Variant report

Variant	nsv933545
Chromosome Location	chr2:50988264-51129525
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	chr2:51083034-51083154	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr2:51106584-51106784	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
4	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
5	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
7	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
8	CEBPB	chr2:51127917-51128117	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
10	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
12	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
13	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
14	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
15	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
16	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
17	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
18	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
19	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
20	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
21	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
22	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
23	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
24	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
25	CTCF	chr2:51099850-51099874	Gliobla	brain:	n/a	n/a
26	CTCF	chr2:51013600-51013750	HEK293	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
27	CTCF	chr2:51009680-51009830	HRE	kidney:	n/a	n/a
28	CTCF	chr2:51013578-51013819	Medullo	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
29	CTCF	chr2:51008900-51009050	Caco-2	colon:	n/a	n/a
30	CTCF	chr2:51099780-51099930	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr2:51099760-51099910	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr2:51013600-51013750	HepG2	liver:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
33	CTCF	chr2:51099880-51100030	HCT-116	colon:	n/a	n/a
34	CTCF	chr2:51099842-51099897	LNCaP	prostate:	n/a	n/a
35	CTCF	chr2:51099780-51099930	Caco-2	colon:	n/a	n/a
36	CTCF	chr2:51009720-51009870	AG04450	lung:	n/a	chr2:51009841-51009854
37	CTCF	chr2:51013660-51013810	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
38	CTCF	chr2:51015540-51015690	HCT-116	colon:	n/a	n/a
39	CTCF	chr2:51099689-51099932	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr2:51013560-51013710	HBMEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
41	CTCF	chr2:51009804-51009856	Hela-S3	cervix:	n/a	chr2:51009841-51009854
42	CTCF	chr2:51099820-51099970	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr2:51086260-51086410	BE2_C	brain:	n/a	n/a
44	CTCF	chr2:51099780-51099930	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr2:51013620-51013770	SK-N-SH_RA	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
46	CTCF	chr2:51040238-51040274	A549	lung:	n/a	n/a
47	CTCF	chr2:51099800-51099950	AG04450	lung:	n/a	n/a
48	CTCF	chr2:51099820-51099970	BE2_C	brain:	n/a	n/a
49	CTCF	chr2:51040080-51040230	GM12874	blood:	n/a	n/a
50	CTCF	chr2:51013580-51013730	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51056884-51056934	A549	lung:	n/a
2	chr2:51056822-51056872	HNPCEpiC	eye:	n/a
3	chr2:50992829-50992879	GM12891	blood:	n/a
4	chr2:50992829-50992879	HCPEpiC	choroid plexus:	n/a
5	chr2:51001003-51001053	HRCEpiC	kidney:	n/a
6	chr2:51001003-51001053	AG04450	lung:	fetal
7	chr2:51074939-51074989	HRCEpiC	kidney:	n/a
8	chr2:51001003-51001053	U87	brain:	n/a
9	chr2:51074939-51074989	BJ	skin:	n/a
10	chr2:51074939-51074989	CMK	blood:	n/a
11	chr2:51057548-51057598	HIPEpiC	eye:	n/a
12	chr2:51074939-51074989	ovcar-3	ovarian:	n/a
13	chr2:51056822-51056872	NHDF-neo	bronchial:	n/a
14	chr2:51001003-51001053	PrEC	prostate:	n/a
15	chr2:51074939-51074989	ProgFib	skin:	n/a
16	chr2:51074881-51074931	U87	brain:	n/a
17	chr2:51074939-51074989	GM12891	blood:	n/a
18	chr2:51057218-51057268	Hela-S3	cervix:	n/a
19	chr2:51074939-51074989	HCM	heart:	n/a
20	chr2:50992829-50992879	HEK293	kidney:	embryo
21	chr2:51074881-51074931	BJ	skin:	n/a
22	chr2:51057548-51057598	HL-60	blood:	n/a
23	chr2:51074881-51074931	NHBE	bronchial:	n/a
24	chr2:51056884-51056934	AG04450	lung:	fetal
25	chr2:51056884-51056934	AG09309	skin:	n/a
26	chr2:51057548-51057598	HCF	heart:	n/a
27	chr2:50992829-50992879	Jurkat	blood:	n/a
28	chr2:51065673-51065723	PFSK-1	brain:	n/a
29	chr2:50992829-50992879	AG09319	gingival:	n/a
30	chr2:51057548-51057598	HUVEC	blood vessel:	n/a
31	chr2:51056884-51056934	Jurkat	blood:	n/a
32	chr2:51074939-51074989	HIPEpiC	eye:	n/a
33	chr2:51057548-51057598	A549	lung:	n/a
34	chr2:51056822-51056872	AG10803	skin:	n/a
35	chr2:51057218-51057268	HMEC	breast:	n/a
36	chr2:51057548-51057598	GM12891	blood:	n/a
37	chr2:51074881-51074931	ovcar-3	ovarian:	n/a
38	chr2:51074939-51074989	RPTEC	kidney:	n/a
39	chr2:51057218-51057268	BE2_C	brain:	n/a
40	chr2:51056884-51056934	H1-hESC	embryonic stem cell:	embryo
41	chr2:51057548-51057598	NT2-D1	testis:	n/a
42	chr2:51057548-51057598	MCF10A-Er-Src	breast:	n/a
43	chr2:51056822-51056872	HCM	heart:	n/a
44	chr2:51057218-51057268	SK-N-SH	brain:	n/a
45	chr2:51065673-51065723	MCF-7	breast:	n/a
46	chr2:51056884-51056934	PANC-1	pancreas:	n/a
47	chr2:51057218-51057268	ProgFib	skin:	n/a
48	chr2:51065673-51065723	K562	blood:	n/a
49	chr2:51065673-51065723	GM19239	blood:	n/a
50	chr2:51001003-51001053	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
2	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
3	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:
4	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
5	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
6	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
7	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
8	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
9	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSHR-5	chr2:51056580-51056816	NONHSAT070648

Variant related genes	Relation type
ENSG00000238165	TF binding region
ENSG00000215968	TF binding region
ENSG00000238165	CpG island
ENSG00000215968	CpG island

Extended variants
information (count: 4938 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4938 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs36008048	chr2:50988276-50988277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143704836	chr2:50988277-50988278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141443109	chr2:50988304-50988305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138509326	chr2:50988371-50988372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs3850330	chr2:50988382-50988383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs555730461	chr2:50988504-50988505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567247320	chr2:50988520-50988521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9679041	chr2:50988546-50988547	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs545552909	chr2:50988548-50988549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565440990	chr2:50988551-50988552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186889606	chr2:50988566-50988567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541350460	chr2:50988570-50988571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560237637	chr2:50988576-50988577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544826565	chr2:50988590-50988591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557924451	chr2:50988607-50988608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112513050	chr2:50988639-50988640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528872021	chr2:50988666-50988667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189968646	chr2:50988672-50988673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112594426	chr2:50988749-50988750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529238648	chr2:50988811-50988812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544603223	chr2:50988873-50988874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72837057	chr2:50988927-50988928	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs533463899	chr2:50988935-50988936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551942006	chr2:50988972-50988973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370211808	chr2:50989028-50989029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141642615	chr2:50989034-50989035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182247109	chr2:50989061-50989062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187324704	chr2:50989062-50989063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567577408	chr2:50989100-50989101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537398848	chr2:50989107-50989108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549750403	chr2:50989111-50989112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9678486	chr2:50989198-50989199	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs538712380	chr2:50989205-50989206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192701850	chr2:50989219-50989220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573074635	chr2:50989253-50989254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201347068	chr2:50989255-50989256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199532042	chr2:50989259-50989260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368336459	chr2:50989260-50989261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149339520	chr2:50989261-50989262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200805154	chr2:50989262-50989263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534141553	chr2:50989289-50989290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs397794864	chr2:50989290-50989291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555598550	chr2:50989346-50989347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34638001	chr2:50989391-50989392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183695662	chr2:50989429-50989430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188215204	chr2:50989451-50989452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs193275061	chr2:50989470-50989471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78838030	chr2:50989526-50989527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150497745	chr2:50989562-50989563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545494811	chr2:50989656-50989657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Breast cancer	21364760	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
Basal cell lymphoma	21115979	CNVD
Cognitive impairment	21505072	CNVD
Psychiatric disorder	19734545	CNVD
Autism	20844286	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Autism	19218893	CNVD
Autism	22209245	CNVD
Neuropsychiatric disorder	21827697	CNVD
Schizophrenia	22118685	CNVD
Autism	20663923	CNVD
Schizophrenia	21285140	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	22885689	CNVD
Autism	20964600	CNVD
Schizophrenia	19521646	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Mental retardation	19896112	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	17989066	CNVD
Autism	19404257	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50982600-50991200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:50983200-50991800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:50983200-50996800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr2:50990800-50991200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:50991200-50991800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:50991200-50992200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr2:50991200-50992600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:50991400-50993400	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr2:50991800-50993000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:50991800-50993400	Enhancers	Brain Cingulate Gyrus	brain
11	chr2:50991800-50997000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr2:50992000-50993000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr2:50992000-50993000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr2:50992200-50992800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr2:50992200-50992800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr2:50992200-50993400	Enhancers	Fetal Kidney	kidney
17	chr2:50992400-50992600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:50992400-50993000	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr2:50992600-50992800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:50992600-50993000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:50992800-50993600	Enhancers	Brain Anterior Caudate	brain
22	chr2:50992800-50994200	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr2:50992800-51000800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:50993000-50994000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:50993000-50994400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr2:50993000-50998800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr2:50993000-50999200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr2:50993000-51000800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr2:50993400-50995600	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr2:50993400-50996000	Weak transcription	Brain Cingulate Gyrus	brain
31	chr2:50993600-50994200	Enhancers	Brain Germinal Matrix	brain
32	chr2:50993600-50996800	Weak transcription	Brain Anterior Caudate	brain
33	chr2:50994000-50996200	Weak transcription	Fetal Brain Female	brain
34	chr2:50994000-50996600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:50994200-50994800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr2:50994400-50995000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr2:50994800-50999800	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr2:50995000-51000600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr2:50995600-50996200	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr2:50995800-50997400	Enhancers	Fetal Brain Male	brain
41	chr2:50996000-50996400	Enhancers	Brain Cingulate Gyrus	brain
42	chr2:50996000-50997200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr2:50996000-50997400	Enhancers	Duodenum Mucosa	Duodenum
44	chr2:50996200-50996600	Enhancers	Fetal Intestine Small	intestine
45	chr2:50996200-50996600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr2:50996200-50996800	Enhancers	Fetal Brain Female	brain
47	chr2:50996400-50997200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:50996400-50997200	Enhancers	Fetal Intestine Large	intestine
49	chr2:50996400-51000800	Weak transcription	Brain Cingulate Gyrus	brain
50	chr2:50996600-50997000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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