Variant report

Variant	nsv874051
Chromosome Location	chr2:51039129-51114704
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	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
3	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
4	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
5	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
6	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
7	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
8	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
9	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
10	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
11	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
12	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
14	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
15	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
16	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
17	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
18	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
19	CEBPB	chr2:51106584-51106784	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
21	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
22	CTCF	chr2:51099800-51099950	HRE	kidney:	n/a	n/a
23	CTCF	chr2:51099880-51100030	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr2:51075262-51075348	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr2:51099809-51099906	Medullo	brain:	n/a	n/a
26	CTCF	chr2:51099842-51099897	LNCaP	prostate:	n/a	n/a
27	CTCF	chr2:51099800-51099950	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr2:51099780-51099930	Caco-2	colon:	n/a	n/a
29	CTCF	chr2:51099940-51100090	NHEK	skin:	n/a	n/a
30	CTCF	chr2:51099740-51099890	HCT-116	colon:	n/a	n/a
31	CTCF	chr2:51086389-51086467	NHEK	skin:	n/a	n/a
32	CTCF	chr2:51099850-51099874	Gliobla	brain:	n/a	n/a
33	CTCF	chr2:51099780-51099930	HMEC	breast:	n/a	n/a
34	CTCF	chr2:51056731-51056889	GM20000	blood:	n/a	n/a
35	CTCF	chr2:51099720-51099870	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr2:51099780-51099930	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr2:51099780-51099930	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr2:51101513-51101543	Lung_OC	lung:	n/a	n/a
39	CTCF	chr2:51086380-51086530	Caco-2	colon:	n/a	n/a
40	CTCF	chr2:51099760-51099910	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr2:51099820-51099970	HAc	cerebellar:	n/a	n/a
42	CTCF	chr2:51099740-51099890	RPTEC	kidney:	n/a	n/a
43	CTCF	chr2:51099820-51099970	SAEC	small airway:	n/a	n/a
44	CTCF	chr2:51040080-51040230	GM12874	blood:	n/a	n/a
45	CTCF	chr2:51040238-51040274	A549	lung:	n/a	n/a
46	CTCF	chr2:51099800-51099950	BE2_C	brain:	n/a	n/a
47	CTCF	chr2:51099800-51099950	AG04450	lung:	n/a	n/a
48	CTCF	chr2:51099760-51099910	AG04449	skin:	n/a	n/a
49	CTCF	chr2:51099757-51100003	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr2:51099780-51099930	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51065673-51065723	Hela-S3	cervix:	n/a
2	chr2:51074939-51074989	HCF	heart:	n/a
3	chr2:51074881-51074931	HUVEC	blood vessel:	n/a
4	chr2:51074881-51074931	MCF-7	breast:	n/a
5	chr2:51074881-51074931	BJ	skin:	n/a
6	chr2:51056822-51056872	HL-60	blood:	n/a
7	chr2:51065673-51065723	HUVEC	blood vessel:	n/a
8	chr2:51074881-51074931	IMR90	lung:	fetal
9	chr2:51057218-51057268	ECC-1	luminal epithelium:	n/a
10	chr2:51065673-51065723	AG09319	gingival:	n/a
11	chr2:51057548-51057598	NHDF-neo	bronchial:	n/a
12	chr2:51057218-51057268	HCT-116	colon:	n/a
13	chr2:51057218-51057268	NT2-D1	testis:	n/a
14	chr2:51056884-51056934	NB4	blood:	n/a
15	chr2:51074881-51074931	MCF10A-Er-Src	breast:	n/a
16	chr2:51074881-51074931	PANC-1	pancreas:	n/a
17	chr2:51057548-51057598	H1-hESC	embryonic stem cell:	embryo
18	chr2:51057218-51057268	ProgFib	skin:	n/a
19	chr2:51056884-51056934	ovcar-3	ovarian:	n/a
20	chr2:51074881-51074931	AG09309	skin:	n/a
21	chr2:51057218-51057268	NHBE	bronchial:	n/a
22	chr2:51065673-51065723	HMEC	breast:	n/a
23	chr2:51056884-51056934	U87	brain:	n/a
24	chr2:51057548-51057598	NB4	blood:	n/a
25	chr2:51056822-51056872	ECC-1	luminal epithelium:	n/a
26	chr2:51074881-51074931	NHDF-neo	bronchial:	n/a
27	chr2:51057548-51057598	GM12891	blood:	n/a
28	chr2:51056822-51056872	AG04450	lung:	fetal
29	chr2:51074939-51074989	BE2_C	brain:	n/a
30	chr2:51065673-51065723	HNPCEpiC	eye:	n/a
31	chr2:51057548-51057598	HAEpiC	amniotic membrane:	n/a
32	chr2:51057218-51057268	PFSK-1	brain:	n/a
33	chr2:51056884-51056934	HUVEC	blood vessel:	n/a
34	chr2:51057218-51057268	HL-60	blood:	n/a
35	chr2:51074881-51074931	ProgFib	skin:	n/a
36	chr2:51074881-51074931	NHBE	bronchial:	n/a
37	chr2:51074881-51074931	NT2-D1	testis:	n/a
38	chr2:51057548-51057598	BE2_C	brain:	n/a
39	chr2:51057548-51057598	ECC-1	luminal epithelium:	n/a
40	chr2:51065673-51065723	NB4	blood:	n/a
41	chr2:51056822-51056872	AG09309	skin:	n/a
42	chr2:51065673-51065723	HRPEpiC	eye:	n/a
43	chr2:51056822-51056872	HCT-116	colon:	n/a
44	chr2:51056822-51056872	ovcar-3	ovarian:	n/a
45	chr2:51057548-51057598	U87	brain:	n/a
46	chr2:51057218-51057268	HCF	heart:	n/a
47	chr2:51074939-51074989	HUVEC	blood vessel:	n/a
48	chr2:51056822-51056872	RPTEC	kidney:	n/a
49	chr2:51057548-51057598	HRE	kidney:	n/a
50	chr2:51074939-51074989	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:
2	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
3	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
4	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
ENSG00000238165	CpG island

Extended variants
information (count: 2825 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2825 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3908115	chr2:51040802-51040803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs3908116	chr2:51040820-51040821	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs139933639	chr2:51040821-51040822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145439896	chr2:51040823-51040824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553889867	chr2:51040884-51040885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571904705	chr2:51040909-51040910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs17041061	chr2:51040985-51040986	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs561219225	chr2:51040999-51041000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189546231	chr2:51041007-51041008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567632706	chr2:51041033-51041034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530184397	chr2:51041046-51041047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138814110	chr2:51041077-51041078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs80145098	chr2:51041078-51041079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368477098	chr2:51041079-51041080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535730808	chr2:51041096-51041097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564875122	chr2:51041119-51041120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570274453	chr2:51041162-51041163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570211494	chr2:51041202-51041203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539190920	chr2:51041240-51041241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537283847	chr2:51041242-51041243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs4971566	chr2:51041246-51041247	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs182183711	chr2:51041279-51041280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535312826	chr2:51041280-51041281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116153576	chr2:51041299-51041300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549724688	chr2:51041324-51041325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35296165	chr2:51041335-51041336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184988293	chr2:51041343-51041344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573578333	chr2:51041368-51041369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147731826	chr2:51041371-51041372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553826767	chr2:51041374-51041375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572239804	chr2:51041383-51041384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536412783	chr2:51041437-51041438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575046923	chr2:51041457-51041458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs3914731	chr2:51041472-51041473	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs556183509	chr2:51041477-51041478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4971699	chr2:51041501-51041502	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs141033035	chr2:51041519-51041520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10708029	chr2:51041575-51041576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs3891419	chr2:51041578-51041579	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs17041064	chr2:51041603-51041604	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs541063804	chr2:51041614-51041615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564931104	chr2:51041623-51041624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559458730	chr2:51041654-51041655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181822825	chr2:51041660-51041661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549509273	chr2:51041667-51041668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72837092	chr2:51041668-51041669	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs150280476	chr2:51041669-51041670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530066829	chr2:51041689-51041690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550059880	chr2:51041719-51041720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571634546	chr2:51041829-51041830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51040800-51041200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:51041200-51041400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:51041400-51051800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:51042000-51042200	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr2:51042200-51042400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr2:51042400-51042600	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr2:51042600-51046400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr2:51046600-51047400	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr2:51047400-51048000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr2:51047600-51048800	Enhancers	Brain Germinal Matrix	brain
11	chr2:51048000-51048800	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr2:51048800-51050000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr2:51048800-51056800	Weak transcription	Brain Germinal Matrix	brain
14	chr2:51050000-51051000	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr2:51050200-51050400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:51050400-51051600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:51051600-51052800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:51051800-51052000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr2:51052000-51052400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:51052400-51054200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:51053000-51058600	Weak transcription	Brain Hippocampus Middle	brain
22	chr2:51054000-51054400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:51054400-51057400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:51056800-51057600	Enhancers	Fetal Brain Male	brain
25	chr2:51056800-51057800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr2:51056800-51057800	Enhancers	Fetal Brain Female	brain
27	chr2:51056800-51059800	Enhancers	Brain Germinal Matrix	brain
28	chr2:51056800-51060000	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr2:51057200-51057400	Enhancers	Brain Anterior Caudate	brain
30	chr2:51057200-51058800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:51057400-51057600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr2:51057400-51058400	Weak transcription	Brain Anterior Caudate	brain
33	chr2:51057600-51058000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:51057600-51058800	Weak transcription	Fetal Brain Male	brain
35	chr2:51057800-51058200	Weak transcription	Fetal Brain Female	brain
36	chr2:51058000-51059600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:51058200-51059800	Enhancers	Fetal Brain Female	brain
38	chr2:51058400-51058800	Enhancers	Brain Anterior Caudate	brain
39	chr2:51058400-51059800	Enhancers	Brain Cingulate Gyrus	brain
40	chr2:51058600-51058800	Enhancers	Brain Hippocampus Middle	brain
41	chr2:51058600-51059400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr2:51058600-51059600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:51058600-51059800	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr2:51058800-51059000	Flanking Active TSS	Brain Hippocampus Middle	brain
45	chr2:51058800-51059400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr2:51058800-51059400	Active TSS	Brain Anterior Caudate	brain
47	chr2:51058800-51060000	Enhancers	Fetal Brain Male	brain
48	chr2:51059000-51059200	Enhancers	Brain Hippocampus Middle	brain
49	chr2:51059200-51059400	Active TSS	Brain Hippocampus Middle	brain
50	chr2:51059400-51059800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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