Variant report

Variant	nsv1010830
Chromosome Location	chr4:96607025-96862878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:775)
CpG islands
(count:794)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:96614717-96615069	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:96614804-96615129	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:96862615-96862654	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:96756891-96757056	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr4:96720077-96720233	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr4:96720028-96720203	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr4:96833916-96833938	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr4:96789068-96789369	HCT-116	colon:	n/a	n/a
9	CBX3	chr4:96789054-96789386	K562	blood:	n/a	n/a
10	CBX3	chr4:96789036-96789470	HCT-116	colon:	n/a	n/a
11	CBX3	chr4:96847445-96847700	K562	blood:	n/a	n/a
12	CEBPB	chr4:96809244-96809518	IMR90	lung:	n/a	chr4:96809374-96809385
13	CEBPB	chr4:96693254-96693466	HepG2	liver:	n/a	chr4:96693362-96693373
14	CEBPB	chr4:96636890-96637488	MCF-7	breast:	n/a	n/a
15	CEBPB	chr4:96636962-96637451	ECC-1	luminal epithelium:	n/a	n/a
16	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
17	CEBPB	chr4:96703666-96703970	HepG2	liver:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
18	CEBPB	chr4:96649198-96649434	HepG2	liver:	n/a	chr4:96649277-96649288 chr4:96649328-96649339
19	CEBPB	chr4:96703580-96703990	A549	lung:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
20	CEBPB	chr4:96719923-96720273	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:96668531-96669056	MCF-7	breast:	n/a	chr4:96669001-96669014
22	CEBPB	chr4:96649188-96649501	A549	lung:	n/a	chr4:96649277-96649288 chr4:96649328-96649339
23	CEBPB	chr4:96703659-96703859	K562	blood:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
24	CEBPB	chr4:96668490-96669010	MCF-7	breast:	n/a	n/a
25	CEBPB	chr4:96637023-96637373	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr4:96702017-96702218	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:96809307-96809514	HepG2	liver:	n/a	chr4:96809374-96809385
28	CEBPB	chr4:96653308-96653672	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr4:96791240-96791451	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr4:96702003-96702220	A549	lung:	n/a	n/a
31	CEBPB	chr4:96703619-96704039	IMR90	lung:	n/a	chr4:96703699-96703710 chr4:96703701-96703710 chr4:96704005-96704016
32	CEBPB	chr4:96702036-96702236	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:96693229-96693518	IMR90	lung:	n/a	chr4:96693362-96693373
34	CEBPB	chr4:96845178-96845472	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:96636884-96637398	MCF-7	breast:	n/a	n/a
36	CHD1	chr4:96719677-96719682	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr4:96723453-96723459	GM12878	blood:	n/a	n/a
38	CHD2	chr4:96719273-96719276	GM12878	blood:	n/a	n/a
39	CTCF	chr4:96756940-96757090	NHEK	skin:	n/a	n/a
40	CTCF	chr4:96756826-96757214	GM12878	blood:	n/a	n/a
41	CTCF	chr4:96756920-96757070	HRE	kidney:	n/a	n/a
42	CTCF	chr4:96797240-96797390	GM12864	blood:	n/a	n/a
43	CTCF	chr4:96756900-96757050	HCT-116	colon:	n/a	n/a
44	CTCF	chr4:96756869-96757153	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr4:96614819-96614938	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr4:96756900-96757050	SAEC	small airway:	n/a	n/a
47	CTCF	chr4:96614840-96614990	NHEK	skin:	n/a	n/a
48	CTCF	chr4:96756940-96757090	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr4:96614800-96614950	HMEC	breast:	n/a	n/a
50	CTCF	chr4:96614820-96614970	AG04450	lung:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:96761377-96761427	IMR90	lung:	fetal
2	chr4:96761377-96761427	IMR90	lung:	fetal
3	chr4:96761229-96761279	ovcar-3	ovarian:	n/a
4	chr4:96761135-96761185	GM12891	blood:	n/a
5	chr4:96836082-96836132	U87	brain:	n/a
6	chr4:96760945-96760995	AG04450	lung:	fetal
7	chr4:96761231-96761281	AG04449	skin:	fetal
8	chr4:96761796-96761846	HCF	heart:	n/a
9	chr4:96761559-96761609	HEEpiC	esophagus:	n/a
10	chr4:96761026-96761076	AG04450	lung:	fetal
11	chr4:96760014-96760064	CMK	blood:	n/a
12	chr4:96761559-96761609	CMK	blood:	n/a
13	chr4:96761377-96761427	U87	brain:	n/a
14	chr4:96678053-96678103	NB4	blood:	n/a
15	chr4:96761264-96761314	PFSK-1	brain:	n/a
16	chr4:96760945-96760995	NB4	blood:	n/a
17	chr4:96761231-96761281	ovcar-3	ovarian:	n/a
18	chr4:96761796-96761846	AG09309	skin:	n/a
19	chr4:96761264-96761314	GM06990	blood:	n/a
20	chr4:96678053-96678103	AG10803	skin:	n/a
21	chr4:96761231-96761281	GM12878	blood:	n/a
22	chr4:96761796-96761846	GM12892	blood:	n/a
23	chr4:96761135-96761185	GM06990	blood:	n/a
24	chr4:96761796-96761846	GM19239	blood:	n/a
25	chr4:96836082-96836132	ovcar-3	ovarian:	n/a
26	chr4:96678053-96678103	Caco-2	colon:	n/a
27	chr4:96760945-96760995	NHBE	bronchial:	n/a
28	chr4:96761231-96761281	SK-N-SH_RA	brain:	n/a
29	chr4:96836082-96836132	HEEpiC	esophagus:	n/a
30	chr4:96678053-96678103	CMK	blood:	n/a
31	chr4:96761598-96761648	HCPEpiC	choroid plexus:	n/a
32	chr4:96836082-96836132	HMEC	breast:	n/a
33	chr4:96760945-96760995	SK-N-SH	brain:	n/a
34	chr4:96836082-96836132	HCM	heart:	n/a
35	chr4:96761796-96761846	NB4	blood:	n/a
36	chr4:96761229-96761279	AG10803	skin:	n/a
37	chr4:96761598-96761648	GM19239	blood:	n/a
38	chr4:96761229-96761279	HIPEpiC	eye:	n/a
39	chr4:96760014-96760064	AG04450	lung:	fetal
40	chr4:96836082-96836132	CMK	blood:	n/a
41	chr4:96761559-96761609	NHBE	bronchial:	n/a
42	chr4:96761598-96761648	HIPEpiC	eye:	n/a
43	chr4:96678053-96678103	NHDF-neo	bronchial:	n/a
44	chr4:96761231-96761281	SK-N-SH	brain:	n/a
45	chr4:96760014-96760064	IMR90	lung:	fetal
46	chr4:96761598-96761648	HRE	kidney:	n/a
47	chr4:96761026-96761076	PrEC	prostate:	n/a
48	chr4:96761026-96761076	LNCaP	prostate:	n/a
49	chr4:96761026-96761076	ovcar-3	ovarian:	n/a
50	chr4:96761264-96761314	AG04449	skin:	fetal

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:96756581..96757503-chr4:96956588..96957342,2	MCF-7	breast:
2	chr4:96614781..96615424-chr4:97273090..97273698,2	MCF-7	breast:
3	chr4:96749923..96752182-chr4:96773061..96775566,2	K562	blood:
4	chr4:96817765..96820012-chr4:96825569..96827518,2	K562	blood:
5	chr4:96720160..96722789-chr4:96726350..96727999,2	K562	blood:
6	chr4:96720160..96722789-chr4:96726350..96727999,2	K562	blood:
7	chr4:96822970..96824843-chr4:96830954..96833894,2	K562	blood:
8	chr4:96674646..96677370-chr4:96678560..96681527,2	MCF-7	breast:
9	chr4:96669276..96670825-chr4:96677264..96679662,2	MCF-7	breast:
10	chr4:96822970..96824843-chr4:96830954..96833894,2	K562	blood:
11	chr4:96749923..96752182-chr4:96773061..96775566,2	K562	blood:
12	chr4:96669276..96670825-chr4:96677264..96679662,2	MCF-7	breast:
13	chr4:96674646..96677370-chr4:96678560..96681527,2	MCF-7	breast:
14	chr4:96817765..96820012-chr4:96825569..96827518,2	K562	blood:

No data

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

Extended variants
information (count: 5630 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5630 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185668831	chr4:96610618-96610619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs13112339	chr4:96610670-96610671	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs560008387	chr4:96610686-96610687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573630117	chr4:96610687-96610688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542387833	chr4:96610696-96610697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs56349891	chr4:96610717-96610718	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs531271500	chr4:96610718-96610719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs13112562	chr4:96610719-96610720	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs564678074	chr4:96610742-96610743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527275794	chr4:96610760-96610761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73842146	chr4:96610846-96610847	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs557147503	chr4:96610883-96610884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567148371	chr4:96610910-96610911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116380756	chr4:96610918-96610919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548091024	chr4:96613017-96613018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs10024303	chr4:96613063-96613064	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs530112308	chr4:96613091-96613092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548642253	chr4:96613117-96613118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376107247	chr4:96613200-96613201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561029615	chr4:96613237-96613238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530162072	chr4:96613238-96613239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550115368	chr4:96613264-96613265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10024516	chr4:96613274-96613275	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs191706201	chr4:96613286-96613287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551089522	chr4:96613328-96613329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112481823	chr4:96613350-96613351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559031432	chr4:96613360-96613361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534797144	chr4:96613408-96613409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184637589	chr4:96613423-96613424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369407032	chr4:96613463-96613464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574558872	chr4:96613481-96613482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567742448	chr4:96613497-96613498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571320590	chr4:96613498-96613499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189524061	chr4:96613505-96613506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192175827	chr4:96613510-96613511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538683195	chr4:96613519-96613520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545828686	chr4:96613552-96613553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565227712	chr4:96613568-96613569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142247456	chr4:96615015-96615016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs72884050	chr4:96615035-96615036	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs532816245	chr4:96615079-96615080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1579619	chr4:96615082-96615083	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs566270224	chr4:96615098-96615099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73842148	chr4:96615101-96615102	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs191037343	chr4:96615154-96615155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115451602	chr4:96615159-96615160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568629587	chr4:96615164-96615165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73842149	chr4:96615180-96615181	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs553593393	chr4:96615215-96615216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557229354	chr4:96615237-96615238	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96610600-96610800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:96610600-96611000	Enhancers	Right Atrium	heart
3	chr4:96613000-96613600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:96615000-96616800	Enhancers	HUVEC	blood vessel
5	chr4:96616800-96622200	Weak transcription	HUVEC	blood vessel
6	chr4:96617800-96618400	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr4:96618400-96618800	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr4:96619200-96620800	Enhancers	Dnd41	blood
9	chr4:96621000-96622600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:96622000-96622400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
11	chr4:96622200-96622400	Enhancers	Ovary	ovary
12	chr4:96622200-96622600	Enhancers	HSMMtube	muscle
13	chr4:96622200-96623600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:96622200-96623600	Enhancers	HUVEC	blood vessel
15	chr4:96622400-96622600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr4:96622400-96623400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:96622400-96623600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr4:96622400-96623600	Enhancers	HSMM	muscle
19	chr4:96622600-96622800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr4:96622600-96623200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:96622600-96623600	Enhancers	HMEC	breast
22	chr4:96622600-96623800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:96622800-96623200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr4:96622800-96623200	Enhancers	NH-A	brain
25	chr4:96622800-96623400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr4:96622800-96623400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:96623000-96623200	Enhancers	Ovary	ovary
28	chr4:96623000-96623400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr4:96623000-96623400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr4:96623000-96623400	Enhancers	Rectal Smooth Muscle	rectum
31	chr4:96623200-96623600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr4:96623200-96623600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr4:96623800-96628000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:96628000-96628200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:96628200-96628400	Enhancers	Aorta	Aorta
36	chr4:96628200-96629000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:96629000-96629200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:96632800-96636400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:96635000-96636600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:96636400-96637600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr4:96636600-96637400	Enhancers	HMEC	breast
42	chr4:96636800-96637400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:96637000-96637600	Enhancers	Placenta Amnion	Placenta Amnion
44	chr4:96637400-96638400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr4:96638400-96638600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr4:96647400-96647600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr4:96647400-96648200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:96647600-96650200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr4:96648200-96648400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr4:96648600-96649200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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