Variant report

Variant	nsv1009270
Chromosome Location	chr2:50972224-51135705
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	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
3	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
5	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
6	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
7	CEBPB	chr2:51106584-51106784	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
9	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
10	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
11	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
12	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
13	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
14	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
15	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
16	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
17	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
18	CEBPB	chr2:51127917-51128117	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
20	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
22	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
23	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
25	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
26	CTCF	chr2:50973760-50973910	WI-38	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
27	CTCF	chr2:50973760-50973910	AG09319	gingival:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973740-50973890	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973760-50973910	GM12871	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973760-50973910	GM12865	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:51013640-51013790	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
32	CTCF	chr2:50973740-50973890	AG10803	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
33	CTCF	chr2:50973760-50973910	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:51099809-51099906	Medullo	brain:	n/a	n/a
35	CTCF	chr2:50973820-50973970	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50973685-50974004	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:51099880-51100030	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr2:50973780-50973930	HEK293	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:51013580-51013730	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
40	CTCF	chr2:51086380-51086530	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:51086380-51086530	Caco-2	colon:	n/a	n/a
42	CTCF	chr2:50973740-50973890	Caco-2	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:51099840-51099990	HRE	kidney:	n/a	n/a
44	CTCF	chr2:50973760-50973910	Caco-2	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:51086389-51086467	NHEK	skin:	n/a	n/a
46	CTCF	chr2:51101513-51101543	Lung_OC	lung:	n/a	n/a
47	CTCF	chr2:50973740-50973890	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50973634-50974016	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973772-50973922	GM19239	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:51099740-51099890	RPTEC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51074881-51074931	SK-N-SH	brain:	n/a
2	chr2:51065673-51065723	A549	lung:	n/a
3	chr2:51074881-51074931	SK-N-SH	brain:	n/a
4	chr2:51065673-51065723	A549	lung:	n/a
5	chr2:51057218-51057268	HEEpiC	esophagus:	n/a
6	chr2:51056884-51056934	GM19239	blood:	n/a
7	chr2:51074939-51074989	AG09309	skin:	n/a
8	chr2:51056884-51056934	ProgFib	skin:	n/a
9	chr2:51056884-51056934	GM12891	blood:	n/a
10	chr2:50992829-50992879	ECC-1	luminal epithelium:	n/a
11	chr2:51057218-51057268	NB4	blood:	n/a
12	chr2:51056884-51056934	U87	brain:	n/a
13	chr2:51074881-51074931	NH-A	brain:	n/a
14	chr2:51001003-51001053	HCPEpiC	choroid plexus:	n/a
15	chr2:50992829-50992879	Caco-2	colon:	n/a
16	chr2:51057548-51057598	HEK293	kidney:	embryo
17	chr2:51056884-51056934	SAEC	small airway:	n/a
18	chr2:51057548-51057598	SK-N-SH_RA	brain:	n/a
19	chr2:51056822-51056872	AoSMC	blood vessel:	n/a
20	chr2:51056884-51056934	AG09309	skin:	n/a
21	chr2:51074881-51074931	HEEpiC	esophagus:	n/a
22	chr2:51074939-51074989	HUVEC	blood vessel:	n/a
23	chr2:51057218-51057268	SKMC	muscle:	n/a
24	chr2:51065673-51065723	SK-N-MC	brain:	n/a
25	chr2:51057548-51057598	HNPCEpiC	eye:	n/a
26	chr2:51074881-51074931	HUVEC	blood vessel:	n/a
27	chr2:51056822-51056872	NHBE	bronchial:	n/a
28	chr2:51065673-51065723	GM12891	blood:	n/a
29	chr2:51074881-51074931	PANC-1	pancreas:	n/a
30	chr2:51074881-51074931	Hepatocyte	liver:	n/a
31	chr2:51056884-51056934	PANC-1	pancreas:	n/a
32	chr2:51057548-51057598	HCPEpiC	choroid plexus:	n/a
33	chr2:51001003-51001053	HCM	heart:	n/a
34	chr2:51001003-51001053	NHBE	bronchial:	n/a
35	chr2:51001003-51001053	HMEC	breast:	n/a
36	chr2:51074881-51074931	AG09309	skin:	n/a
37	chr2:51057548-51057598	GM19239	blood:	n/a
38	chr2:51001003-51001053	PrEC	prostate:	n/a
39	chr2:51057218-51057268	HCT-116	colon:	n/a
40	chr2:51001003-51001053	BJ	skin:	n/a
41	chr2:51057218-51057268	HNPCEpiC	eye:	n/a
42	chr2:51057548-51057598	AG04449	skin:	fetal
43	chr2:51056884-51056934	HCT-116	colon:	n/a
44	chr2:51057548-51057598	CMK	blood:	n/a
45	chr2:51056822-51056872	ECC-1	luminal epithelium:	n/a
46	chr2:51056822-51056872	LNCaP	prostate:	n/a
47	chr2:51056884-51056934	T-47D	breast:	n/a
48	chr2:50992829-50992879	SK-N-SH	brain:	n/a
49	chr2:51056822-51056872	K562	blood:	n/a
50	chr2:50992829-50992879	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
2	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
3	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:
4	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
5	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
6	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
7	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
8	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
9	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
10	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
11	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
12	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
13	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
14	chr2:51084150..51086897-chr2:51088805..51090362,2	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: 5823 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:5823 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555039284	chr2:50972252-50972253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534688789	chr2:50972268-50972269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576553613	chr2:50972271-50972272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543841453	chr2:50972283-50972284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558952185	chr2:50972306-50972307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78180195	chr2:50972336-50972337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73933049	chr2:50972337-50972338	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs146343843	chr2:50972344-50972345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184602191	chr2:50972347-50972348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138286779	chr2:50972357-50972358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530479764	chr2:50972434-50972435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577359936	chr2:50972437-50972438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34515222	chr2:50972438-50972439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551768206	chr2:50972443-50972444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563709766	chr2:50972444-50972445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs397814947	chr2:50972446-50972447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528397944	chr2:50972449-50972450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74430630	chr2:50972453-50972454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78972802	chr2:50972454-50972455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546856702	chr2:50972462-50972463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568201961	chr2:50972523-50972524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28403015	chr2:50972541-50972542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113304221	chr2:50972562-50972563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535635451	chr2:50972582-50972583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76405494	chr2:50972584-50972585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76260536	chr2:50972652-50972653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530035666	chr2:50972654-50972655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191420681	chr2:50972688-50972689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142981411	chr2:50972725-50972726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535044874	chr2:50972748-50972749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183593141	chr2:50972751-50972752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112094276	chr2:50972791-50972792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369568081	chr2:50972829-50972830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557224857	chr2:50972845-50972846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374036933	chr2:50972867-50972868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577623623	chr2:50972874-50972875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540170946	chr2:50972883-50972884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543111916	chr2:50972888-50972889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112182252	chr2:50972890-50972891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542416832	chr2:50972950-50972951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189583596	chr2:50972957-50972958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575017297	chr2:50972986-50972987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545469123	chr2:50972998-50972999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs3914735	chr2:50972999-50973000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs371181350	chr2:50973001-50973002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111719483	chr2:50973014-50973015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546626127	chr2:50973040-50973041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs3861564	chr2:50973082-50973083	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs144316120	chr2:50973088-50973089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550768103	chr2:50973116-50973117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Breast cancer	21990379	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
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	17989066	CNVD
Autism	19404257	CNVD

Chromatin state (count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50972200-50975800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:50972200-50978200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:50974200-50974400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:50974200-50974400	Weak transcription	Brain Germinal Matrix	brain
5	chr2:50974400-50974600	Enhancers	Brain Hippocampus Middle	brain
6	chr2:50974400-50975200	Enhancers	HSMMtube	muscle
7	chr2:50974400-50976200	Enhancers	Brain Germinal Matrix	brain
8	chr2:50974400-50978200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:50975000-50976000	Enhancers	Fetal Muscle Leg	muscle
10	chr2:50975000-50976800	Enhancers	Fetal Brain Female	brain
11	chr2:50975200-50975800	Enhancers	Fetal Brain Male	brain
12	chr2:50975200-50977200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr2:50975400-50975600	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr2:50975400-50975800	Enhancers	Brain Hippocampus Middle	brain
15	chr2:50975600-50975800	Enhancers	Fetal Stomach	stomach
16	chr2:50975600-50975800	Enhancers	Psoas Muscle	Psoas
17	chr2:50975600-50976200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
18	chr2:50975800-50976200	Active TSS	Brain Anterior Caudate	brain
19	chr2:50975800-50976200	Active TSS	Brain Hippocampus Middle	brain
20	chr2:50975800-50976200	Active TSS	Brain Substantia Nigra	brain
21	chr2:50975800-50976200	Enhancers	Fetal Kidney	kidney
22	chr2:50975800-50976600	Weak transcription	Fetal Stomach	stomach
23	chr2:50975800-50977000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr2:50975800-50978400	Weak transcription	Fetal Brain Male	brain
25	chr2:50976000-50977200	Enhancers	Brain Cingulate Gyrus	brain
26	chr2:50976000-50978000	Weak transcription	Psoas Muscle	Psoas
27	chr2:50976000-50978600	Weak transcription	Fetal Muscle Leg	muscle
28	chr2:50976200-50976600	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr2:50976200-50976800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:50976200-50977400	Enhancers	Brain Hippocampus Middle	brain
31	chr2:50976200-50978200	Weak transcription	Brain Germinal Matrix	brain
32	chr2:50976200-50982800	Weak transcription	Brain Substantia Nigra	brain
33	chr2:50976400-50976600	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr2:50976600-50979800	Enhancers	Fetal Stomach	stomach
35	chr2:50976600-50983200	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr2:50976800-50977400	Weak transcription	Fetal Brain Female	brain
37	chr2:50976800-50978200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr2:50976800-50978200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr2:50977000-50982200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:50977200-50978400	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr2:50977400-50983600	Weak transcription	Brain Hippocampus Middle	brain
42	chr2:50977400-50984400	Enhancers	Fetal Brain Female	brain
43	chr2:50978200-50978800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr2:50978200-50979200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr2:50978200-50979200	Enhancers	Colon Smooth Muscle	Colon
46	chr2:50978200-50979400	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr2:50978200-50979600	Enhancers	Rectal Smooth Muscle	rectum
48	chr2:50978200-50980400	Enhancers	Brain Germinal Matrix	brain
49	chr2:50978200-50980400	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr2:50978400-50978800	Enhancers	NH-A	brain

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