Variant report

Variant	nsv581845
Chromosome Location	chr2:50902931-50983186
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	chr2:50955596-50955702	K562	blood:	n/a	n/a
2	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
4	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
5	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
7	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
9	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
11	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
12	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr2:50973780-50973930	WI-38	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
14	CTCF	chr2:50973780-50973930	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
15	CTCF	chr2:50973760-50973910	AG09319	gingival:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
16	CTCF	chr2:50973760-50973910	HCPEpiC	choroid plexus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
17	CTCF	chr2:50973740-50973890	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
18	CTCF	chr2:50973760-50973910	GM06990	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
19	CTCF	chr2:50907104-50907160	GM20000	blood:	n/a	n/a
20	CTCF	chr2:50973740-50973890	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
21	CTCF	chr2:50973800-50973950	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
22	CTCF	chr2:50973760-50973910	GM12865	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973760-50973910	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50973740-50973890	HFF	foreskin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:50973780-50973930	HMEC	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50973760-50973910	GM12875	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
27	CTCF	chr2:50973740-50973931	GM10266	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973732-50973938	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973760-50973910	BJ	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973760-50973910	NHEK	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50973728-50973980	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
32	CTCF	chr2:50978500-50978650	BE2_C	brain:	n/a	n/a
33	CTCF	chr2:50973752-50973932	GM12891	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:50973800-50973950	GM12869	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50973800-50973950	GM12864	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50973720-50973870	HEK293	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:50973740-50973890	AG09319	gingival:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
38	CTCF	chr2:50973641-50974055	H1-hESC	embryonic stem cell:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50973740-50973890	NHEK	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:50973820-50973970	HEEpiC	esophagus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:50973740-50973890	WERI-Rb-1	eye:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:50973746-50973953	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:50973760-50973910	GM12878	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973741-50973938	GM19240	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973729-50973949	NHEK	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:50973740-50973890	AG10803	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50978545-50978604	Medullo	brain:	n/a	n/a
48	CTCF	chr2:50973685-50974004	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973740-50973890	RPTEC	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50973740-50973890	GM12871	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50956659-50956709	MCF-7	breast:	n/a
2	chr2:50956659-50956709	HRCEpiC	kidney:	n/a
3	chr2:50956659-50956709	HAEpiC	amniotic membrane:	n/a
4	chr2:50956659-50956709	MCF10A-Er-Src	breast:	n/a
5	chr2:50956659-50956709	HRPEpiC	eye:	n/a
6	chr2:50956659-50956709	HCF	heart:	n/a
7	chr2:50956659-50956709	SK-N-MC	brain:	n/a
8	chr2:50956659-50956709	HL-60	blood:	n/a
9	chr2:50956659-50956709	PANC-1	pancreas:	n/a
10	chr2:50956659-50956709	HEEpiC	esophagus:	n/a
11	chr2:50956659-50956709	HCT-116	colon:	n/a
12	chr2:50956659-50956709	ECC-1	luminal epithelium:	n/a
13	chr2:50956659-50956709	NH-A	brain:	n/a
14	chr2:50956659-50956709	PFSK-1	brain:	n/a
15	chr2:50956659-50956709	AG09319	gingival:	n/a
16	chr2:50956659-50956709	BE2_C	brain:	n/a
17	chr2:50956659-50956709	IMR90	lung:	fetal
18	chr2:50956659-50956709	PrEC	prostate:	n/a
19	chr2:50956659-50956709	Caco-2	colon:	n/a
20	chr2:50956659-50956709	ovcar-3	ovarian:	n/a
21	chr2:50956659-50956709	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:50956659-50956709	NB4	blood:	n/a
23	chr2:50956659-50956709	GM12891	blood:	n/a
24	chr2:50956659-50956709	SKMC	muscle:	n/a
25	chr2:50956659-50956709	AG04450	lung:	fetal
26	chr2:50956659-50956709	HCM	heart:	n/a
27	chr2:50956659-50956709	SK-N-SH_RA	brain:	n/a
28	chr2:50956659-50956709	CMK	blood:	n/a
29	chr2:50956659-50956709	AG09309	skin:	n/a
30	chr2:50956659-50956709	NT2-D1	testis:	n/a
31	chr2:50956659-50956709	GM12878	blood:	n/a
32	chr2:50956659-50956709	HRE	kidney:	n/a
33	chr2:50956659-50956709	GM06990	blood:	n/a
34	chr2:50956659-50956709	K562	blood:	n/a
35	chr2:50956659-50956709	AoSMC	blood vessel:	n/a
36	chr2:50956659-50956709	U87	brain:	n/a
37	chr2:50956659-50956709	Jurkat	blood:	n/a
38	chr2:50956659-50956709	HNPCEpiC	eye:	n/a
39	chr2:50956659-50956709	HEK293	kidney:	embryo
40	chr2:50956659-50956709	SAEC	small airway:	n/a
41	chr2:50956659-50956709	ProgFib	skin:	n/a
42	chr2:50956659-50956709	AG10803	skin:	n/a
43	chr2:50956659-50956709	HCPEpiC	choroid plexus:	n/a
44	chr2:50956659-50956709	NHDF-neo	bronchial:	n/a
45	chr2:50956659-50956709	BJ	skin:	n/a
46	chr2:50956659-50956709	HUVEC	blood vessel:	n/a
47	chr2:50956659-50956709	H1-hESC	embryonic stem cell:	embryo
48	chr2:50956659-50956709	HepG2	liver:	n/a
49	chr2:50956659-50956709	GM19239	blood:	n/a
50	chr2:50956659-50956709	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
2	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
3	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
4	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
5	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
6	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000216191	TF binding region
ENSG00000216191	CpG island
ENSG00000216191	chromatin interactions

Extended variants
information (count: 2644 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:2644 , 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	rs148319363	chr2:50904205-50904206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114264277	chr2:50904242-50904243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181864980	chr2:50904251-50904252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185102536	chr2:50904255-50904256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552112300	chr2:50904289-50904290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570813328	chr2:50904295-50904296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528745580	chr2:50904310-50904311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547206815	chr2:50904315-50904316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143249298	chr2:50904318-50904319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147501929	chr2:50904331-50904332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138542529	chr2:50904332-50904333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568934109	chr2:50904333-50904334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187998759	chr2:50904374-50904375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200886641	chr2:50904380-50904381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557761114	chr2:50904397-50904398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144054884	chr2:50904437-50904438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150690203	chr2:50904460-50904461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181459654	chr2:50904465-50904466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573750570	chr2:50904474-50904475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566766980	chr2:50904525-50904526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551279730	chr2:50904582-50904583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186823435	chr2:50905402-50905403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564186251	chr2:50905458-50905459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535098556	chr2:50905463-50905464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573145114	chr2:50905488-50905489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs28531883	chr2:50905523-50905524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540578346	chr2:50905542-50905543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562245438	chr2:50905570-50905571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2216788	chr2:50905575-50905576	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs551208242	chr2:50905577-50905578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563059827	chr2:50905591-50905592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533090202	chr2:50905599-50905600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551499905	chr2:50905639-50905640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566504731	chr2:50905646-50905647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533563392	chr2:50905656-50905657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78250746	chr2:50905668-50905669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs377249631	chr2:50905689-50905690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9284754	chr2:50905758-50905759	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs369263595	chr2:50905760-50905761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569612142	chr2:50905804-50905805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537713856	chr2:50905805-50905806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146712639	chr2:50905830-50905831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369354108	chr2:50905872-50905873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532940467	chr2:50905889-50905890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577411744	chr2:50905973-50905974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139422267	chr2:50905981-50905982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557978267	chr2:50905997-50905998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190641721	chr2:50906021-50906022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540288380	chr2:50906040-50906041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142735980	chr2:50906046-50906047	Enhancers	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
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
Acute myeloid leukemia	20729466	CNVD
Bipolar disorder	19114987	CNVD
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50904200-50904600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr2:50905400-50905800	Enhancers	Brain Hippocampus Middle	brain
3	chr2:50905600-50906200	Enhancers	Brain Anterior Caudate	brain
4	chr2:50905800-50906200	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr2:50913400-50914000	Enhancers	Brain Angular Gyrus	brain
6	chr2:50913400-50914600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr2:50913600-50914800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr2:50913600-50916000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr2:50913600-50916200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr2:50913800-50915800	Enhancers	Brain Anterior Caudate	brain
11	chr2:50913800-50916200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr2:50914000-50914200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:50914000-50914200	Enhancers	Brain Cingulate Gyrus	brain
14	chr2:50914000-50914400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:50914000-50917800	Weak transcription	Brain Angular Gyrus	brain
16	chr2:50914200-50915200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:50914200-50916000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr2:50914200-50918600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr2:50914400-50918400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr2:50914600-50914800	Enhancers	H9 Cell Line	embryonic stem cell
21	chr2:50914600-50914800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr2:50914600-50915200	Enhancers	Fetal Heart	heart
23	chr2:50914800-50915200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr2:50914800-50915200	Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr2:50914800-50915800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr2:50915000-50915200	Enhancers	Brain Substantia Nigra	brain
27	chr2:50915000-50915400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr2:50915000-50915600	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr2:50915200-50915600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr2:50915200-50915800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:50915200-50916000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:50915600-50915800	Enhancers	H9 Cell Line	embryonic stem cell
33	chr2:50915600-50916000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr2:50915600-50916200	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr2:50915800-50917800	Weak transcription	Brain Anterior Caudate	brain
36	chr2:50915800-50918600	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr2:50915800-50918800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr2:50916000-50918600	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr2:50916000-50918800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr2:50916000-50948000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:50916200-50923800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr2:50917600-50917800	Enhancers	Brain Hippocampus Middle	brain
43	chr2:50917600-50918000	Weak transcription	Brain Substantia Nigra	brain
44	chr2:50917600-50918400	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr2:50917800-50918400	Enhancers	Brain Angular Gyrus	brain
46	chr2:50917800-50918600	Enhancers	Brain Anterior Caudate	brain
47	chr2:50918000-50918200	Enhancers	Brain Substantia Nigra	brain
48	chr2:50918200-50918800	Weak transcription	Brain Substantia Nigra	brain
49	chr2:50918400-50918600	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr2:50918400-50918800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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