Variant report

Variant	nsv872859
Chromosome Location	chr1:194377156-194590401
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:592)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:194504737-194505069	K562	blood:	n/a	n/a
2	ATF1	chr1:194539567-194539748	K562	blood:	n/a	n/a
3	BACH1	chr1:194402542-194402548	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr1:194447109-194447326	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:194504591-194504863	K562	blood:	n/a	n/a
6	CBX3	chr1:194479720-194479912	K562	blood:	n/a	n/a
7	CBX3	chr1:194479655-194479980	K562	blood:	n/a	n/a
8	CBX3	chr1:194388807-194389300	HCT-116	colon:	n/a	n/a
9	CBX3	chr1:194388867-194389138	K562	blood:	n/a	n/a
10	CCNT2	chr1:194517300-194517500	K562	blood:	n/a	n/a
11	CEBPB	chr1:194465951-194466182	IMR90	lung:	n/a	chr1:194466086-194466097
12	CEBPB	chr1:194380325-194380663	IMR90	lung:	n/a	chr1:194380492-194380501 chr1:194380490-194380501 chr1:194380490-194380503
13	CEBPB	chr1:194424471-194424668	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:194531531-194531792	HepG2	liver:	n/a	chr1:194531632-194531643
15	CEBPB	chr1:194514268-194514460	K562	blood:	n/a	chr1:194514354-194514365
16	CEBPB	chr1:194424423-194424710	IMR90	lung:	n/a	n/a
17	CEBPB	chr1:194574883-194575091	HepG2	liver:	n/a	chr1:194574939-194574950
18	CEBPB	chr1:194397513-194397819	HepG2	liver:	n/a	chr1:194397683-194397694
19	CEBPB	chr1:194380328-194380670	HepG2	liver:	n/a	chr1:194380492-194380501 chr1:194380490-194380501 chr1:194380490-194380503
20	CEBPB	chr1:194383847-194384061	H1-hESC	embryonic stem cell:	n/a	chr1:194383907-194383918
21	CEBPB	chr1:194538154-194538433	HepG2	liver:	n/a	chr1:194538275-194538286 chr1:194538274-194538287
22	CEBPB	chr1:194531495-194531766	A549	lung:	n/a	chr1:194531632-194531643
23	CEBPB	chr1:194380423-194380607	K562	blood:	n/a	chr1:194380492-194380501 chr1:194380490-194380501 chr1:194380490-194380503
24	CEBPB	chr1:194574845-194575007	A549	lung:	n/a	chr1:194574939-194574950
25	CEBPB	chr1:194424402-194424677	A549	lung:	n/a	n/a
26	CEBPB	chr1:194465936-194466208	HepG2	liver:	n/a	chr1:194466086-194466097
27	CEBPB	chr1:194383802-194384002	HepG2	liver:	n/a	chr1:194383907-194383918
28	CEBPB	chr1:194514201-194514523	HepG2	liver:	n/a	chr1:194514354-194514365
29	CEBPB	chr1:194397494-194397754	A549	lung:	n/a	chr1:194397683-194397694
30	CEBPB	chr1:194574841-194575055	H1-hESC	embryonic stem cell:	n/a	chr1:194574939-194574950
31	CEBPD	chr1:194504482-194504872	K562	blood:	n/a	n/a
32	CTCF	chr1:194507732-194507869	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:194537880-194538030	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr1:194537840-194537990	HRE	kidney:	n/a	n/a
35	CTCF	chr1:194537840-194537990	HCT-116	colon:	n/a	n/a
36	CTCF	chr1:194537940-194538090	BE2_C	brain:	n/a	n/a
37	CTCF	chr1:194537880-194538030	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr1:194436060-194436210	NB4	blood:	n/a	n/a
39	CTCF	chr1:194435980-194436130	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr1:194507653-194507951	GM12878	blood:	n/a	n/a
41	CTCF	chr1:194435840-194435990	A549	lung:	n/a	n/a
42	CTCF	chr1:194435960-194436110	HPF	lung:	n/a	n/a
43	CTCF	chr1:194435947-194436110	Medullo	brain:	n/a	n/a
44	CTCF	chr1:194507760-194507910	NHEK	skin:	n/a	n/a
45	CTCF	chr1:194379013-194379114	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:194435864-194436187	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr1:194493940-194494090	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:194507570-194507916	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:194435940-194436090	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr1:194435980-194436130	HCM	heart:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:194400632-194400682	HCM	heart:	n/a
2	chr1:194400632-194400682	Caco-2	colon:	n/a
3	chr1:194400632-194400682	AG09309	skin:	n/a
4	chr1:194400632-194400682	HAEpiC	amniotic membrane:	n/a
5	chr1:194400632-194400682	HRPEpiC	eye:	n/a
6	chr1:194400632-194400682	GM19239	blood:	n/a
7	chr1:194400632-194400682	AG10803	skin:	n/a
8	chr1:194400632-194400682	MCF-7	breast:	n/a
9	chr1:194400632-194400682	NT2-D1	testis:	n/a
10	chr1:194400632-194400682	HCT-116	colon:	n/a
11	chr1:194400632-194400682	HEEpiC	esophagus:	n/a
12	chr1:194400632-194400682	RPTEC	kidney:	n/a
13	chr1:194400632-194400682	BJ	skin:	n/a
14	chr1:194400632-194400682	CMK	blood:	n/a
15	chr1:194400632-194400682	GM12892	blood:	n/a
16	chr1:194400632-194400682	Jurkat	blood:	n/a
17	chr1:194400632-194400682	HepG2	liver:	n/a
18	chr1:194400632-194400682	U87	brain:	n/a
19	chr1:194400632-194400682	Hepatocyte	liver:	n/a
20	chr1:194400632-194400682	T-47D	breast:	n/a
21	chr1:194400632-194400682	HRE	kidney:	n/a
22	chr1:194400632-194400682	PrEC	prostate:	n/a
23	chr1:194400632-194400682	PFSK-1	brain:	n/a
24	chr1:194400632-194400682	NH-A	brain:	n/a
25	chr1:194400632-194400682	HCPEpiC	choroid plexus:	n/a
26	chr1:194400632-194400682	LNCaP	prostate:	n/a
27	chr1:194400632-194400682	SKMC	muscle:	n/a
28	chr1:194400632-194400682	IMR90	lung:	fetal
29	chr1:194400632-194400682	PANC-1	pancreas:	n/a
30	chr1:194400632-194400682	GM06990	blood:	n/a
31	chr1:194400632-194400682	HMEC	breast:	n/a
32	chr1:194400632-194400682	SK-N-SH_RA	brain:	n/a
33	chr1:194400632-194400682	HRCEpiC	kidney:	n/a
34	chr1:194400632-194400682	SK-N-MC	brain:	n/a
35	chr1:194400632-194400682	SAEC	small airway:	n/a
36	chr1:194400632-194400682	K562	blood:	n/a
37	chr1:194400632-194400682	HNPCEpiC	eye:	n/a
38	chr1:194400632-194400682	NHBE	bronchial:	n/a
39	chr1:194400632-194400682	GM12891	blood:	n/a
40	chr1:194400632-194400682	NB4	blood:	n/a
41	chr1:194400632-194400682	ECC-1	luminal epithelium:	n/a
42	chr1:194400632-194400682	GM12878	blood:	n/a
43	chr1:194400632-194400682	AoSMC	blood vessel:	n/a
44	chr1:194400632-194400682	NHDF-neo	bronchial:	n/a
45	chr1:194400632-194400682	MCF10A-Er-Src	breast:	n/a
46	chr1:194400632-194400682	AG04449	skin:	fetal
47	chr1:194400632-194400682	SK-N-SH	brain:	n/a
48	chr1:194400632-194400682	HCF	heart:	n/a
49	chr1:194400632-194400682	AG09319	gingival:	n/a
50	chr1:194400632-194400682	ovcar-3	ovarian:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:194417615..194420407-chr1:194420472..194422250,2	K562	blood:
2	chr1:194519474..194521221-chr1:194527873..194530649,2	K562	blood:
3	chr1:194441258..194442954-chr1:194443825..194445745,2	K562	blood:
4	chr1:194532647..194534539-chr1:194535882..194538033,2	K562	blood:
5	chr1:194490383..194492848-chr1:194494979..194497910,2	K562	blood:
6	chr1:194436232..194436752-chr8:43092409..43092930,2	MCF-7	breast:
7	chr1:194425454..194427984-chr1:194432751..194435016,2	K562	blood:
8	chr1:194490383..194492848-chr1:194494979..194497910,2	K562	blood:
9	chr1:194441258..194442954-chr1:194443825..194445745,2	K562	blood:
10	chr1:194470680..194473383-chr1:194480491..194482592,2	K562	blood:
11	chr1:194557101..194559742-chr1:194559800..194562767,2	K562	blood:
12	chr1:194583954..194584474-chr4:116457976..116458496,2	MCF-7	breast:
13	chr1:194450165..194451814-chr1:194453131..194454944,2	MCF-7	breast:
14	chr1:194553579..194555823-chr1:194557889..194560513,2	K562	blood:
15	chr1:194425454..194428460-chr1:194432154..194435016,3	K562	blood:
16	chr1:194583954..194584474-chr4:146024840..146025360,2	MCF-7	breast:
17	chr1:194553579..194555823-chr1:194557889..194560513,2	K562	blood:
18	chr1:194565462..194567193-chr1:194826327..194828767,2	K562	blood:
19	chr1:194417615..194420407-chr1:194420472..194422250,2	K562	blood:
20	chr1:194583454..194584474-chr7:89057256..89058256,3	MCF-7	breast:
21	chr1:194519474..194521221-chr1:194527873..194530649,2	K562	blood:
22	chr1:194583474..194584454-chr2:31059867..31060367,2	MCF-7	breast:
23	chr1:194450165..194451814-chr1:194453131..194454944,2	MCF-7	breast:
24	chr1:194470680..194473383-chr1:194480491..194482592,2	K562	blood:
25	chr1:194425454..194427984-chr1:194432751..194435016,2	K562	blood:
26	chr1:194557101..194559742-chr1:194559800..194562767,2	K562	blood:
27	chr1:194532647..194534539-chr1:194535882..194538033,2	K562	blood:
28	chr1:194425454..194428460-chr1:194432154..194435016,3	K562	blood:
29	chr1:194583954..194584474-chr11:21332888..21333408,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-983P	TF binding region
RNU6-983P	CpG island

Extended variants
information (count: 2153 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2153 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4460614	chr1:194377156-194377157	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188317299	chr1:194377211-194377212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560049613	chr1:194377215-194377216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527299090	chr1:194377216-194377217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61816708	chr1:194377232-194377233	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs192205789	chr1:194377253-194377254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567274677	chr1:194377280-194377281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs58912027	chr1:194377339-194377340	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs78065549	chr1:194377402-194377403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370918720	chr1:194377418-194377419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs377555204	chr1:194377425-194377426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74133948	chr1:194377433-194377434	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs114698188	chr1:194377434-194377435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs59472106	chr1:194377454-194377455	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs184484224	chr1:194377474-194377475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576488603	chr1:194377504-194377505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544014612	chr1:194377511-194377512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs57295120	chr1:194377512-194377513	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs58776407	chr1:194377527-194377528	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs541705052	chr1:194377562-194377563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559812074	chr1:194377563-194377564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79158952	chr1:194377575-194377576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188610340	chr1:194377581-194377582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs60002272	chr1:194377587-194377588	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs192660290	chr1:194377602-194377603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140304396	chr1:194377639-194377640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564690497	chr1:194377658-194377659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561214497	chr1:194377692-194377693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142670808	chr1:194377701-194377702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79166562	chr1:194377734-194377735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543238705	chr1:194377746-194377747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184320214	chr1:194377779-194377780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189072527	chr1:194377796-194377797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570154111	chr1:194377825-194377826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116118927	chr1:194377847-194377848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559104754	chr1:194377853-194377854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61700513	chr1:194377860-194377861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs75874780	chr1:194377876-194377877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553611275	chr1:194377885-194377886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575067657	chr1:194377895-194377896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542601013	chr1:194377897-194377898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201775346	chr1:194377910-194377911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147541109	chr1:194377925-194377926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192160840	chr1:194377931-194377932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367871170	chr1:194377932-194377933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183881710	chr1:194377955-194377956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116004635	chr1:194377982-194377983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531966380	chr1:194378011-194378012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547302609	chr1:194378027-194378028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12039872	chr1:194378048-194378049	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:194376600-194380200	Weak transcription	Fetal Lung	lung
2	chr1:194380200-194380600	Enhancers	Fetal Lung	lung
3	chr1:194380600-194383200	Weak transcription	Fetal Lung	lung
4	chr1:194383200-194383400	ZNF genes & repeats	Fetal Lung	lung
5	chr1:194388800-194389200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:194389200-194389600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:194389600-194390000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr1:194390000-194400600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr1:194400400-194400600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:194406600-194406800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:194411000-194413800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:194411400-194411800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr1:194411400-194412000	Enhancers	Brain Substantia Nigra	brain
14	chr1:194411400-194412200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr1:194411400-194413400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:194411600-194412000	Enhancers	Brain Angular Gyrus	brain
17	chr1:194411600-194412000	Enhancers	Brain Anterior Caudate	brain
18	chr1:194411600-194412000	Enhancers	Brain Hippocampus Middle	brain
19	chr1:194411600-194412000	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr1:194411600-194412400	Enhancers	Brain Germinal Matrix	brain
21	chr1:194411600-194412400	Enhancers	Fetal Brain Female	brain
22	chr1:194411800-194412000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr1:194412000-194412400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr1:194412000-194412400	Active TSS	Brain Substantia Nigra	brain
25	chr1:194412000-194412600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr1:194412000-194412600	Active TSS	Brain Angular Gyrus	brain
27	chr1:194412000-194412800	Active TSS	Brain Anterior Caudate	brain
28	chr1:194412000-194412800	Active TSS	Brain Hippocampus Middle	brain
29	chr1:194412200-194412400	Active TSS	Brain Cingulate Gyrus	brain
30	chr1:194412200-194412600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr1:194412200-194412600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr1:194412200-194412600	Active TSS	Brain Inferior Temporal Lobe	brain
33	chr1:194412200-194412800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr1:194412400-194412600	Flanking Active TSS	Brain Cingulate Gyrus	brain
35	chr1:194412400-194412600	Flanking Active TSS	Brain Substantia Nigra	brain
36	chr1:194412400-194413200	Weak transcription	Brain Germinal Matrix	brain
37	chr1:194412600-194412800	Enhancers	Brain Cingulate Gyrus	brain
38	chr1:194412600-194413200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr1:194412600-194413600	Enhancers	Brain Substantia Nigra	brain
40	chr1:194412600-194413800	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr1:194412800-194413400	Enhancers	Brain Anterior Caudate	brain
42	chr1:194413200-194413400	Enhancers	Brain Germinal Matrix	brain
43	chr1:194413200-194413800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr1:194413600-194413800	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr1:194437200-194437600	Active TSS	Right Atrium	heart
46	chr1:194443200-194444400	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr1:194443200-194444400	Enhancers	Fetal Brain Male	brain
48	chr1:194443200-194445800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr1:194443800-194444200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:194444000-194444200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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