chr4:78156196-78156246	A549	lung:	n/a
8	chr4:78156196-78156246	NHBE	bronchial:	n/a
9	chr4:78156196-78156246	BE2_C	brain:	n/a
10	chr4:78156196-78156246	SKMC	muscle:	n/a
11	chr4:78156196-78156246	ovcar-3	ovarian:	n/a
12	chr4:78156196-78156246	PrEC	prostate:	n/a
13	chr4:78156196-78156246	SK-N-SH_RA	brain:	n/a
14	chr4:78156196-78156246	LNCaP	prostate:	n/a
15	chr4:78156196-78156246	Hepatocyte	liver:	n/a
16	chr4:78156196-78156246	Jurkat	blood:	n/a
17	chr4:78156196-78156246	HRPEpiC	eye:	n/a
18	chr4:78156196-78156246	HPAEpiC	pulmonary alveolar:	n/a
19	chr4:78156196-78156246	AG09319	gingival:	n/a
20	chr4:78156196-78156246	MCF10A-Er-Src	breast:	n/a
21	chr4:78156196-78156246	NT2-D1	testis:	n/a
22	chr4:78156196-78156246	HepG2	liver:	n/a
23	chr4:78156196-78156246	HRCEpiC	kidney:	n/a
24	chr4:78156196-78156246	HUVEC	blood vessel:	n/a
25	chr4:78156196-78156246	GM12878	blood:	n/a
26	chr4:78156196-78156246	NB4	blood:	n/a
27	chr4:78156196-78156246	PANC-1	pancreas:	n/a
28	chr4:78156196-78156246	T-47D	breast:	n/a
29	chr4:78156196-78156246	GM19239	blood:	n/a
30	chr4:78156196-78156246	HEK293	kidney:	embryo
31	chr4:78156196-78156246	HCT-116	colon:	n/a
32	chr4:78156196-78156246	AoSMC	blood vessel:	n/a
33	chr4:78156196-78156246	AG04449	skin:	fetal
34	chr4:78156196-78156246	ProgFib	skin:	n/a
35	chr4:78156196-78156246	HCF	heart:	n/a
36	chr4:78156196-78156246	HNPCEpiC	eye:	n/a
37	chr4:78156196-78156246	SK-N-MC	brain:	n/a
38	chr4:78156196-78156246	PFSK-1	brain:	n/a
39	chr4:78156196-78156246	HRE	kidney:	n/a
40	chr4:78156196-78156246	NH-A	brain:	n/a
41	chr4:78156196-78156246	H1-hESC	embryonic stem cell:	embryo
42	chr4:78156196-78156246	Hela-S3	cervix:	n/a
43	chr4:78156196-78156246	HCPEpiC	choroid plexus:	n/a
44	chr4:78156196-78156246	HMEC	breast:	n/a
45	chr4:78156196-78156246	NHDF-neo	bronchial:	n/a
46	chr4:78156196-78156246	GM12892	blood:	n/a
47	chr4:78156196-78156246	MCF-7	breast:	n/a
48	chr4:78156196-78156246	RPTEC	kidney:	n/a
49	chr4:78156196-78156246	AG10803	skin:	n/a
50	chr4:78156196-78156246	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:78155142..78157870-chr4:78168469..78170209,2	MCF-7	breast:
2	chr4:78161324..78162321-chr4:78279149..78280134,4	MCF-7	breast:
3	chr4:78122483..78124874-chr4:78125132..78127042,2	MCF-7	breast:
4	chr4:78161416..78162110-chr4:78226527..78227315,3	MCF-7	breast:
5	chr4:78016448..78019261-chr4:78148834..78151500,2	MCF-7	breast:
6	chr4:78161398..78162211-chr4:78229720..78230660,3	MCF-7	breast:
7	chr4:78174499..78176837-chr4:78205161..78207032,2	MCF-7	breast:
8	chr4:78130169..78132632-chr4:78133437..78136630,3	K562	blood:
9	chr4:78149304..78151645-chr4:78154973..78157716,3	K562	blood:
10	chr4:78130169..78132632-chr4:78133437..78136630,3	K562	blood:
11	chr4:78155252..78157365-chr4:78224145..78227144,3	MCF-7	breast:
12	chr4:78161284..78162458-chr4:78229777..78230742,7	K562	blood:
13	chr4:78161473..78162127-chr4:78394685..78395318,2	K562	blood:
14	chr4:78161365..78162334-chr4:78279195..78280134,7	K562	blood:
15	chr4:78177354..78179710-chr4:78180664..78183643,2	MCF-7	breast:
16	chr4:78174499..78176837-chr4:78205161..78207032,2	MCF-7	breast:
17	chr4:78155142..78157870-chr4:78168469..78170209,2	MCF-7	breast:
18	chr4:78161311..78162711-chr4:78226629..78227614,14	MCF-7	breast:
19	chr4:78149304..78151645-chr4:78154973..78157716,3	K562	blood:
20	chr4:78161188..78162532-chr4:78229476..78230856,15	MCF-7	breast:
21	chr4:78132153..78134677-chr4:78134780..78136645,2	MCF-7	breast:
22	chr4:78160754..78162321-chr4:78226906..78228617,2	MCF-7	breast:
23	chr4:77996630..77998488-chr4:78129645..78132473,2	MCF-7	breast:
24	chr4:78158067..78160012-chr4:78227264..78228770,2	MCF-7	breast:
25	chr4:77994973..77997901-chr4:78150275..78153619,3	MCF-7	breast:
26	chr4:78162165..78163774-chr4:78227168..78228953,2	MCF-7	breast:
27	chr4:78182930..78185790-chr4:78187841..78189605,2	K562	blood:
28	chr4:78132153..78134677-chr4:78134780..78136645,2	MCF-7	breast:
29	chr4:78177354..78179710-chr4:78180664..78183643,2	MCF-7	breast:
30	chr4:78016602..78017111-chr4:78134180..78134764,2	MCF-7	breast:
31	chr4:78161721..78162270-chr4:78279119..78279681,2	MCF-7	breast:
32	chr4:78182930..78185790-chr4:78187841..78189605,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNI-4	chr4:78137569-78138031	NONHSAT097051

Variant related genes	Relation type
ENSG00000270669	TF binding region
ENSG00000270669	CpG island
ENSG00000118816	chromatin interactions

Extended variants
information (count: 3986 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3986 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370222592	chr4:78126477-78126478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539350864	chr4:78126498-78126499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552770639	chr4:78126574-78126575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141212620	chr4:78126583-78126584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373235373	chr4:78126585-78126586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377495417	chr4:78126600-78126601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538475399	chr4:78126654-78126655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4596264	chr4:78126655-78126656	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs573727013	chr4:78126665-78126666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10675804	chr4:78126696-78126697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537839597	chr4:78126723-78126724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548014640	chr4:78126732-78126733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144989595	chr4:78126733-78126734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4859475	chr4:78126749-78126750	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs573018250	chr4:78126763-78126764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192510779	chr4:78126771-78126772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183206869	chr4:78126828-78126829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575083346	chr4:78126843-78126844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533761668	chr4:78126875-78126876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77815598	chr4:78126932-78126933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561224661	chr4:78126945-78126946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188040905	chr4:78126980-78126981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376253109	chr4:78127011-78127012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193051941	chr4:78127053-78127054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547111682	chr4:78127054-78127055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560551897	chr4:78127091-78127092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532827308	chr4:78127119-78127120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10030727	chr4:78127149-78127150	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs10030735	chr4:78127169-78127170	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs556417326	chr4:78127186-78127187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184542580	chr4:78127196-78127197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375960360	chr4:78127201-78127202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148049523	chr4:78127219-78127220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375425158	chr4:78127232-78127233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567207553	chr4:78127255-78127256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368735062	chr4:78127262-78127263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575588123	chr4:78127268-78127269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568899134	chr4:78127312-78127313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141795270	chr4:78127356-78127357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150133101	chr4:78127405-78127406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201619076	chr4:78127424-78127425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35388917	chr4:78127427-78127428	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs138580288	chr4:78127428-78127429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558421488	chr4:78127430-78127431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575193129	chr4:78127440-78127441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543958305	chr4:78127472-78127473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554759180	chr4:78127512-78127513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34623364	chr4:78127528-78127529	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs540743322	chr4:78127561-78127562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73826748	chr4:78127572-78127573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	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
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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78125200-78127800	Weak transcription	Fetal Muscle Leg	muscle
2	chr4:78125200-78143600	Weak transcription	Primary B cells from cord blood	blood
3	chr4:78126200-78130600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:78130600-78131000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:78130600-78131000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:78130800-78131400	Enhancers	H9 Cell Line	embryonic stem cell
7	chr4:78131000-78131400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
8	chr4:78135200-78135400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:78135200-78135400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:78136200-78136800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:78136400-78136600	Enhancers	Fetal Heart	heart
12	chr4:78136400-78136800	Enhancers	Fetal Muscle Leg	muscle
13	chr4:78136600-78139600	Weak transcription	Fetal Heart	heart
14	chr4:78136800-78139200	Weak transcription	Fetal Muscle Leg	muscle
15	chr4:78139200-78140600	Enhancers	Fetal Muscle Leg	muscle
16	chr4:78139600-78140000	Enhancers	Fetal Heart	heart
17	chr4:78140000-78140200	Weak transcription	Fetal Heart	heart
18	chr4:78140200-78144000	Enhancers	Fetal Heart	heart
19	chr4:78140600-78141800	Weak transcription	Fetal Muscle Leg	muscle
20	chr4:78141800-78142800	Enhancers	Fetal Muscle Leg	muscle
21	chr4:78141800-78143200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:78142000-78143000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr4:78142000-78143000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:78142200-78142400	Enhancers	Aorta	Aorta
25	chr4:78142200-78142800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:78142200-78142800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr4:78142200-78143200	Bivalent Enhancer	Osteobl	bone
28	chr4:78142400-78142600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr4:78142600-78143200	Enhancers	Fetal Lung	lung
30	chr4:78142800-78145600	Weak transcription	Fetal Muscle Leg	muscle
31	chr4:78143200-78143400	Enhancers	Aorta	Aorta
32	chr4:78143200-78143400	Enhancers	Fetal Muscle Trunk	muscle
33	chr4:78145600-78147200	Enhancers	Fetal Muscle Leg	muscle
34	chr4:78146000-78146200	Enhancers	Fetal Muscle Trunk	muscle
35	chr4:78146000-78146600	Enhancers	Right Atrium	heart
36	chr4:78146000-78147400	Enhancers	Fetal Heart	heart
37	chr4:78146200-78147800	Weak transcription	Fetal Muscle Trunk	muscle
38	chr4:78147400-78152200	Weak transcription	Fetal Heart	heart
39	chr4:78147600-78148000	Weak transcription	Primary B cells from cord blood	blood
40	chr4:78147800-78148800	ZNF genes & repeats	Fetal Muscle Trunk	muscle
41	chr4:78148000-78149000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr4:78148600-78148800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:78148600-78148800	Enhancers	HMEC	breast
44	chr4:78148800-78153600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:78149000-78156400	Weak transcription	Primary B cells from cord blood	blood
46	chr4:78149200-78150400	Weak transcription	HMEC	breast
47	chr4:78150000-78150800	Enhancers	Esophagus	oesophagus
48	chr4:78150000-78151000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr4:78150400-78151200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:78150400-78151200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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