Variant report

Variant	nsv879631
Chromosome Location	chr4:97114706-97263153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:184)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:283 , 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	BACH1	chr4:97219633-97219647	K562	blood:	n/a	n/a
2	BATF	chr4:97181320-97181623	GM12878	blood:	n/a	n/a
3	CCNT2	chr4:97232230-97232431	K562	blood:	n/a	n/a
4	CEBPB	chr4:97181245-97181515	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr4:97232224-97232424	HepG2	liver:	n/a	chr4:97232323-97232334
6	CEBPB	chr4:97121791-97122057	HepG2	liver:	n/a	chr4:97121932-97121945 chr4:97121932-97121945 chr4:97121933-97121944
7	CEBPB	chr4:97169804-97170043	HepG2	liver:	n/a	chr4:97169952-97169963
8	CEBPB	chr4:97121782-97122027	K562	blood:	n/a	chr4:97121932-97121945 chr4:97121932-97121945 chr4:97121933-97121944
9	CEBPB	chr4:97169823-97170116	IMR90	lung:	n/a	chr4:97169952-97169963
10	CEBPB	chr4:97212163-97212391	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:97196970-97197200	IMR90	lung:	n/a	chr4:97197086-97197097 chr4:97197086-97197099 chr4:97197088-97197099
12	CEBPB	chr4:97196996-97197265	HepG2	liver:	n/a	chr4:97197086-97197097 chr4:97197086-97197099 chr4:97197088-97197099
13	CEBPZ	chr4:97142345-97142434	HepG2	liver:	n/a	n/a
14	CHD2	chr4:97148728-97148991	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr4:97181136-97181419	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr4:97208240-97208390	BJ	skin:	n/a	n/a
17	CTCF	chr4:97149800-97149950	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:97149760-97149910	MCF-7	breast:	n/a	n/a
19	CTCF	chr4:97215300-97215450	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr4:97149720-97149870	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr4:97236100-97236250	AG10803	skin:	n/a	n/a
22	CTCF	chr4:97218381-97218400	GM13977	blood:	n/a	n/a
23	CTCF	chr4:97185140-97185290	K562	blood:	n/a	n/a
24	CTCF	chr4:97149816-97149926	MCF-7	breast:	n/a	n/a
25	CTCF	chr4:97149760-97149910	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr4:97149746-97150037	GM12878	blood:	n/a	n/a
27	CTCF	chr4:97253051-97253085	GM10266	blood:	n/a	n/a
28	CTCF	chr4:97149740-97149890	HCT-116	colon:	n/a	n/a
29	CTCF	chr4:97149860-97150010	HEK293	kidney:	n/a	n/a
30	CTCF	chr4:97149806-97149963	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:97240429-97240511	Medullo	brain:	n/a	n/a
32	CUX1	chr4:97220938-97220944	GM12878	blood:	n/a	n/a
33	E2F4	chr4:97164842-97164849	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr4:97159747-97159877	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr4:97231416-97231604	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr4:97219961-97220271	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr4:97154282-97154437	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr4:97121319-97121407	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr4:97255051-97255216	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr4:97140627-97140736	MCF10A-Er-Src	breast:	n/a	n/a
41	EBF1	chr4:97237065-97237135	GM12878	blood:	n/a	chr4:97237097-97237108
42	EGR1	chr4:97149652-97150139	MCF-7	breast:	n/a	n/a
43	EGR1	chr4:97149622-97150148	HCT-116	colon:	n/a	n/a
44	EGR1	chr4:97149617-97150082	MCF-7	breast:	n/a	n/a
45	ELF1	chr4:97149606-97149993	MCF-7	breast:	n/a	n/a
46	ELF1	chr4:97149509-97150091	MCF-7	breast:	n/a	n/a
47	EP300	chr4:97117755-97117756	GM12878	blood:	n/a	n/a
48	EP300	chr4:97117354-97118151	ECC-1	luminal epithelium:	n/a	n/a
49	EP300	chr4:97226021-97226772	SK-N-SH	brain:	n/a	chr4:97226725-97226735 chr4:97226140-97226154
50	EP300	chr4:97148661-97149093	H1-hESC	embryonic stem cell:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:97148730-97148780	HMEC	breast:	n/a
2	chr4:97148730-97148780	HMEC	breast:	n/a
3	chr4:97148730-97148780	HRPEpiC	eye:	n/a
4	chr4:97141368-97141418	NHBE	bronchial:	n/a
5	chr4:97141368-97141418	GM12892	blood:	n/a
6	chr4:97182116-97182166	HEK293	kidney:	embryo
7	chr4:97141368-97141418	PFSK-1	brain:	n/a
8	chr4:97141368-97141418	GM19239	blood:	n/a
9	chr4:97148730-97148780	AG10803	skin:	n/a
10	chr4:97141368-97141418	MCF10A-Er-Src	breast:	n/a
11	chr4:97141368-97141418	Jurkat	blood:	n/a
12	chr4:97182116-97182166	NH-A	brain:	n/a
13	chr4:97182116-97182166	H1-hESC	embryonic stem cell:	embryo
14	chr4:97182116-97182166	IMR90	lung:	fetal
15	chr4:97141368-97141418	GM12878	blood:	n/a
16	chr4:97141368-97141418	HCT-116	colon:	n/a
17	chr4:97141368-97141418	RPTEC	kidney:	n/a
18	chr4:97182116-97182166	HCM	heart:	n/a
19	chr4:97141368-97141418	HMEC	breast:	n/a
20	chr4:97148730-97148780	Hela-S3	cervix:	n/a
21	chr4:97141368-97141418	PANC-1	pancreas:	n/a
22	chr4:97148730-97148780	GM19239	blood:	n/a
23	chr4:97182116-97182166	NB4	blood:	n/a
24	chr4:97148730-97148780	T-47D	breast:	n/a
25	chr4:97141368-97141418	ovcar-3	ovarian:	n/a
26	chr4:97148730-97148780	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:97141368-97141418	SK-N-SH	brain:	n/a
28	chr4:97148730-97148780	SKMC	muscle:	n/a
29	chr4:97148730-97148780	SAEC	small airway:	n/a
30	chr4:97182116-97182166	HL-60	blood:	n/a
31	chr4:97148730-97148780	AG09319	gingival:	n/a
32	chr4:97182116-97182166	PANC-1	pancreas:	n/a
33	chr4:97141368-97141418	SKMC	muscle:	n/a
34	chr4:97148730-97148780	A549	lung:	n/a
35	chr4:97141368-97141418	AG09309	skin:	n/a
36	chr4:97148730-97148780	HIPEpiC	eye:	n/a
37	chr4:97182116-97182166	AG10803	skin:	n/a
38	chr4:97148730-97148780	HL-60	blood:	n/a
39	chr4:97182116-97182166	SAEC	small airway:	n/a
40	chr4:97141368-97141418	ECC-1	luminal epithelium:	n/a
41	chr4:97148730-97148780	ProgFib	skin:	n/a
42	chr4:97141368-97141418	HEK293	kidney:	embryo
43	chr4:97182116-97182166	HCPEpiC	choroid plexus:	n/a
44	chr4:97182116-97182166	HRPEpiC	eye:	n/a
45	chr4:97182116-97182166	SK-N-MC	brain:	n/a
46	chr4:97141368-97141418	U87	brain:	n/a
47	chr4:97182116-97182166	RPTEC	kidney:	n/a
48	chr4:97182116-97182166	LNCaP	prostate:	n/a
49	chr4:97148730-97148780	MCF10A-Er-Src	breast:	n/a
50	chr4:97141368-97141418	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:97204222..97205966-chr4:97206787..97209522,2	K562	blood:
2	chr4:97103707..97106316-chr4:97112297..97115167,2	K562	blood:
3	chr4:97174563..97176732-chr4:97282381..97284958,2	K562	blood:
4	chr4:97204222..97205966-chr4:97206787..97209522,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDHA2-1	chr4:97231883-97231945	ENSG00000248510
2	lnc-PDHA2-3	chr4:97133430-97134251	NONHSAT097469

No data

Variant related genes	Relation type
ENSG00000250655	TF binding region
ENSG00000248510	TF binding region
ENSG00000250655	CpG island
ENSG00000248510	CpG island

Extended variants
information (count: 2617 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2617 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6532594	chr4:97114706-97114707	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576899318	chr4:97114769-97114770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186122701	chr4:97116037-97116038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535279675	chr4:97116048-97116049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190602918	chr4:97116202-97116203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576911776	chr4:97116216-97116217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556855870	chr4:97116264-97116265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539392309	chr4:97116306-97116307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552677908	chr4:97116331-97116332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572725358	chr4:97116332-97116333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541356537	chr4:97116377-97116378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551755091	chr4:97116436-97116437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554782911	chr4:97116464-97116465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575147101	chr4:97116514-97116515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574648214	chr4:97116575-97116576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140810560	chr4:97117816-97117817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533088412	chr4:97117838-97117839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs78172707	chr4:97117858-97117859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73842457	chr4:97117866-97117867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191805471	chr4:97117875-97117876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535053004	chr4:97117934-97117935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548485811	chr4:97117947-97117948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182495390	chr4:97117969-97117970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537327933	chr4:97117974-97117975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140885732	chr4:97117976-97117977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373477482	chr4:97118002-97118003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78587588	chr4:97118003-97118004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547527268	chr4:97118088-97118089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74797393	chr4:97118181-97118182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539933975	chr4:97118182-97118183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553146075	chr4:97118189-97118190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527336996	chr4:97118195-97118196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543479924	chr4:97132649-97132650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186356091	chr4:97132673-97132674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs195697	chr4:97132695-97132696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139304320	chr4:97132756-97132757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577250894	chr4:97132757-97132758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546078804	chr4:97132769-97132770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1820369	chr4:97132784-97132785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1820368	chr4:97132787-97132788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34739838	chr4:97132802-97132803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561111436	chr4:97132832-97132833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186803789	chr4:97132854-97132855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528268264	chr4:97132945-97132946	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs140598495	chr4:97132946-97132947	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs150414841	chr4:97132950-97132951	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs190057299	chr4:97133014-97133015	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs530608567	chr4:97133029-97133030	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs540646254	chr4:97133041-97133042	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs138131662	chr4:97133042-97133043	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	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
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20688739	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:97114200-97114800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr4:97116000-97116400	Enhancers	Fetal Heart	heart
3	chr4:97116000-97116600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr4:97116200-97116600	Enhancers	HSMMtube	muscle
5	chr4:97117800-97118200	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr4:97132600-97133200	Enhancers	Dnd41	blood
7	chr4:97132600-97133800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:97132800-97133600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:97133200-97133600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:97133600-97137600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:97137600-97138600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:97138000-97138400	Enhancers	Stomach Mucosa	stomach
13	chr4:97138000-97139000	Enhancers	Brain Germinal Matrix	brain
14	chr4:97141200-97141600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr4:97141200-97141800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr4:97141200-97141800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr4:97141200-97142400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:97141400-97141800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:97141600-97141800	Enhancers	Brain Cingulate Gyrus	brain
20	chr4:97141600-97142400	Enhancers	H9 Cell Line	embryonic stem cell
21	chr4:97148600-97149400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr4:97148600-97149800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:97149000-97149400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr4:97149000-97150000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr4:97149000-97150000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr4:97149200-97149800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr4:97149800-97150000	Enhancers	H9 Cell Line	embryonic stem cell
28	chr4:97158000-97158400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
29	chr4:97158400-97158600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:97161200-97161600	Enhancers	Fetal Lung	lung
31	chr4:97164600-97167000	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr4:97172000-97172200	Enhancers	Gastric	stomach
33	chr4:97172200-97183200	Weak transcription	Gastric	stomach
34	chr4:97176200-97176600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr4:97176600-97181200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr4:97181000-97182600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr4:97181000-97184200	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr4:97181200-97181400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr4:97181200-97181800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr4:97181200-97182000	Enhancers	Fetal Intestine Large	intestine
41	chr4:97181200-97182600	Enhancers	H1 Cell Line	embryonic stem cell
42	chr4:97181200-97182600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr4:97181200-97183000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr4:97181200-97183200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr4:97181400-97181600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr4:97181400-97181600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:97181400-97182600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr4:97181400-97183200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr4:97181600-97182400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:97181600-97185000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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