Variant report

Variant	nsv879629
Chromosome Location	chr4:96747135-96818263
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:278)
CpG islands
(count:674)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:278 , 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	chr4:96756891-96757056	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr4:96789068-96789369	HCT-116	colon:	n/a	n/a
3	CBX3	chr4:96789036-96789470	HCT-116	colon:	n/a	n/a
4	CBX3	chr4:96789054-96789386	K562	blood:	n/a	n/a
5	CEBPB	chr4:96809244-96809518	IMR90	lung:	n/a	chr4:96809374-96809385
6	CEBPB	chr4:96791240-96791451	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr4:96809307-96809514	HepG2	liver:	n/a	chr4:96809374-96809385
8	CEBPB	chr4:96781173-96781373	HepG2	liver:	n/a	chr4:96781272-96781281 chr4:96781270-96781281 chr4:96781272-96781281 chr4:96781270-96781283 chr4:96781270-96781283 chr4:96781272-96781281 chr4:96781272-96781281 chr4:96781272-96781283 chr4:96781272-96781283
9	CTCF	chr4:96756960-96757110	GM12865	blood:	n/a	n/a
10	CTCF	chr4:96756920-96757070	NB4	blood:	n/a	n/a
11	CTCF	chr4:96756940-96757090	HEK293	kidney:	n/a	n/a
12	CTCF	chr4:96756986-96757050	GM13976	blood:	n/a	n/a
13	CTCF	chr4:96757020-96757170	GM12868	blood:	n/a	n/a
14	CTCF	chr4:96756920-96757070	HEK293	kidney:	n/a	n/a
15	CTCF	chr4:96756980-96757130	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr4:96756980-96757130	GM12865	blood:	n/a	n/a
17	CTCF	chr4:96756900-96757050	HCT-116	colon:	n/a	n/a
18	CTCF	chr4:96756963-96757084	Spleen_OC	spleen:	n/a	n/a
19	CTCF	chr4:96756976-96757084	LNCaP	prostate:	n/a	n/a
20	CTCF	chr4:96756980-96757130	GM12878	blood:	n/a	n/a
21	CTCF	chr4:96756948-96757089	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr4:96804480-96804630	AG04450	lung:	n/a	n/a
23	CTCF	chr4:96756960-96757110	GM12874	blood:	n/a	n/a
24	CTCF	chr4:96756971-96757100	GM13977	blood:	n/a	n/a
25	CTCF	chr4:96756940-96757090	RPTEC	kidney:	n/a	n/a
26	CTCF	chr4:96756925-96757120	MCF-7	breast:	n/a	n/a
27	CTCF	chr4:96756960-96757110	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr4:96756960-96757110	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr4:96756920-96757070	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr4:96756784-96757181	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:96756980-96757130	HAc	cerebellar:	n/a	n/a
32	CTCF	chr4:96756940-96757090	GM12865	blood:	n/a	n/a
33	CTCF	chr4:96756920-96757070	HVMF	connective:	n/a	n/a
34	CTCF	chr4:96756960-96757110	HL-60	blood:	n/a	n/a
35	CTCF	chr4:96756920-96757070	GM12874	blood:	n/a	n/a
36	CTCF	chr4:96756960-96757110	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr4:96756980-96757130	GM12872	blood:	n/a	n/a
38	CTCF	chr4:96756940-96757090	HCM	heart:	n/a	n/a
39	CTCF	chr4:96756900-96757050	GM12872	blood:	n/a	n/a
40	CTCF	chr4:96756826-96757214	GM12878	blood:	n/a	n/a
41	CTCF	chr4:96756960-96757110	GM12878	blood:	n/a	n/a
42	CTCF	chr4:96757000-96757055	GM10266	blood:	n/a	n/a
43	CTCF	chr4:96808520-96808670	GM12872	blood:	n/a	n/a
44	CTCF	chr4:96756960-96757110	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:96756960-96757110	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr4:96756914-96757140	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr4:96757020-96757170	BJ	skin:	n/a	n/a
48	CTCF	chr4:96756940-96757090	HPF	lung:	n/a	n/a
49	CTCF	chr4:96756937-96757112	Gliobla	brain:	n/a	n/a
50	CTCF	chr4:96756920-96757070	Caco-2	colon:	n/a	n/a

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:96761377-96761427	K562	blood:	n/a
2	chr4:96761231-96761281	GM12878	blood:	n/a
3	chr4:96760945-96760995	LNCaP	prostate:	n/a
4	chr4:96761377-96761427	K562	blood:	n/a
5	chr4:96761231-96761281	GM12878	blood:	n/a
6	chr4:96760945-96760995	LNCaP	prostate:	n/a
7	chr4:96761231-96761281	K562	blood:	n/a
8	chr4:96761231-96761281	HPAEpiC	pulmonary alveolar:	n/a
9	chr4:96760945-96760995	K562	blood:	n/a
10	chr4:96761264-96761314	AG04450	lung:	fetal
11	chr4:96761796-96761846	ProgFib	skin:	n/a
12	chr4:96761231-96761281	HepG2	liver:	n/a
13	chr4:96760014-96760064	HEEpiC	esophagus:	n/a
14	chr4:96761135-96761185	Caco-2	colon:	n/a
15	chr4:96761135-96761185	SKMC	muscle:	n/a
16	chr4:96761231-96761281	HCPEpiC	choroid plexus:	n/a
17	chr4:96761135-96761185	HepG2	liver:	n/a
18	chr4:96760945-96760995	GM12891	blood:	n/a
19	chr4:96761026-96761076	PrEC	prostate:	n/a
20	chr4:96761598-96761648	HEEpiC	esophagus:	n/a
21	chr4:96760945-96760995	HIPEpiC	eye:	n/a
22	chr4:96761231-96761281	HMEC	breast:	n/a
23	chr4:96761796-96761846	ECC-1	luminal epithelium:	n/a
24	chr4:96761135-96761185	NHDF-neo	bronchial:	n/a
25	chr4:96760945-96760995	SK-N-SH_RA	brain:	n/a
26	chr4:96760945-96760995	NH-A	brain:	n/a
27	chr4:96761796-96761846	HCF	heart:	n/a
28	chr4:96760014-96760064	ProgFib	skin:	n/a
29	chr4:96760945-96760995	HCPEpiC	choroid plexus:	n/a
30	chr4:96760945-96760995	CMK	blood:	n/a
31	chr4:96761135-96761185	BJ	skin:	n/a
32	chr4:96761135-96761185	GM12892	blood:	n/a
33	chr4:96761796-96761846	Caco-2	colon:	n/a
34	chr4:96760014-96760064	GM12891	blood:	n/a
35	chr4:96761026-96761076	HRE	kidney:	n/a
36	chr4:96761026-96761076	AoSMC	blood vessel:	n/a
37	chr4:96760014-96760064	ECC-1	luminal epithelium:	n/a
38	chr4:96761231-96761281	LNCaP	prostate:	n/a
39	chr4:96761135-96761185	Hepatocyte	liver:	n/a
40	chr4:96761598-96761648	GM06990	blood:	n/a
41	chr4:96761598-96761648	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:96760945-96760995	HMEC	breast:	n/a
43	chr4:96761264-96761314	HUVEC	blood vessel:	n/a
44	chr4:96760014-96760064	HRPEpiC	eye:	n/a
45	chr4:96760014-96760064	HMEC	breast:	n/a
46	chr4:96761796-96761846	HEK293	kidney:	embryo
47	chr4:96761796-96761846	HMEC	breast:	n/a
48	chr4:96761135-96761185	K562	blood:	n/a
49	chr4:96761559-96761609	PANC-1	pancreas:	n/a
50	chr4:96761559-96761609	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:96817765..96820012-chr4:96825569..96827518,2	K562	blood:
2	chr4:96749923..96752182-chr4:96773061..96775566,2	K562	blood:
3	chr4:96756581..96757503-chr4:96956588..96957342,2	MCF-7	breast:
4	chr4:96749923..96752182-chr4:96773061..96775566,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-1059P	TF binding region
PDHA2	TF binding region
RNU6-1059P	CpG island
PDHA2	CpG island

Extended variants
information (count: 1176 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1176 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10019259	chr4:96747135-96747136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553615416	chr4:96747136-96747137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10019264	chr4:96747153-96747154	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs542016485	chr4:96747173-96747174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561507284	chr4:96747193-96747194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184416593	chr4:96747221-96747222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530879229	chr4:96747230-96747231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573685293	chr4:96747310-96747311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544319905	chr4:96747347-96747348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368944689	chr4:96747348-96747349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546233533	chr4:96747354-96747355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537997735	chr4:96750870-96750871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556238484	chr4:96750900-96750901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1436540	chr4:96750932-96750933	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs545606897	chr4:96750943-96750944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572898677	chr4:96751011-96751012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541798925	chr4:96751031-96751032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555410697	chr4:96751070-96751071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568611331	chr4:96751118-96751119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181736430	chr4:96751162-96751163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10212823	chr4:96751176-96751177	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs5860442	chr4:96751201-96751202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112332994	chr4:96751203-96751204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111956131	chr4:96751204-96751205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140294686	chr4:96751220-96751221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74489746	chr4:96751232-96751233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540208596	chr4:96751240-96751241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186603005	chr4:96751271-96751272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1436539	chr4:96751309-96751310	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs528570505	chr4:96751366-96751367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191510731	chr4:96751371-96751372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115194770	chr4:96751376-96751377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528980444	chr4:96751388-96751389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181111309	chr4:96751389-96751390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs377478171	chr4:96751417-96751418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs17024641	chr4:96751439-96751440	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs116432604	chr4:96751483-96751484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144018234	chr4:96751495-96751496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185119291	chr4:96751497-96751498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189688756	chr4:96751515-96751516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77921706	chr4:96751529-96751530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539615143	chr4:96751532-96751533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377292591	chr4:96751539-96751540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183451082	chr4:96751545-96751546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62309086	chr4:96751559-96751560	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs535560026	chr4:96751589-96751590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs17473405	chr4:96751622-96751623	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs575288066	chr4:96751623-96751624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187690984	chr4:96751627-96751628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs62309087	chr4:96751661-96751662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96746600-96747400	Enhancers	Brain Germinal Matrix	brain
2	chr4:96746800-96747200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr4:96750800-96751600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:96751000-96751400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr4:96751000-96751600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:96751000-96751600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:96751200-96751400	Enhancers	Brain Hippocampus Middle	brain
8	chr4:96751400-96755000	Weak transcription	Brain Hippocampus Middle	brain
9	chr4:96751600-96754800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:96751800-96752200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:96752000-96752400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr4:96752000-96752600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr4:96752200-96752600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr4:96752200-96752600	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr4:96752400-96755000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr4:96752600-96755000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:96752600-96756800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr4:96754800-96755400	Enhancers	Brain Angular Gyrus	brain
19	chr4:96754800-96756000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:96755000-96755200	Enhancers	Brain Substantia Nigra	brain
21	chr4:96755000-96755400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr4:96755000-96755400	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr4:96755000-96755400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:96755000-96755400	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr4:96755000-96755600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr4:96755000-96756000	Enhancers	Brain Hippocampus Middle	brain
27	chr4:96755400-96756600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:96755400-96756800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr4:96755400-96756800	Weak transcription	Brain Substantia Nigra	brain
30	chr4:96756000-96758600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:96756800-96757000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:96756800-96757200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr4:96756800-96757200	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr4:96756800-96757200	Enhancers	Brain Substantia Nigra	brain
35	chr4:96757000-96757200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:96757000-96759200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:96757200-96759400	Weak transcription	Brain Substantia Nigra	brain
38	chr4:96758600-96760200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr4:96758600-96760600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr4:96758600-96760800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr4:96758800-96760200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr4:96758800-96760200	Enhancers	Fetal Heart	heart
43	chr4:96758800-96761000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr4:96759000-96759600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr4:96759200-96760000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:96759200-96760200	Enhancers	H1 Cell Line	embryonic stem cell
47	chr4:96759400-96759600	Enhancers	Brain Substantia Nigra	brain
48	chr4:96759400-96759800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:96759400-96760200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr4:96759400-96760200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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