Variant report

Variant	nsv874122
Chromosome Location	chr2:52667944-52730021
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:134)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:134 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr2:52675296-52675528	GM12878	blood:	n/a	n/a
2	BHLHE40	chr2:52675363-52675413	K562	blood:	n/a	n/a
3	CEBPB	chr2:52669548-52669834	A549	lung:	n/a	n/a
4	CEBPB	chr2:52683689-52684029	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:52682200-52682504	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:52698898-52699465	HepG2	liver:	n/a	chr2:52699035-52699046
7	CEBPB	chr2:52692381-52692934	Hela-S3	cervix:	n/a	chr2:52692711-52692723 chr2:52692721-52692732
8	CEBPB	chr2:52698901-52699369	A549	lung:	n/a	chr2:52699035-52699046
9	CEBPB	chr2:52679211-52679275	A549	lung:	n/a	n/a
10	CEBPB	chr2:52669548-52669831	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:52682169-52682476	IMR90	lung:	n/a	n/a
12	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
13	CEBPB	chr2:52702812-52703040	A549	lung:	n/a	chr2:52702847-52702858 chr2:52702907-52702918 chr2:52703014-52703026
14	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
15	CEBPB	chr2:52669525-52669824	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:52699331-52699366	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:52683698-52683958	A549	lung:	n/a	n/a
18	CEBPB	chr2:52682180-52682454	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:52682177-52682409	A549	lung:	n/a	n/a
20	CHD2	chr2:52697733-52697749	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr2:52706240-52706390	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr2:52706560-52706710	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr2:52704400-52704550	GM12869	blood:	n/a	n/a
24	CTCF	chr2:52706340-52706490	AG04450	lung:	n/a	n/a
25	CTCF	chr2:52684000-52684150	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr2:52706320-52706470	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr2:52684785-52684804	LNCaP	prostate:	n/a	n/a
28	CTCF	chr2:52706386-52706414	Medullo	brain:	n/a	n/a
29	CTCF	chr2:52706289-52706362	Medullo	brain:	n/a	n/a
30	CTCF	chr2:52706319-52706404	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr2:52684764-52684817	GM10266	blood:	n/a	n/a
32	CTCF	chr2:52683920-52684070	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr2:52684738-52684835	GM10248	blood:	n/a	n/a
34	CTCF	chr2:52706200-52706350	HPF	lung:	n/a	n/a
35	CTCF	chr2:52706320-52706470	NHEK	skin:	n/a	n/a
36	CTCF	chr2:52706240-52706390	HCFaa	heart:	n/a	n/a
37	CTCF	chr2:52706200-52706350	HCT-116	colon:	n/a	n/a
38	CTCF	chr2:52706300-52706450	HMF	breast:	n/a	n/a
39	CTCF	chr2:52706340-52706490	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr2:52706260-52706410	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:52701560-52701710	Caco-2	colon:	n/a	n/a
42	CTCF	chr2:52701720-52701870	Caco-2	colon:	n/a	n/a
43	E2F4	chr2:52716051-52716210	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr2:52726538-52726745	MCF10A-Er-Src	breast:	n/a	n/a
45	EBF1	chr2:52675396-52675574	GM12878	blood:	n/a	n/a
46	EP300	chr2:52725664-52725727	GM12878	blood:	n/a	n/a
47	EP300	chr2:52692584-52692937	Hela-S3	cervix:	n/a	chr2:52692839-52692848 chr2:52692838-52692847
48	EP300	chr2:52693206-52693207	GM12878	blood:	n/a	n/a
49	FOS	chr2:52702533-52702974	MCF10A-Er-Src	breast:	n/a	chr2:52702666-52702674
50	FOS	chr2:52702589-52702949	MCF10A-Er-Src	breast:	n/a	chr2:52702666-52702674

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52695221-52695271	AG04450	lung:	fetal
2	chr2:52695221-52695271	GM12892	blood:	n/a
3	chr2:52695221-52695271	ECC-1	luminal epithelium:	n/a
4	chr2:52695221-52695271	HepG2	liver:	n/a
5	chr2:52695221-52695271	HUVEC	blood vessel:	n/a
6	chr2:52695221-52695271	SK-N-SH	brain:	n/a
7	chr2:52695221-52695271	HCPEpiC	choroid plexus:	n/a
8	chr2:52695221-52695271	HIPEpiC	eye:	n/a
9	chr2:52695221-52695271	AG10803	skin:	n/a
10	chr2:52695221-52695271	NB4	blood:	n/a
11	chr2:52695221-52695271	AG09309	skin:	n/a
12	chr2:52695221-52695271	HCT-116	colon:	n/a
13	chr2:52695221-52695271	PrEC	prostate:	n/a
14	chr2:52695221-52695271	AG04449	skin:	fetal
15	chr2:52695221-52695271	HRPEpiC	eye:	n/a
16	chr2:52695221-52695271	HAEpiC	amniotic membrane:	n/a
17	chr2:52695221-52695271	RPTEC	kidney:	n/a
18	chr2:52695221-52695271	HL-60	blood:	n/a
19	chr2:52695221-52695271	H1-hESC	embryonic stem cell:	embryo
20	chr2:52695221-52695271	GM06990	blood:	n/a
21	chr2:52695221-52695271	NHBE	bronchial:	n/a
22	chr2:52695221-52695271	AoSMC	blood vessel:	n/a
23	chr2:52695221-52695271	HEK293	kidney:	embryo
24	chr2:52695221-52695271	SK-N-MC	brain:	n/a
25	chr2:52695221-52695271	HNPCEpiC	eye:	n/a
26	chr2:52695221-52695271	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:52695221-52695271	ProgFib	skin:	n/a
28	chr2:52695221-52695271	Jurkat	blood:	n/a
29	chr2:52695221-52695271	HCM	heart:	n/a
30	chr2:52695221-52695271	NHDF-neo	bronchial:	n/a
31	chr2:52695221-52695271	ovcar-3	ovarian:	n/a
32	chr2:52695221-52695271	AG09319	gingival:	n/a
33	chr2:52695221-52695271	GM12891	blood:	n/a
34	chr2:52695221-52695271	HCF	heart:	n/a
35	chr2:52695221-52695271	SAEC	small airway:	n/a
36	chr2:52695221-52695271	NT2-D1	testis:	n/a
37	chr2:52695221-52695271	Hepatocyte	liver:	n/a
38	chr2:52695221-52695271	HRCEpiC	kidney:	n/a
39	chr2:52695221-52695271	PFSK-1	brain:	n/a
40	chr2:52695221-52695271	HEEpiC	esophagus:	n/a
41	chr2:52695221-52695271	K562	blood:	n/a
42	chr2:52695221-52695271	GM12878	blood:	n/a
43	chr2:52695221-52695271	MCF-7	breast:	n/a
44	chr2:52695221-52695271	GM19239	blood:	n/a
45	chr2:52695221-52695271	Caco-2	colon:	n/a
46	chr2:52695221-52695271	BE2_C	brain:	n/a
47	chr2:52695221-52695271	NH-A	brain:	n/a
48	chr2:52695221-52695271	A549	lung:	n/a
49	chr2:52695221-52695271	HMEC	breast:	n/a
50	chr2:52695221-52695271	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:56708428..56710649-chr2:52687376..52688939,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

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	chr2:52721826-52722000	XLOC_002095
4	lnc-ASB3-3	chr2:52725741-52725923	XLOC_002095
5	lnc-ASB3-3	chr2:52722903-52722974	XLOC_002095

No data

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

Extended variants
information (count: 1996 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1996 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17731986	chr2:52667944-52667945	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112956612	chr2:52667950-52667951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111974329	chr2:52667962-52667963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200401378	chr2:52667970-52667971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373796012	chr2:52667981-52667982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562344186	chr2:52668018-52668019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116116243	chr2:52668070-52668071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551344973	chr2:52668081-52668082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377172717	chr2:52668160-52668161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188244527	chr2:52668185-52668186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146990662	chr2:52668196-52668197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565611539	chr2:52668222-52668223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs193082465	chr2:52668227-52668228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138096371	chr2:52668238-52668239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532605287	chr2:52668255-52668256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185271522	chr2:52668268-52668269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543812413	chr2:52668274-52668275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189825502	chr2:52668279-52668280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562549606	chr2:52668285-52668286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs143771209	chr2:52668326-52668327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545762327	chr2:52668418-52668419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553357871	chr2:52668433-52668434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150165839	chr2:52668445-52668446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542351472	chr2:52668448-52668449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116858775	chr2:52668468-52668469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562017277	chr2:52668469-52668470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544830089	chr2:52668500-52668501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530976812	chr2:52668503-52668504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138619056	chr2:52668516-52668517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11897609	chr2:52668522-52668523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113742930	chr2:52668560-52668561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551289610	chr2:52668593-52668594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551866732	chr2:52668607-52668608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76613247	chr2:52668611-52668612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4971598	chr2:52668651-52668652	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs111289988	chr2:52668660-52668661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548220841	chr2:52668674-52668675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149352921	chr2:52668690-52668691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183623568	chr2:52668702-52668703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374105335	chr2:52668704-52668705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188296472	chr2:52668726-52668727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144663477	chr2:52668815-52668816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138348019	chr2:52668849-52668850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115394306	chr2:52668909-52668910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181833576	chr2:52668962-52668963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533342231	chr2:52668966-52668967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544827255	chr2:52668968-52668969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142839882	chr2:52668985-52668986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10208214	chr2:52668988-52668989	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs563446784	chr2:52672416-52672417	Enhancers	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:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52665000-52668200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:52666400-52669000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr2:52667200-52668600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:52667200-52668600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr2:52667600-52668600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr2:52667800-52668600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr2:52667800-52669000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr2:52668200-52668600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:52668200-52668600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr2:52672400-52674000	Enhancers	Fetal Heart	heart
11	chr2:52674200-52682800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr2:52679000-52679200	Enhancers	Liver	Liver
13	chr2:52679200-52680400	Flanking Active TSS	Liver	Liver
14	chr2:52680400-52684400	Enhancers	Liver	Liver
15	chr2:52681800-52684600	Enhancers	Fetal Intestine Large	intestine
16	chr2:52682400-52684600	Enhancers	Fetal Intestine Small	intestine
17	chr2:52682800-52683000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr2:52683000-52683800	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr2:52683200-52684200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr2:52683400-52684200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:52683400-52684200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr2:52683400-52684400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr2:52683400-52684400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr2:52683400-52685400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr2:52683600-52684000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:52683600-52684000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:52683600-52684400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr2:52683600-52684400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:52683600-52685400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr2:52683600-52686200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:52683800-52684200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr2:52683800-52684200	Enhancers	H9 Cell Line	embryonic stem cell
33	chr2:52684000-52685200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr2:52684000-52694000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr2:52684200-52685200	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr2:52684200-52685200	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr2:52684200-52685200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr2:52684200-52692200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr2:52684400-52685200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr2:52684400-52689200	Weak transcription	Liver	Liver
41	chr2:52684400-52690800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr2:52684400-52694400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr2:52685200-52685400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr2:52685200-52686000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr2:52685200-52686200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr2:52685200-52686200	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr2:52685400-52694000	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr2:52687200-52688000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:52689200-52690600	Enhancers	Liver	Liver
50	chr2:52690600-52691000	Flanking Active TSS	Liver	Liver

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