Variant report

Variant	nsv530832
Chromosome Location	chr2:50892847-50982172
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	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
4	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
5	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
6	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
11	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
12	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr2:50973734-50974070	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
14	CTCF	chr2:50973740-50973890	HFF	foreskin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
15	CTCF	chr2:50973641-50974055	H1-hESC	embryonic stem cell:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
16	CTCF	chr2:50973800-50973950	GM12874	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
17	CTCF	chr2:50973760-50973910	GM06990	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
18	CTCF	chr2:50902120-50902270	GM12874	blood:	n/a	n/a
19	CTCF	chr2:50973720-50974002	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
20	CTCF	chr2:50973760-50973910	HCFaa	heart:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
21	CTCF	chr2:50902100-50902250	GM12873	blood:	n/a	n/a
22	CTCF	chr2:50973751-50973938	GM12892	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973760-50973910	AG09319	gingival:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50902180-50902330	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr2:50902100-50902250	GM12874	blood:	n/a	n/a
26	CTCF	chr2:50902120-50902270	K562	blood:	n/a	n/a
27	CTCF	chr2:50973733-50973949	ProgFib	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973800-50973950	GM12869	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973760-50973910	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50902100-50902250	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr2:50902197-50902266	Medullo	brain:	n/a	n/a
32	CTCF	chr2:50973720-50973870	HEK293	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
33	CTCF	chr2:50902156-50902295	GM19239	blood:	n/a	n/a
34	CTCF	chr2:50973720-50973870	HPF	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50902163-50902293	Gliobla	brain:	n/a	n/a
36	CTCF	chr2:50973752-50973928	H1-hESC	embryonic stem cell:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:50973740-50973890	HAc	cerebellar:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
38	CTCF	chr2:50902060-50902290	GM12864	blood:	n/a	n/a
39	CTCF	chr2:50973780-50973930	GM12874	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:50973780-50973930	BE2_C	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:50973741-50973938	GM19240	blood:	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	NHEK	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973740-50973890	AoAF	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973732-50973965	GM19238	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:50973820-50973970	HEEpiC	esophagus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50973800-50973950	GM12864	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50902100-50902250	HepG2	liver:	n/a	n/a
49	CTCF	chr2:50902100-50902250	SAEC	small airway:	n/a	n/a
50	CTCF	chr2:50973760-50973923	K562	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	RPTEC	kidney:	n/a
2	chr2:50956659-50956709	GM12891	blood:	n/a
3	chr2:50956659-50956709	HIPEpiC	eye:	n/a
4	chr2:50956659-50956709	HUVEC	blood vessel:	n/a
5	chr2:50956659-50956709	ProgFib	skin:	n/a
6	chr2:50956659-50956709	GM12878	blood:	n/a
7	chr2:50956659-50956709	Hela-S3	cervix:	n/a
8	chr2:50956659-50956709	Hepatocyte	liver:	n/a
9	chr2:50956659-50956709	NT2-D1	testis:	n/a
10	chr2:50956659-50956709	NHDF-neo	bronchial:	n/a
11	chr2:50956659-50956709	HCPEpiC	choroid plexus:	n/a
12	chr2:50956659-50956709	AG09319	gingival:	n/a
13	chr2:50956659-50956709	SK-N-SH_RA	brain:	n/a
14	chr2:50956659-50956709	U87	brain:	n/a
15	chr2:50956659-50956709	H1-hESC	embryonic stem cell:	embryo
16	chr2:50956659-50956709	HL-60	blood:	n/a
17	chr2:50956659-50956709	PANC-1	pancreas:	n/a
18	chr2:50956659-50956709	SK-N-MC	brain:	n/a
19	chr2:50956659-50956709	SKMC	muscle:	n/a
20	chr2:50956659-50956709	NB4	blood:	n/a
21	chr2:50956659-50956709	BJ	skin:	n/a
22	chr2:50956659-50956709	AG04449	skin:	fetal
23	chr2:50956659-50956709	CMK	blood:	n/a
24	chr2:50956659-50956709	GM12892	blood:	n/a
25	chr2:50956659-50956709	PrEC	prostate:	n/a
26	chr2:50956659-50956709	T-47D	breast:	n/a
27	chr2:50956659-50956709	IMR90	lung:	fetal
28	chr2:50956659-50956709	AoSMC	blood vessel:	n/a
29	chr2:50956659-50956709	BE2_C	brain:	n/a
30	chr2:50956659-50956709	LNCaP	prostate:	n/a
31	chr2:50956659-50956709	GM19239	blood:	n/a
32	chr2:50956659-50956709	ECC-1	luminal epithelium:	n/a
33	chr2:50956659-50956709	A549	lung:	n/a
34	chr2:50956659-50956709	HAEpiC	amniotic membrane:	n/a
35	chr2:50956659-50956709	HEEpiC	esophagus:	n/a
36	chr2:50956659-50956709	HNPCEpiC	eye:	n/a
37	chr2:50956659-50956709	HEK293	kidney:	embryo
38	chr2:50956659-50956709	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:50956659-50956709	HCM	heart:	n/a
40	chr2:50956659-50956709	K562	blood:	n/a
41	chr2:50956659-50956709	AG10803	skin:	n/a
42	chr2:50956659-50956709	MCF-7	breast:	n/a
43	chr2:50956659-50956709	AG04450	lung:	fetal
44	chr2:50956659-50956709	ovcar-3	ovarian:	n/a
45	chr2:50956659-50956709	HRPEpiC	eye:	n/a
46	chr2:50956659-50956709	HCF	heart:	n/a
47	chr2:50956659-50956709	NH-A	brain:	n/a
48	chr2:50956659-50956709	AG09309	skin:	n/a
49	chr2:50956659-50956709	HMEC	breast:	n/a
50	chr2:50956659-50956709	GM06990	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	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
4	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
5	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
6	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:

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

Extended variants
information (count: 2861 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:2861 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567373567	chr2:50892849-50892850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537516423	chr2:50892850-50892851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529664577	chr2:50892862-50892863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201748361	chr2:50892947-50892948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1518542	chr2:50892999-50893000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs571140655	chr2:50893000-50893001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368975319	chr2:50893097-50893098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538954767	chr2:50893116-50893117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553649261	chr2:50893166-50893167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141761785	chr2:50893170-50893171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542424465	chr2:50893199-50893200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184296437	chr2:50893284-50893285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190008163	chr2:50893337-50893338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78223588	chr2:50893401-50893402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144995863	chr2:50893414-50893415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533152574	chr2:50893451-50893452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545762643	chr2:50893482-50893483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181274324	chr2:50893531-50893532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545989772	chr2:50893533-50893534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371467425	chr2:50893534-50893535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527948084	chr2:50893538-50893539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186110517	chr2:50893564-50893565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574367957	chr2:50893567-50893568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538433245	chr2:50893655-50893656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35877581	chr2:50893683-50893684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562665369	chr2:50893691-50893692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375296092	chr2:50893692-50893693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567827125	chr2:50893722-50893723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531469687	chr2:50893737-50893738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138833686	chr2:50893826-50893827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190484134	chr2:50893827-50893828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181965582	chr2:50893858-50893859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141952000	chr2:50893880-50893881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12612961	chr2:50893882-50893883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs577272334	chr2:50893887-50893888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536111914	chr2:50893895-50893896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545937440	chr2:50893943-50893944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs202154192	chr2:50893978-50893979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76585796	chr2:50893990-50893991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149259633	chr2:50894014-50894015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200409431	chr2:50894015-50894016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200857518	chr2:50894016-50894017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61084942	chr2:50894017-50894018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs386354971	chr2:50894019-50894020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34096569	chr2:50894044-50894045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374525163	chr2:50894045-50894046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576138653	chr2:50894054-50894055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35135340	chr2:50894080-50894081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139299807	chr2:50894098-50894099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187259699	chr2:50894101-50894102	Weak transcription	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:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50890400-50899200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:50890800-50895000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:50894800-50895800	Enhancers	Brain Angular Gyrus	brain
4	chr2:50895000-50895200	Enhancers	Brain Germinal Matrix	brain
5	chr2:50895000-50895600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:50895000-50895800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr2:50895200-50896200	Enhancers	Brain Substantia Nigra	brain
8	chr2:50895600-50896000	Enhancers	Brain Cingulate Gyrus	brain
9	chr2:50895800-50896000	Enhancers	Brain Germinal Matrix	brain
10	chr2:50896000-50896400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:50899200-50899600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:50899200-50899800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:50899600-50899800	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr2:50904200-50904600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr2:50905400-50905800	Enhancers	Brain Hippocampus Middle	brain
16	chr2:50905600-50906200	Enhancers	Brain Anterior Caudate	brain
17	chr2:50905800-50906200	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr2:50913400-50914000	Enhancers	Brain Angular Gyrus	brain
19	chr2:50913400-50914600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:50913600-50914800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr2:50913600-50916000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:50913600-50916200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr2:50913800-50915800	Enhancers	Brain Anterior Caudate	brain
24	chr2:50913800-50916200	Enhancers	H1 Cell Line	embryonic stem cell
25	chr2:50914000-50914200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:50914000-50914200	Enhancers	Brain Cingulate Gyrus	brain
27	chr2:50914000-50914400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:50914000-50917800	Weak transcription	Brain Angular Gyrus	brain
29	chr2:50914200-50915200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr2:50914200-50916000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:50914200-50918600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr2:50914400-50918400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:50914600-50914800	Enhancers	H9 Cell Line	embryonic stem cell
34	chr2:50914600-50914800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr2:50914600-50915200	Enhancers	Fetal Heart	heart
36	chr2:50914800-50915200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr2:50914800-50915200	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr2:50914800-50915800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:50915000-50915200	Enhancers	Brain Substantia Nigra	brain
40	chr2:50915000-50915400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr2:50915000-50915600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr2:50915200-50915600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr2:50915200-50915800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:50915200-50916000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr2:50915600-50915800	Enhancers	H9 Cell Line	embryonic stem cell
46	chr2:50915600-50916000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr2:50915600-50916200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr2:50915800-50917800	Weak transcription	Brain Anterior Caudate	brain
49	chr2:50915800-50918600	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr2:50915800-50918800	Weak transcription	H9 Cell Line	embryonic stem cell

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