Variant report

Variant	nsv581854
Chromosome Location	chr2:51019232-51093536
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	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
3	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
4	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
5	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
6	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
7	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
8	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
9	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
10	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
11	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
13	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
14	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
15	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
16	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
17	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
18	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
19	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
20	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
21	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
22	CTCF	chr2:51075262-51075348	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr2:51086400-51086492	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr2:51086360-51086510	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr2:51040238-51040274	A549	lung:	n/a	n/a
26	CTCF	chr2:51056731-51056889	GM20000	blood:	n/a	n/a
27	CTCF	chr2:51086260-51086410	BE2_C	brain:	n/a	n/a
28	CTCF	chr2:51086389-51086467	NHEK	skin:	n/a	n/a
29	CTCF	chr2:51086380-51086530	Caco-2	colon:	n/a	n/a
30	CTCF	chr2:51040080-51040230	GM12874	blood:	n/a	n/a
31	CTCF	chr2:51086380-51086530	HCT-116	colon:	n/a	n/a
32	EBF1	chr2:51056677-51056926	GM12878	blood:	n/a	n/a
33	EBF1	chr2:51056723-51056916	GM12878	blood:	n/a	n/a
34	ESR1	chr2:51036670-51036984	ECC-1	luminal epithelium:	n/a	n/a
35	ESR1	chr2:51036590-51036975	ECC-1	luminal epithelium:	n/a	n/a
36	ESR1	chr2:51031536-51031804	ECC-1	luminal epithelium:	n/a	chr2:51031705-51031722 chr2:51031705-51031720 chr2:51031704-51031721
37	ESR1	chr2:51036616-51037084	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr2:51036504-51036992	ECC-1	luminal epithelium:	n/a	n/a
39	FOS	chr2:51084537-51084734	MCF10A-Er-Src	breast:	n/a	chr2:51084610-51084619
40	FOS	chr2:51082559-51082872	MCF10A-Er-Src	breast:	n/a	chr2:51082783-51082795
41	FOS	chr2:51033298-51033583	MCF10A-Er-Src	breast:	n/a	chr2:51033465-51033474 chr2:51033466-51033474 chr2:51033466-51033473 chr2:51033466-51033475
42	FOS	chr2:51033342-51033592	MCF10A-Er-Src	breast:	n/a	chr2:51033465-51033474 chr2:51033466-51033474 chr2:51033466-51033473 chr2:51033466-51033475
43	FOS	chr2:51084616-51084639	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr2:51033293-51033592	MCF10A-Er-Src	breast:	n/a	chr2:51033465-51033474 chr2:51033466-51033474 chr2:51033466-51033473 chr2:51033466-51033475
45	FOS	chr2:51082596-51082827	MCF10A-Er-Src	breast:	n/a	chr2:51082783-51082795
46	FOS	chr2:51082581-51082816	MCF10A-Er-Src	breast:	n/a	chr2:51082783-51082795
47	FOXA2	chr2:51054779-51055152	A549	lung:	n/a	n/a
48	GABPA	chr2:51056700-51057037	Hela-S3	cervix:	n/a	n/a
49	GABPA	chr2:51056770-51056919	HepG2	liver:	n/a	n/a
50	GABPA	chr2:51056730-51056923	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51056884-51056934	ProgFib	skin:	n/a
2	chr2:51056822-51056872	SK-N-SH	brain:	n/a
3	chr2:51057548-51057598	AG04450	lung:	fetal
4	chr2:51056884-51056934	AoSMC	blood vessel:	n/a
5	chr2:51057548-51057598	RPTEC	kidney:	n/a
6	chr2:51057548-51057598	Caco-2	colon:	n/a
7	chr2:51057548-51057598	BE2_C	brain:	n/a
8	chr2:51074881-51074931	NT2-D1	testis:	n/a
9	chr2:51074939-51074989	SK-N-MC	brain:	n/a
10	chr2:51065673-51065723	H1-hESC	embryonic stem cell:	embryo
11	chr2:51074939-51074989	HL-60	blood:	n/a
12	chr2:51056822-51056872	GM12878	blood:	n/a
13	chr2:51057218-51057268	PANC-1	pancreas:	n/a
14	chr2:51074939-51074989	RPTEC	kidney:	n/a
15	chr2:51074939-51074989	GM12878	blood:	n/a
16	chr2:51056884-51056934	GM19239	blood:	n/a
17	chr2:51057218-51057268	NHDF-neo	bronchial:	n/a
18	chr2:51065673-51065723	RPTEC	kidney:	n/a
19	chr2:51074939-51074989	HNPCEpiC	eye:	n/a
20	chr2:51074881-51074931	CMK	blood:	n/a
21	chr2:51074881-51074931	Caco-2	colon:	n/a
22	chr2:51057548-51057598	HL-60	blood:	n/a
23	chr2:51074939-51074989	HRPEpiC	eye:	n/a
24	chr2:51074939-51074989	AG10803	skin:	n/a
25	chr2:51056884-51056934	AG09309	skin:	n/a
26	chr2:51074881-51074931	HCM	heart:	n/a
27	chr2:51074939-51074989	HRCEpiC	kidney:	n/a
28	chr2:51057218-51057268	SK-N-SH_RA	brain:	n/a
29	chr2:51056822-51056872	HCM	heart:	n/a
30	chr2:51074881-51074931	SAEC	small airway:	n/a
31	chr2:51057548-51057598	HAEpiC	amniotic membrane:	n/a
32	chr2:51065673-51065723	HAEpiC	amniotic membrane:	n/a
33	chr2:51056822-51056872	SAEC	small airway:	n/a
34	chr2:51056884-51056934	AG09319	gingival:	n/a
35	chr2:51056822-51056872	Hepatocyte	liver:	n/a
36	chr2:51065673-51065723	SKMC	muscle:	n/a
37	chr2:51056884-51056934	HCM	heart:	n/a
38	chr2:51057218-51057268	Hela-S3	cervix:	n/a
39	chr2:51056884-51056934	HRPEpiC	eye:	n/a
40	chr2:51065673-51065723	A549	lung:	n/a
41	chr2:51056822-51056872	HCPEpiC	choroid plexus:	n/a
42	chr2:51074939-51074989	AG09319	gingival:	n/a
43	chr2:51074881-51074931	HEK293	kidney:	embryo
44	chr2:51056822-51056872	SK-N-SH_RA	brain:	n/a
45	chr2:51074881-51074931	HRCEpiC	kidney:	n/a
46	chr2:51057548-51057598	HCM	heart:	n/a
47	chr2:51057218-51057268	HCF	heart:	n/a
48	chr2:51056884-51056934	ECC-1	luminal epithelium:	n/a
49	chr2:51056822-51056872	Caco-2	colon:	n/a
50	chr2:51065673-51065723	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
2	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
3	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
4	chr2:51018306..51019906-chr2:51022210..51025087,2	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: 2616 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2616 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9751737	chr2:51019232-51019233	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536401333	chr2:51019295-51019296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540534569	chr2:51019310-51019311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573688820	chr2:51019322-51019323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144293950	chr2:51019329-51019330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528881876	chr2:51019378-51019379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147836071	chr2:51019380-51019381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375758665	chr2:51019385-51019386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562594454	chr2:51019389-51019390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148870517	chr2:51019406-51019407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552332981	chr2:51019410-51019411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143620789	chr2:51019416-51019417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76963028	chr2:51019418-51019419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556245246	chr2:51019430-51019431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151001205	chr2:51019459-51019460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568319759	chr2:51019500-51019501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535841644	chr2:51019501-51019502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557118760	chr2:51019503-51019504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140948666	chr2:51019542-51019543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188512716	chr2:51019556-51019557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13017116	chr2:51019601-51019602	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs72837080	chr2:51019670-51019671	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs375696616	chr2:51019736-51019737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527478027	chr2:51019745-51019746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35196243	chr2:51019748-51019749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555632160	chr2:51019774-51019775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573892304	chr2:51019781-51019782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544179123	chr2:51019795-51019796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201162796	chr2:51019814-51019815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562170695	chr2:51019823-51019824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532836666	chr2:51019857-51019858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181560453	chr2:51019889-51019890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564299541	chr2:51019893-51019894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528689016	chr2:51019912-51019913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138872571	chr2:51019913-51019914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4125974	chr2:51019920-51019921	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs186574468	chr2:51019924-51019925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374609078	chr2:51019962-51019963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201451713	chr2:51019997-51019998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535993773	chr2:51020001-51020002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550932222	chr2:51020046-51020047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569288562	chr2:51020056-51020057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192358138	chr2:51020074-51020075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142084061	chr2:51020082-51020083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs80005564	chr2:51020096-51020097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533980476	chr2:51020112-51020113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555306849	chr2:51020166-51020167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549874748	chr2:51020196-51020197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183734115	chr2:51020209-51020210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs377208723	chr2:51020216-51020217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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

Chromatin state (count:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51014000-51020000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr2:51016200-51021000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:51016200-51021000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr2:51018000-51023200	Weak transcription	Fetal Brain Male	brain
5	chr2:51020000-51021000	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr2:51020600-51022800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr2:51020600-51023400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr2:51020800-51021000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:51020800-51021400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr2:51020800-51021600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr2:51020800-51022800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:51020800-51023000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:51021000-51021200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr2:51021000-51021400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:51021000-51021400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
16	chr2:51021000-51023200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr2:51021200-51021600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr2:51021200-51021800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr2:51021200-51021800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr2:51021400-51022200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:51021400-51023000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr2:51021600-51022200	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr2:51021800-51022200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr2:51021800-51022800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr2:51022200-51022400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr2:51022200-51022400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:51022200-51022600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:51022400-51023200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:51023000-51024200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr2:51023200-51023400	Enhancers	Fetal Brain Male	brain
31	chr2:51023400-51023600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:51030400-51031800	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr2:51030800-51032200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:51031600-51032200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:51031600-51032400	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr2:51031800-51032200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr2:51031800-51036600	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr2:51032200-51036800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:51036600-51037000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr2:51036800-51037200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:51040800-51041200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr2:51041200-51041400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr2:51041400-51051800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr2:51042000-51042200	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr2:51042200-51042400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr2:51042400-51042600	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr2:51042600-51046400	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr2:51046600-51047400	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr2:51047400-51048000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr2:51047600-51048800	Enhancers	Brain Germinal Matrix	brain

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