Variant report

Variant	nsv874120
Chromosome Location	chr2:52659874-52745557
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	chr2:52667276-52667711	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr2:52667277-52667714	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr2:52667333-52667627	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr2:52667354-52667508	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr2:52675296-52675528	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:52675363-52675413	K562	blood:	n/a	n/a
7	CEBPB	chr2:52699331-52699366	IMR90	lung:	n/a	n/a
8	CEBPB	chr2:52741949-52742162	A549	lung:	n/a	n/a
9	CEBPB	chr2:52702580-52703046	HepG2	liver:	n/a	chr2:52702675-52702692 chr2:52702847-52702858 chr2:52702676-52702689 chr2:52702676-52702687 chr2:52702646-52702657 chr2:52702907-52702918 chr2:52703014-52703026
10	CEBPB	chr2:52682169-52682476	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:52682200-52682504	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:52682177-52682409	A549	lung:	n/a	n/a
13	CEBPB	chr2:52698901-52699369	A549	lung:	n/a	chr2:52699035-52699046
14	CEBPB	chr2:52682180-52682454	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:52702812-52703040	A549	lung:	n/a	chr2:52702847-52702858 chr2:52702907-52702918 chr2:52703014-52703026
16	CEBPB	chr2:52679211-52679275	A549	lung:	n/a	n/a
17	CEBPB	chr2:52698898-52699465	HepG2	liver:	n/a	chr2:52699035-52699046
18	CEBPB	chr2:52667215-52667804	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:52666378-52666692	H1-hESC	embryonic stem cell:	n/a	chr2:52666669-52666680 chr2:52666671-52666680 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666671-52666682
20	CEBPB	chr2:52666489-52666836	Hela-S3	cervix:	n/a	chr2:52666669-52666680 chr2:52666671-52666680 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666671-52666682
21	CEBPB	chr2:52702578-52703057	IMR90	lung:	n/a	chr2:52702675-52702692 chr2:52702847-52702858 chr2:52702676-52702689 chr2:52702676-52702687 chr2:52702646-52702657 chr2:52702907-52702918 chr2:52703014-52703026
22	CEBPB	chr2:52683689-52684029	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:52669525-52669824	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:52683698-52683958	A549	lung:	n/a	n/a
25	CEBPB	chr2:52666595-52666817	K562	blood:	n/a	chr2:52666669-52666680 chr2:52666671-52666680 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666671-52666682
26	CEBPB	chr2:52669548-52669831	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:52692381-52692934	Hela-S3	cervix:	n/a	chr2:52692711-52692723 chr2:52692721-52692732
28	CEBPB	chr2:52667357-52667802	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr2:52669548-52669834	A549	lung:	n/a	n/a
30	CEBPB	chr2:52666507-52666820	HepG2	liver:	n/a	chr2:52666669-52666680 chr2:52666671-52666680 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666671-52666682
31	CHD2	chr2:52697733-52697749	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr2:52667317-52667650	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr2:52706260-52706410	HCT-116	colon:	n/a	n/a
34	CTCF	chr2:52684000-52684150	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr2:52706320-52706470	NHEK	skin:	n/a	n/a
36	CTCF	chr2:52663856-52663913	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr2:52706340-52706490	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr2:52684785-52684804	LNCaP	prostate:	n/a	n/a
39	CTCF	chr2:52706319-52706404	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr2:52706200-52706350	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:52684764-52684817	GM10266	blood:	n/a	n/a
42	CTCF	chr2:52683920-52684070	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr2:52663734-52663860	GM12878	blood:	n/a	n/a
44	CTCF	chr2:52684738-52684835	GM10248	blood:	n/a	n/a
45	CTCF	chr2:52704400-52704550	GM12869	blood:	n/a	n/a
46	CTCF	chr2:52706240-52706390	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr2:52706240-52706390	HCFaa	heart:	n/a	n/a
48	CTCF	chr2:52701560-52701710	Caco-2	colon:	n/a	n/a
49	CTCF	chr2:52706560-52706710	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr2:52663784-52663843	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52695221-52695271	NH-A	brain:	n/a
2	chr2:52695221-52695271	GM12891	blood:	n/a
3	chr2:52695221-52695271	SAEC	small airway:	n/a
4	chr2:52695221-52695271	SKMC	muscle:	n/a
5	chr2:52695221-52695271	ovcar-3	ovarian:	n/a
6	chr2:52695221-52695271	A549	lung:	n/a
7	chr2:52695221-52695271	GM06990	blood:	n/a
8	chr2:52695221-52695271	HEEpiC	esophagus:	n/a
9	chr2:52695221-52695271	GM12878	blood:	n/a
10	chr2:52695221-52695271	CMK	blood:	n/a
11	chr2:52695221-52695271	AG09319	gingival:	n/a
12	chr2:52695221-52695271	NHBE	bronchial:	n/a
13	chr2:52695221-52695271	NB4	blood:	n/a
14	chr2:52695221-52695271	GM12892	blood:	n/a
15	chr2:52695221-52695271	HCPEpiC	choroid plexus:	n/a
16	chr2:52695221-52695271	PANC-1	pancreas:	n/a
17	chr2:52695221-52695271	Hela-S3	cervix:	n/a
18	chr2:52695221-52695271	NHDF-neo	bronchial:	n/a
19	chr2:52695221-52695271	IMR90	lung:	fetal
20	chr2:52695221-52695271	AG04449	skin:	fetal
21	chr2:52695221-52695271	HepG2	liver:	n/a
22	chr2:52695221-52695271	MCF-7	breast:	n/a
23	chr2:52695221-52695271	HMEC	breast:	n/a
24	chr2:52695221-52695271	SK-N-SH_RA	brain:	n/a
25	chr2:52695221-52695271	SK-N-SH	brain:	n/a
26	chr2:52695221-52695271	BE2_C	brain:	n/a
27	chr2:52695221-52695271	GM19239	blood:	n/a
28	chr2:52695221-52695271	HEK293	kidney:	embryo
29	chr2:52695221-52695271	PFSK-1	brain:	n/a
30	chr2:52695221-52695271	SK-N-MC	brain:	n/a
31	chr2:52695221-52695271	AoSMC	blood vessel:	n/a
32	chr2:52695221-52695271	PrEC	prostate:	n/a
33	chr2:52695221-52695271	RPTEC	kidney:	n/a
34	chr2:52695221-52695271	H1-hESC	embryonic stem cell:	embryo
35	chr2:52695221-52695271	HCT-116	colon:	n/a
36	chr2:52695221-52695271	ProgFib	skin:	n/a
37	chr2:52695221-52695271	HUVEC	blood vessel:	n/a
38	chr2:52695221-52695271	HRE	kidney:	n/a
39	chr2:52695221-52695271	NT2-D1	testis:	n/a
40	chr2:52695221-52695271	HPAEpiC	pulmonary alveolar:	n/a
41	chr2:52695221-52695271	Jurkat	blood:	n/a
42	chr2:52695221-52695271	AG04450	lung:	fetal
43	chr2:52695221-52695271	HRPEpiC	eye:	n/a
44	chr2:52695221-52695271	U87	brain:	n/a
45	chr2:52695221-52695271	HRCEpiC	kidney:	n/a
46	chr2:52695221-52695271	ECC-1	luminal epithelium:	n/a
47	chr2:52695221-52695271	HNPCEpiC	eye:	n/a
48	chr2:52695221-52695271	Hepatocyte	liver:	n/a
49	chr2:52695221-52695271	Caco-2	colon:	n/a
50	chr2:52695221-52695271	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:52727791..52731753-chr2:52732140..52733978,3	K562	blood:
2	chr2:52727791..52730786-chr2:52732300..52733978,2	K562	blood:
3	chr17:56708428..56710649-chr2:52687376..52688939,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB3-3	chr2:52727682-52727890	XLOC_002095
2	lnc-ASB3-10	chr2:52701211-52701549	NONHSAT070672
3	lnc-ASB3-3	chr2:52725741-52725923	XLOC_002095
4	lnc-ASB3-3	chr2:52722903-52722974	XLOC_002095
5	lnc-ASB3-3	chr2:52721826-52722000	XLOC_002095

Variant related genes	Relation type
ENSG00000225842	TF binding region
ENSG00000236837	TF binding region
ENSG00000225842	CpG island
ENSG00000236837	CpG island
ENSG00000212195	chromatin interactions
ENSG00000236837	chromatin interactions
RAB9B	miRNA target sites
RAD23B	miRNA target sites
RABEP1	miRNA target sites

Extended variants
information (count: 3045 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3045 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6730865	chr2:52659874-52659875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560170038	chr2:52659900-52659901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142414735	chr2:52659904-52659905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550562544	chr2:52659919-52659920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570414979	chr2:52659924-52659925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539164981	chr2:52659929-52659930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184580432	chr2:52659933-52659934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10183375	chr2:52659938-52659939	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs535352527	chr2:52659993-52659994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555421013	chr2:52660009-52660010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190363288	chr2:52660019-52660020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs151294432	chr2:52660024-52660025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560326683	chr2:52660030-52660031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6715943	chr2:52660031-52660032	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs578019032	chr2:52660037-52660038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540765377	chr2:52660061-52660062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560661866	chr2:52660093-52660094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145889787	chr2:52660111-52660112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549604960	chr2:52660126-52660127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563002050	chr2:52660129-52660130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182558971	chr2:52660135-52660136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs60922533	chr2:52660148-52660149	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs185010514	chr2:52660155-52660156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539128203	chr2:52660167-52660168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138550886	chr2:52660242-52660243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140240274	chr2:52660252-52660253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376542995	chr2:52660274-52660275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145204993	chr2:52660294-52660295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555546408	chr2:52660338-52660339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551697333	chr2:52660368-52660369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575421680	chr2:52660409-52660410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538169662	chr2:52660413-52660414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557852639	chr2:52660427-52660428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs578101572	chr2:52660447-52660448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188944819	chr2:52660456-52660457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181091333	chr2:52660475-52660476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368995935	chr2:52660492-52660493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535449121	chr2:52660505-52660506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574193495	chr2:52660531-52660532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542822362	chr2:52660568-52660569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs137994774	chr2:52660598-52660599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115450286	chr2:52660606-52660607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545716385	chr2:52660615-52660616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185409353	chr2:52660620-52660621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374294405	chr2:52660647-52660648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532810415	chr2:52660651-52660652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546190843	chr2:52660694-52660695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566189969	chr2:52660695-52660696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377739837	chr2:52660700-52660701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190220813	chr2:52660706-52660707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52656000-52667200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr2:52658200-52663000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:52658600-52667200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:52662800-52666000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
5	chr2:52663000-52663200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:52664600-52665000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
7	chr2:52665000-52668200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr2:52666000-52667200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr2:52666400-52667800	Enhancers	Hela-S3	cervix
10	chr2:52666400-52669000	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr2:52667200-52667400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr2:52667200-52667600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr2:52667200-52667800	Enhancers	NH-A	brain
14	chr2:52667200-52668600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr2:52667200-52668600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr2:52667400-52667600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr2:52667400-52667800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr2:52667600-52667800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr2:52667600-52667800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr2:52667600-52668600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr2:52667800-52668600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr2:52667800-52669000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:52668200-52668600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr2:52668200-52668600	Enhancers	H9 Cell Line	embryonic stem cell
25	chr2:52672400-52674000	Enhancers	Fetal Heart	heart
26	chr2:52674200-52682800	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr2:52679000-52679200	Enhancers	Liver	Liver
28	chr2:52679200-52680400	Flanking Active TSS	Liver	Liver
29	chr2:52680400-52684400	Enhancers	Liver	Liver
30	chr2:52681800-52684600	Enhancers	Fetal Intestine Large	intestine
31	chr2:52682400-52684600	Enhancers	Fetal Intestine Small	intestine
32	chr2:52682800-52683000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr2:52683000-52683800	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr2:52683200-52684200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr2:52683400-52684200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:52683400-52684200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:52683400-52684400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:52683400-52684400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr2:52683400-52685400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr2:52683600-52684000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:52683600-52684000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:52683600-52684400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr2:52683600-52684400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:52683600-52685400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr2:52683600-52686200	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr2:52683800-52684200	Enhancers	H1 Cell Line	embryonic stem cell
47	chr2:52683800-52684200	Enhancers	H9 Cell Line	embryonic stem cell
48	chr2:52684000-52685200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr2:52684000-52694000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr2:52684200-52685200	Weak transcription	H9 Cell Line	embryonic stem cell

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