Variant report

Variant	nsv830686
Chromosome Location	chr6:72336896-72534267
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:241)
CpG islands
(count:245)
Chromatin interactive
region (count:9)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:241 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr6:72408628-72408652	K562	blood:	n/a	n/a
2	BHLHE40	chr6:72408618-72408690	HepG2	liver:	n/a	n/a
3	BHLHE40	chr6:72422217-72422261	GM12878	blood:	n/a	n/a
4	CBX3	chr6:72520692-72520833	K562	blood:	n/a	n/a
5	CEBPB	chr6:72352542-72352796	K562	blood:	n/a	chr6:72352664-72352673
6	CEBPB	chr6:72340076-72340304	A549	lung:	n/a	chr6:72340212-72340223
7	CEBPB	chr6:72352505-72352848	H1-hESC	embryonic stem cell:	n/a	chr6:72352664-72352673
8	CEBPB	chr6:72479522-72479843	HepG2	liver:	n/a	chr6:72479680-72479691
9	CEBPB	chr6:72375856-72375923	HepG2	liver:	n/a	chr6:72375898-72375909
10	CEBPB	chr6:72340058-72340270	HepG2	liver:	n/a	chr6:72340212-72340223
11	CEBPB	chr6:72375737-72376047	Hela-S3	cervix:	n/a	chr6:72375898-72375909
12	CEBPB	chr6:72352488-72352839	IMR90	lung:	n/a	chr6:72352664-72352673
13	CEBPB	chr6:72516048-72516382	HepG2	liver:	n/a	chr6:72516207-72516218
14	CEBPB	chr6:72352521-72352805	Hela-S3	cervix:	n/a	chr6:72352664-72352673
15	CEBPB	chr6:72352510-72352856	ECC-1	luminal epithelium:	n/a	chr6:72352664-72352673
16	CEBPB	chr6:72383825-72384086	IMR90	lung:	n/a	chr6:72383924-72383935
17	CEBPB	chr6:72352486-72352847	HepG2	liver:	n/a	chr6:72352664-72352673
18	CEBPB	chr6:72383764-72384091	HepG2	liver:	n/a	chr6:72383924-72383935
19	CEBPB	chr6:72383802-72384083	A549	lung:	n/a	chr6:72383924-72383935
20	CEBPB	chr6:72352500-72352818	A549	lung:	n/a	chr6:72352664-72352673
21	CHD2	chr6:72455458-72455540	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr6:72396159-72396248	Fibrobl	skin:	n/a	n/a
23	CTCF	chr6:72352200-72352350	BE2_C	brain:	n/a	n/a
24	CTCF	chr6:72369860-72370010	NHLF	lung:	n/a	n/a
25	CTCF	chr6:72438587-72438645	GM10266	blood:	n/a	n/a
26	CTCF	chr6:72499376-72499440	GM10248	blood:	n/a	n/a
27	CTCF	chr6:72512960-72513110	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr6:72513080-72513230	HEK293	kidney:	n/a	n/a
29	CTCF	chr6:72501911-72502020	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr6:72513017-72513031	GM12878	blood:	n/a	n/a
31	CTCF	chr6:72490435-72490462	GM20000	blood:	n/a	n/a
32	CTCF	chr6:72346858-72346911	GM20000	blood:	n/a	n/a
33	CTCF	chr6:72344691-72344909	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr6:72344738-72344823	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr6:72392020-72392170	GM12867	blood:	n/a	n/a
36	CTCF	chr6:72453927-72453998	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr6:72442223-72442256	GM10248	blood:	n/a	n/a
38	CTCF	chr6:72495203-72495282	Kidney_OC	kidney:	n/a	n/a
39	E2F4	chr6:72431466-72431656	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr6:72467260-72467429	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr6:72476393-72476544	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr6:72487537-72487783	MCF10A-Er-Src	breast:	n/a	n/a
43	EBF1	chr6:72447730-72448042	GM12878	blood:	n/a	chr6:72447890-72447901
44	EBF1	chr6:72441394-72441677	GM12878	blood:	n/a	chr6:72441516-72441525 chr6:72441514-72441525 chr6:72441514-72441527
45	EBF1	chr6:72389912-72390093	GM12878	blood:	n/a	chr6:72389999-72390010 chr6:72390000-72390009 chr6:72389998-72390011 chr6:72390000-72390009
46	EBF1	chr6:72437674-72437946	GM12878	blood:	n/a	chr6:72437797-72437808
47	EP300	chr6:72384731-72384763	GM12878	blood:	n/a	n/a
48	EP300	chr6:72368915-72368980	GM12878	blood:	n/a	n/a
49	ESR1	chr6:72434356-72434630	ECC-1	luminal epithelium:	n/a	n/a
50	FOS	chr6:72427364-72427365	MCF10A-Er-Src	breast:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:72396953-72397003	HMEC	breast:	n/a
2	chr6:72396953-72397003	HMEC	breast:	n/a
3	chr6:72385611-72385661	RPTEC	kidney:	n/a
4	chr6:72396953-72397003	SK-N-SH	brain:	n/a
5	chr6:72385611-72385661	GM06990	blood:	n/a
6	chr6:72385611-72385661	ECC-1	luminal epithelium:	n/a
7	chr6:72385611-72385661	HMEC	breast:	n/a
8	chr6:72385611-72385661	ProgFib	skin:	n/a
9	chr6:72396953-72397003	GM12892	blood:	n/a
10	chr6:72396953-72397003	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:72396953-72397003	LNCaP	prostate:	n/a
12	chr6:72385611-72385661	GM12878	blood:	n/a
13	chr6:72396915-72396965	HCT-116	colon:	n/a
14	chr6:72385611-72385661	HEK293	kidney:	embryo
15	chr6:72396953-72397003	RPTEC	kidney:	n/a
16	chr6:72455356-72455406	HMEC	breast:	n/a
17	chr6:72455356-72455406	HL-60	blood:	n/a
18	chr6:72385611-72385661	SK-N-MC	brain:	n/a
19	chr6:72396915-72396965	SKMC	muscle:	n/a
20	chr6:72396953-72397003	GM06990	blood:	n/a
21	chr6:72385611-72385661	HL-60	blood:	n/a
22	chr6:72396953-72397003	HAEpiC	amniotic membrane:	n/a
23	chr6:72455356-72455406	GM19239	blood:	n/a
24	chr6:72396953-72397003	AoSMC	blood vessel:	n/a
25	chr6:72396915-72396965	GM19239	blood:	n/a
26	chr6:72455356-72455406	LNCaP	prostate:	n/a
27	chr6:72455356-72455406	Hepatocyte	liver:	n/a
28	chr6:72396915-72396965	HCPEpiC	choroid plexus:	n/a
29	chr6:72455356-72455406	HRCEpiC	kidney:	n/a
30	chr6:72396953-72397003	HL-60	blood:	n/a
31	chr6:72455356-72455406	AoSMC	blood vessel:	n/a
32	chr6:72455356-72455406	ProgFib	skin:	n/a
33	chr6:72396915-72396965	AoSMC	blood vessel:	n/a
34	chr6:72396915-72396965	HEEpiC	esophagus:	n/a
35	chr6:72455356-72455406	PrEC	prostate:	n/a
36	chr6:72396915-72396965	GM12891	blood:	n/a
37	chr6:72455356-72455406	NHBE	bronchial:	n/a
38	chr6:72396953-72397003	SK-N-MC	brain:	n/a
39	chr6:72396953-72397003	CMK	blood:	n/a
40	chr6:72455356-72455406	HCT-116	colon:	n/a
41	chr6:72455356-72455406	GM06990	blood:	n/a
42	chr6:72455356-72455406	SK-N-MC	brain:	n/a
43	chr6:72396915-72396965	ProgFib	skin:	n/a
44	chr6:72385611-72385661	HCF	heart:	n/a
45	chr6:72396953-72397003	HUVEC	blood vessel:	n/a
46	chr6:72455356-72455406	AG09319	gingival:	n/a
47	chr6:72385611-72385661	NHBE	bronchial:	n/a
48	chr6:72455356-72455406	GM12892	blood:	n/a
49	chr6:72396953-72397003	U87	brain:	n/a
50	chr6:72455356-72455406	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:72468655..72471627-chr6:72474083..72475719,2	K562	blood:
2	chr6:72426583..72429293-chr6:72434141..72436449,2	K562	blood:
3	chr6:72426583..72429293-chr6:72434141..72436449,2	K562	blood:
4	chr5:5329436..5329951-chr6:72381859..72382388,2	MCF-7	breast:
5	chr6:72345004..72347382-chr6:72350554..72353265,2	K562	blood:
6	chr6:72345004..72347382-chr6:72350554..72353265,2	K562	blood:
7	chr6:72364309..72367260-chr6:72370089..72372248,2	K562	blood:
8	chr6:72468655..72471627-chr6:72474083..72475719,2	K562	blood:
9	chr6:72364309..72367260-chr6:72370089..72372248,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RIMS1-2	chr6:72412257-72412412	NONHSAT113522
2	lnc-RIMS1-2	chr6:72433582-72434014	NONHSAT113522

No data

Variant related genes	Relation type
RNU4-66P	TF binding region
RNU4-66P	CpG island

Extended variants
information (count: 2885 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2885 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531174097	chr6:72336920-72336921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76542713	chr6:72336923-72336924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191417438	chr6:72336927-72336928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556542310	chr6:72336933-72336934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74893974	chr6:72336937-72336938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34237597	chr6:72336940-72336941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542548396	chr6:72336957-72336958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10942957	chr6:72337017-72337018	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs570535741	chr6:72337019-72337020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs199965987	chr6:72337051-72337052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535937119	chr6:72337108-72337109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572928198	chr6:72337121-72337122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540442066	chr6:72337124-72337125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183607492	chr6:72337135-72337136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577427031	chr6:72337157-72337158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544572931	chr6:72337159-72337160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562869876	chr6:72337244-72337245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530159140	chr6:72337260-72337261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548585749	chr6:72337295-72337296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs118081514	chr6:72337310-72337311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572492109	chr6:72337330-72337331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527853455	chr6:72337380-72337381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114448490	chr6:72344655-72344656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564176862	chr6:72344770-72344771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181055144	chr6:72344775-72344776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79011628	chr6:72344787-72344788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs272218	chr6:72344796-72344797	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs272217	chr6:72344869-72344870	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs272216	chr6:72344926-72344927	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs201731518	chr6:72344991-72344992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35694339	chr6:72344994-72344995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs272215	chr6:72345232-72345233	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs183399996	chr6:72345286-72345287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375048628	chr6:72345336-72345337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574783381	chr6:72345437-72345438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs199825149	chr6:72345491-72345492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs526950	chr6:72345562-72345563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1096051	chr6:72345631-72345632	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs694021	chr6:72345636-72345637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2840969	chr6:72345669-72345670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113745332	chr6:72345707-72345708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543401904	chr6:72345718-72345719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2631350	chr6:72345724-72345725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34663956	chr6:72345753-72345754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527843435	chr6:72345763-72345764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145846063	chr6:72345787-72345788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149037668	chr6:72345788-72345789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142046958	chr6:72345801-72345802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550443193	chr6:72345840-72345841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1096052	chr6:72345858-72345859	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:72336800-72337400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr6:72344600-72344800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:72344800-72345000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:72345200-72346000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:72345200-72346200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:72349800-72350800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:72351400-72352400	Enhancers	HUVEC	blood vessel
8	chr6:72355800-72356600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr6:72356200-72356600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:72359600-72360200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr6:72359800-72360200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr6:72369600-72372000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr6:72369800-72371000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:72369800-72372000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:72370200-72370800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:72370400-72370800	Enhancers	Adipose Nuclei	Adipose
17	chr6:72372000-72375400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr6:72372000-72383200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:72373600-72374000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr6:72373800-72375000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:72374000-72374800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr6:72374800-72375000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr6:72375000-72375200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr6:72375400-72376400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr6:72377600-72378200	Enhancers	Fetal Intestine Small	intestine
26	chr6:72378200-72382200	Weak transcription	Fetal Intestine Small	intestine
27	chr6:72381800-72385400	Enhancers	Fetal Intestine Large	intestine
28	chr6:72382200-72382600	Enhancers	Fetal Intestine Small	intestine
29	chr6:72382600-72383400	Weak transcription	Fetal Intestine Small	intestine
30	chr6:72383200-72385400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr6:72383400-72383600	Enhancers	Fetal Intestine Small	intestine
32	chr6:72383600-72385400	Weak transcription	Fetal Intestine Small	intestine
33	chr6:72383800-72384000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:72384000-72384200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr6:72384200-72384800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:72384200-72385000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr6:72384600-72385600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr6:72384800-72385000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:72384800-72385400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr6:72384800-72385600	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr6:72384800-72385800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr6:72385000-72385200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:72385000-72385600	Enhancers	H9 Cell Line	embryonic stem cell
44	chr6:72385000-72385800	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr6:72385000-72386200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr6:72385000-72388000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr6:72385200-72385600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr6:72385400-72385600	Weak transcription	Fetal Intestine Large	intestine
49	chr6:72385400-72385600	Enhancers	Fetal Intestine Small	intestine
50	chr6:72385600-72386000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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