Variant report

Variant	nsv1013464
Chromosome Location	chr2:52398592-52585274
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	ARID3A	chr2:52467445-52467547	K562	blood:	n/a	n/a
2	BACH1	chr2:52562997-52563330	H1-hESC	embryonic stem cell:	n/a	chr2:52563100-52563114
3	BACH1	chr2:52565069-52565261	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr2:52412674-52412755	GM12878	blood:	n/a	n/a
5	CBX3	chr2:52554738-52555164	HCT-116	colon:	n/a	n/a
6	CEBPB	chr2:52568912-52569271	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:52516875-52517234	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr2:52568887-52569285	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:52569536-52570532	IMR90	lung:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
10	CEBPB	chr2:52562704-52563282	ECC-1	luminal epithelium:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52563266-52563277 chr2:52562956-52562967
11	CEBPB	chr2:52434940-52435407	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:52488046-52488388	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:52424571-52424862	HepG2	liver:	n/a	chr2:52424680-52424691
14	CEBPB	chr2:52570175-52570518	H1-hESC	embryonic stem cell:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
15	CEBPB	chr2:52475235-52475401	A549	lung:	n/a	chr2:52475269-52475280
16	CEBPB	chr2:52447440-52447956	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr2:52437849-52438049	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:52569009-52569163	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:52484634-52484917	A549	lung:	n/a	chr2:52484762-52484773 chr2:52484763-52484772 chr2:52484761-52484774 chr2:52484761-52484772
20	CEBPB	chr2:52562807-52563121	A549	lung:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
21	CEBPB	chr2:52570177-52570534	HepG2	liver:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
22	CEBPB	chr2:52475213-52475267	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr2:52516375-52516634	IMR90	lung:	n/a	chr2:52516470-52516481
24	CEBPB	chr2:52496637-52496874	HepG2	liver:	n/a	chr2:52496760-52496771
25	CEBPB	chr2:52484592-52484943	HepG2	liver:	n/a	chr2:52484762-52484773 chr2:52484763-52484772 chr2:52484761-52484774 chr2:52484761-52484772
26	CEBPB	chr2:52516417-52516634	HepG2	liver:	n/a	chr2:52516470-52516481
27	CEBPB	chr2:52562773-52563118	HepG2	liver:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
28	CEBPB	chr2:52496591-52497101	IMR90	lung:	n/a	chr2:52496760-52496771
29	CEBPB	chr2:52484597-52484933	IMR90	lung:	n/a	chr2:52484762-52484773 chr2:52484763-52484772 chr2:52484761-52484774 chr2:52484761-52484772
30	CEBPB	chr2:52496622-52496897	A549	lung:	n/a	chr2:52496760-52496771
31	CEBPB	chr2:52562730-52563288	ECC-1	luminal epithelium:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52563266-52563277 chr2:52562956-52562967
32	CEBPB	chr2:52508166-52508428	IMR90	lung:	n/a	chr2:52508316-52508327
33	CEBPB	chr2:52570199-52570514	A549	lung:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
34	CEBPB	chr2:52497321-52497563	HepG2	liver:	n/a	chr2:52497433-52497444
35	CEBPB	chr2:52562875-52563266	H1-hESC	embryonic stem cell:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
36	CEBPB	chr2:52570208-52570547	Hela-S3	cervix:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
37	CEBPB	chr2:52516890-52517212	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:52493705-52493946	IMR90	lung:	n/a	n/a
39	CEBPB	chr2:52570882-52571236	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr2:52508157-52508457	HepG2	liver:	n/a	chr2:52508316-52508327
41	CEBPB	chr2:52562815-52563192	IMR90	lung:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
42	CEBPB	chr2:52447446-52447926	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr2:52475176-52475438	HepG2	liver:	n/a	chr2:52475269-52475280
44	CEBPB	chr2:52424565-52424782	Hela-S3	cervix:	n/a	chr2:52424680-52424691
45	CEBPB	chr2:52424527-52424851	IMR90	lung:	n/a	chr2:52424680-52424691
46	CEBPB	chr2:52424578-52424825	A549	lung:	n/a	chr2:52424680-52424691
47	CHD2	chr2:52480885-52480914	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr2:52567480-52567630	AG04449	skin:	n/a	n/a
49	CTCF	chr2:52491844-52491921	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr2:52491780-52491930	HCT-116	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52571550-52571600	PANC-1	pancreas:	n/a
2	chr2:52480467-52480517	NH-A	brain:	n/a
3	chr2:52571550-52571600	ovcar-3	ovarian:	n/a
4	chr2:52480467-52480517	AG09309	skin:	n/a
5	chr2:52571550-52571600	HCT-116	colon:	n/a
6	chr2:52571550-52571600	NHDF-neo	bronchial:	n/a
7	chr2:52480467-52480517	PANC-1	pancreas:	n/a
8	chr2:52571550-52571600	NT2-D1	testis:	n/a
9	chr2:52571550-52571600	ECC-1	luminal epithelium:	n/a
10	chr2:52480467-52480517	HEEpiC	esophagus:	n/a
11	chr2:52571550-52571600	PFSK-1	brain:	n/a
12	chr2:52571550-52571600	K562	blood:	n/a
13	chr2:52571550-52571600	GM12892	blood:	n/a
14	chr2:52480467-52480517	T-47D	breast:	n/a
15	chr2:52480467-52480517	IMR90	lung:	fetal
16	chr2:52480467-52480517	AG04450	lung:	fetal
17	chr2:52571550-52571600	Hepatocyte	liver:	n/a
18	chr2:52480467-52480517	A549	lung:	n/a
19	chr2:52480467-52480517	MCF10A-Er-Src	breast:	n/a
20	chr2:52480467-52480517	HRE	kidney:	n/a
21	chr2:52571550-52571600	HL-60	blood:	n/a
22	chr2:52571550-52571600	CMK	blood:	n/a
23	chr2:52480467-52480517	Jurkat	blood:	n/a
24	chr2:52480467-52480517	CMK	blood:	n/a
25	chr2:52571550-52571600	HNPCEpiC	eye:	n/a
26	chr2:52571550-52571600	LNCaP	prostate:	n/a
27	chr2:52571550-52571600	AoSMC	blood vessel:	n/a
28	chr2:52480467-52480517	HCF	heart:	n/a
29	chr2:52571550-52571600	GM06990	blood:	n/a
30	chr2:52480467-52480517	Hepatocyte	liver:	n/a
31	chr2:52571550-52571600	HCPEpiC	choroid plexus:	n/a
32	chr2:52571550-52571600	H1-hESC	embryonic stem cell:	embryo
33	chr2:52571550-52571600	HepG2	liver:	n/a
34	chr2:52480467-52480517	U87	brain:	n/a
35	chr2:52571550-52571600	SK-N-SH_RA	brain:	n/a
36	chr2:52571550-52571600	SKMC	muscle:	n/a
37	chr2:52571550-52571600	HRCEpiC	kidney:	n/a
38	chr2:52571550-52571600	ProgFib	skin:	n/a
39	chr2:52480467-52480517	PFSK-1	brain:	n/a
40	chr2:52571550-52571600	NH-A	brain:	n/a
41	chr2:52480467-52480517	HAEpiC	amniotic membrane:	n/a
42	chr2:52480467-52480517	HIPEpiC	eye:	n/a
43	chr2:52571550-52571600	MCF10A-Er-Src	breast:	n/a
44	chr2:52571550-52571600	BE2_C	brain:	n/a
45	chr2:52571550-52571600	HRE	kidney:	n/a
46	chr2:52480467-52480517	MCF-7	breast:	n/a
47	chr2:52480467-52480517	ECC-1	luminal epithelium:	n/a
48	chr2:52571550-52571600	AG04450	lung:	fetal
49	chr2:52480467-52480517	GM19239	blood:	n/a
50	chr2:52480467-52480517	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:52521422..52524399-chr2:52528510..52532522,3	K562	blood:
2	chr2:52476747..52479271-chr2:52487226..52489997,2	K562	blood:
3	chr2:52476747..52479271-chr2:52487226..52489997,2	K562	blood:
4	chr2:52444137..52446093-chr2:52447228..52448981,2	K562	blood:
5	chr2:52521422..52524399-chr2:52528510..52532522,3	K562	blood:
6	chr2:52444137..52446093-chr2:52447228..52448981,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB3-11	chr2:52581186-52581394	NONHSAT070669
2	lnc-CHAC2-4	chr2:52580012-52580100	ENSG00000231918.1
3	lnc-CHAC2-4	chr2:52543370-52543438	ENSG00000231918.1
4	lnc-CHAC2-10	chr2:52453760-52453813	NONHSAT070667
5	lnc-CHAC2-4	chr2:52576463-52578424	ENSG00000231918.1
6	lnc-ASB3-11	chr2:52576407-52576478	NONHSAT070669
7	lnc-ASB3-11	chr2:52575330-52575504	NONHSAT070669
8	lnc-CHAC2-10	chr2:52470105-52470654	NONHSAT070667
9	lnc-ASB3-11	chr2:52579245-52579427	NONHSAT070669

Variant related genes	Relation type
ENSG00000202195	TF binding region
ENSG00000202195	CpG island

Extended variants
information (count: 3642 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3642 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142204331	chr2:52408022-52408023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144387789	chr2:52408053-52408054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369012013	chr2:52408108-52408109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147863064	chr2:52408167-52408168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190232762	chr2:52408169-52408170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552642766	chr2:52408230-52408231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140389271	chr2:52408251-52408252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535274347	chr2:52408265-52408266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192959329	chr2:52408272-52408273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550116075	chr2:52408314-52408315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575417556	chr2:52408331-52408332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544542439	chr2:52408332-52408333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377512366	chr2:52408336-52408337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150366208	chr2:52408349-52408350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116075628	chr2:52408350-52408351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79627398	chr2:52408357-52408358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs76079538	chr2:52412858-52412859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554581219	chr2:52412862-52412863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567778954	chr2:52412873-52412874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116412047	chr2:52412933-52412934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs62140762	chr2:52412944-52412945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs576636220	chr2:52412961-52412962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs151001809	chr2:52412962-52412963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376064184	chr2:52412964-52412965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs72796297	chr2:52412965-52412966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556336619	chr2:52412968-52412969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185815624	chr2:52412974-52412975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562135882	chr2:52412999-52413000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529561059	chr2:52419216-52419217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541398183	chr2:52419235-52419236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561351091	chr2:52419272-52419273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560879172	chr2:52419320-52419321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550641958	chr2:52419364-52419365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570480064	chr2:52419448-52419449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533134181	chr2:52419455-52419456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530613373	chr2:52419477-52419478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375569831	chr2:52419481-52419482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144190984	chr2:52419503-52419504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544158358	chr2:52419515-52419516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535749227	chr2:52419548-52419549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564471773	chr2:52419574-52419575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555754942	chr2:52419660-52419661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569264549	chr2:52419680-52419681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533458072	chr2:52419707-52419708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537897845	chr2:52419725-52419726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558212639	chr2:52419752-52419753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs578063706	chr2:52419759-52419760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540790119	chr2:52419812-52419813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145289736	chr2:52419881-52419882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10182256	chr2:52419886-52419887	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

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
small cell lung cancer	20016488	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52408000-52408400	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr2:52408000-52408400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:52412800-52413000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:52419200-52419400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:52419200-52421200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr2:52419200-52421200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:52419400-52420400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr2:52420400-52421600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr2:52427600-52427800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:52434800-52435000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:52435000-52435200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr2:52435200-52435400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:52435400-52435600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:52435600-52435800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:52436800-52437200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr2:52436800-52438600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:52437400-52438000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr2:52442000-52443800	Enhancers	Fetal Heart	heart
19	chr2:52443800-52448600	Weak transcription	Fetal Heart	heart
20	chr2:52448600-52449800	Enhancers	Fetal Heart	heart
21	chr2:52449400-52449800	Enhancers	NHDF-Ad	bronchial
22	chr2:52449600-52450000	Active TSS	Primary T helper naive cells from peripheral blood	blood
23	chr2:52451600-52452600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:52452600-52454600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:52454600-52455200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:52463200-52464000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr2:52463400-52463800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr2:52463400-52463800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr2:52463800-52464000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr2:52463800-52464600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr2:52463800-52466000	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr2:52464000-52464400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr2:52464400-52465000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr2:52464600-52464800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr2:52464800-52465800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr2:52465000-52466200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr2:52465800-52466000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr2:52465800-52466400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr2:52465800-52466400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr2:52466000-52466200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr2:52466000-52466400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr2:52466000-52466400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr2:52466000-52466400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr2:52466200-52466400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:52479400-52479600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr2:52479600-52480600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr2:52480400-52481200	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr2:52480600-52481000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr2:52480600-52481000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr2:52480600-52481200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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