Variant report

Variant	nsv525262
Chromosome Location	chr2:51105852-51214993
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	chr2:51155966-51156146	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr2:51179768-51180665	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr2:51214813-51214934	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr2:51185262-51185455	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:51185020-51185401	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
6	CEBPB	chr2:51163450-51163794	HepG2	liver:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
7	CEBPB	chr2:51185023-51185436	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
8	CEBPB	chr2:51185019-51185391	H1-hESC	embryonic stem cell:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
9	CEBPB	chr2:51196305-51196335	K562	blood:	n/a	n/a
10	CEBPB	chr2:51185014-51185411	Hela-S3	cervix:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
11	CEBPB	chr2:51185072-51185406	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
12	CEBPB	chr2:51172595-51172790	HepG2	liver:	n/a	chr2:51172679-51172690
13	CEBPB	chr2:51179763-51180618	IMR90	lung:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
14	CEBPB	chr2:51196130-51196480	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:51180217-51180418	K562	blood:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
16	CEBPB	chr2:51180205-51180442	H1-hESC	embryonic stem cell:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
17	CEBPB	chr2:51196131-51196377	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr2:51185063-51185361	K562	blood:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
19	CEBPB	chr2:51196168-51196459	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:51185077-51185269	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185201-51185210 chr2:51185201-51185210
21	CEBPB	chr2:51180127-51180593	ECC-1	luminal epithelium:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
22	CEBPB	chr2:51179690-51180699	HCT-116	colon:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
23	CEBPB	chr2:51180165-51180469	A549	lung:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
24	CEBPB	chr2:51184978-51185335	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
25	CEBPB	chr2:51184080-51184410	A549	lung:	n/a	chr2:51184131-51184142
26	CEBPB	chr2:51179722-51180770	HCT-116	colon:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
27	CEBPB	chr2:51185008-51185377	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
28	CEBPB	chr2:51180120-51180462	HepG2	liver:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
29	CEBPB	chr2:51185052-51185376	ECC-1	luminal epithelium:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
30	CEBPB	chr2:51185053-51185350	ECC-1	luminal epithelium:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
31	CEBPB	chr2:51185005-51185419	IMR90	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
32	CEBPB	chr2:51185039-51185390	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
33	CEBPB	chr2:51106584-51106784	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:51184010-51184263	HepG2	liver:	n/a	chr2:51184131-51184142
35	CEBPB	chr2:51185035-51185357	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
36	CEBPB	chr2:51127917-51128117	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:51163520-51163763	A549	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
38	CEBPB	chr2:51179698-51180729	Hela-S3	cervix:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
39	CEBPB	chr2:51178589-51178949	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr2:51163327-51163752	IMR90	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163420-51163433 chr2:51163616-51163627
41	CEBPB	chr2:51180081-51180588	ECC-1	luminal epithelium:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
42	CHD2	chr2:51179784-51180498	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr2:51164960-51165110	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr2:51146320-51146470	AG04449	skin:	n/a	n/a
45	CTCF	chr2:51181940-51182090	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr2:51146780-51146930	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr2:51181680-51181830	GM12868	blood:	n/a	n/a
48	CTCF	chr2:51159644-51159672	GM13977	blood:	n/a	n/a
49	CTCF	chr2:51146900-51147050	HPAF	blood vessel:	n/a	n/a
50	CUX1	chr2:51158632-51158662	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51144781..51146893-chr2:51147491..51149076,2	K562	blood:
2	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
3	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
4	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
5	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
6	chr2:51144781..51146893-chr2:51147491..51149076,2	K562	blood:
7	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
8	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:
9	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
10	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
11	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000216011	TF binding region
ENSG00000272385	TF binding region

Extended variants
information (count: 4177 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:4177 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13027232	chr2:51105852-51105853	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531662310	chr2:51105869-51105870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571598070	chr2:51105883-51105884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543918949	chr2:51105892-51105893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74606890	chr2:51105900-51105901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148788210	chr2:51105940-51105941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547235078	chr2:51105943-51105944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185029662	chr2:51105951-51105952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372868708	chr2:51105963-51105964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545129125	chr2:51105976-51105977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527763617	chr2:51105994-51105995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569653474	chr2:51105995-51105996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536711209	chr2:51106016-51106017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13027132	chr2:51106026-51106027	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs190719938	chr2:51106051-51106052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17570759	chr2:51106092-51106093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs554448831	chr2:51106126-51106127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548124898	chr2:51106184-51106185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567993617	chr2:51106188-51106189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182226756	chr2:51106214-51106215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543347414	chr2:51106228-51106229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10210089	chr2:51106285-51106286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs576399826	chr2:51106286-51106287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549010072	chr2:51106301-51106302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543480130	chr2:51106376-51106377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79228872	chr2:51106384-51106385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs60188414	chr2:51106471-51106472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6719841	chr2:51106479-51106480	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs79927354	chr2:51106480-51106481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559123916	chr2:51106489-51106490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529907665	chr2:51106497-51106498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141567439	chr2:51106504-51106505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186389762	chr2:51106564-51106565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571126523	chr2:51106622-51106623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150517090	chr2:51106636-51106637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551934305	chr2:51106747-51106748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570519218	chr2:51106759-51106760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368717806	chr2:51106764-51106765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34654700	chr2:51106777-51106778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573605437	chr2:51106782-51106783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144977552	chr2:51106783-51106784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557735350	chr2:51106813-51106814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566299324	chr2:51106832-51106833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144348338	chr2:51106885-51106886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372776443	chr2:51106891-51106892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555221923	chr2:51106900-51106901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112734125	chr2:51106935-51106936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72840217	chr2:51106940-51106941	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs375243892	chr2:51106964-51106965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11888865	chr2:51106969-51106970	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:108)

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
Schizophrenia	17989066	CNVD
Autism	19404257	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51083200-51108400	Weak transcription	Fetal Brain Female	brain
2	chr2:51108600-51109000	Enhancers	Brain Germinal Matrix	brain
3	chr2:51110800-51114000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr2:51111000-51111200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr2:51111000-51113200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:51111000-51113400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:51111200-51111800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:51111800-51112400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr2:51111800-51112800	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr2:51112800-51113600	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr2:51113600-51114400	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr2:51114400-51114800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr2:51122600-51132800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr2:51129200-51129400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:51129200-51130000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:51129400-51134000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:51130000-51134800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:51134000-51135000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr2:51134600-51135000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:51134800-51136800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:51135000-51137400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr2:51136400-51137000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr2:51136400-51137000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr2:51136400-51137200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr2:51136400-51137200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr2:51136600-51137000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr2:51136600-51137000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:51136600-51137000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr2:51136600-51137200	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr2:51136800-51140000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:51137000-51140400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr2:51137200-51151400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr2:51137400-51138200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr2:51138200-51138400	Enhancers	Fetal Brain Female	brain
35	chr2:51138200-51141200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr2:51138400-51147800	Weak transcription	Fetal Brain Female	brain
37	chr2:51139600-51140800	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr2:51140000-51140400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:51140800-51142600	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr2:51141200-51141400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:51142600-51142800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr2:51144600-51147200	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr2:51147200-51147400	Enhancers	Brain Germinal Matrix	brain
44	chr2:51147200-51149000	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr2:51147400-51149800	Weak transcription	Brain Germinal Matrix	brain
46	chr2:51147800-51148200	Enhancers	Fetal Brain Female	brain
47	chr2:51148400-51148600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr2:51148600-51149800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr2:51149000-51149400	Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr2:51149400-51149600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet

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