Variant report

Variant	nsv878727
Chromosome Location	chr4:19058288-19230465
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:19197286-19197699	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:19197235-19197676	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:19137800-19138204	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:19137962-19138101	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:19148249-19148491	IMR90	lung:	n/a	chr4:19148352-19148363
6	CEBPB	chr4:19134973-19135293	H1-hESC	embryonic stem cell:	n/a	chr4:19135127-19135138
7	CEBPB	chr4:19115665-19115921	HepG2	liver:	n/a	chr4:19115855-19115866 chr4:19115855-19115866 chr4:19115691-19115704
8	CEBPB	chr4:19196878-19197790	H1-hESC	embryonic stem cell:	n/a	chr4:19197052-19197065
9	CEBPB	chr4:19134958-19135299	IMR90	lung:	n/a	chr4:19135127-19135138
10	CEBPB	chr4:19143247-19143482	IMR90	lung:	n/a	chr4:19143358-19143369 chr4:19143357-19143370 chr4:19143357-19143368
11	CEBPB	chr4:19149012-19149189	HepG2	liver:	n/a	chr4:19149089-19149098 chr4:19149087-19149098
12	CEBPB	chr4:19226065-19226352	H1-hESC	embryonic stem cell:	n/a	chr4:19226205-19226216
13	CEBPB	chr4:19147751-19148518	HepG2	liver:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879 chr4:19148352-19148363
14	CEBPB	chr4:19134974-19135295	A549	lung:	n/a	chr4:19135127-19135138
15	CEBPB	chr4:19185777-19186242	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr4:19146661-19146739	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:19197001-19197141	IMR90	lung:	n/a	chr4:19197052-19197065
18	CEBPB	chr4:19226069-19226374	Hela-S3	cervix:	n/a	chr4:19226205-19226216
19	CEBPB	chr4:19226085-19226381	IMR90	lung:	n/a	chr4:19226205-19226216
20	CEBPB	chr4:19148242-19148497	Hela-S3	cervix:	n/a	chr4:19148352-19148363
21	CEBPB	chr4:19132498-19132945	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:19147718-19148107	ECC-1	luminal epithelium:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879
23	CEBPB	chr4:19187049-19187517	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr4:19134971-19135274	K562	blood:	n/a	chr4:19135127-19135138
25	CEBPB	chr4:19147696-19148020	H1-hESC	embryonic stem cell:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879
26	CEBPB	chr4:19123587-19124188	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:19143246-19143469	HepG2	liver:	n/a	chr4:19143358-19143369 chr4:19143357-19143370 chr4:19143357-19143368
28	CEBPB	chr4:19226059-19226306	K562	blood:	n/a	chr4:19226205-19226216
29	CEBPB	chr4:19115771-19115787	K562	blood:	n/a	n/a
30	CEBPB	chr4:19219629-19219706	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr4:19226066-19226394	HepG2	liver:	n/a	chr4:19226205-19226216
32	CEBPB	chr4:19134953-19135308	HepG2	liver:	n/a	chr4:19135127-19135138
33	CEBPB	chr4:19122665-19122865	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:19147727-19148019	IMR90	lung:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879
35	CHD2	chr4:19197288-19197935	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr4:19197218-19197812	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTBP2	chr4:19197170-19197696	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr4:19226578-19226734	Hela-S3	cervix:	n/a	chr4:19226642-19226650 chr4:19226638-19226654 chr4:19226639-19226660 chr4:19226637-19226655
39	CTCF	chr4:19226360-19226510	HAc	cerebellar:	n/a	n/a
40	CTCF	chr4:19226380-19226530	BE2_C	brain:	n/a	n/a
41	CTCF	chr4:19093260-19093410	Caco-2	colon:	n/a	n/a
42	CTCF	chr4:19166088-19166211	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:19158580-19158730	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr4:19215300-19215450	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr4:19226340-19226490	HVMF	connective:	n/a	n/a
46	CTCF	chr4:19226580-19226730	SK-N-SH_RA	brain:	n/a	chr4:19226642-19226650 chr4:19226638-19226654 chr4:19226639-19226660 chr4:19226637-19226655
47	CTCF	chr4:19226100-19226250	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr4:19226220-19226370	WI-38	lung:	n/a	n/a
49	CTCF	chr4:19226620-19226770	HA-sp	spinal cord:	n/a	chr4:19226642-19226650 chr4:19226638-19226654 chr4:19226639-19226660 chr4:19226637-19226655
50	CTCF	chr4:19214280-19214430	HRPEpiC	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:19134792-19134842	H1-hESC	embryonic stem cell:	embryo
2	chr4:19197380-19197430	PANC-1	pancreas:	n/a
3	chr4:19197380-19197430	HCF	heart:	n/a
4	chr4:19134792-19134842	GM12892	blood:	n/a
5	chr4:19134792-19134842	HRE	kidney:	n/a
6	chr4:19197380-19197430	ovcar-3	ovarian:	n/a
7	chr4:19134792-19134842	PANC-1	pancreas:	n/a
8	chr4:19134792-19134842	Hela-S3	cervix:	n/a
9	chr4:19134792-19134842	HUVEC	blood vessel:	n/a
10	chr4:19134792-19134842	HL-60	blood:	n/a
11	chr4:19197380-19197430	BJ	skin:	n/a
12	chr4:19134792-19134842	HAEpiC	amniotic membrane:	n/a
13	chr4:19134792-19134842	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:19134792-19134842	SK-N-SH_RA	brain:	n/a
15	chr4:19134792-19134842	MCF10A-Er-Src	breast:	n/a
16	chr4:19134792-19134842	NHDF-neo	bronchial:	n/a
17	chr4:19134792-19134842	HEK293	kidney:	embryo
18	chr4:19197380-19197430	MCF10A-Er-Src	breast:	n/a
19	chr4:19197380-19197430	SKMC	muscle:	n/a
20	chr4:19134792-19134842	HepG2	liver:	n/a
21	chr4:19134792-19134842	GM12891	blood:	n/a
22	chr4:19197380-19197430	A549	lung:	n/a
23	chr4:19197380-19197430	AoSMC	blood vessel:	n/a
24	chr4:19197380-19197430	HRE	kidney:	n/a
25	chr4:19197380-19197430	PFSK-1	brain:	n/a
26	chr4:19197380-19197430	MCF-7	breast:	n/a
27	chr4:19134792-19134842	BE2_C	brain:	n/a
28	chr4:19197380-19197430	K562	blood:	n/a
29	chr4:19134792-19134842	AG09319	gingival:	n/a
30	chr4:19134792-19134842	HRCEpiC	kidney:	n/a
31	chr4:19134792-19134842	HCT-116	colon:	n/a
32	chr4:19134792-19134842	NH-A	brain:	n/a
33	chr4:19197380-19197430	NT2-D1	testis:	n/a
34	chr4:19134792-19134842	NHBE	bronchial:	n/a
35	chr4:19134792-19134842	SKMC	muscle:	n/a
36	chr4:19197380-19197430	HMEC	breast:	n/a
37	chr4:19197380-19197430	H1-hESC	embryonic stem cell:	embryo
38	chr4:19197380-19197430	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:19134792-19134842	CMK	blood:	n/a
40	chr4:19134792-19134842	AG10803	skin:	n/a
41	chr4:19134792-19134842	AoSMC	blood vessel:	n/a
42	chr4:19197380-19197430	SK-N-SH_RA	brain:	n/a
43	chr4:19197380-19197430	HepG2	liver:	n/a
44	chr4:19197380-19197430	HRPEpiC	eye:	n/a
45	chr4:19197380-19197430	HCPEpiC	choroid plexus:	n/a
46	chr4:19197380-19197430	Hela-S3	cervix:	n/a
47	chr4:19197380-19197430	HAEpiC	amniotic membrane:	n/a
48	chr4:19197380-19197430	CMK	blood:	n/a
49	chr4:19134792-19134842	NB4	blood:	n/a
50	chr4:19197380-19197430	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:19118666..19120200-chr4:19121807..19124671,2	K562	blood:
2	chr4:19118666..19120200-chr4:19121807..19124671,2	K562	blood:
3	chr4:19078847..19080844-chr4:19084174..19086115,2	MCF-7	breast:
4	chr4:19078847..19080844-chr4:19084174..19086115,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LCORL-2	chr4:19173958-19174149	ENSG00000248238

Variant related genes	Relation type
RNA5SP157	TF binding region
RNA5SP157	CpG island

Extended variants
information (count: 2350 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2350 , 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	rs16898044	chr4:19058288-19058289	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551013414	chr4:19058296-19058297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569120139	chr4:19058331-19058332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536960439	chr4:19058350-19058351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371806290	chr4:19058356-19058357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554916974	chr4:19058376-19058377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563800828	chr4:19058386-19058387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577669326	chr4:19058388-19058389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115858347	chr4:19058455-19058456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs17537533	chr4:19058515-19058516	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs115376216	chr4:19072403-19072404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547788330	chr4:19072410-19072411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541520021	chr4:19072435-19072436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111896622	chr4:19072469-19072470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369999152	chr4:19072477-19072478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373751556	chr4:19072535-19072536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188951953	chr4:19072604-19072605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527992343	chr4:19072610-19072611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372820193	chr4:19072611-19072612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368528030	chr4:19072620-19072621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527343919	chr4:19072799-19072800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116329535	chr4:19072834-19072835	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs192455068	chr4:19072865-19072866	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs531467277	chr4:19072907-19072908	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs549587359	chr4:19072909-19072910	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs556714845	chr4:19072944-19072945	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs117268163	chr4:19072955-19072956	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs183159480	chr4:19073033-19073034	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs187491090	chr4:19073040-19073041	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs114034041	chr4:19073052-19073053	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs539538915	chr4:19073066-19073067	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs191941576	chr4:19073122-19073123	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs184717407	chr4:19073133-19073134	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs189234021	chr4:19073173-19073174	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs574325712	chr4:19073188-19073189	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs138613224	chr4:19073194-19073195	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs542215969	chr4:19073197-19073198	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs372613090	chr4:19073248-19073249	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs141746835	chr4:19073249-19073250	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs146230338	chr4:19073271-19073272	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs555812250	chr4:19073366-19073367	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs114672715	chr4:19073368-19073369	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs369782958	chr4:19073417-19073418	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs192610719	chr4:19073434-19073435	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs531501931	chr4:19073443-19073444	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs73801199	chr4:19073449-19073450	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs561637803	chr4:19073495-19073496	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs139207049	chr4:19073529-19073530	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs555822627	chr4:19075401-19075402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192495255	chr4:19075402-19075403	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Glioma	20126413	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:19058000-19058600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:19072400-19072800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:19072800-19073200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:19073200-19073600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:19075400-19076200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr4:19075600-19076000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:19075600-19076200	Enhancers	Fetal Kidney	kidney
8	chr4:19075800-19076200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr4:19076000-19077600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:19077600-19078200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:19079400-19079600	ZNF genes & repeats	Primary B cells from cord blood	blood
12	chr4:19079400-19079600	ZNF genes & repeats	Primary T cells from cord blood	blood
13	chr4:19079400-19079600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
14	chr4:19079400-19079600	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr4:19079400-19079600	Active TSS	HUVEC	blood vessel
16	chr4:19079400-19079600	Flanking Bivalent TSS/Enh	K562	blood
17	chr4:19079400-19079600	Enhancers	Osteobl	bone
18	chr4:19097000-19097600	Enhancers	H9 Cell Line	embryonic stem cell
19	chr4:19097000-19097800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:19097000-19098000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:19097000-19098000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr4:19097200-19097600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:19097200-19097800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr4:19097200-19097800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:19097200-19097800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr4:19097200-19098000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:19097200-19098400	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:19097600-19098000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr4:19097800-19099400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr4:19098000-19099200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:19099400-19099600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:19099400-19100200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:19111800-19112000	Enhancers	Fetal Kidney	kidney
34	chr4:19112000-19113600	Weak transcription	Fetal Kidney	kidney
35	chr4:19132200-19132800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:19133800-19136800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr4:19134200-19134400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr4:19134200-19135200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr4:19134400-19135000	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr4:19134400-19135000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr4:19134400-19135200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr4:19134600-19135000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr4:19135000-19136200	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr4:19135000-19136200	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr4:19135000-19136200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr4:19135200-19136200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr4:19136200-19136400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr4:19136200-19136400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr4:19136200-19136600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr4:19136200-19136600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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