Variant report

Variant	nsv932839
Chromosome Location	chr2:50181785-50225697
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:184)
CpG islands
(count:366)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:184 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr2:50201138-50201446	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr2:50201231-50201453	GM12878	blood:	n/a	n/a
3	BACH1	chr2:50187267-50187290	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:50194769-50194798	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:50194055-50194251	HepG2	liver:	n/a	n/a
6	CTCF	chr2:50189926-50190074	HepG2	liver:	n/a	n/a
7	CTCF	chr2:50189920-50190070	WERI-Rb-1	eye:	n/a	n/a
8	CTCF	chr2:50189895-50190097	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr2:50189900-50190050	HepG2	liver:	n/a	n/a
10	CTCF	chr2:50189965-50190041	MCF-7	breast:	n/a	n/a
11	CTCF	chr2:50189888-50190094	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr2:50201354-50201402	MCF-7	breast:	n/a	n/a
13	CTCF	chr2:50201327-50201436	A549	lung:	n/a	n/a
14	CTCF	chr2:50189935-50190057	MCF-7	breast:	n/a	n/a
15	CTCF	chr2:50189988-50190018	GM12892	blood:	n/a	n/a
16	CTCF	chr2:50201387-50201411	MCF-7	breast:	n/a	n/a
17	CTCF	chr2:50201339-50201442	MCF-7	breast:	n/a	n/a
18	CTCF	chr2:50189964-50190051	MCF-7	breast:	n/a	n/a
19	CTCF	chr2:50189886-50190131	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr2:50204400-50204550	WI-38	lung:	n/a	n/a
21	CTCF	chr2:50189920-50190070	HepG2	liver:	n/a	n/a
22	CTCF	chr2:50189940-50190043	MCF-7	breast:	n/a	n/a
23	CTCF	chr2:50189950-50190021	HepG2	liver:	n/a	n/a
24	CTCF	chr2:50205620-50205770	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr2:50189973-50190032	A549	lung:	n/a	n/a
26	E2F4	chr2:50211398-50211489	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F6	chr2:50201245-50201581	A549	lung:	n/a	n/a
28	E2F6	chr2:50201129-50201637	A549	lung:	n/a	chr2:50201592-50201601
29	EBF1	chr2:50200115-50200227	GM12878	blood:	n/a	n/a
30	ELF1	chr2:50201257-50201496	GM12878	blood:	n/a	n/a
31	EP300	chr2:50199438-50200387	SK-N-SH	brain:	n/a	chr2:50199740-50199754
32	EP300	chr2:50199705-50200249	SK-N-SH_RA	brain:	n/a	chr2:50199740-50199754
33	EP300	chr2:50201159-50201524	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr2:50199649-50200294	SK-N-SH_RA	brain:	n/a	chr2:50199740-50199754
35	EP300	chr2:50201124-50201533	SK-N-SH_RA	brain:	n/a	n/a
36	FOS	chr2:50208070-50208137	MCF10A-Er-Src	breast:	n/a	chr2:50208096-50208105 chr2:50208097-50208105 chr2:50208096-50208106 chr2:50208097-50208104 chr2:50208095-50208107
37	FOXA2	chr2:50201291-50201557	A549	lung:	n/a	n/a
38	FOXP2	chr2:50201240-50201525	PFSK-1	brain:	n/a	n/a
39	FOXP2	chr2:50201284-50201514	SK-N-MC	brain:	n/a	n/a
40	FOXP2	chr2:50201193-50201591	SK-N-MC	brain:	n/a	n/a
41	GABPA	chr2:50201148-50201629	A549	lung:	n/a	n/a
42	GABPA	chr2:50201180-50201629	A549	lung:	n/a	n/a
43	GABPA	chr2:50201248-50201488	HepG2	liver:	n/a	n/a
44	GABPA	chr2:50201251-50201460	HepG2	liver:	n/a	n/a
45	GATA2	chr2:50200922-50201708	SH-SY5Y	brain:	n/a	chr2:50201391-50201401
46	GATA2	chr2:50199572-50200231	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr2:50199627-50200327	SK-N-SH	brain:	n/a	n/a
48	GATA3	chr2:50199729-50200220	SK-N-SH	brain:	n/a	n/a
49	GATA3	chr2:50182536-50182567	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr2:50199670-50200211	SH-SY5Y	brain:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50201413-50201463	AG04449	skin:	fetal
2	chr2:50187352-50187402	MCF10A-Er-Src	breast:	n/a
3	chr2:50201505-50201555	GM12892	blood:	n/a
4	chr2:50201479-50201529	AG09309	skin:	n/a
5	chr2:50201479-50201529	HRPEpiC	eye:	n/a
6	chr2:50201413-50201463	HRPEpiC	eye:	n/a
7	chr2:50201505-50201555	IMR90	lung:	fetal
8	chr2:50201511-50201561	AG04450	lung:	fetal
9	chr2:50201505-50201555	HRE	kidney:	n/a
10	chr2:50187352-50187402	ECC-1	luminal epithelium:	n/a
11	chr2:50201413-50201463	HNPCEpiC	eye:	n/a
12	chr2:50201479-50201529	Hela-S3	cervix:	n/a
13	chr2:50201479-50201529	NH-A	brain:	n/a
14	chr2:50201505-50201555	HUVEC	blood vessel:	n/a
15	chr2:50201511-50201561	AG09309	skin:	n/a
16	chr2:50201511-50201561	IMR90	lung:	fetal
17	chr2:50201382-50201432	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:50201505-50201555	SK-N-SH_RA	brain:	n/a
19	chr2:50201479-50201529	HAEpiC	amniotic membrane:	n/a
20	chr2:50201413-50201463	SKMC	muscle:	n/a
21	chr2:50201505-50201555	PFSK-1	brain:	n/a
22	chr2:50201479-50201529	HMEC	breast:	n/a
23	chr2:50201413-50201463	HAEpiC	amniotic membrane:	n/a
24	chr2:50201511-50201561	U87	brain:	n/a
25	chr2:50201511-50201561	HUVEC	blood vessel:	n/a
26	chr2:50201505-50201555	AG10803	skin:	n/a
27	chr2:50201505-50201555	HMEC	breast:	n/a
28	chr2:50187352-50187402	NB4	blood:	n/a
29	chr2:50187352-50187402	MCF-7	breast:	n/a
30	chr2:50201511-50201561	SK-N-MC	brain:	n/a
31	chr2:50201479-50201529	HNPCEpiC	eye:	n/a
32	chr2:50201511-50201561	NH-A	brain:	n/a
33	chr2:50201505-50201555	RPTEC	kidney:	n/a
34	chr2:50201505-50201555	ovcar-3	ovarian:	n/a
35	chr2:50187352-50187402	HNPCEpiC	eye:	n/a
36	chr2:50201479-50201529	HCPEpiC	choroid plexus:	n/a
37	chr2:50201479-50201529	SK-N-SH_RA	brain:	n/a
38	chr2:50201505-50201555	BJ	skin:	n/a
39	chr2:50187352-50187402	HUVEC	blood vessel:	n/a
40	chr2:50201505-50201555	HCM	heart:	n/a
41	chr2:50187352-50187402	AG04449	skin:	fetal
42	chr2:50201413-50201463	SK-N-SH_RA	brain:	n/a
43	chr2:50187352-50187402	HMEC	breast:	n/a
44	chr2:50201382-50201432	AG09309	skin:	n/a
45	chr2:50201511-50201561	GM19239	blood:	n/a
46	chr2:50201413-50201463	SAEC	small airway:	n/a
47	chr2:50201505-50201555	CMK	blood:	n/a
48	chr2:50201413-50201463	MCF10A-Er-Src	breast:	n/a
49	chr2:50201479-50201529	NB4	blood:	n/a
50	chr2:50201505-50201555	LNCaP	prostate:	n/a

No data

Variant related genes	Relation type
NRXN1	TF binding region
NRXN1	CpG island

Extended variants
information (count: 1338 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1338 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534992252	chr2:50181800-50181801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373239124	chr2:50181810-50181811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181545527	chr2:50181846-50181847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567315780	chr2:50181852-50181853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537650407	chr2:50181880-50181881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75009026	chr2:50181896-50181897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148991575	chr2:50181906-50181907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538917385	chr2:50181967-50181968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115934127	chr2:50182005-50182006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566747205	chr2:50182035-50182036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534341016	chr2:50182095-50182096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555588692	chr2:50182116-50182117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574031043	chr2:50182194-50182195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186522886	chr2:50182204-50182205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74740315	chr2:50182275-50182276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79201970	chr2:50182283-50182284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74896756	chr2:50182346-50182347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117990439	chr2:50182357-50182358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548408831	chr2:50182395-50182396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527299268	chr2:50182413-50182414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144113970	chr2:50182414-50182415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571112464	chr2:50182434-50182435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531405093	chr2:50182451-50182452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190920647	chr2:50182525-50182526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571443091	chr2:50182531-50182532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567084996	chr2:50182544-50182545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532492678	chr2:50182545-50182546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182346619	chr2:50182558-50182559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369453243	chr2:50182720-50182721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146924002	chr2:50182723-50182724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199747653	chr2:50182746-50182747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553894990	chr2:50182747-50182748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34383466	chr2:50182750-50182751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs397873451	chr2:50182759-50182760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533943296	chr2:50182788-50182789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62132441	chr2:50182809-50182810	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs77836533	chr2:50182812-50182813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556426340	chr2:50182813-50182814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576200310	chr2:50182853-50182854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs137936783	chr2:50182860-50182861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72369095	chr2:50182862-50182863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577807715	chr2:50183023-50183024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370022794	chr2:50183026-50183027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545158610	chr2:50183033-50183034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554175188	chr2:50183036-50183037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34617676	chr2:50183078-50183079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544842843	chr2:50183083-50183084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10165762	chr2:50183085-50183086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370116442	chr2:50183128-50183129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565092441	chr2:50183138-50183139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Bladder cancer	21909424	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50141600-50187400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr2:50176000-50185600	Weak transcription	Fetal Brain Female	brain
3	chr2:50176200-50186600	Weak transcription	Brain Angular Gyrus	brain
4	chr2:50178400-50186600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr2:50181600-50182000	Enhancers	Fetal Brain Male	brain
6	chr2:50181800-50182000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:50182000-50184200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:50182000-50185200	Weak transcription	Fetal Brain Male	brain
9	chr2:50184200-50189000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:50185200-50185800	Enhancers	Fetal Brain Male	brain
11	chr2:50185200-50188800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:50185400-50185600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr2:50185400-50185600	Enhancers	Brain Cingulate Gyrus	brain
14	chr2:50185600-50186000	Enhancers	Fetal Brain Female	brain
15	chr2:50185600-50186400	Weak transcription	Brain Cingulate Gyrus	brain
16	chr2:50185600-50187200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:50185800-50188200	Weak transcription	Fetal Brain Male	brain
18	chr2:50186000-50186200	Weak transcription	Fetal Brain Female	brain
19	chr2:50186200-50187600	Enhancers	Fetal Brain Female	brain
20	chr2:50186400-50186600	Enhancers	Fetal Muscle Leg	muscle
21	chr2:50186400-50186800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr2:50186400-50187600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr2:50186400-50188000	Enhancers	Brain Cingulate Gyrus	brain
24	chr2:50186400-50188600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr2:50186600-50187400	Enhancers	H9 Cell Line	embryonic stem cell
26	chr2:50186600-50187600	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr2:50186600-50188000	Enhancers	Brain Anterior Caudate	brain
28	chr2:50186600-50188600	Enhancers	Brain Angular Gyrus	brain
29	chr2:50186800-50187200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr2:50186800-50187200	Enhancers	Brain Substantia Nigra	brain
31	chr2:50186800-50188400	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr2:50186800-50188800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:50187000-50187400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr2:50187000-50187400	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr2:50187000-50187600	Enhancers	Brain Hippocampus Middle	brain
36	chr2:50187000-50188000	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr2:50187200-50187400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr2:50187200-50187400	Flanking Active TSS	Brain Substantia Nigra	brain
39	chr2:50187200-50187600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:50187200-50187800	Enhancers	Brain Germinal Matrix	brain
41	chr2:50187200-50188000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr2:50187400-50188000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr2:50187400-50188000	Active TSS	Brain Substantia Nigra	brain
44	chr2:50187400-50188200	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr2:50187400-50188800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr2:50187400-50189800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr2:50187600-50187800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:50187600-50187800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
49	chr2:50187600-50188000	Flanking Active TSS	Brain Hippocampus Middle	brain
50	chr2:50187600-50199800	Weak transcription	Fetal Brain Female	brain

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