Variant report

Variant	nsv1005102
Chromosome Location	chr3:85729640-85829412
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	ARID3A	chr3:85808773-85808957	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:85775448-85775854	HepG2	liver:	n/a	n/a
3	CEBPB	chr3:85761031-85761231	A549	lung:	n/a	n/a
4	CEBPB	chr3:85782496-85782758	HepG2	liver:	n/a	chr3:85782605-85782616 chr3:85782605-85782618
5	CEBPB	chr3:85740359-85740732	Hela-S3	cervix:	n/a	chr3:85740534-85740545 chr3:85740548-85740559
6	CEBPB	chr3:85740389-85740673	H1-hESC	embryonic stem cell:	n/a	chr3:85740534-85740545 chr3:85740548-85740559
7	CEBPB	chr3:85777024-85777302	A549	lung:	n/a	chr3:85777131-85777144 chr3:85777132-85777143 chr3:85777130-85777147
8	CEBPB	chr3:85776958-85777314	IMR90	lung:	n/a	chr3:85777131-85777144 chr3:85777132-85777143 chr3:85777130-85777147
9	CEBPB	chr3:85775455-85775813	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:85774128-85774136	A549	lung:	n/a	n/a
11	CEBPB	chr3:85775542-85775726	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:85808496-85808696	A549	lung:	n/a	chr3:85808591-85808604 chr3:85808591-85808602
13	CEBPB	chr3:85740352-85740683	A549	lung:	n/a	chr3:85740534-85740545 chr3:85740548-85740559
14	CEBPB	chr3:85773942-85774177	HepG2	liver:	n/a	chr3:85774099-85774112 chr3:85774099-85774110
15	CEBPB	chr3:85740335-85740646	ECC-1	luminal epithelium:	n/a	chr3:85740534-85740545 chr3:85740548-85740559
16	CEBPB	chr3:85827947-85828147	HepG2	liver:	n/a	chr3:85828058-85828067 chr3:85828057-85828068
17	CEBPB	chr3:85773985-85774188	K562	blood:	n/a	chr3:85774099-85774112 chr3:85774099-85774110
18	CEBPB	chr3:85740366-85740735	HepG2	liver:	n/a	chr3:85740534-85740545 chr3:85740548-85740559
19	CEBPB	chr3:85761045-85761288	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:85757553-85757873	H1-hESC	embryonic stem cell:	n/a	chr3:85757704-85757715
21	CEBPB	chr3:85740362-85740740	IMR90	lung:	n/a	chr3:85740534-85740545 chr3:85740548-85740559
22	CEBPB	chr3:85740401-85740692	MCF-7	breast:	n/a	chr3:85740534-85740545 chr3:85740548-85740559
23	CEBPB	chr3:85808414-85808753	HepG2	liver:	n/a	chr3:85808591-85808604 chr3:85808591-85808602
24	CEBPB	chr3:85740365-85740729	A549	lung:	n/a	chr3:85740534-85740545 chr3:85740548-85740559
25	CEBPB	chr3:85740303-85740671	ECC-1	luminal epithelium:	n/a	chr3:85740534-85740545 chr3:85740548-85740559
26	CEBPB	chr3:85770960-85771149	HepG2	liver:	n/a	chr3:85771103-85771114
27	CEBPB	chr3:85740266-85740663	A549	lung:	n/a	chr3:85740534-85740545 chr3:85740548-85740559
28	CEBPB	chr3:85740422-85740637	K562	blood:	n/a	chr3:85740534-85740545 chr3:85740548-85740559
29	CEBPB	chr3:85761016-85761240	IMR90	lung:	n/a	n/a
30	CEBPB	chr3:85775512-85775666	A549	lung:	n/a	n/a
31	CEBPB	chr3:85775455-85775841	HepG2	liver:	n/a	n/a
32	CEBPB	chr3:85776997-85777310	HepG2	liver:	n/a	chr3:85777131-85777144 chr3:85777132-85777143 chr3:85777130-85777147
33	CEBPB	chr3:85757520-85757837	HepG2	liver:	n/a	chr3:85757704-85757715
34	CTCF	chr3:85793336-85793368	GM20000	blood:	n/a	n/a
35	CTCF	chr3:85802940-85803090	AG10803	skin:	n/a	n/a
36	CTCF	chr3:85766934-85767035	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:85748600-85748750	GM12875	blood:	n/a	n/a
38	CTCF	chr3:85763100-85763128	Lung_OC	lung:	n/a	n/a
39	CTCF	chr3:85747690-85747719	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr3:85774346-85774369	K562	blood:	n/a	n/a
41	CTCF	chr3:85763131-85763137	Lung_OC	lung:	n/a	n/a
42	CTCF	chr3:85762514-85762570	GM10248	blood:	n/a	n/a
43	CTCF	chr3:85775200-85775350	HMEC	breast:	n/a	n/a
44	CTCF	chr3:85756161-85756257	Fibrobl	skin:	n/a	n/a
45	CTCF	chr3:85766945-85767032	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:85794850-85794877	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr3:85771430-85771460	GM10248	blood:	n/a	n/a
48	E2F4	chr3:85735738-85735755	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr3:85745612-85745640	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr3:85824444-85824633	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:85792009-85792059	HMEC	breast:	n/a
2	chr3:85792009-85792059	BJ	skin:	n/a
3	chr3:85792009-85792059	Hepatocyte	liver:	n/a
4	chr3:85792009-85792059	HUVEC	blood vessel:	n/a
5	chr3:85792009-85792059	Hela-S3	cervix:	n/a
6	chr3:85792009-85792059	HepG2	liver:	n/a
7	chr3:85792009-85792059	BE2_C	brain:	n/a
8	chr3:85792009-85792059	MCF10A-Er-Src	breast:	n/a
9	chr3:85792009-85792059	AG09319	gingival:	n/a
10	chr3:85792009-85792059	MCF-7	breast:	n/a
11	chr3:85792009-85792059	HIPEpiC	eye:	n/a
12	chr3:85792009-85792059	PANC-1	pancreas:	n/a
13	chr3:85792009-85792059	T-47D	breast:	n/a
14	chr3:85792009-85792059	CMK	blood:	n/a
15	chr3:85792009-85792059	AG04450	lung:	fetal
16	chr3:85792009-85792059	GM12892	blood:	n/a
17	chr3:85792009-85792059	SK-N-SH	brain:	n/a
18	chr3:85792009-85792059	SK-N-SH_RA	brain:	n/a
19	chr3:85792009-85792059	HL-60	blood:	n/a
20	chr3:85792009-85792059	HRCEpiC	kidney:	n/a
21	chr3:85792009-85792059	HAEpiC	amniotic membrane:	n/a
22	chr3:85792009-85792059	ovcar-3	ovarian:	n/a
23	chr3:85792009-85792059	HEEpiC	esophagus:	n/a
24	chr3:85792009-85792059	GM19239	blood:	n/a
25	chr3:85792009-85792059	SKMC	muscle:	n/a
26	chr3:85792009-85792059	NT2-D1	testis:	n/a
27	chr3:85792009-85792059	HPAEpiC	pulmonary alveolar:	n/a
28	chr3:85792009-85792059	U87	brain:	n/a
29	chr3:85792009-85792059	PFSK-1	brain:	n/a
30	chr3:85792009-85792059	AG09309	skin:	n/a
31	chr3:85792009-85792059	Caco-2	colon:	n/a
32	chr3:85792009-85792059	ProgFib	skin:	n/a
33	chr3:85792009-85792059	LNCaP	prostate:	n/a
34	chr3:85792009-85792059	A549	lung:	n/a
35	chr3:85792009-85792059	K562	blood:	n/a
36	chr3:85792009-85792059	AG04449	skin:	fetal
37	chr3:85792009-85792059	HCM	heart:	n/a
38	chr3:85792009-85792059	HRE	kidney:	n/a
39	chr3:85792009-85792059	Jurkat	blood:	n/a
40	chr3:85792009-85792059	SK-N-MC	brain:	n/a
41	chr3:85792009-85792059	RPTEC	kidney:	n/a
42	chr3:85792009-85792059	HEK293	kidney:	embryo
43	chr3:85792009-85792059	AG10803	skin:	n/a
44	chr3:85792009-85792059	HCPEpiC	choroid plexus:	n/a
45	chr3:85792009-85792059	NH-A	brain:	n/a
46	chr3:85792009-85792059	HRPEpiC	eye:	n/a
47	chr3:85792009-85792059	HCF	heart:	n/a
48	chr3:85792009-85792059	ECC-1	luminal epithelium:	n/a
49	chr3:85792009-85792059	PrEC	prostate:	n/a
50	chr3:85792009-85792059	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:85801276..85804011-chr3:85805861..85807546,2	MCF-7	breast:
2	chr3:85775563..85777702-chr3:85778192..85780972,2	MCF-7	breast:
3	chr3:85801802..85803723-chr3:85806304..85808705,2	MCF-7	breast:
4	chr3:85801276..85804011-chr3:85805861..85807546,2	MCF-7	breast:
5	chr3:85801802..85803723-chr3:85806304..85808705,2	MCF-7	breast:

Variant related genes	Relation type
CADM2	TF binding region
CADM2	CpG island
ENSG00000175161	chromatin interactions

Extended variants
information (count: 2228 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2228 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370136381	chr3:85729670-85729671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546725184	chr3:85729683-85729684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187692528	chr3:85729713-85729714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113636574	chr3:85729733-85729734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192803432	chr3:85729756-85729757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184858627	chr3:85729767-85729768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568490136	chr3:85729799-85729800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565049078	chr3:85729800-85729801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536104410	chr3:85729846-85729847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373598844	chr3:85729855-85729856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143904660	chr3:85729905-85729906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554283745	chr3:85729918-85729919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188522157	chr3:85729945-85729946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572867887	chr3:85729966-85729967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146420098	chr3:85730059-85730060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138691509	chr3:85730131-85730132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577555304	chr3:85730184-85730185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544921163	chr3:85730189-85730190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563205390	chr3:85730248-85730249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114321229	chr3:85730295-85730296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7615008	chr3:85730335-85730336	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs560287079	chr3:85730340-85730341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192011445	chr3:85730385-85730386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552292428	chr3:85730409-85730410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184231127	chr3:85730433-85730434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371527078	chr3:85730476-85730477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376554617	chr3:85730516-85730517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560057713	chr3:85730525-85730526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149434424	chr3:85730584-85730585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368312318	chr3:85730595-85730596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550446020	chr3:85730622-85730623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372903176	chr3:85730689-85730690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547856124	chr3:85730702-85730703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568778031	chr3:85730715-85730716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189378058	chr3:85730723-85730724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375839175	chr3:85730760-85730761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554503475	chr3:85730766-85730767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369752917	chr3:85730771-85730772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373271040	chr3:85730789-85730790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116098983	chr3:85730815-85730816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533879292	chr3:85730836-85730837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558734697	chr3:85730894-85730895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577493966	chr3:85730899-85730900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544780414	chr3:85730903-85730904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556814317	chr3:85730998-85730999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575027479	chr3:85731014-85731015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542165962	chr3:85731056-85731057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560528197	chr3:85731057-85731058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572394499	chr3:85731073-85731074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564360348	chr3:85731089-85731090	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Prostate cancer	21307934	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85720200-85730400	Weak transcription	Brain Hippocampus Middle	brain
2	chr3:85725200-85730400	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:85730200-85731400	Enhancers	Brain Anterior Caudate	brain
4	chr3:85730400-85731000	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr3:85730400-85731400	Enhancers	Brain Hippocampus Middle	brain
6	chr3:85731200-85731600	Enhancers	Brain Angular Gyrus	brain
7	chr3:85731400-85736800	Weak transcription	Brain Hippocampus Middle	brain
8	chr3:85747400-85748200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr3:85748200-85748800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr3:85748400-85748800	ZNF genes & repeats	Brain Hippocampus Middle	brain
11	chr3:85748800-85753200	Weak transcription	Brain Hippocampus Middle	brain
12	chr3:85751200-85753400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr3:85751800-85752000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr3:85752000-85752600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr3:85752400-85753200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr3:85752600-85752800	Enhancers	Brain Cingulate Gyrus	brain
17	chr3:85752600-85753200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr3:85752800-85753000	Enhancers	Brain Angular Gyrus	brain
19	chr3:85752800-85753200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr3:85752800-85753200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr3:85753200-85753600	Enhancers	Brain Hippocampus Middle	brain
22	chr3:85753200-85756800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr3:85753200-85756800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr3:85753200-85756800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr3:85753200-85757000	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr3:85753400-85754400	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr3:85753600-85753800	Enhancers	Brain Angular Gyrus	brain
28	chr3:85753600-85753800	Enhancers	Brain Cingulate Gyrus	brain
29	chr3:85753600-85758600	Weak transcription	Brain Hippocampus Middle	brain
30	chr3:85754400-85754800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr3:85754400-85755600	Enhancers	Brain Germinal Matrix	brain
32	chr3:85754800-85757000	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr3:85755600-85759200	Weak transcription	Brain Germinal Matrix	brain
34	chr3:85756800-85757400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:85756800-85758600	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr3:85756800-85759200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr3:85757000-85759000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr3:85757000-85759200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr3:85757000-85759200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr3:85757200-85758800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr3:85757400-85757800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr3:85757600-85759000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr3:85757800-85759000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr3:85758000-85758600	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr3:85758400-85758600	Enhancers	Brain Anterior Caudate	brain
46	chr3:85758600-85759000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr3:85758600-85759200	Enhancers	Brain Hippocampus Middle	brain
48	chr3:85758600-85759400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr3:85758600-85759400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr3:85758600-85759400	Enhancers	Brain Substantia Nigra	brain

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