Variant report

Variant	nsv899128
Chromosome Location	chr12:59636969-59766169
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:454)
CpG islands
(count:245)
Chromatin interactive
region (count:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:59711326-59712140	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr12:59715232-59716577	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr12:59712703-59713078	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:59676806-59677328	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr12:59688446-59688498	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr12:59651136-59651360	HepG2	liver:	n/a	chr12:59651173-59651184 chr12:59651172-59651183 chr12:59651302-59651314
7	CEBPB	chr12:59711472-59711762	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr12:59715106-59715383	HepG2	liver:	n/a	chr12:59715258-59715269 chr12:59715259-59715270
9	CEBPB	chr12:59676742-59677102	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:59714782-59714836	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr12:59715120-59715444	H1-hESC	embryonic stem cell:	n/a	chr12:59715258-59715269 chr12:59715259-59715270
12	CEBPB	chr12:59676821-59677075	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD1	chr12:59720305-59720376	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr12:59716571-59717024	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr12:59721521-59721835	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr12:59720721-59720725	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr12:59713313-59713383	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr12:59714901-59715583	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr12:59709990-59710190	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr12:59712533-59712578	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr12:59716233-59717084	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr12:59711509-59712122	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr12:59740124-59740318	K562	blood:	n/a	n/a
24	CTCF	chr12:59740140-59740290	NHEK	skin:	n/a	n/a
25	CTCF	chr12:59739980-59740130	HMEC	breast:	n/a	n/a
26	CTCF	chr12:59740080-59740230	GM06990	blood:	n/a	n/a
27	CTCF	chr12:59668580-59668730	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr12:59740180-59740330	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr12:59740140-59740290	HMEC	breast:	n/a	n/a
30	CTCF	chr12:59739980-59740130	RPTEC	kidney:	n/a	n/a
31	CTCF	chr12:59694991-59695008	LNCaP	prostate:	n/a	n/a
32	CTCF	chr12:59675420-59675570	HRE	kidney:	n/a	chr12:59675518-59675528
33	CTCF	chr12:59740113-59740350	Gliobla	brain:	n/a	n/a
34	CTCF	chr12:59740157-59740322	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:59740120-59740270	GM12872	blood:	n/a	n/a
36	CTCF	chr12:59740420-59740570	HCT-116	colon:	n/a	n/a
37	CTCF	chr12:59698160-59698310	BJ	skin:	n/a	n/a
38	CTCF	chr12:59740180-59740330	NB4	blood:	n/a	n/a
39	CTCF	chr12:59740160-59740310	GM12865	blood:	n/a	n/a
40	CTCF	chr12:59740120-59740270	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr12:59740160-59740310	HVMF	connective:	n/a	n/a
42	CTCF	chr12:59740098-59740391	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr12:59698300-59698450	NB4	blood:	n/a	n/a
44	CTCF	chr12:59740163-59740301	GM10266	blood:	n/a	n/a
45	CTCF	chr12:59695276-59695336	GM20000	blood:	n/a	n/a
46	CTCF	chr12:59695269-59695275	GM20000	blood:	n/a	n/a
47	CTCF	chr12:59740180-59740330	GM12873	blood:	n/a	n/a
48	CTCF	chr12:59740180-59740330	RPTEC	kidney:	n/a	n/a
49	CTCF	chr12:59739980-59740250	HMF	breast:	n/a	n/a
50	CTCF	chr12:59740180-59740330	GM12870	blood:	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	chr12:59730539-59730589	BE2_C	brain:	n/a
2	chr12:59730539-59730589	BE2_C	brain:	n/a
3	chr12:59715992-59716042	HepG2	liver:	n/a
4	chr12:59676888-59676938	Hela-S3	cervix:	n/a
5	chr12:59676888-59676938	HCF	heart:	n/a
6	chr12:59676888-59676938	AG10803	skin:	n/a
7	chr12:59715992-59716042	GM19239	blood:	n/a
8	chr12:59676888-59676938	SK-N-MC	brain:	n/a
9	chr12:59721694-59721744	MCF10A-Er-Src	breast:	n/a
10	chr12:59730539-59730589	NH-A	brain:	n/a
11	chr12:59721694-59721744	U87	brain:	n/a
12	chr12:59715992-59716042	K562	blood:	n/a
13	chr12:59730539-59730589	HIPEpiC	eye:	n/a
14	chr12:59715992-59716042	PFSK-1	brain:	n/a
15	chr12:59730539-59730589	HCM	heart:	n/a
16	chr12:59715992-59716042	SK-N-SH_RA	brain:	n/a
17	chr12:59715992-59716042	H1-hESC	embryonic stem cell:	embryo
18	chr12:59721694-59721744	PrEC	prostate:	n/a
19	chr12:59721694-59721744	HNPCEpiC	eye:	n/a
20	chr12:59676888-59676938	H1-hESC	embryonic stem cell:	embryo
21	chr12:59730539-59730589	AG04450	lung:	fetal
22	chr12:59721694-59721744	HRPEpiC	eye:	n/a
23	chr12:59721694-59721744	HRE	kidney:	n/a
24	chr12:59715992-59716042	PrEC	prostate:	n/a
25	chr12:59730539-59730589	AG09309	skin:	n/a
26	chr12:59730539-59730589	Jurkat	blood:	n/a
27	chr12:59715992-59716042	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:59730539-59730589	AG09319	gingival:	n/a
29	chr12:59730539-59730589	HRPEpiC	eye:	n/a
30	chr12:59676888-59676938	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:59721694-59721744	Hepatocyte	liver:	n/a
32	chr12:59721694-59721744	IMR90	lung:	fetal
33	chr12:59676888-59676938	K562	blood:	n/a
34	chr12:59676888-59676938	SKMC	muscle:	n/a
35	chr12:59730539-59730589	ECC-1	luminal epithelium:	n/a
36	chr12:59715992-59716042	NT2-D1	testis:	n/a
37	chr12:59721694-59721744	SK-N-SH_RA	brain:	n/a
38	chr12:59676888-59676938	LNCaP	prostate:	n/a
39	chr12:59715992-59716042	LNCaP	prostate:	n/a
40	chr12:59676888-59676938	SK-N-SH_RA	brain:	n/a
41	chr12:59715992-59716042	AG09319	gingival:	n/a
42	chr12:59730539-59730589	HPAEpiC	pulmonary alveolar:	n/a
43	chr12:59721694-59721744	SAEC	small airway:	n/a
44	chr12:59676888-59676938	Jurkat	blood:	n/a
45	chr12:59721694-59721744	K562	blood:	n/a
46	chr12:59676888-59676938	IMR90	lung:	fetal
47	chr12:59715992-59716042	RPTEC	kidney:	n/a
48	chr12:59676888-59676938	HMEC	breast:	n/a
49	chr12:59676888-59676938	NB4	blood:	n/a
50	chr12:59730539-59730589	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:59567506..59568224-chr12:59739584..59740478,2	MCF-7	breast:
2	chr12:59655684..59657205-chr12:59659679..59661187,2	MCF-7	breast:
3	chr12:59692138..59694777-chr12:59713415..59715358,2	MCF-7	breast:
4	chr12:59655684..59657205-chr12:59659679..59661187,2	MCF-7	breast:
5	chr12:59653805..59656189-chr12:59672943..59675327,2	MCF-7	breast:
6	chr12:59692138..59694777-chr12:59713415..59715358,2	MCF-7	breast:
7	chr12:59673431..59675592-chr12:59677210..59679968,2	MCF-7	breast:
8	chr12:59673431..59675592-chr12:59677210..59679968,2	MCF-7	breast:
9	chr12:59764978..59768337-chr12:59768399..59771459,3	MCF-7	breast:
10	chr12:59653805..59656189-chr12:59672943..59675327,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-272B17.2.1-1	chr12:59759999-59760050	ENSG00000258214
2	lnc-SLC16A7-4	chr12:59714688-59717255	NONHSAT029042
3	lnc-SLC16A7-4	chr12:59712962-59714552	NONHSAT029042

No data

Variant related genes	Relation type
RNU6-279P	TF binding region
RNU6-279P	CpG island

Extended variants
information (count: 3164 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3164 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4548712	chr12:59638812-59638813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34181987	chr12:59638858-59638859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546427593	chr12:59638863-59638864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149892752	chr12:59638876-59638877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs28861990	chr12:59638880-59638881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187248324	chr12:59638933-59638934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146438767	chr12:59638981-59638982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562178052	chr12:59639011-59639012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529271980	chr12:59639016-59639017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544154179	chr12:59639038-59639039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557088027	chr12:59639051-59639052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533099626	chr12:59639053-59639054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376512435	chr12:59639068-59639069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10783951	chr12:59639076-59639077	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs192063342	chr12:59639103-59639104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527462570	chr12:59639138-59639139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546203574	chr12:59639141-59639142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184659737	chr12:59639159-59639160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567338977	chr12:59639166-59639167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189421099	chr12:59639177-59639178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140790574	chr12:59639198-59639199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571253903	chr12:59639216-59639217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192676298	chr12:59639235-59639236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558414469	chr12:59639238-59639239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185687704	chr12:59639247-59639248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540794381	chr12:59639286-59639287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372054573	chr12:59639289-59639290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373792851	chr12:59639294-59639295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11495535	chr12:59639347-59639348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11536185	chr12:59639353-59639354	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs79572122	chr12:59639354-59639355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189046497	chr12:59639390-59639391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75087737	chr12:59639405-59639406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180996636	chr12:59639442-59639443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545007415	chr12:59639450-59639451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560358805	chr12:59639475-59639476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527514422	chr12:59639480-59639481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549112876	chr12:59639507-59639508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560973318	chr12:59639521-59639522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531474061	chr12:59639533-59639534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145181400	chr12:59639563-59639564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34238449	chr12:59639573-59639574	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs149000623	chr12:59639594-59639595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2221157	chr12:59639613-59639614	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs76235983	chr12:59639632-59639633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534140393	chr12:59639671-59639672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375468852	chr12:59639672-59639673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573894072	chr12:59639717-59639718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537979341	chr12:59639731-59639732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556226114	chr12:59639769-59639770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21215367	CNVD

Chromatin state (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59638800-59644200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr12:59642400-59642600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:59642400-59642600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr12:59642600-59646600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr12:59644000-59644800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr12:59644000-59645000	Enhancers	Brain Hippocampus Middle	brain
7	chr12:59644200-59644600	Enhancers	Brain Angular Gyrus	brain
8	chr12:59644200-59644600	Enhancers	Brain Anterior Caudate	brain
9	chr12:59644200-59644800	Enhancers	H9 Cell Line	embryonic stem cell
10	chr12:59644200-59644800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr12:59644200-59644800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr12:59644200-59644800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr12:59644400-59644600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:59644400-59644800	Enhancers	Brain Cingulate Gyrus	brain
15	chr12:59644600-59646600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:59645000-59646000	Weak transcription	Brain Hippocampus Middle	brain
17	chr12:59646000-59647400	ZNF genes & repeats	Brain Hippocampus Middle	brain
18	chr12:59646600-59647200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
19	chr12:59646600-59647400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr12:59646600-59648000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:59646800-59647400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr12:59676600-59677400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr12:59676600-59677400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr12:59676600-59677600	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr12:59676600-59677600	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr12:59676800-59677200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr12:59676800-59677400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:59676800-59677600	Enhancers	H1 Cell Line	embryonic stem cell
29	chr12:59677000-59677400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr12:59677000-59677400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:59677000-59677400	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr12:59677400-59679400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:59683600-59688000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:59684000-59684200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr12:59684200-59684800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr12:59684800-59685600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr12:59686400-59687000	Enhancers	Gastric	stomach
38	chr12:59687000-59687200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr12:59687000-59692200	Weak transcription	Gastric	stomach
40	chr12:59688000-59688200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:59688200-59688600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:59688600-59689000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:59690200-59690400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr12:59690400-59692200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr12:59692200-59692400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr12:59692200-59692400	Enhancers	Gastric	stomach
47	chr12:59697400-59698600	Enhancers	Fetal Heart	heart
48	chr12:59698200-59698400	Enhancers	Aorta	Aorta
49	chr12:59704600-59707400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr12:59705400-59707400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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