Variant report

Variant	nsv879647
Chromosome Location	chr4:98435389-98569259
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:324)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr4:98508998-98509375	GM12878	blood:	n/a	n/a
2	CEBPB	chr4:98503490-98503558	H1-hESC	embryonic stem cell:	n/a	chr4:98503500-98503511 chr4:98503499-98503512
3	CEBPB	chr4:98550616-98550860	A549	lung:	n/a	n/a
4	CEBPB	chr4:98503368-98503620	HepG2	liver:	n/a	chr4:98503500-98503511 chr4:98503499-98503512
5	CEBPB	chr4:98550602-98550799	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr4:98511464-98511776	MCF-7	breast:	n/a	n/a
7	CEBPB	chr4:98539500-98539574	H1-hESC	embryonic stem cell:	n/a	chr4:98539512-98539523
8	CEBPB	chr4:98467950-98468187	HepG2	liver:	n/a	chr4:98468073-98468084
9	CEBPB	chr4:98510925-98511719	MCF-7	breast:	n/a	n/a
10	CEBPB	chr4:98539434-98539658	HepG2	liver:	n/a	chr4:98539512-98539523
11	CEBPB	chr4:98510992-98511342	MCF-7	breast:	n/a	n/a
12	CEBPB	chr4:98467897-98468197	IMR90	lung:	n/a	chr4:98468073-98468084
13	CEBPB	chr4:98551808-98552192	Hela-S3	cervix:	n/a	n/a
14	CHD1	chr4:98522881-98522890	GM12878	blood:	n/a	n/a
15	CTCF	chr4:98470160-98470310	MCF-7	breast:	n/a	n/a
16	CTCF	chr4:98470332-98470380	LNCaP	prostate:	n/a	n/a
17	CTCF	chr4:98470220-98470370	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr4:98528859-98528993	MCF-7	breast:	n/a	n/a
19	CTCF	chr4:98509180-98509330	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr4:98470160-98470310	BE2_C	brain:	n/a	n/a
21	CTCF	chr4:98470240-98470390	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr4:98470240-98470390	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr4:98528780-98528930	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:98470260-98470410	HMEC	breast:	n/a	n/a
25	CTCF	chr4:98470220-98470370	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr4:98470200-98470350	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr4:98470280-98470430	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr4:98470220-98470370	HMEC	breast:	n/a	n/a
29	CTCF	chr4:98568740-98568890	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr4:98528780-98528930	BE2_C	brain:	n/a	n/a
31	CTCF	chr4:98470340-98470490	RPTEC	kidney:	n/a	n/a
32	CTCF	chr4:98470240-98470390	HCFaa	heart:	n/a	n/a
33	CTCF	chr4:98470220-98470370	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr4:98470287-98470384	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr4:98487508-98487591	LNCaP	prostate:	n/a	n/a
36	CTCF	chr4:98470220-98470370	NHEK	skin:	n/a	n/a
37	CTCF	chr4:98470254-98470361	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:98450689-98450738	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr4:98470160-98470310	NHEK	skin:	n/a	n/a
40	CTCF	chr4:98470220-98470370	HRE	kidney:	n/a	n/a
41	CTCF	chr4:98528860-98529010	A549	lung:	n/a	n/a
42	CTCF	chr4:98452840-98452878	GM13976	blood:	n/a	n/a
43	CTCF	chr4:98470280-98470430	HCT-116	colon:	n/a	n/a
44	CTCF	chr4:98470200-98470350	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr4:98492982-98493028	Lung_OC	lung:	n/a	n/a
46	CTCF	chr4:98470160-98470310	HAc	cerebellar:	n/a	n/a
47	CTCF	chr4:98470220-98470370	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:98470260-98470410	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr4:98470260-98470410	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr4:98470240-98470390	HEEpiC	esophagus:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:98479820-98479870	IMR90	lung:	fetal
2	chr4:98479820-98479870	PrEC	prostate:	n/a
3	chr4:98479820-98479870	GM12892	blood:	n/a
4	chr4:98479820-98479870	AG09319	gingival:	n/a
5	chr4:98479820-98479870	ProgFib	skin:	n/a
6	chr4:98479820-98479870	SK-N-MC	brain:	n/a
7	chr4:98479820-98479870	AG04450	lung:	fetal
8	chr4:98479820-98479870	MCF-7	breast:	n/a
9	chr4:98479820-98479870	HNPCEpiC	eye:	n/a
10	chr4:98479820-98479870	HIPEpiC	eye:	n/a
11	chr4:98479820-98479870	HRCEpiC	kidney:	n/a
12	chr4:98479820-98479870	GM12891	blood:	n/a
13	chr4:98479820-98479870	SK-N-SH_RA	brain:	n/a
14	chr4:98479820-98479870	RPTEC	kidney:	n/a
15	chr4:98479820-98479870	HUVEC	blood vessel:	n/a
16	chr4:98479820-98479870	HRPEpiC	eye:	n/a
17	chr4:98479820-98479870	H1-hESC	embryonic stem cell:	embryo
18	chr4:98479820-98479870	PANC-1	pancreas:	n/a
19	chr4:98479820-98479870	HEEpiC	esophagus:	n/a
20	chr4:98479820-98479870	Hepatocyte	liver:	n/a
21	chr4:98479820-98479870	SK-N-SH	brain:	n/a
22	chr4:98479820-98479870	NHDF-neo	bronchial:	n/a
23	chr4:98479820-98479870	HL-60	blood:	n/a
24	chr4:98479820-98479870	HCF	heart:	n/a
25	chr4:98479820-98479870	HCT-116	colon:	n/a
26	chr4:98479820-98479870	PFSK-1	brain:	n/a
27	chr4:98479820-98479870	HMEC	breast:	n/a
28	chr4:98479820-98479870	GM12878	blood:	n/a
29	chr4:98479820-98479870	LNCaP	prostate:	n/a
30	chr4:98479820-98479870	AoSMC	blood vessel:	n/a
31	chr4:98479820-98479870	GM19239	blood:	n/a
32	chr4:98479820-98479870	T-47D	breast:	n/a
33	chr4:98479820-98479870	Caco-2	colon:	n/a
34	chr4:98479820-98479870	NH-A	brain:	n/a
35	chr4:98479820-98479870	AG09309	skin:	n/a
36	chr4:98479820-98479870	HRE	kidney:	n/a
37	chr4:98479820-98479870	ECC-1	luminal epithelium:	n/a
38	chr4:98479820-98479870	HCPEpiC	choroid plexus:	n/a
39	chr4:98479820-98479870	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:98479820-98479870	NB4	blood:	n/a
41	chr4:98479820-98479870	U87	brain:	n/a
42	chr4:98479820-98479870	Jurkat	blood:	n/a
43	chr4:98479820-98479870	CMK	blood:	n/a
44	chr4:98479820-98479870	ovcar-3	ovarian:	n/a
45	chr4:98479820-98479870	A549	lung:	n/a
46	chr4:98479820-98479870	BJ	skin:	n/a
47	chr4:98479820-98479870	NHBE	bronchial:	n/a
48	chr4:98479820-98479870	MCF10A-Er-Src	breast:	n/a
49	chr4:98479820-98479870	HCM	heart:	n/a
50	chr4:98479820-98479870	K562	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:98505232..98506917-chr4:98508304..98511467,3	MCF-7	breast:
2	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
3	chr4:98522959..98525428-chr4:98528956..98531903,2	K562	blood:
4	chr4:98505232..98506917-chr4:98508304..98511467,3	MCF-7	breast:
5	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
6	chr4:98562115..98565020-chr4:98567699..98570313,2	MCF-7	breast:
7	chr4:98522959..98525428-chr4:98528956..98531903,2	K562	blood:
8	chr4:98562115..98565020-chr4:98567699..98570313,2	MCF-7	breast:
9	chr4:98401691..98403419-chr4:98441466..98443377,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000254044	TF binding region
ENSG00000254044	CpG island

Extended variants
information (count: 1560 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1560 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138309501	chr4:98437017-98437018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531949514	chr4:98437079-98437080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549943963	chr4:98437088-98437089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6830060	chr4:98437107-98437108	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs35564795	chr4:98437231-98437232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535672602	chr4:98437235-98437236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547842514	chr4:98437397-98437398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75986953	chr4:98437409-98437410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533782020	chr4:98437415-98437416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149144289	chr4:98437428-98437429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577051482	chr4:98437509-98437510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538170541	chr4:98437565-98437566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143213191	chr4:98437589-98437590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574648819	chr4:98437596-98437597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535286630	chr4:98446005-98446006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs62315844	chr4:98446007-98446008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112999909	chr4:98446047-98446048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559973090	chr4:98446086-98446087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562455964	chr4:98446220-98446221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557845609	chr4:98446236-98446237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192758905	chr4:98446251-98446252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537052655	chr4:98446252-98446253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555782601	chr4:98446261-98446262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148809604	chr4:98446353-98446354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541252079	chr4:98446519-98446520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559928466	chr4:98446544-98446545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575100678	chr4:98446565-98446566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111775223	chr4:98446574-98446575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545878534	chr4:98446599-98446600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184450825	chr4:98446645-98446646	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs551722999	chr4:98446687-98446688	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs80130813	chr4:98446701-98446702	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs78583855	chr4:98446714-98446715	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs188473606	chr4:98446748-98446749	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs137857683	chr4:98446749-98446750	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs142444566	chr4:98446787-98446788	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs12501678	chr4:98446792-98446793	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs565510176	chr4:98446841-98446842	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs539259223	chr4:98446887-98446888	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs113801414	chr4:98446900-98446901	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs200719682	chr4:98446917-98446918	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs147885501	chr4:98446948-98446949	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs569863079	chr4:98446983-98446984	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs537042083	chr4:98447017-98447018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141557916	chr4:98447071-98447072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191842425	chr4:98447088-98447089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147028235	chr4:98447113-98447114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs36053233	chr4:98447121-98447122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs34760817	chr4:98447192-98447193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184313895	chr4:98447224-98447225	Weak transcription	n/a	n/a	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
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
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
Melanoma	20688739	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98437000-98437600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:98446000-98446600	Enhancers	HUVEC	blood vessel
3	chr4:98446400-98446800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:98446600-98447000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr4:98446600-98447000	Flanking Active TSS	HUVEC	blood vessel
6	chr4:98447000-98447200	Enhancers	HUVEC	blood vessel
7	chr4:98447200-98451600	Weak transcription	HUVEC	blood vessel
8	chr4:98451600-98452600	Enhancers	HUVEC	blood vessel
9	chr4:98451800-98452200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:98465800-98466400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr4:98465800-98466600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:98465800-98466800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:98465800-98467000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr4:98466000-98466600	Enhancers	H1 Cell Line	embryonic stem cell
15	chr4:98466000-98466600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr4:98466000-98466800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr4:98466000-98467200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:98466200-98466800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr4:98466200-98466800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr4:98466800-98478600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr4:98470600-98472800	Enhancers	Dnd41	blood
22	chr4:98478400-98480000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr4:98478400-98481400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr4:98478600-98479800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr4:98478600-98480200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr4:98478600-98480600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr4:98478600-98480800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr4:98478600-98481400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr4:98478800-98480000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr4:98478800-98480000	Enhancers	H9 Cell Line	embryonic stem cell
31	chr4:98479000-98481200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr4:98479600-98480000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:98481600-98483800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr4:98486600-98487000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr4:98495000-98495800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr4:98495200-98495600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:98495200-98495600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr4:98506400-98507000	Enhancers	Dnd41	blood
39	chr4:98508800-98509000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:98509000-98509400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:98509400-98510600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:98510600-98511600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:98510800-98511200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:98510800-98511600	Enhancers	HMEC	breast
45	chr4:98514200-98514800	ZNF genes & repeats	Pancreas	Pancrea
46	chr4:98514400-98515000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr4:98548600-98549400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:98548800-98549200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:98548800-98549400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr4:98548800-98549400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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