Variant report

Variant	nsv879986
Chromosome Location	chr4:132640243-132716060
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:253)
CpG islands
(count:2384)
Chromatin interactive
region (count:0)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:132643327-132643727	GM12878	blood:	n/a	n/a
2	CCNT2	chr4:132646067-132646366	K562	blood:	n/a	n/a
3	CHD2	chr4:132646072-132646353	GM12878	blood:	n/a	n/a
4	CHD2	chr4:132646065-132646272	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr4:132663911-132663984	GM12891	blood:	n/a	n/a
6	CTCF	chr4:132693300-132693367	Lung_OC	lung:	n/a	n/a
7	CTCF	chr4:132680481-132680506	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr4:132664464-132664625	LNCaP	prostate:	n/a	chr4:132664549-132664562
9	CTCF	chr4:132697034-132697131	GM10248	blood:	n/a	n/a
10	CTCF	chr4:132694129-132694165	GM20000	blood:	n/a	n/a
11	CTCF	chr4:132685297-132685357	LNCaP	prostate:	n/a	n/a
12	CTCF	chr4:132656296-132656315	LNCaP	prostate:	n/a	n/a
13	CTCF	chr4:132671917-132672049	LNCaP	prostate:	n/a	chr4:132671985-132671998
14	CTCF	chr4:132656337-132656391	LNCaP	prostate:	n/a	n/a
15	CTCF	chr4:132664482-132664598	LNCaP	prostate:	n/a	chr4:132664549-132664562
16	CTCF	chr4:132684958-132685024	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr4:132651343-132651348	GM10248	blood:	n/a	n/a
18	CTCF	chr4:132656263-132656342	GM10248	blood:	n/a	n/a
19	CTCF	chr4:132671870-132672056	LNCaP	prostate:	n/a	chr4:132671985-132671998
20	E2F6	chr4:132646712-132646865	K562	blood:	n/a	n/a
21	EP300	chr4:132695427-132695985	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr4:132695549-132695979	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chr4:132695209-132696216	SK-N-SH	brain:	n/a	n/a
24	EP300	chr4:132641457-132641845	GM12878	blood:	n/a	n/a
25	ESR1	chr4:132646144-132646379	T-47D	breast:	n/a	n/a
26	FOS	chr4:132713900-132714099	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr4:132713900-132713928	MCF10A-Er-Src	breast:	n/a	n/a
28	FOSL2	chr4:132671224-132671521	HepG2	liver:	n/a	n/a
29	FOSL2	chr4:132663766-132664083	HepG2	liver:	n/a	n/a
30	FOXA1	chr4:132689820-132690101	HepG2	liver:	n/a	n/a
31	FOXP2	chr4:132695556-132695964	SK-N-MC	brain:	n/a	n/a
32	GATA2	chr4:132695553-132696126	SH-SY5Y	brain:	n/a	n/a
33	GATA3	chr4:132695579-132696183	SH-SY5Y	brain:	n/a	n/a
34	HEY1	chr4:132651079-132651270	K562	blood:	n/a	n/a
35	HEY1	chr4:132660960-132661201	HepG2	liver:	n/a	n/a
36	HEY1	chr4:132655977-132656218	HepG2	liver:	n/a	n/a
37	HEY1	chr4:132646146-132646336	HepG2	liver:	n/a	n/a
38	HEY1	chr4:132648596-132649072	HepG2	liver:	n/a	n/a
39	HEY1	chr4:132658465-132658706	HepG2	liver:	n/a	n/a
40	HEY1	chr4:132648601-132648997	K562	blood:	n/a	n/a
41	HEY1	chr4:132648681-132648865	K562	blood:	n/a	n/a
42	HEY1	chr4:132651064-132651326	HepG2	liver:	n/a	n/a
43	HEY1	chr4:132646169-132646415	K562	blood:	n/a	n/a
44	IRF4	chr4:132714884-132715175	GM12878	blood:	n/a	n/a
45	JUN	chr4:132700963-132701024	HepG2	liver:	n/a	chr4:132700988-132701001
46	JUND	chr4:132695358-132696019	SK-N-SH	brain:	n/a	n/a
47	JUND	chr4:132700849-132701175	HepG2	liver:	n/a	n/a
48	JUND	chr4:132642970-132643176	HepG2	liver:	n/a	n/a
49	JUND	chr4:132646170-132646446	A549	lung:	n/a	n/a
50	MAFK	chr4:132702290-132702368	HepG2	liver:	n/a	chr4:132702296-132702312 chr4:132702297-132702308 chr4:132702296-132702307 chr4:132702295-132702309 chr4:132702296-132702307

(count:2384 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132643925-132643975	Hela-S3	cervix:	n/a
2	chr4:132677675-132677725	SK-N-SH_RA	brain:	n/a
3	chr4:132651902-132651952	SAEC	small airway:	n/a
4	chr4:132652001-132652051	SK-N-MC	brain:	n/a
5	chr4:132652113-132652163	AG09319	gingival:	n/a
6	chr4:132643925-132643975	Hela-S3	cervix:	n/a
7	chr4:132677675-132677725	SK-N-SH_RA	brain:	n/a
8	chr4:132651902-132651952	SAEC	small airway:	n/a
9	chr4:132652001-132652051	SK-N-MC	brain:	n/a
10	chr4:132652113-132652163	AG09319	gingival:	n/a
11	chr4:132677681-132677731	HRE	kidney:	n/a
12	chr4:132661931-132661981	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:132647121-132647171	T-47D	breast:	n/a
14	chr4:132651902-132651952	HRE	kidney:	n/a
15	chr4:132649479-132649529	NT2-D1	testis:	n/a
16	chr4:132661961-132662011	NHBE	bronchial:	n/a
17	chr4:132649229-132649279	NB4	blood:	n/a
18	chr4:132661931-132661981	HEEpiC	esophagus:	n/a
19	chr4:132650897-132650947	LNCaP	prostate:	n/a
20	chr4:132653123-132653173	HCPEpiC	choroid plexus:	n/a
21	chr4:132671417-132671467	GM12892	blood:	n/a
22	chr4:132649551-132649601	HAEpiC	amniotic membrane:	n/a
23	chr4:132653123-132653173	PANC-1	pancreas:	n/a
24	chr4:132653123-132653173	NHDF-neo	bronchial:	n/a
25	chr4:132666907-132666957	HAEpiC	amniotic membrane:	n/a
26	chr4:132653123-132653173	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:132686909-132686959	U87	brain:	n/a
28	chr4:132665367-132665417	SK-N-SH	brain:	n/a
29	chr4:132671715-132671765	HRE	kidney:	n/a
30	chr4:132646574-132646624	NH-A	brain:	n/a
31	chr4:132653123-132653173	HRE	kidney:	n/a
32	chr4:132663979-132664029	AoSMC	blood vessel:	n/a
33	chr4:132684138-132684188	PrEC	prostate:	n/a
34	chr4:132646360-132646410	SK-N-SH	brain:	n/a
35	chr4:132646574-132646624	HEK293	kidney:	embryo
36	chr4:132686116-132686166	H1-hESC	embryonic stem cell:	embryo
37	chr4:132648785-132648835	HMEC	breast:	n/a
38	chr4:132677681-132677731	HAEpiC	amniotic membrane:	n/a
39	chr4:132650897-132650947	Hela-S3	cervix:	n/a
40	chr4:132653123-132653173	HRCEpiC	kidney:	n/a
41	chr4:132663979-132664029	PrEC	prostate:	n/a
42	chr4:132677675-132677725	Jurkat	blood:	n/a
43	chr4:132684138-132684188	SKMC	muscle:	n/a
44	chr4:132642641-132642691	HEEpiC	esophagus:	n/a
45	chr4:132654638-132654688	Jurkat	blood:	n/a
46	chr4:132649479-132649529	AG10803	skin:	n/a
47	chr4:132661931-132661981	MCF-7	breast:	n/a
48	chr4:132686909-132686959	GM19239	blood:	n/a
49	chr4:132652113-132652163	ovcar-3	ovarian:	n/a
50	chr4:132669467-132669517	RPTEC	kidney:	n/a

No data

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-62N21.1.1-12	chr4:132641417-132641698	NONHSAT098317
2	lnc-PCDH10-4	chr4:132694701-132694847	NONHSAT098323
3	lnc-PCDH10-16	chr4:132678560-132678792	NONHSAT098318
4	lnc-PCDH10-4	chr4:132694720-132694847	XLOC_003690
5	lnc-PCDH10-4	chr4:132694457-132694847	XLOC_003690
6	lnc-PCDH10-4	chr4:132712365-132712637	XLOC_003690
7	lnc-PCDH10-14	chr4:132689388-132689733	NONHSAT098321
8	lnc-PCDH10-4	chr4:132695748-132696191	XLOC_003690
9	lnc-PCDH10-4	chr4:132694702-132694847	XLOC_003690
10	lnc-PCDH10-4	chr4:132695435-132695524	XLOC_003690
11	lnc-PCDH10-4	chr4:132695434-132695524	NONHSAT098323
12	lnc-PCDH10-4	chr4:132695748-132695847	XLOC_003690
13	lnc-PCDH10-4	chr4:132695620-132696191	NONHSAT098323

No data

Variant related genes	Relation type
ENSG00000252014	TF binding region
RN7SL205P	TF binding region
ENSG00000251676	TF binding region
ENSG00000249416	TF binding region
ENSG00000252014	CpG island
RN7SL205P	CpG island
ENSG00000251676	CpG island
ENSG00000249416	CpG island
MBNL1	miRNA target sites

Extended variants
information (count: 1244 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1244 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573964503	chr4:132641426-132641427	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs10440356	chr4:132641436-132641437	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs2863563	chr4:132641469-132641470	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs2863564	chr4:132641470-132641471	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs559795937	chr4:132641483-132641484	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs1913007	chr4:132641498-132641499	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs2863565	chr4:132641505-132641506	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs2863566	chr4:132641512-132641513	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs114598910	chr4:132641525-132641526	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs2863567	chr4:132641546-132641547	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs565166992	chr4:132641572-132641573	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs532838441	chr4:132641614-132641615	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs542628107	chr4:132641615-132641616	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs3978151	chr4:132641651-132641652	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs2863568	chr4:132641755-132641756	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs549481455	chr4:132641761-132641762	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs2863569	chr4:132641794-132641795	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs569594916	chr4:132641801-132641802	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs2902504	chr4:132641813-132641814	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs549498267	chr4:132642642-132642643	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs148299003	chr4:132642644-132642645	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs376705928	chr4:132642679-132642680	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs567725820	chr4:132642874-132642875	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs35783481	chr4:132642883-132642884	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs75341453	chr4:132642892-132642893	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs565545677	chr4:132642893-132642894	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs557167239	chr4:132642899-132642900	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs534472433	chr4:132642903-132642904	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs200687384	chr4:132642908-132642909	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs544470177	chr4:132642932-132642933	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs190604399	chr4:132642936-132642937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs528958187	chr4:132642972-132642973	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs542728118	chr4:132642976-132642977	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs559048999	chr4:132642977-132642978	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs78464716	chr4:132642978-132642979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs554262412	chr4:132643038-132643039	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs4863849	chr4:132643039-132643040	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs200412922	chr4:132643082-132643083	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs571561053	chr4:132643119-132643120	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs182916163	chr4:132643125-132643126	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs57077437	chr4:132643151-132643152	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs28782861	chr4:132643180-132643181	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs188317617	chr4:132643189-132643190	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs192204281	chr4:132643202-132643203	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs553441782	chr4:132643231-132643232	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs566481978	chr4:132643260-132643261	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs538646065	chr4:132643278-132643279	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs13434514	chr4:132643282-132643283	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs575516044	chr4:132643291-132643292	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs544916144	chr4:132643303-132643304	Enhancers	TF binding region	1 gene(s)	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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	19492091	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132643200-132644000	Enhancers	GM12878-XiMat	blood
2	chr4:132643400-132643600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:132643600-132644000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:132643800-132646000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:132644000-132644200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:132645800-132646800	Active TSS	Rectal Mucosa Donor 31	rectum
7	chr4:132646000-132646400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:132646000-132646400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr4:132646000-132646400	Active TSS	Primary T helper cells fromperipheralblood	blood
10	chr4:132646000-132646400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
11	chr4:132646000-132646400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr4:132646000-132646400	Active TSS	Ovary	ovary
13	chr4:132646000-132646400	Active TSS	Stomach Smooth Muscle	stomach
14	chr4:132646000-132647000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:132646200-132646400	ZNF genes & repeats	Gastric	stomach
16	chr4:132646200-132646400	Active TSS	Right Ventricle	heart
17	chr4:132646200-132646600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr4:132648200-132649200	Active TSS	HMEC	breast
19	chr4:132650400-132650600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:132663800-132664000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
21	chr4:132663800-132664000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:132663800-132664000	ZNF genes & repeats	Dnd41	blood
23	chr4:132663800-132664800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr4:132663800-132664800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr4:132664000-132664400	Weak transcription	Dnd41	blood
26	chr4:132664400-132664800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:132664600-132664800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
28	chr4:132664600-132664800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr4:132664800-132671200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:132664800-132671200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr4:132664800-132671200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:132664800-132671200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:132664800-132671200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr4:132671200-132671600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:132671200-132671600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
36	chr4:132671200-132671600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr4:132671200-132671600	ZNF genes & repeats	Placenta	Placenta
38	chr4:132671200-132671800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr4:132671200-132672000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:132671600-132672400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr4:132671600-132672600	Weak transcription	Placenta	Placenta
42	chr4:132685800-132686200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:132694800-132696200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr4:132695200-132696000	Enhancers	NH-A	brain
45	chr4:132695200-132696200	Enhancers	Muscle Satellite Cultured Cells	--
46	chr4:132695400-132695800	Enhancers	Fetal Stomach	stomach
47	chr4:132695400-132696000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:132695400-132696000	Enhancers	HMEC	breast
49	chr4:132695400-132696000	Enhancers	NHEK	skin
50	chr4:132695400-132696200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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