Variant report

Variant	nsv1025981
Chromosome Location	chr4:188364844-188451578
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	BACH1	chr4:188413248-188413433	K562	blood:	n/a	chr4:188413338-188413352
2	CEBPB	chr4:188405573-188406437	IMR90	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
3	CEBPB	chr4:188440459-188440698	IMR90	lung:	n/a	n/a
4	CEBPB	chr4:188376676-188376735	HepG2	liver:	n/a	chr4:188376676-188376689 chr4:188376676-188376687 chr4:188376678-188376689
5	CEBPB	chr4:188405582-188405932	A549	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
6	CEBPB	chr4:188399632-188400363	IMR90	lung:	n/a	n/a
7	CEBPB	chr4:188406167-188406450	A549	lung:	n/a	n/a
8	CEBPB	chr4:188440289-188440620	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:188405581-188406417	HepG2	liver:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
10	CEBPB	chr4:188405764-188405895	H1-hESC	embryonic stem cell:	n/a	chr4:188405878-188405889 chr4:188405877-188405890
11	CEBPB	chr4:188401324-188401855	IMR90	lung:	n/a	n/a
12	CTCF	chr4:188412728-188412816	NHEK	skin:	n/a	n/a
13	CTCF	chr4:188383305-188383331	GM19239	blood:	n/a	n/a
14	CTCF	chr4:188426682-188426755	LNCaP	prostate:	n/a	n/a
15	CTCF	chr4:188442915-188443011	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr4:188443124-188443168	Medullo	brain:	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	chr4:188438067-188438123	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr4:188372133-188372215	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr4:188395046-188395246	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr4:188418016-188418170	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F6	chr4:188426476-188426590	K562	blood:	n/a	n/a
24	EP300	chr4:188413842-188413867	GM12878	blood:	n/a	n/a
25	EP300	chr4:188413364-188413589	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr4:188421092-188421565	T-47D	breast:	n/a	n/a
27	EP300	chr4:188437667-188437686	GM12878	blood:	n/a	n/a
28	EP300	chr4:188401602-188401920	T-47D	breast:	n/a	n/a
29	EP300	chr4:188399901-188400574	T-47D	breast:	n/a	chr4:188400130-188400139
30	EP300	chr4:188399817-188400577	SK-N-SH	brain:	n/a	chr4:188400130-188400139
31	FOS	chr4:188399962-188400354	MCF10A-Er-Src	breast:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
32	FOS	chr4:188399962-188400312	MCF10A-Er-Src	breast:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
33	FOS	chr4:188399945-188400441	MCF10A-Er-Src	breast:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
34	FOS	chr4:188401433-188402312	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr4:188401411-188402262	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr4:188401061-188401145	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr4:188413155-188413419	MCF10A-Er-Src	breast:	n/a	chr4:188413339-188413351 chr4:188413341-188413349 chr4:188413340-188413350 chr4:188413340-188413350
38	FOS	chr4:188399944-188400346	MCF10A-Er-Src	breast:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
39	FOS	chr4:188401415-188402310	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:188401535-188402265	MCF10A-Er-Src	breast:	n/a	n/a
41	FOSL2	chr4:188399844-188400429	A549	lung:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
42	FOSL2	chr4:188401888-188402360	SK-N-SH	brain:	n/a	n/a
43	FOSL2	chr4:188399880-188400454	SK-N-SH	brain:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
44	FOXA1	chr4:188421080-188421491	T-47D	breast:	n/a	n/a
45	FOXA1	chr4:188400709-188401005	T-47D	breast:	n/a	n/a
46	FOXA1	chr4:188401546-188402068	T-47D	breast:	n/a	chr4:188401842-188401857
47	FOXA1	chr4:188401641-188402083	HepG2	liver:	n/a	chr4:188401842-188401857
48	FOXA1	chr4:188400738-188400883	T-47D	breast:	n/a	n/a
49	FOXA1	chr4:188401680-188402066	HepG2	liver:	n/a	chr4:188401842-188401857
50	FOXA1	chr4:188399892-188400407	T-47D	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188426506-188426556	NH-A	brain:	n/a
2	chr4:188426506-188426556	NH-A	brain:	n/a
3	chr4:188426506-188426556	Jurkat	blood:	n/a
4	chr4:188398437-188398487	HMEC	breast:	n/a
5	chr4:188398437-188398487	SAEC	small airway:	n/a
6	chr4:188426506-188426556	PANC-1	pancreas:	n/a
7	chr4:188426437-188426487	A549	lung:	n/a
8	chr4:188398437-188398487	HNPCEpiC	eye:	n/a
9	chr4:188428637-188428687	HMEC	breast:	n/a
10	chr4:188398437-188398487	HUVEC	blood vessel:	n/a
11	chr4:188401038-188401088	Jurkat	blood:	n/a
12	chr4:188426506-188426556	NHBE	bronchial:	n/a
13	chr4:188428637-188428687	HepG2	liver:	n/a
14	chr4:188423066-188423116	U87	brain:	n/a
15	chr4:188401038-188401088	HRCEpiC	kidney:	n/a
16	chr4:188398437-188398487	CMK	blood:	n/a
17	chr4:188423066-188423116	AG09309	skin:	n/a
18	chr4:188426506-188426556	SK-N-SH	brain:	n/a
19	chr4:188428637-188428687	HCF	heart:	n/a
20	chr4:188423066-188423116	HIPEpiC	eye:	n/a
21	chr4:188427966-188428016	Hela-S3	cervix:	n/a
22	chr4:188398437-188398487	PFSK-1	brain:	n/a
23	chr4:188391387-188391437	GM12878	blood:	n/a
24	chr4:188398437-188398487	NT2-D1	testis:	n/a
25	chr4:188426278-188426328	NB4	blood:	n/a
26	chr4:188426278-188426328	AG04450	lung:	fetal
27	chr4:188391387-188391437	AG09319	gingival:	n/a
28	chr4:188426278-188426328	NHBE	bronchial:	n/a
29	chr4:188401038-188401088	GM06990	blood:	n/a
30	chr4:188426437-188426487	ProgFib	skin:	n/a
31	chr4:188401038-188401088	IMR90	lung:	fetal
32	chr4:188391387-188391437	HCF	heart:	n/a
33	chr4:188426278-188426328	T-47D	breast:	n/a
34	chr4:188401038-188401088	H1-hESC	embryonic stem cell:	embryo
35	chr4:188426506-188426556	AG10803	skin:	n/a
36	chr4:188426506-188426556	K562	blood:	n/a
37	chr4:188401038-188401088	HEEpiC	esophagus:	n/a
38	chr4:188427966-188428016	H1-hESC	embryonic stem cell:	embryo
39	chr4:188398437-188398487	RPTEC	kidney:	n/a
40	chr4:188426437-188426487	ovcar-3	ovarian:	n/a
41	chr4:188428637-188428687	SK-N-SH	brain:	n/a
42	chr4:188398437-188398487	GM12891	blood:	n/a
43	chr4:188428637-188428687	AoSMC	blood vessel:	n/a
44	chr4:188401038-188401088	HL-60	blood:	n/a
45	chr4:188428637-188428687	CMK	blood:	n/a
46	chr4:188391387-188391437	Hepatocyte	liver:	n/a
47	chr4:188427966-188428016	HCT-116	colon:	n/a
48	chr4:188426278-188426328	AG09309	skin:	n/a
49	chr4:188391387-188391437	GM19239	blood:	n/a
50	chr4:188428637-188428687	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
2	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
3	chr4:188390078..188391598-chr8:43091410..43092931,3	MCF-7	breast:
4	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
5	chr4:188426813..188429681-chrX:150150480..150152156,2	MCF-7	breast:
6	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
7	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
8	chr4:188391078..188391578-chr8:43092429..43092931,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-12	chr4:188370524-188371133	l_2817_chr4:188360138-188372335_testes
2	lnc-ZFP42-12	chr4:188371277-188372335	l_2817_chr4:188360138-188372335_testes
3	lnc-TRIML2-5	chr4:188437307-188437878	XLOC_004219
4	lnc-ZFP42-11	chr4:188419171-188419708	NONHSAT099698
5	lnc-TRIML2-12	chr4:188364965-188365452	NONHSAT099697
6	lnc-ZFP42-11	chr4:188419753-188420210	NONHSAT099698
7	lnc-TRIML2-5	chr4:188438236-188438362	XLOC_004219

Variant related genes	Relation type
ENSG00000251490	TF binding region
ENSG00000251643	TF binding region
ENSG00000251490	CpG island
ENSG00000251643	CpG island
ENSG00000029993	chromatin interactions
ANP32E	miRNA target sites
ANTXR1	miRNA target sites

Extended variants
information (count: 1685 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1685 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534500995	chr4:188364966-188364967	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs559268129	chr4:188364983-188364984	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs11132452	chr4:188365049-188365050	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs569151942	chr4:188365094-188365095	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs191583802	chr4:188365113-188365114	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs57537371	chr4:188365124-188365125	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs142910861	chr4:188365226-188365227	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs77932738	chr4:188365234-188365235	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs553400904	chr4:188365276-188365277	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs573013482	chr4:188365311-188365312	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs1864603	chr4:188365395-188365396	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs147397818	chr4:188365419-188365420	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs554208312	chr4:188365510-188365511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116084954	chr4:188365557-188365558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561432316	chr4:188365576-188365577	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs139665851	chr4:188365596-188365597	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs546894310	chr4:188365602-188365603	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs560274129	chr4:188365613-188365614	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs79992110	chr4:188365640-188365641	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs181115710	chr4:188365669-188365670	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs568914227	chr4:188365680-188365681	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs142541594	chr4:188365738-188365739	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs548420709	chr4:188365767-188365768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376310816	chr4:188365811-188365812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116361538	chr4:188365886-188365887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186101721	chr4:188365895-188365896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35270210	chr4:188365961-188365962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553582956	chr4:188366069-188366070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115662447	chr4:188366093-188366094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538793064	chr4:188366099-188366100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558517539	chr4:188366130-188366131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6821124	chr4:188366141-188366142	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs78664985	chr4:188366150-188366151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150533583	chr4:188366151-188366152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575065452	chr4:188366164-188366165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540800549	chr4:188366165-188366166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540647505	chr4:188368767-188368768	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs146835447	chr4:188368770-188368771	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs183012605	chr4:188368811-188368812	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs73025730	chr4:188368819-188368820	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs187472997	chr4:188368843-188368844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs3055865	chr4:188370533-188370534	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs552757671	chr4:188370534-188370535	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs150477607	chr4:188370541-188370542	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs138346478	chr4:188370547-188370548	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs34676546	chr4:188370557-188370558	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs536628843	chr4:188370584-188370585	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs193077213	chr4:188370597-188370598	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs560564057	chr4:188370620-188370621	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs542946494	chr4:188370641-188370642	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cognitive impairment	21505072	CNVD

Chromatin state (count:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188365000-188365400	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr4:188365400-188366200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr4:188370800-188371200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr4:188370800-188372000	Enhancers	Fetal Lung	lung
5	chr4:188374800-188375200	Enhancers	Brain Germinal Matrix	brain
6	chr4:188374800-188375200	Enhancers	Fetal Heart	heart
7	chr4:188375000-188375400	Enhancers	HSMMtube	muscle
8	chr4:188385600-188385800	Enhancers	Fetal Lung	lung
9	chr4:188385600-188386400	Enhancers	Adipose Nuclei	Adipose
10	chr4:188385600-188386400	Enhancers	Fetal Stomach	stomach
11	chr4:188385600-188386800	Enhancers	Aorta	Aorta
12	chr4:188385800-188386400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:188386400-188386600	Enhancers	Fetal Lung	lung
14	chr4:188386400-188394600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr4:188389600-188390800	Enhancers	Fetal Heart	heart
16	chr4:188389600-188391200	Enhancers	HSMMtube	muscle
17	chr4:188390400-188390600	Enhancers	Fetal Muscle Leg	muscle
18	chr4:188390400-188391000	Enhancers	Colon Smooth Muscle	Colon
19	chr4:188390400-188391600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr4:188390600-188390800	Enhancers	HSMM	muscle
21	chr4:188390600-188391200	Weak transcription	Fetal Muscle Leg	muscle
22	chr4:188390600-188391200	Enhancers	Rectal Smooth Muscle	rectum
23	chr4:188390800-188391200	Flanking Active TSS	Fetal Heart	heart
24	chr4:188391200-188391600	Enhancers	Fetal Heart	heart
25	chr4:188391200-188391600	Flanking Active TSS	HSMMtube	muscle
26	chr4:188391200-188392000	Enhancers	Fetal Muscle Leg	muscle
27	chr4:188391400-188391600	Enhancers	HSMM	muscle
28	chr4:188391600-188392200	Enhancers	HSMMtube	muscle
29	chr4:188391600-188399600	Weak transcription	Fetal Heart	heart
30	chr4:188391800-188392000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:188392000-188399600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:188392200-188398600	Weak transcription	HSMMtube	muscle
33	chr4:188394600-188396400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:188396400-188398400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr4:188397600-188400000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:188397800-188398000	Enhancers	Aorta	Aorta
37	chr4:188397800-188402000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:188398000-188399000	Weak transcription	Aorta	Aorta
39	chr4:188398200-188398400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr4:188398400-188398600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:188398400-188399600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:188398400-188399600	Enhancers	Stomach Smooth Muscle	stomach
43	chr4:188398600-188398800	Active TSS	HSMMtube	muscle
44	chr4:188398600-188399600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr4:188398800-188399400	Flanking Active TSS	HSMMtube	muscle
46	chr4:188398800-188401800	Enhancers	Colon Smooth Muscle	Colon
47	chr4:188399000-188399600	Enhancers	HSMM	muscle
48	chr4:188399000-188399600	Enhancers	NHLF	lung
49	chr4:188399000-188400200	Enhancers	Aorta	Aorta
50	chr4:188399000-188402200	Enhancers	Fetal Stomach	stomach

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