Variant report

Variant	nsv878726
Chromosome Location	chr4:19038807-19304946
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	chr4:19137800-19138204	GM12878	blood:	n/a	n/a
2	ATF2	chr4:19197235-19197676	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:19197286-19197699	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:19137962-19138101	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:19219629-19219706	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr4:19132498-19132945	IMR90	lung:	n/a	n/a
7	CEBPB	chr4:19134974-19135295	A549	lung:	n/a	chr4:19135127-19135138
8	CEBPB	chr4:19196878-19197790	H1-hESC	embryonic stem cell:	n/a	chr4:19197052-19197065
9	CEBPB	chr4:19286887-19287044	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:19226059-19226306	K562	blood:	n/a	chr4:19226205-19226216
11	CEBPB	chr4:19146661-19146739	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:19226066-19226394	HepG2	liver:	n/a	chr4:19226205-19226216
13	CEBPB	chr4:19288115-19288116	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr4:19143247-19143482	IMR90	lung:	n/a	chr4:19143358-19143369 chr4:19143357-19143370 chr4:19143357-19143368
15	CEBPB	chr4:19147718-19148107	ECC-1	luminal epithelium:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879
16	CEBPB	chr4:19147727-19148019	IMR90	lung:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879
17	CEBPB	chr4:19185777-19186242	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr4:19123587-19124188	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:19226065-19226352	H1-hESC	embryonic stem cell:	n/a	chr4:19226205-19226216
20	CEBPB	chr4:19148249-19148491	IMR90	lung:	n/a	chr4:19148352-19148363
21	CEBPB	chr4:19147696-19148020	H1-hESC	embryonic stem cell:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879
22	CEBPB	chr4:19147751-19148518	HepG2	liver:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879 chr4:19148352-19148363
23	CEBPB	chr4:19134973-19135293	H1-hESC	embryonic stem cell:	n/a	chr4:19135127-19135138
24	CEBPB	chr4:19187049-19187517	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr4:19134958-19135299	IMR90	lung:	n/a	chr4:19135127-19135138
26	CEBPB	chr4:19143246-19143469	HepG2	liver:	n/a	chr4:19143358-19143369 chr4:19143357-19143370 chr4:19143357-19143368
27	CEBPB	chr4:19148242-19148497	Hela-S3	cervix:	n/a	chr4:19148352-19148363
28	CEBPB	chr4:19226069-19226374	Hela-S3	cervix:	n/a	chr4:19226205-19226216
29	CEBPB	chr4:19303235-19303482	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr4:19303074-19303531	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:19115771-19115787	K562	blood:	n/a	n/a
32	CEBPB	chr4:19115665-19115921	HepG2	liver:	n/a	chr4:19115855-19115866 chr4:19115855-19115866 chr4:19115691-19115704
33	CEBPB	chr4:19134953-19135308	HepG2	liver:	n/a	chr4:19135127-19135138
34	CEBPB	chr4:19265137-19265337	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:19197001-19197141	IMR90	lung:	n/a	chr4:19197052-19197065
36	CEBPB	chr4:19226085-19226381	IMR90	lung:	n/a	chr4:19226205-19226216
37	CEBPB	chr4:19149012-19149189	HepG2	liver:	n/a	chr4:19149089-19149098 chr4:19149087-19149098
38	CEBPB	chr4:19134971-19135274	K562	blood:	n/a	chr4:19135127-19135138
39	CEBPB	chr4:19122665-19122865	HepG2	liver:	n/a	n/a
40	CHD2	chr4:19197288-19197935	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr4:19197218-19197812	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTBP2	chr4:19197170-19197696	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr4:19226500-19226650	K562	blood:	n/a	chr4:19226642-19226650
44	CTCF	chr4:19226280-19226430	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr4:19226346-19226393	GM13976	blood:	n/a	n/a
46	CTCF	chr4:19226246-19226851	IMR90	lung:	n/a	chr4:19226642-19226650 chr4:19226638-19226654 chr4:19226639-19226660 chr4:19226637-19226655
47	CTCF	chr4:19115880-19116030	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:19214340-19214490	HRE	kidney:	n/a	n/a
49	CTCF	chr4:19226500-19226650	AoAF	blood vessel:	n/a	chr4:19226642-19226650
50	CTCF	chr4:19226280-19226430	GM12864	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:19197380-19197430	HRCEpiC	kidney:	n/a
2	chr4:19197380-19197430	AG04450	lung:	fetal
3	chr4:19134792-19134842	HEEpiC	esophagus:	n/a
4	chr4:19197380-19197430	HIPEpiC	eye:	n/a
5	chr4:19197380-19197430	HCPEpiC	choroid plexus:	n/a
6	chr4:19197380-19197430	ovcar-3	ovarian:	n/a
7	chr4:19134792-19134842	NH-A	brain:	n/a
8	chr4:19134792-19134842	NT2-D1	testis:	n/a
9	chr4:19134792-19134842	HMEC	breast:	n/a
10	chr4:19197380-19197430	HCM	heart:	n/a
11	chr4:19197380-19197430	HRE	kidney:	n/a
12	chr4:19197380-19197430	HepG2	liver:	n/a
13	chr4:19134792-19134842	IMR90	lung:	fetal
14	chr4:19197380-19197430	MCF-7	breast:	n/a
15	chr4:19197380-19197430	ECC-1	luminal epithelium:	n/a
16	chr4:19197380-19197430	BE2_C	brain:	n/a
17	chr4:19134792-19134842	ovcar-3	ovarian:	n/a
18	chr4:19134792-19134842	HCT-116	colon:	n/a
19	chr4:19134792-19134842	GM12891	blood:	n/a
20	chr4:19134792-19134842	AG04449	skin:	fetal
21	chr4:19134792-19134842	SKMC	muscle:	n/a
22	chr4:19197380-19197430	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:19134792-19134842	AG09309	skin:	n/a
24	chr4:19134792-19134842	HEK293	kidney:	embryo
25	chr4:19197380-19197430	HMEC	breast:	n/a
26	chr4:19134792-19134842	HNPCEpiC	eye:	n/a
27	chr4:19134792-19134842	PANC-1	pancreas:	n/a
28	chr4:19134792-19134842	K562	blood:	n/a
29	chr4:19197380-19197430	PFSK-1	brain:	n/a
30	chr4:19197380-19197430	SKMC	muscle:	n/a
31	chr4:19197380-19197430	Hela-S3	cervix:	n/a
32	chr4:19197380-19197430	AG09319	gingival:	n/a
33	chr4:19197380-19197430	ProgFib	skin:	n/a
34	chr4:19134792-19134842	AoSMC	blood vessel:	n/a
35	chr4:19134792-19134842	AG04450	lung:	fetal
36	chr4:19197380-19197430	CMK	blood:	n/a
37	chr4:19134792-19134842	HAEpiC	amniotic membrane:	n/a
38	chr4:19197380-19197430	AG10803	skin:	n/a
39	chr4:19197380-19197430	NHDF-neo	bronchial:	n/a
40	chr4:19134792-19134842	HUVEC	blood vessel:	n/a
41	chr4:19134792-19134842	PFSK-1	brain:	n/a
42	chr4:19134792-19134842	CMK	blood:	n/a
43	chr4:19197380-19197430	NHBE	bronchial:	n/a
44	chr4:19197380-19197430	NT2-D1	testis:	n/a
45	chr4:19134792-19134842	A549	lung:	n/a
46	chr4:19197380-19197430	IMR90	lung:	fetal
47	chr4:19197380-19197430	SK-N-SH_RA	brain:	n/a
48	chr4:19197380-19197430	HUVEC	blood vessel:	n/a
49	chr4:19197380-19197430	H1-hESC	embryonic stem cell:	embryo
50	chr4:19197380-19197430	NB4	blood:	n/a

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	chr4:19258834..19261386-chr4:19628228..19629933,2	K562	blood:
4	chr4:19078847..19080844-chr4:19084174..19086115,2	MCF-7	breast:
5	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: 4003 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:4003 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs207342	chr4:19038807-19038808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575118085	chr4:19038821-19038822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542143226	chr4:19038824-19038825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138392947	chr4:19038846-19038847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6844497	chr4:19038858-19038859	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs528760630	chr4:19038873-19038874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142386468	chr4:19038880-19038881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564595634	chr4:19038897-19038898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370241037	chr4:19038930-19038931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547374279	chr4:19038938-19038939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs80156578	chr4:19038941-19038942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532012354	chr4:19038970-19038971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183231948	chr4:19039008-19039009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562338521	chr4:19039054-19039055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530040298	chr4:19039060-19039061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77326503	chr4:19039065-19039066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186136045	chr4:19039179-19039180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs207341	chr4:19039193-19039194	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs527450433	chr4:19039199-19039200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552715333	chr4:19039230-19039231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568628874	chr4:19039262-19039263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570878798	chr4:19039295-19039296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537950546	chr4:19039355-19039356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550182944	chr4:19039402-19039403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568340424	chr4:19039440-19039441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148290610	chr4:19039483-19039484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554008363	chr4:19039507-19039508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs28710904	chr4:19039512-19039513	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs539595591	chr4:19039626-19039627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190844979	chr4:19039647-19039648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141369239	chr4:19039670-19039671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543959896	chr4:19039775-19039776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562533524	chr4:19039815-19039816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574326425	chr4:19039904-19039905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569459492	chr4:19039925-19039926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116836089	chr4:19039950-19039951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560449777	chr4:19039975-19039976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs527487224	chr4:19039990-19039991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183922641	chr4:19040074-19040075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368655582	chr4:19040108-19040109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs536417630	chr4:19040143-19040144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs16898019	chr4:19040287-19040288	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs531860827	chr4:19040298-19040299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187784964	chr4:19040305-19040306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375603218	chr4:19040308-19040309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367891925	chr4:19040347-19040348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs117860162	chr4:19040377-19040378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192454956	chr4:19040410-19040411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535416482	chr4:19040442-19040443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547685765	chr4:19040452-19040453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:19036400-19039800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:19038000-19039600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr4:19039600-19040200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr4:19039800-19040200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:19039800-19040200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr4:19040200-19041000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr4:19041000-19041600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr4:19043000-19043200	ZNF genes & repeats	Pancreas	Pancrea
9	chr4:19048800-19049200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:19048800-19049600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:19049200-19052800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:19049600-19056200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:19052600-19054000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr4:19052600-19054000	Enhancers	Fetal Kidney	kidney
15	chr4:19052800-19054000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:19052800-19054200	Enhancers	Fetal Lung	lung
17	chr4:19053000-19054000	Enhancers	Colon Smooth Muscle	Colon
18	chr4:19053000-19054200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr4:19053200-19053800	Enhancers	Fetal Stomach	stomach
20	chr4:19053400-19053800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:19053400-19053800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr4:19053400-19054000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:19053400-19054000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr4:19053400-19054000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr4:19053600-19054000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:19053600-19054000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr4:19053600-19054000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr4:19053600-19054000	Enhancers	Brain Germinal Matrix	brain
29	chr4:19053600-19054200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr4:19053800-19054200	Enhancers	Fetal Brain Male	brain
31	chr4:19054000-19054600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:19054000-19056200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr4:19054000-19056400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:19054200-19056400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr4:19054200-19056600	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr4:19054600-19055600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:19055600-19056000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:19056000-19056200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:19056200-19057200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:19056200-19057200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr4:19056200-19057800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr4:19056400-19057200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:19056400-19057400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr4:19056600-19056800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:19057200-19057600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:19057600-19058000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr4:19058000-19058600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:19072400-19072800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:19072800-19073200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:19073200-19073600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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