Variant report

Variant	nsv1032478
Chromosome Location	chr4:188219548-188272422
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:101)
CpG islands
(count:305)
Chromatin interactive
region (count:4)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:101 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:188263083-188263269	HepG2	liver:	n/a	n/a
2	CEBPB	chr4:188253347-188253499	Hela-S3	cervix:	n/a	chr4:188253450-188253461
3	CEBPB	chr4:188223685-188224011	IMR90	lung:	n/a	n/a
4	CEBPB	chr4:188253393-188253593	HepG2	liver:	n/a	chr4:188253450-188253461
5	CEBPB	chr4:188254417-188254534	K562	blood:	n/a	n/a
6	CEBPB	chr4:188254340-188254476	A549	lung:	n/a	chr4:188254404-188254415
7	CEBPB	chr4:188254254-188254599	IMR90	lung:	n/a	chr4:188254404-188254415
8	CEBPB	chr4:188234147-188234350	IMR90	lung:	n/a	n/a
9	CEBPB	chr4:188254264-188254489	HepG2	liver:	n/a	chr4:188254404-188254415
10	CTCF	chr4:188246064-188246219	MCF-7	breast:	n/a	n/a
11	CTCF	chr4:188257800-188257917	LNCaP	prostate:	n/a	n/a
12	CTCF	chr4:188241480-188241630	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr4:188230720-188230870	AG10803	skin:	n/a	n/a
14	CTCF	chr4:188257708-188257915	A549	lung:	n/a	n/a
15	CTCF	chr4:188230709-188230813	NHEK	skin:	n/a	n/a
16	CTCF	chr4:188230727-188230815	ProgFib	skin:	n/a	n/a
17	CTCF	chr4:188228292-188228390	Fibrobl	skin:	n/a	n/a
18	CTCF	chr4:188246107-188246174	MCF-7	breast:	n/a	n/a
19	CTCF	chr4:188243900-188244050	HepG2	liver:	n/a	n/a
20	CTCF	chr4:188249940-188250090	GM12864	blood:	n/a	n/a
21	CTCF	chr4:188228291-188228408	NHEK	skin:	n/a	n/a
22	CTCF	chr4:188229160-188229310	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr4:188228280-188228430	HMEC	breast:	n/a	n/a
24	CTCF	chr4:188243900-188244050	BE2_C	brain:	n/a	n/a
25	CTCF	chr4:188228280-188228430	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr4:188243984-188244028	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr4:188230711-188230796	Gliobla	brain:	n/a	n/a
28	CTCF	chr4:188230700-188230850	AG04449	skin:	n/a	n/a
29	E2F4	chr4:188253764-188253823	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr4:188261646-188262204	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr4:188265864-188266016	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr4:188227007-188227153	MCF10A-Er-Src	breast:	n/a	chr4:188227077-188227084 chr4:188227076-188227084 chr4:188227076-188227085 chr4:188227075-188227084
33	FOS	chr4:188230811-188231011	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr4:188226960-188227128	MCF10A-Er-Src	breast:	n/a	chr4:188227077-188227084 chr4:188227076-188227084 chr4:188227076-188227085 chr4:188227075-188227084
35	FOS	chr4:188254326-188254667	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr4:188254316-188254686	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr4:188230726-188231129	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr4:188228368-188228512	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:188239885-188240193	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:188240035-188240194	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr4:188228345-188228500	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr4:188254265-188254675	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr4:188254324-188254701	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr4:188230726-188230921	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr4:188230743-188230969	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr4:188240003-188240203	MCF10A-Er-Src	breast:	n/a	n/a
47	FOSL2	chr4:188254322-188254695	SK-N-SH	brain:	n/a	n/a
48	FOXA1	chr4:188229964-188230240	T-47D	breast:	n/a	n/a
49	GABPA	chr4:188257677-188257971	Hela-S3	cervix:	n/a	n/a
50	GATA3	chr4:188229793-188230344	T-47D	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188256637-188256687	HNPCEpiC	eye:	n/a
2	chr4:188256708-188256758	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:188256708-188256758	NH-A	brain:	n/a
4	chr4:188256637-188256687	HRCEpiC	kidney:	n/a
5	chr4:188223108-188223158	CMK	blood:	n/a
6	chr4:188230390-188230440	HEK293	kidney:	embryo
7	chr4:188256708-188256758	BJ	skin:	n/a
8	chr4:188223108-188223158	HRPEpiC	eye:	n/a
9	chr4:188256765-188256815	HRPEpiC	eye:	n/a
10	chr4:188223108-188223158	Hepatocyte	liver:	n/a
11	chr4:188256708-188256758	MCF-7	breast:	n/a
12	chr4:188256708-188256758	HCPEpiC	choroid plexus:	n/a
13	chr4:188256708-188256758	HRCEpiC	kidney:	n/a
14	chr4:188256765-188256815	PFSK-1	brain:	n/a
15	chr4:188256765-188256815	Hepatocyte	liver:	n/a
16	chr4:188223108-188223158	Caco-2	colon:	n/a
17	chr4:188256765-188256815	GM12891	blood:	n/a
18	chr4:188256765-188256815	NHBE	bronchial:	n/a
19	chr4:188256708-188256758	HNPCEpiC	eye:	n/a
20	chr4:188256765-188256815	ProgFib	skin:	n/a
21	chr4:188256637-188256687	MCF-7	breast:	n/a
22	chr4:188256765-188256815	SK-N-MC	brain:	n/a
23	chr4:188256637-188256687	SKMC	muscle:	n/a
24	chr4:188223108-188223158	HCT-116	colon:	n/a
25	chr4:188256765-188256815	AG04449	skin:	fetal
26	chr4:188256708-188256758	AoSMC	blood vessel:	n/a
27	chr4:188256708-188256758	SKMC	muscle:	n/a
28	chr4:188256637-188256687	AG09309	skin:	n/a
29	chr4:188256765-188256815	BJ	skin:	n/a
30	chr4:188230390-188230440	GM12892	blood:	n/a
31	chr4:188256765-188256815	PANC-1	pancreas:	n/a
32	chr4:188256708-188256758	PFSK-1	brain:	n/a
33	chr4:188256708-188256758	Caco-2	colon:	n/a
34	chr4:188256708-188256758	LNCaP	prostate:	n/a
35	chr4:188256708-188256758	HEK293	kidney:	embryo
36	chr4:188223108-188223158	SKMC	muscle:	n/a
37	chr4:188256637-188256687	HIPEpiC	eye:	n/a
38	chr4:188223108-188223158	GM12878	blood:	n/a
39	chr4:188256765-188256815	GM19239	blood:	n/a
40	chr4:188256765-188256815	HCT-116	colon:	n/a
41	chr4:188256708-188256758	Hela-S3	cervix:	n/a
42	chr4:188256765-188256815	HCPEpiC	choroid plexus:	n/a
43	chr4:188223108-188223158	LNCaP	prostate:	n/a
44	chr4:188223108-188223158	HEK293	kidney:	embryo
45	chr4:188230390-188230440	A549	lung:	n/a
46	chr4:188256765-188256815	HCF	heart:	n/a
47	chr4:188256708-188256758	NHDF-neo	bronchial:	n/a
48	chr4:188223108-188223158	U87	brain:	n/a
49	chr4:188256765-188256815	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:188256708-188256758	GM19239	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188261472..188262979-chr4:188266588..188269425,2	K562	blood:
2	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:
3	chr4:188261472..188262979-chr4:188266588..188269425,2	K562	blood:
4	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-13	chr4:188251486-188251546	NONHSAT099691
2	lnc-FAT1-3	chr4:188225792-188226855	XLOC_004217
3	lnc-ZFP42-13	chr4:188252448-188253478	NONHSAT099691
4	lnc-ZFP42-13	chr4:188228509-188228694	NONHSAT099691
5	lnc-FAT1-3	chr4:188225237-188225621	XLOC_004217
6	lnc-FAT1-3	chr4:188228260-188228423	XLOC_004217
7	lnc-ZFP42-13	chr4:188237423-188237596	NONHSAT099691
8	lnc-FAT1-3	chr4:188230336-188230836	XLOC_004217

No data

Variant related genes	Relation type
ENSG00000250658	TF binding region
ENSG00000250658	CpG island

Extended variants
information (count: 2068 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2068 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562800785	chr4:188219557-188219558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531898898	chr4:188219575-188219576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375363440	chr4:188219597-188219598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548735896	chr4:188219623-188219624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562122261	chr4:188219628-188219629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs28695617	chr4:188219632-188219633	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs547168203	chr4:188219636-188219637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138259829	chr4:188219656-188219657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539391389	chr4:188219684-188219685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549814601	chr4:188219688-188219689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115966475	chr4:188219718-188219719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370906910	chr4:188219750-188219751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183155975	chr4:188219803-188219804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572133810	chr4:188219805-188219806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10028172	chr4:188219807-188219808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540823887	chr4:188219816-188219817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116375051	chr4:188219819-188219820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553972406	chr4:188219820-188219821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143842479	chr4:188219863-188219864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545758054	chr4:188219864-188219865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562564308	chr4:188219900-188219901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576054987	chr4:188219902-188219903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367794132	chr4:188219969-188219970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543833670	chr4:188220033-188220034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187991606	chr4:188220089-188220090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1564043	chr4:188220110-188220111	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs190645612	chr4:188220114-188220115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574583677	chr4:188220173-188220174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183353642	chr4:188220182-188220183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564127442	chr4:188220191-188220192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150576143	chr4:188220208-188220209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1564044	chr4:188220209-188220210	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs187792707	chr4:188220210-188220211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1564045	chr4:188220214-188220215	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs1975896	chr4:188220227-188220228	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs548998462	chr4:188220231-188220232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1975897	chr4:188220255-188220256	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs534471783	chr4:188220281-188220282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557547451	chr4:188220319-188220320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4862794	chr4:188220352-188220353	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs72721171	chr4:188220360-188220361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192186723	chr4:188220367-188220368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13110850	chr4:188220370-188220371	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs576018341	chr4:188220549-188220550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542253363	chr4:188220557-188220558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555735315	chr4:188220634-188220635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2219662	chr4:188220635-188220636	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs564693505	chr4:188220640-188220641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533597717	chr4:188220645-188220646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35586195	chr4:188220662-188220663	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188216400-188223000	Weak transcription	Fetal Lung	lung
2	chr4:188217800-188230400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:188218600-188227600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:188218600-188234000	Weak transcription	Aorta	Aorta
5	chr4:188219600-188219800	Enhancers	Fetal Kidney	kidney
6	chr4:188219800-188223600	Weak transcription	Fetal Kidney	kidney
7	chr4:188223000-188223400	Enhancers	Fetal Lung	lung
8	chr4:188223200-188223400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:188223200-188223400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr4:188223200-188223400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:188223200-188223800	Enhancers	Right Atrium	heart
12	chr4:188223200-188224000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:188223200-188224000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr4:188223200-188224000	Enhancers	Ovary	ovary
15	chr4:188223400-188223600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr4:188223400-188223800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:188223400-188223800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:188223400-188223800	Active TSS	Fetal Brain Male	brain
19	chr4:188223400-188223800	Enhancers	NHDF-Ad	bronchial
20	chr4:188223400-188224000	Flanking Active TSS	Fetal Lung	lung
21	chr4:188223400-188224200	Enhancers	Adipose Nuclei	Adipose
22	chr4:188223400-188224600	Enhancers	Muscle Satellite Cultured Cells	--
23	chr4:188223400-188224600	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr4:188223400-188224600	Enhancers	NHLF	lung
25	chr4:188223400-188224600	Enhancers	Osteobl	bone
26	chr4:188223400-188225000	Enhancers	Fetal Muscle Leg	muscle
27	chr4:188223400-188225600	Enhancers	Fetal Stomach	stomach
28	chr4:188223600-188223800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:188223600-188224000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr4:188223600-188224800	Enhancers	Fetal Kidney	kidney
31	chr4:188223800-188224200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr4:188223800-188224600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr4:188224000-188224600	Weak transcription	Ovary	ovary
34	chr4:188224000-188225800	Enhancers	Fetal Lung	lung
35	chr4:188224000-188228200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:188224200-188224400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr4:188224400-188224600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr4:188224600-188224800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr4:188224600-188224800	Enhancers	Ovary	ovary
40	chr4:188224600-188227200	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr4:188224600-188227400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:188224600-188228200	Weak transcription	Osteobl	bone
43	chr4:188224600-188229600	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr4:188225800-188226200	Weak transcription	Fetal Lung	lung
45	chr4:188226200-188226800	Enhancers	Fetal Lung	lung
46	chr4:188226600-188227400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr4:188226600-188228600	Enhancers	HMEC	breast
48	chr4:188227200-188227800	Enhancers	H9 Cell Line	embryonic stem cell
49	chr4:188227200-188228600	Enhancers	Muscle Satellite Cultured Cells	--
50	chr4:188227400-188228200	Enhancers	NHEK	skin

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