Variant report

Variant	nsv1023240
Chromosome Location	chr4:188417210-188497858
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	CEBPB	chr4:188479534-188479869	IMR90	lung:	n/a	n/a
2	CEBPB	chr4:188474103-188474183	K562	blood:	n/a	n/a
3	CEBPB	chr4:188492564-188492757	K562	blood:	n/a	chr4:188492666-188492677
4	CEBPB	chr4:188440459-188440698	IMR90	lung:	n/a	n/a
5	CEBPB	chr4:188492567-188492769	HepG2	liver:	n/a	chr4:188492666-188492677
6	CEBPB	chr4:188440289-188440620	HepG2	liver:	n/a	n/a
7	CTCF	chr4:188458860-188459010	BJ	skin:	n/a	n/a
8	CTCF	chr4:188451786-188451820	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr4:188443124-188443168	Medullo	brain:	n/a	n/a
10	CTCF	chr4:188476228-188476262	GM20000	blood:	n/a	n/a
11	CTCF	chr4:188442915-188443011	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr4:188475140-188475290	AG04450	lung:	n/a	n/a
13	CTCF	chr4:188458880-188459030	HVMF	connective:	n/a	n/a
14	CTCF	chr4:188458895-188458970	Fibrobl	skin:	n/a	n/a
15	CTCF	chr4:188451774-188451781	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr4:188426682-188426755	LNCaP	prostate:	n/a	n/a
17	CTCF	chr4:188441212-188441256	LNCaP	prostate:	n/a	n/a
18	CUX1	chr4:188425013-188425025	GM12878	blood:	n/a	n/a
19	E2F4	chr4:188418016-188418170	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr4:188438067-188438123	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F6	chr4:188426476-188426590	K562	blood:	n/a	n/a
22	EP300	chr4:188421092-188421565	T-47D	breast:	n/a	n/a
23	EP300	chr4:188437667-188437686	GM12878	blood:	n/a	n/a
24	FOS	chr4:188476455-188476656	MCF10A-Er-Src	breast:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554
25	FOS	chr4:188479536-188479878	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
26	FOS	chr4:188479576-188479879	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
27	FOS	chr4:188479536-188479871	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
28	FOS	chr4:188476506-188476656	MCF10A-Er-Src	breast:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554
29	FOS	chr4:188479537-188479903	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
30	FOSL2	chr4:188476250-188476756	A549	lung:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554
31	FOXA1	chr4:188421066-188421547	T-47D	breast:	n/a	n/a
32	FOXA1	chr4:188482506-188482661	T-47D	breast:	n/a	n/a
33	FOXA1	chr4:188421080-188421491	T-47D	breast:	n/a	n/a
34	FOXA2	chr4:188476383-188476791	A549	lung:	n/a	n/a
35	GATA3	chr4:188421105-188421613	T-47D	breast:	n/a	n/a
36	GATA3	chr4:188476912-188477168	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr4:188421035-188421573	T-47D	breast:	n/a	n/a
38	JUN	chr4:188475494-188475577	K562	blood:	n/a	n/a
39	JUN	chr4:188484429-188484629	K562	blood:	n/a	n/a
40	JUN	chr4:188432774-188433012	K562	blood:	n/a	n/a
41	JUND	chr4:188476398-188476661	HepG2	liver:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554 chr4:188476544-188476555
42	JUND	chr4:188452451-188452524	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAFF	chr4:188456784-188456861	HepG2	liver:	n/a	n/a
44	MAFK	chr4:188497530-188497696	HepG2	liver:	n/a	n/a
45	MAFK	chr4:188418003-188418158	IMR90	lung:	n/a	n/a
46	MAFK	chr4:188417930-188418197	HepG2	liver:	n/a	n/a
47	MAFK	chr4:188456684-188456898	HepG2	liver:	n/a	chr4:188456792-188456812 chr4:188456792-188456803
48	MAX	chr4:188479935-188480096	NB4	blood:	n/a	n/a
49	MAZ	chr4:188471769-188471776	HepG2	liver:	n/a	n/a
50	MXI1	chr4:188418866-188418872	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188426278-188426328	HRE	kidney:	n/a
2	chr4:188428637-188428687	AG04449	skin:	fetal
3	chr4:188426278-188426328	HRE	kidney:	n/a
4	chr4:188428637-188428687	AG04449	skin:	fetal
5	chr4:188428637-188428687	LNCaP	prostate:	n/a
6	chr4:188428637-188428687	HAEpiC	amniotic membrane:	n/a
7	chr4:188462685-188462735	AG04450	lung:	fetal
8	chr4:188426506-188426556	SK-N-SH_RA	brain:	n/a
9	chr4:188427966-188428016	MCF10A-Er-Src	breast:	n/a
10	chr4:188426437-188426487	HIPEpiC	eye:	n/a
11	chr4:188426278-188426328	SAEC	small airway:	n/a
12	chr4:188426437-188426487	PANC-1	pancreas:	n/a
13	chr4:188426437-188426487	AoSMC	blood vessel:	n/a
14	chr4:188423066-188423116	NT2-D1	testis:	n/a
15	chr4:188426437-188426487	HNPCEpiC	eye:	n/a
16	chr4:188428637-188428687	HUVEC	blood vessel:	n/a
17	chr4:188423066-188423116	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:188426278-188426328	IMR90	lung:	fetal
19	chr4:188426506-188426556	PFSK-1	brain:	n/a
20	chr4:188462685-188462735	HL-60	blood:	n/a
21	chr4:188423066-188423116	HEEpiC	esophagus:	n/a
22	chr4:188426278-188426328	HEK293	kidney:	embryo
23	chr4:188426506-188426556	GM12878	blood:	n/a
24	chr4:188426437-188426487	HCT-116	colon:	n/a
25	chr4:188423066-188423116	HAEpiC	amniotic membrane:	n/a
26	chr4:188426437-188426487	HL-60	blood:	n/a
27	chr4:188427966-188428016	A549	lung:	n/a
28	chr4:188426278-188426328	HCT-116	colon:	n/a
29	chr4:188427966-188428016	HepG2	liver:	n/a
30	chr4:188428637-188428687	MCF10A-Er-Src	breast:	n/a
31	chr4:188462685-188462735	T-47D	breast:	n/a
32	chr4:188426506-188426556	SAEC	small airway:	n/a
33	chr4:188428637-188428687	HCPEpiC	choroid plexus:	n/a
34	chr4:188426278-188426328	NHDF-neo	bronchial:	n/a
35	chr4:188426437-188426487	CMK	blood:	n/a
36	chr4:188426437-188426487	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:188426437-188426487	AG09309	skin:	n/a
38	chr4:188426506-188426556	HRE	kidney:	n/a
39	chr4:188426437-188426487	ECC-1	luminal epithelium:	n/a
40	chr4:188428637-188428687	GM19239	blood:	n/a
41	chr4:188426506-188426556	NHDF-neo	bronchial:	n/a
42	chr4:188426278-188426328	Jurkat	blood:	n/a
43	chr4:188428637-188428687	A549	lung:	n/a
44	chr4:188426278-188426328	K562	blood:	n/a
45	chr4:188462685-188462735	H1-hESC	embryonic stem cell:	embryo
46	chr4:188462685-188462735	AG09309	skin:	n/a
47	chr4:188423066-188423116	NH-A	brain:	n/a
48	chr4:188462685-188462735	HMEC	breast:	n/a
49	chr4:188428637-188428687	SK-N-SH	brain:	n/a
50	chr4:188427966-188428016	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:188426813..188429681-chrX:150150480..150152156,2	MCF-7	breast:
2	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
3	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-11	chr4:188419171-188419708	NONHSAT099698
2	lnc-TRIML2-5	chr4:188438236-188438362	XLOC_004219
3	lnc-TRIML2-5	chr4:188437307-188437878	XLOC_004219
4	lnc-TRIML2-4	chr4:188454033-188454357	NR_110436
5	lnc-TRIML2-4	chr4:188454032-188454357	ENSG00000250590
6	lnc-TRIML2-4	chr4:188479391-188479418	NONHSAT099704
7	lnc-TRIML2-4	chr4:188476215-188476298	ENSG00000250590
8	lnc-ZFP42-11	chr4:188419753-188420210	NONHSAT099698
9	lnc-TRIML2-4	chr4:188476930-188477058	ENSG00000250590
10	lnc-TRIML2-4	chr4:188454036-188454357	ENSG00000250590
11	lnc-TRIML2-4	chr4:188476930-188477103	ENSG00000250590
12	lnc-ZFP42-10	chr4:188493477-188493987	NONHSAT099705
13	lnc-TRIML2-4	chr4:188477065-188477112	ENSG00000250590
14	lnc-TRIML2-4	chr4:188454032-188454357	ENSG00000250590
15	lnc-TRIML2-4	chr4:188478901-188479074	ENSG00000250590
16	lnc-TRIML2-4	chr4:188479231-188479418	ENSG00000250590

Variant related genes	Relation type
ENSG00000251490	TF binding region
ENSG00000250590	TF binding region
ENSG00000251490	CpG island
ENSG00000250590	CpG island
ENSG00000029993	chromatin interactions
ANP32E	miRNA target sites
ANTXR1	miRNA target sites

Extended variants
information (count: 1508 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1508 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185174152	chr4:188417243-188417244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536728884	chr4:188417283-188417284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10022277	chr4:188417303-188417304	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs144721397	chr4:188417337-188417338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12651364	chr4:188417385-188417386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571562952	chr4:188417394-188417395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532590642	chr4:188417456-188417457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77867835	chr4:188417458-188417459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368908592	chr4:188417461-188417462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376672004	chr4:188417474-188417475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538180998	chr4:188417525-188417526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75641094	chr4:188417535-188417536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574723154	chr4:188417553-188417554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539928607	chr4:188417570-188417571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559859781	chr4:188417714-188417715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189569671	chr4:188417732-188417733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs180822837	chr4:188417735-188417736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566187148	chr4:188417815-188417816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562358972	chr4:188417846-188417847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114090151	chr4:188417873-188417874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149995084	chr4:188417878-188417879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561911108	chr4:188417922-188417923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536315011	chr4:188417955-188417956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145068510	chr4:188418042-188418043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547619016	chr4:188418047-188418048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555154570	chr4:188418053-188418054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186473363	chr4:188418072-188418073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11132460	chr4:188418073-188418074	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs539153930	chr4:188418091-188418092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552518328	chr4:188418093-188418094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149120970	chr4:188418155-188418156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538512652	chr4:188418198-188418199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144740818	chr4:188418225-188418226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76237835	chr4:188418233-188418234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534078650	chr4:188418245-188418246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553953636	chr4:188418278-188418279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576494044	chr4:188418296-188418297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545602198	chr4:188418411-188418412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191402933	chr4:188418441-188418442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575995139	chr4:188418479-188418480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138673979	chr4:188418507-188418508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12648376	chr4:188418541-188418542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570102975	chr4:188418559-188418560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371546402	chr4:188418635-188418636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140267162	chr4:188418661-188418662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527595469	chr4:188418707-188418708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547581553	chr4:188418714-188418715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1549810	chr4:188418718-188418719	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs183595846	chr4:188418777-188418778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371885753	chr4:188418781-188418782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Autism	20808228	CNVD
Cognitive impairment	21505072	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188416800-188417800	Enhancers	Fetal Lung	lung
2	chr4:188417800-188420800	Weak transcription	Fetal Lung	lung
3	chr4:188420800-188421200	Enhancers	Fetal Lung	lung
4	chr4:188421200-188422400	Weak transcription	Fetal Lung	lung
5	chr4:188421800-188422400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:188422200-188423200	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr4:188422400-188423200	Enhancers	Fetal Lung	lung
8	chr4:188422400-188426000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:188422600-188423400	Enhancers	Adipose Nuclei	Adipose
10	chr4:188423000-188423400	Enhancers	Ovary	ovary
11	chr4:188425600-188426800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:188425800-188426800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:188426000-188426400	Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr4:188426000-188426600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:188426200-188426600	Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr4:188426200-188426800	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr4:188426200-188426800	ZNF genes & repeats	Placenta	Placenta
18	chr4:188426200-188427400	Active TSS	H1 Cell Line	embryonic stem cell
19	chr4:188426200-188427400	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr4:188426200-188427400	Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr4:188432000-188433000	Enhancers	Adipose Nuclei	Adipose
22	chr4:188433000-188433400	Enhancers	A549	lung
23	chr4:188451200-188451800	Enhancers	Fetal Muscle Trunk	muscle
24	chr4:188454000-188454200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr4:188454200-188455200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr4:188454600-188456200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:188455000-188455800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr4:188455000-188455800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr4:188455000-188456200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr4:188455200-188456000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr4:188462000-188462600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:188462000-188462800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr4:188462200-188462600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr4:188462200-188462600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:188462200-188463600	Enhancers	Muscle Satellite Cultured Cells	--
36	chr4:188462400-188462600	Enhancers	HSMM	muscle
37	chr4:188462400-188462600	Enhancers	NHDF-Ad	bronchial
38	chr4:188462400-188462800	Enhancers	HSMMtube	muscle
39	chr4:188462600-188463000	Flanking Active TSS	HSMM	muscle
40	chr4:188462600-188463000	Flanking Active TSS	NHDF-Ad	bronchial
41	chr4:188462600-188463600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr4:188462800-188463000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:188462800-188463200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:188462800-188463200	Flanking Active TSS	HSMMtube	muscle
45	chr4:188462800-188463600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr4:188463000-188463600	Enhancers	HSMM	muscle
47	chr4:188463000-188463600	Enhancers	NHDF-Ad	bronchial
48	chr4:188463200-188463600	Enhancers	HSMMtube	muscle
49	chr4:188463200-188468600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr4:188463600-188465600	Weak transcription	Muscle Satellite Cultured Cells	--

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