Variant report

Variant	nsv881303
Chromosome Location	chr4:165746041-165809314
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:359)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:165797902-165798295	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr4:165798206-165798475	GM12878	blood:	n/a	n/a
3	CEBPB	chr4:165801664-165801932	HepG2	liver:	n/a	chr4:165801839-165801856 chr4:165801842-165801855 chr4:165801797-165801808
4	CEBPB	chr4:165802030-165802424	MCF-7	breast:	n/a	n/a
5	CEBPB	chr4:165801600-165801995	H1-hESC	embryonic stem cell:	n/a	chr4:165801839-165801856 chr4:165801842-165801855 chr4:165801797-165801808
6	CEBPB	chr4:165787890-165788501	H1-hESC	embryonic stem cell:	n/a	chr4:165788490-165788498
7	CHD1	chr4:165801109-165801557	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD1	chr4:165798069-165800388	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD1	chr4:165800716-165800843	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr4:165798043-165798606	GM12878	blood:	n/a	n/a
11	CHD2	chr4:165801727-165801927	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr4:165777004-165777041	MCF-7	breast:	n/a	n/a
13	CTCF	chr4:165805297-165805503	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr4:165808228-165808276	GM20000	blood:	n/a	n/a
15	CTCF	chr4:165805340-165805490	HMEC	breast:	n/a	n/a
16	CTCF	chr4:165805380-165805530	GM12875	blood:	n/a	n/a
17	CTCF	chr4:165805330-165805562	Gliobla	brain:	n/a	n/a
18	CTCF	chr4:165805340-165805490	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr4:165805360-165805510	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr4:165805300-165805450	GM12870	blood:	n/a	n/a
21	CTCF	chr4:165805360-165805510	HRE	kidney:	n/a	n/a
22	CTCF	chr4:165805570-165805604	Lung_OC	lung:	n/a	n/a
23	CTCF	chr4:165805336-165805508	HepG2	liver:	n/a	n/a
24	CTCF	chr4:165805400-165805550	GM12866	blood:	n/a	n/a
25	CTCF	chr4:165805400-165805550	K562	blood:	n/a	n/a
26	CTCF	chr4:165805380-165805530	Caco-2	colon:	n/a	n/a
27	CTCF	chr4:165805318-165805555	HepG2	liver:	n/a	n/a
28	CTCF	chr4:165805320-165805470	AG10803	skin:	n/a	n/a
29	CTCF	chr4:165805342-165805547	LNCaP	prostate:	n/a	n/a
30	CTCF	chr4:165805320-165805470	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr4:165805340-165805490	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr4:165805360-165805510	HMEC	breast:	n/a	n/a
33	CTCF	chr4:165805420-165805570	HVMF	connective:	n/a	n/a
34	CTCF	chr4:165805400-165805498	NHEK	skin:	n/a	n/a
35	CTCF	chr4:165805360-165805510	AG10803	skin:	n/a	n/a
36	CTCF	chr4:165805340-165805490	GM12872	blood:	n/a	n/a
37	CTCF	chr4:165805380-165805530	RPTEC	kidney:	n/a	n/a
38	CTCF	chr4:165805320-165805470	GM12873	blood:	n/a	n/a
39	CTCF	chr4:165805340-165805490	AG09309	skin:	n/a	n/a
40	CTCF	chr4:165805319-165805560	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:165805340-165805490	HAc	cerebellar:	n/a	n/a
42	CTCF	chr4:165805340-165805490	GM12867	blood:	n/a	n/a
43	CTCF	chr4:165805360-165805510	GM12878	blood:	n/a	n/a
44	CTCF	chr4:165773537-165773575	GM10248	blood:	n/a	n/a
45	CTCF	chr4:165805323-165805526	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr4:165805324-165805555	GM10266	blood:	n/a	n/a
47	CTCF	chr4:165805340-165805490	GM12873	blood:	n/a	n/a
48	CTCF	chr4:165805340-165805490	AG04449	skin:	n/a	n/a
49	CTCF	chr4:165777004-165777018	GM19240	blood:	n/a	n/a
50	CTCF	chr4:165805316-165805561	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:165770585-165770635	SAEC	small airway:	n/a
2	chr4:165798316-165798366	AG04449	skin:	fetal
3	chr4:165798316-165798366	PANC-1	pancreas:	n/a
4	chr4:165749663-165749713	PANC-1	pancreas:	n/a
5	chr4:165770585-165770635	NT2-D1	testis:	n/a
6	chr4:165749663-165749713	IMR90	lung:	fetal
7	chr4:165770585-165770635	K562	blood:	n/a
8	chr4:165770585-165770635	AG04449	skin:	fetal
9	chr4:165798316-165798366	PFSK-1	brain:	n/a
10	chr4:165770585-165770635	GM12892	blood:	n/a
11	chr4:165749663-165749713	H1-hESC	embryonic stem cell:	embryo
12	chr4:165798316-165798366	ECC-1	luminal epithelium:	n/a
13	chr4:165749663-165749713	HIPEpiC	eye:	n/a
14	chr4:165798316-165798366	U87	brain:	n/a
15	chr4:165798316-165798366	Caco-2	colon:	n/a
16	chr4:165798316-165798366	NB4	blood:	n/a
17	chr4:165798316-165798366	BJ	skin:	n/a
18	chr4:165770585-165770635	AG10803	skin:	n/a
19	chr4:165770585-165770635	HCT-116	colon:	n/a
20	chr4:165770585-165770635	SK-N-MC	brain:	n/a
21	chr4:165749663-165749713	AG09319	gingival:	n/a
22	chr4:165770585-165770635	H1-hESC	embryonic stem cell:	embryo
23	chr4:165798316-165798366	HEK293	kidney:	embryo
24	chr4:165749663-165749713	NT2-D1	testis:	n/a
25	chr4:165798316-165798366	AG04450	lung:	fetal
26	chr4:165770585-165770635	BE2_C	brain:	n/a
27	chr4:165770585-165770635	NHDF-neo	bronchial:	n/a
28	chr4:165749663-165749713	MCF-7	breast:	n/a
29	chr4:165770585-165770635	Hepatocyte	liver:	n/a
30	chr4:165749663-165749713	HCF	heart:	n/a
31	chr4:165798316-165798366	AG09309	skin:	n/a
32	chr4:165798316-165798366	SK-N-SH	brain:	n/a
33	chr4:165749663-165749713	GM12892	blood:	n/a
34	chr4:165770585-165770635	HIPEpiC	eye:	n/a
35	chr4:165798316-165798366	GM19239	blood:	n/a
36	chr4:165798316-165798366	HEEpiC	esophagus:	n/a
37	chr4:165770585-165770635	BJ	skin:	n/a
38	chr4:165749663-165749713	HCPEpiC	choroid plexus:	n/a
39	chr4:165749663-165749713	NHBE	bronchial:	n/a
40	chr4:165770585-165770635	HL-60	blood:	n/a
41	chr4:165798316-165798366	SK-N-MC	brain:	n/a
42	chr4:165749663-165749713	MCF10A-Er-Src	breast:	n/a
43	chr4:165798316-165798366	A549	lung:	n/a
44	chr4:165749663-165749713	HMEC	breast:	n/a
45	chr4:165749663-165749713	RPTEC	kidney:	n/a
46	chr4:165749663-165749713	AoSMC	blood vessel:	n/a
47	chr4:165798316-165798366	HAEpiC	amniotic membrane:	n/a
48	chr4:165770585-165770635	HEEpiC	esophagus:	n/a
49	chr4:165770585-165770635	AoSMC	blood vessel:	n/a
50	chr4:165770585-165770635	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:165772859..165774381-chr4:165791100..165793270,2	MCF-7	breast:
2	chr4:165800303..165802984-chr4:165804742..165807562,2	K562	blood:
3	chr4:165786297..165787799-chr4:165799445..165800981,2	MCF-7	breast:
4	chr4:165700977..165701537-chr4:165804617..165805893,3	MCF-7	breast:
5	chr4:165800303..165802984-chr4:165804742..165807562,2	K562	blood:
6	chr4:165772859..165774381-chr4:165791100..165793270,2	MCF-7	breast:
7	chr4:165786297..165787799-chr4:165799445..165800981,2	MCF-7	breast:
8	chr4:165700661..165701216-chr4:165804953..165805488,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf39-1	chr4:165798346-165798559	ENSG00000248329
2	lnc-C4orf39-1	chr4:165800023-165800066	FPKM1_group_24404_transcript_2
3	lnc-C4orf39-1	chr4:165798156-165798559	ENSG00000248329
4	lnc-C4orf39-1	chr4:165798394-165798559	ENSG00000248329
5	lnc-C4orf39-1	chr4:165798156-165798559	NONHSAT099080
6	lnc-C4orf39-1	chr4:165800072-165800161	NONHSAT099080
7	lnc-C4orf39-1	chr4:165798158-165798562	FPKM1_group_24404_transcript_2
8	lnc-C4orf39-1	chr4:165800072-165800161	ENSG00000248329
9	lnc-C4orf39-1	chr4:165800072-165800408	ENSG00000248329
10	lnc-C4orf39-1	chr4:165800072-165800161	ENSG00000248329

No data

Variant related genes	Relation type
ENSG00000248329	TF binding region
ENSG00000248329	CpG island
VANGL1	miRNA target sites
NSF	miRNA target sites
DENR	miRNA target sites
FANCC	miRNA target sites
EZH2	miRNA target sites

Extended variants
information (count: 2343 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2343 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12500207	chr4:165746041-165746042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147354454	chr4:165746060-165746061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529528792	chr4:165746074-165746075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547824426	chr4:165746078-165746079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562941614	chr4:165746122-165746123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530524395	chr4:165746123-165746124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551948220	chr4:165746131-165746132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570642985	chr4:165746145-165746146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191285595	chr4:165746184-165746185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546754649	chr4:165746193-165746194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574025352	chr4:165746209-165746210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568301992	chr4:165746210-165746211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6536869	chr4:165746214-165746215	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs181012232	chr4:165746216-165746217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs28594917	chr4:165746228-165746229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35875470	chr4:165746232-165746233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs137857195	chr4:165746275-165746276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114390967	chr4:165746276-165746277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374040050	chr4:165746278-165746279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555248796	chr4:165746289-165746290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573266605	chr4:165746301-165746302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540504537	chr4:165746372-165746373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562299252	chr4:165746391-165746392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141693694	chr4:165746522-165746523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs72695856	chr4:165746523-165746524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185218100	chr4:165746551-165746552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540466849	chr4:165746599-165746600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376809897	chr4:165746603-165746604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550557660	chr4:165746604-165746605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs70952652	chr4:165746610-165746611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150527200	chr4:165746616-165746617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139507641	chr4:165746618-165746619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558159185	chr4:165746676-165746677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552272530	chr4:165746700-165746701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191208276	chr4:165746744-165746745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183331653	chr4:165746778-165746779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149832892	chr4:165746837-165746838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113200702	chr4:165746838-165746839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187707515	chr4:165746916-165746917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144785152	chr4:165746949-165746950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550857858	chr4:165746968-165746969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569294850	chr4:165746998-165746999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372450389	chr4:165747015-165747016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558116746	chr4:165747018-165747019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4692012	chr4:165747026-165747027	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs534297409	chr4:165747052-165747053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555686493	chr4:165747094-165747095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573856932	chr4:165747099-165747100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544522389	chr4:165747117-165747118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564999145	chr4:165747118-165747119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Breast cancer	17603634	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	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
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
Congenital diaphragmatic hernia	21085971	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
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165737000-165749000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:165741600-165748800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr4:165742000-165749000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:165743600-165746800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr4:165743800-165746800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr4:165743800-165749200	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr4:165744000-165748800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr4:165744200-165748800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr4:165744200-165748800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr4:165744400-165749000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr4:165744400-165749000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:165746000-165748800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr4:165746800-165747200	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr4:165746800-165747200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:165747200-165748600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr4:165747200-165748800	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr4:165748600-165749600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr4:165748800-165749000	Enhancers	H9 Cell Line	embryonic stem cell
19	chr4:165748800-165749000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr4:165748800-165749600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr4:165748800-165749600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr4:165748800-165749600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr4:165748800-165750000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr4:165749000-165749200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:165749000-165749400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr4:165749000-165749600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr4:165749000-165749800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:165749000-165751600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr4:165749200-165749600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr4:165749200-165749600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:165749600-165749800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:165749800-165765400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:165752400-165752600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr4:165753800-165754600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr4:165764200-165765600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr4:165764600-165764800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr4:165764600-165765000	Enhancers	H9 Cell Line	embryonic stem cell
38	chr4:165764600-165765000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr4:165764600-165765600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr4:165764600-165765800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr4:165764600-165765800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr4:165764600-165765800	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr4:165764800-165765800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr4:165765000-165765400	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr4:165765000-165765400	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr4:165765400-165765600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr4:165765400-165765600	Enhancers	H9 Cell Line	embryonic stem cell
48	chr4:165765400-165765600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr4:165765400-165765800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:165765600-165765800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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