Variant report

Variant	nsv874115
Chromosome Location	chr2:52553023-52609707
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	BACH1	chr2:52565069-52565261	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:52562997-52563330	H1-hESC	embryonic stem cell:	n/a	chr2:52563100-52563114
3	CBX3	chr2:52554738-52555164	HCT-116	colon:	n/a	n/a
4	CEBPB	chr2:52568912-52569271	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:52562815-52563192	IMR90	lung:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
6	CEBPB	chr2:52570177-52570534	HepG2	liver:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
7	CEBPB	chr2:52562773-52563118	HepG2	liver:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
8	CEBPB	chr2:52570199-52570514	A549	lung:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
9	CEBPB	chr2:52569009-52569163	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:52562875-52563266	H1-hESC	embryonic stem cell:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
11	CEBPB	chr2:52570882-52571236	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr2:52570208-52570547	Hela-S3	cervix:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
13	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
14	CEBPB	chr2:52569536-52570532	IMR90	lung:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
15	CEBPB	chr2:52568887-52569285	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:52562807-52563121	A549	lung:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
17	CEBPB	chr2:52562730-52563288	ECC-1	luminal epithelium:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52563266-52563277 chr2:52562956-52562967
18	CEBPB	chr2:52562704-52563282	ECC-1	luminal epithelium:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52563266-52563277 chr2:52562956-52562967
19	CTCF	chr2:52567460-52567610	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr2:52567497-52567583	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr2:52567240-52567390	HAc	cerebellar:	n/a	n/a
22	CTCF	chr2:52567480-52567630	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr2:52567400-52567550	BE2_C	brain:	n/a	n/a
24	CTCF	chr2:52566062-52566160	GM13976	blood:	n/a	n/a
25	CTCF	chr2:52567440-52567590	AG04450	lung:	n/a	n/a
26	CTCF	chr2:52594040-52594190	GM12869	blood:	n/a	n/a
27	CTCF	chr2:52567430-52567681	IMR90	lung:	n/a	n/a
28	CTCF	chr2:52567440-52567590	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr2:52567480-52567630	AG04449	skin:	n/a	n/a
30	CTCF	chr2:52567460-52567610	HAc	cerebellar:	n/a	n/a
31	CTCF	chr2:52585340-52585400	GM20000	blood:	n/a	n/a
32	E2F4	chr2:52562812-52562995	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr2:52567940-52568322	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr2:52580808-52581008	MCF10A-Er-Src	breast:	n/a	n/a
35	EP300	chr2:52562566-52563428	ECC-1	luminal epithelium:	n/a	chr2:52562953-52562967 chr2:52562811-52562825 chr2:52563102-52563111
36	EP300	chr2:52596370-52596765	T-47D	breast:	n/a	n/a
37	FOS	chr2:52602791-52602978	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr2:52562813-52563273	MCF10A-Er-Src	breast:	n/a	chr2:52563103-52563112 chr2:52563102-52563111
39	FOS	chr2:52562948-52563267	MCF10A-Er-Src	breast:	n/a	chr2:52563103-52563112 chr2:52563102-52563111
40	FOS	chr2:52562813-52563272	MCF10A-Er-Src	breast:	n/a	chr2:52563103-52563112 chr2:52563102-52563111
41	FOS	chr2:52562851-52563273	MCF10A-Er-Src	breast:	n/a	chr2:52563103-52563112 chr2:52563102-52563111
42	FOS	chr2:52572336-52572536	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr2:52564135-52564316	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr2:52602723-52603030	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr2:52567971-52568310	MCF10A-Er-Src	breast:	n/a	chr2:52568163-52568171 chr2:52568162-52568172 chr2:52568162-52568172 chr2:52568161-52568173
46	FOS	chr2:52602718-52602926	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr2:52602694-52603019	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr2:52568000-52568309	MCF10A-Er-Src	breast:	n/a	chr2:52568163-52568171 chr2:52568162-52568172 chr2:52568162-52568172 chr2:52568161-52568173
49	FOS	chr2:52567989-52568292	MCF10A-Er-Src	breast:	n/a	chr2:52568163-52568171 chr2:52568162-52568172 chr2:52568162-52568172 chr2:52568161-52568173
50	FOS	chr2:52564169-52564368	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52571550-52571600	HCF	heart:	n/a
2	chr2:52571550-52571600	AG09309	skin:	n/a
3	chr2:52571550-52571600	T-47D	breast:	n/a
4	chr2:52571550-52571600	GM12878	blood:	n/a
5	chr2:52571550-52571600	HRPEpiC	eye:	n/a
6	chr2:52571550-52571600	NHDF-neo	bronchial:	n/a
7	chr2:52571550-52571600	HepG2	liver:	n/a
8	chr2:52571550-52571600	NT2-D1	testis:	n/a
9	chr2:52571550-52571600	GM06990	blood:	n/a
10	chr2:52571550-52571600	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:52571550-52571600	Caco-2	colon:	n/a
12	chr2:52571550-52571600	GM12891	blood:	n/a
13	chr2:52571550-52571600	ECC-1	luminal epithelium:	n/a
14	chr2:52571550-52571600	A549	lung:	n/a
15	chr2:52571550-52571600	HCT-116	colon:	n/a
16	chr2:52571550-52571600	HEEpiC	esophagus:	n/a
17	chr2:52571550-52571600	SK-N-SH_RA	brain:	n/a
18	chr2:52571550-52571600	IMR90	lung:	fetal
19	chr2:52571550-52571600	HRE	kidney:	n/a
20	chr2:52571550-52571600	AG09319	gingival:	n/a
21	chr2:52571550-52571600	GM19239	blood:	n/a
22	chr2:52571550-52571600	Hepatocyte	liver:	n/a
23	chr2:52571550-52571600	U87	brain:	n/a
24	chr2:52571550-52571600	CMK	blood:	n/a
25	chr2:52571550-52571600	LNCaP	prostate:	n/a
26	chr2:52571550-52571600	SAEC	small airway:	n/a
27	chr2:52571550-52571600	NH-A	brain:	n/a
28	chr2:52571550-52571600	ProgFib	skin:	n/a
29	chr2:52571550-52571600	HEK293	kidney:	embryo
30	chr2:52571550-52571600	SK-N-SH	brain:	n/a
31	chr2:52571550-52571600	HIPEpiC	eye:	n/a
32	chr2:52571550-52571600	AG04450	lung:	fetal
33	chr2:52571550-52571600	Hela-S3	cervix:	n/a
34	chr2:52571550-52571600	MCF10A-Er-Src	breast:	n/a
35	chr2:52571550-52571600	NB4	blood:	n/a
36	chr2:52571550-52571600	BE2_C	brain:	n/a
37	chr2:52571550-52571600	PrEC	prostate:	n/a
38	chr2:52571550-52571600	PFSK-1	brain:	n/a
39	chr2:52571550-52571600	SK-N-MC	brain:	n/a
40	chr2:52571550-52571600	HCPEpiC	choroid plexus:	n/a
41	chr2:52571550-52571600	ovcar-3	ovarian:	n/a
42	chr2:52571550-52571600	AG04449	skin:	fetal
43	chr2:52571550-52571600	SKMC	muscle:	n/a
44	chr2:52571550-52571600	HL-60	blood:	n/a
45	chr2:52571550-52571600	HCM	heart:	n/a
46	chr2:52571550-52571600	Jurkat	blood:	n/a
47	chr2:52571550-52571600	HMEC	breast:	n/a
48	chr2:52571550-52571600	MCF-7	breast:	n/a
49	chr2:52571550-52571600	H1-hESC	embryonic stem cell:	embryo
50	chr2:52571550-52571600	AG10803	skin:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-4	chr2:52580012-52580100	ENSG00000231918.1
2	lnc-ASB3-11	chr2:52575330-52575504	NONHSAT070669
3	lnc-CHAC2-3	chr2:52600256-52600309	XLOC_001468
4	lnc-ASB3-11	chr2:52581186-52581394	NONHSAT070669
5	lnc-ASB3-11	chr2:52579245-52579427	NONHSAT070669
6	lnc-ASB3-11	chr2:52576407-52576478	NONHSAT070669
7	lnc-CHAC2-4	chr2:52576463-52578424	ENSG00000231918.1

Variant related genes	Relation type
ENSG00000225444	TF binding region
ENSG00000225444	CpG island

Extended variants
information (count: 2302 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2302 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs118035019	chr2:52553801-52553802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs530472118	chr2:52553820-52553821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370510488	chr2:52553823-52553824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562180939	chr2:52553839-52553840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531286278	chr2:52553906-52553907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375152715	chr2:52553931-52553932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376826721	chr2:52553993-52553994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577104407	chr2:52561018-52561019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546165498	chr2:52561027-52561028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144978897	chr2:52561058-52561059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528490637	chr2:52561081-52561082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373522097	chr2:52561087-52561088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1424789	chr2:52561123-52561124	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs1424790	chr2:52561159-52561160	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs531004518	chr2:52561165-52561166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185825696	chr2:52561181-52561182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538696291	chr2:52561186-52561187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149115597	chr2:52561190-52561191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77136183	chr2:52561214-52561215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142203845	chr2:52561231-52561232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76394380	chr2:52561234-52561235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547294144	chr2:52561316-52561317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565505189	chr2:52561406-52561407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34767062	chr2:52561415-52561416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534610899	chr2:52561422-52561423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565813790	chr2:52561433-52561434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs59902490	chr2:52561458-52561459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571504557	chr2:52561543-52561544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554659674	chr2:52561545-52561546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534591155	chr2:52561551-52561552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574632475	chr2:52561555-52561556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147883612	chr2:52561581-52561582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111268328	chr2:52561659-52561660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556912853	chr2:52561689-52561690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141526516	chr2:52561692-52561693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187402521	chr2:52561712-52561713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192252847	chr2:52561713-52561714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147075314	chr2:52561722-52561723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111677360	chr2:52561769-52561770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562812583	chr2:52561778-52561779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs56333115	chr2:52561783-52561784	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs561835610	chr2:52561852-52561853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367851740	chr2:52561853-52561854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544769262	chr2:52561896-52561897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564494257	chr2:52561897-52561898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200494763	chr2:52561909-52561910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533589046	chr2:52561914-52561915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546937033	chr2:52561929-52561930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567173918	chr2:52561959-52561960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138400728	chr2:52562014-52562015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52553800-52554000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:52561000-52561400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:52561400-52561600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:52561400-52562200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr2:52561600-52565000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:52561600-52565200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:52561600-52565800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:52562200-52562600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:52562200-52565000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr2:52562200-52565200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr2:52562400-52562800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr2:52562600-52562800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:52562600-52563400	Enhancers	H1 Cell Line	embryonic stem cell
14	chr2:52562600-52563800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr2:52562600-52565200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr2:52562600-52567600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr2:52562800-52563800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:52562800-52565000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr2:52563000-52564800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:52563400-52563800	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr2:52563800-52564200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr2:52563800-52564600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr2:52563800-52564600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr2:52564200-52564400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr2:52564200-52564600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr2:52564200-52564600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:52564200-52565000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr2:52564200-52565000	Enhancers	H9 Cell Line	embryonic stem cell
29	chr2:52564400-52572400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr2:52564600-52565000	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr2:52564600-52565200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr2:52564600-52565600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr2:52564600-52569400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr2:52564800-52565000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:52565000-52565200	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr2:52565000-52565800	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr2:52565000-52566200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:52565000-52566400	Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr2:52565000-52566400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr2:52565000-52566600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr2:52565000-52577800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr2:52565200-52565400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr2:52565200-52565800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:52565200-52566200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr2:52565200-52566400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr2:52565200-52566400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr2:52565400-52565600	Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr2:52565600-52566400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr2:52565600-52567400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr2:52565800-52566200	Enhancers	H9 Cell Line	embryonic stem cell

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