Variant report

Variant	nsv564757
Chromosome Location	chr14:47267652-47490379
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	chr14:47354811-47355132	K562	blood:	n/a	n/a
2	BACH1	chr14:47354745-47355139	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr14:47356455-47356637	GM12878	blood:	n/a	chr14:47356567-47356578
4	BATF	chr14:47356425-47356723	GM12878	blood:	n/a	chr14:47356567-47356578
5	BCL11A	chr14:47287397-47287658	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr14:47303861-47303947	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr14:47280156-47280467	HepG2	liver:	n/a	chr14:47280326-47280337 chr14:47280326-47280339 chr14:47280326-47280339
8	CEBPB	chr14:47362170-47362344	H1-hESC	embryonic stem cell:	n/a	chr14:47362259-47362270
9	CEBPB	chr14:47366505-47366846	HepG2	liver:	n/a	chr14:47366671-47366680 chr14:47366671-47366682 chr14:47366669-47366682 chr14:47366669-47366680
10	CEBPB	chr14:47393718-47394047	IMR90	lung:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
11	CEBPB	chr14:47362090-47362394	IMR90	lung:	n/a	chr14:47362259-47362270
12	CEBPB	chr14:47423059-47423295	HepG2	liver:	n/a	chr14:47423216-47423225 chr14:47423214-47423225 chr14:47423214-47423227
13	CEBPB	chr14:47303627-47303827	HepG2	liver:	n/a	chr14:47303681-47303692
14	CEBPB	chr14:47380994-47381232	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:47454833-47454920	A549	lung:	n/a	n/a
16	CEBPB	chr14:47393713-47394028	HepG2	liver:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
17	CEBPB	chr14:47393770-47394030	H1-hESC	embryonic stem cell:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
18	CEBPB	chr14:47404933-47405117	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr14:47362166-47362402	A549	lung:	n/a	chr14:47362259-47362270
20	CEBPB	chr14:47404877-47405212	IMR90	lung:	n/a	n/a
21	CEBPB	chr14:47288787-47289125	A549	lung:	n/a	chr14:47288961-47288972
22	CEBPB	chr14:47366550-47366832	A549	lung:	n/a	chr14:47366671-47366680 chr14:47366671-47366682 chr14:47366669-47366682 chr14:47366669-47366680
23	CEBPB	chr14:47366543-47366799	H1-hESC	embryonic stem cell:	n/a	chr14:47366671-47366682 chr14:47366669-47366682 chr14:47366669-47366680 chr14:47366671-47366680
24	CEBPB	chr14:47303607-47303836	A549	lung:	n/a	chr14:47303681-47303692
25	CEBPB	chr14:47404882-47405242	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:47485719-47485919	A549	lung:	n/a	chr14:47485846-47485857 chr14:47485886-47485898
27	CEBPB	chr14:47393758-47394044	A549	lung:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
28	CEBPB	chr14:47485732-47485940	HepG2	liver:	n/a	chr14:47485846-47485857 chr14:47485886-47485898
29	CEBPB	chr14:47288797-47289144	HepG2	liver:	n/a	chr14:47288961-47288972
30	CEBPB	chr14:47353274-47353450	A549	lung:	n/a	n/a
31	CEBPB	chr14:47366501-47366839	IMR90	lung:	n/a	chr14:47366671-47366680 chr14:47366671-47366682 chr14:47366669-47366682 chr14:47366669-47366680
32	CEBPB	chr14:47362102-47362436	HepG2	liver:	n/a	chr14:47362259-47362270
33	CEBPB	chr14:47353249-47353482	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:47434809-47435009	HepG2	liver:	n/a	chr14:47434916-47434933
35	CTCF	chr14:47450422-47450496	GM20000	blood:	n/a	n/a
36	CTCF	chr14:47420480-47420630	BE2_C	brain:	n/a	n/a
37	CTCF	chr14:47389840-47389990	GM12875	blood:	n/a	n/a
38	CTCF	chr14:47420360-47420510	A549	lung:	n/a	n/a
39	CTCF	chr14:47420526-47420542	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr14:47420440-47420590	HCT-116	colon:	n/a	n/a
41	CTCF	chr14:47393000-47393150	HCPEpiC	choroid plexus:	n/a	chr14:47393063-47393084
42	CTCF	chr14:47389880-47390030	GM12864	blood:	n/a	n/a
43	CTCF	chr14:47389780-47389930	BE2_C	brain:	n/a	n/a
44	CTCF	chr14:47438574-47438603	Lung_OC	lung:	n/a	n/a
45	CTCF	chr14:47389800-47389950	GM12873	blood:	n/a	n/a
46	CTCF	chr14:47389920-47390070	MCF-7	breast:	n/a	n/a
47	CTCF	chr14:47389800-47389950	HCT-116	colon:	n/a	n/a
48	CTCF	chr14:47420400-47420550	HEK293	kidney:	n/a	n/a
49	CTCF	chr14:47389900-47390050	HRE	kidney:	n/a	n/a
50	CTCF	chr14:47420620-47420770	HRE	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:47310377-47310427	Hepatocyte	liver:	n/a
2	chr14:47411755-47411805	PANC-1	pancreas:	n/a
3	chr14:47311141-47311191	AG09319	gingival:	n/a
4	chr14:47411755-47411805	NT2-D1	testis:	n/a
5	chr14:47310377-47310427	Caco-2	colon:	n/a
6	chr14:47411755-47411805	MCF10A-Er-Src	breast:	n/a
7	chr14:47310377-47310427	SK-N-MC	brain:	n/a
8	chr14:47411755-47411805	AG04449	skin:	fetal
9	chr14:47411755-47411805	SAEC	small airway:	n/a
10	chr14:47411755-47411805	NHDF-neo	bronchial:	n/a
11	chr14:47411755-47411805	CMK	blood:	n/a
12	chr14:47310377-47310427	K562	blood:	n/a
13	chr14:47311141-47311191	SK-N-SH	brain:	n/a
14	chr14:47411755-47411805	AoSMC	blood vessel:	n/a
15	chr14:47311141-47311191	HAEpiC	amniotic membrane:	n/a
16	chr14:47310377-47310427	Jurkat	blood:	n/a
17	chr14:47311141-47311191	H1-hESC	embryonic stem cell:	embryo
18	chr14:47311141-47311191	PFSK-1	brain:	n/a
19	chr14:47411755-47411805	HMEC	breast:	n/a
20	chr14:47411755-47411805	HIPEpiC	eye:	n/a
21	chr14:47411755-47411805	IMR90	lung:	fetal
22	chr14:47310377-47310427	NB4	blood:	n/a
23	chr14:47310377-47310427	RPTEC	kidney:	n/a
24	chr14:47310377-47310427	GM12892	blood:	n/a
25	chr14:47311141-47311191	PrEC	prostate:	n/a
26	chr14:47311141-47311191	AG04450	lung:	fetal
27	chr14:47311141-47311191	ECC-1	luminal epithelium:	n/a
28	chr14:47411755-47411805	AG10803	skin:	n/a
29	chr14:47411755-47411805	K562	blood:	n/a
30	chr14:47310377-47310427	MCF10A-Er-Src	breast:	n/a
31	chr14:47411755-47411805	GM19239	blood:	n/a
32	chr14:47311141-47311191	NH-A	brain:	n/a
33	chr14:47411755-47411805	HUVEC	blood vessel:	n/a
34	chr14:47310377-47310427	SAEC	small airway:	n/a
35	chr14:47311141-47311191	Hela-S3	cervix:	n/a
36	chr14:47411755-47411805	HCF	heart:	n/a
37	chr14:47411755-47411805	Hepatocyte	liver:	n/a
38	chr14:47311141-47311191	HEEpiC	esophagus:	n/a
39	chr14:47411755-47411805	AG09319	gingival:	n/a
40	chr14:47411755-47411805	GM12878	blood:	n/a
41	chr14:47311141-47311191	Caco-2	colon:	n/a
42	chr14:47310377-47310427	HRPEpiC	eye:	n/a
43	chr14:47411755-47411805	NB4	blood:	n/a
44	chr14:47311141-47311191	HCF	heart:	n/a
45	chr14:47411755-47411805	T-47D	breast:	n/a
46	chr14:47310377-47310427	MCF-7	breast:	n/a
47	chr14:47311141-47311191	SK-N-MC	brain:	n/a
48	chr14:47411755-47411805	RPTEC	kidney:	n/a
49	chr14:47411755-47411805	MCF-7	breast:	n/a
50	chr14:47411755-47411805	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:47409007..47410877-chr14:47415123..47417216,2	K562	blood:
2	chr14:47417689..47420302-chr14:47420799..47423183,3	MCF-7	breast:
3	chr14:47417689..47420302-chr14:47420799..47423183,3	MCF-7	breast:
4	chr14:47409007..47410877-chr14:47415123..47417216,2	K562	blood:
5	chr14:47401862..47402382-chr2:190007804..190008571,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-11	chr14:47465657-47466377	NONHSAT036685

Variant related genes	Relation type
RPA2P1	TF binding region
ENSG00000251735	TF binding region
MDGA2	TF binding region
RPA2P1	CpG island
ENSG00000251735	CpG island
MDGA2	CpG island

Extended variants
information (count: 3292 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3292 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531042715	chr14:47272414-47272415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs543192809	chr14:47272418-47272419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12587412	chr14:47272423-47272424	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs372279931	chr14:47272434-47272435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528586475	chr14:47272441-47272442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546643572	chr14:47272489-47272490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201289579	chr14:47272518-47272519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs12587459	chr14:47272604-47272605	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs187003332	chr14:47272645-47272646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550647358	chr14:47272691-47272692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569111165	chr14:47272699-47272700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143153219	chr14:47272715-47272716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs75062257	chr14:47272717-47272718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566640887	chr14:47272790-47272791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146891880	chr14:47272793-47272794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192295589	chr14:47272810-47272811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184079189	chr14:47272815-47272816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139732767	chr14:47272850-47272851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557405049	chr14:47272865-47272866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368179258	chr14:47272887-47272888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1491906	chr14:47272890-47272891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369794278	chr14:47272906-47272907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185037007	chr14:47272926-47272927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574120514	chr14:47272938-47272939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150040430	chr14:47272995-47272996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35630007	chr14:47273018-47273019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73248930	chr14:47273048-47273049	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs145321730	chr14:47273089-47273090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573060489	chr14:47273121-47273122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540370040	chr14:47273146-47273147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556476646	chr14:47273166-47273167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532428597	chr14:47273232-47273233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550936020	chr14:47273328-47273329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562705475	chr14:47273341-47273342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145248017	chr14:47273350-47273351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548454911	chr14:47273358-47273359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143309197	chr14:47273381-47273382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs72676628	chr14:47285214-47285215	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs571468280	chr14:47285266-47285267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs180908136	chr14:47285310-47285311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574831773	chr14:47285344-47285345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375927050	chr14:47285351-47285352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149422910	chr14:47285420-47285421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186328371	chr14:47285433-47285434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569435425	chr14:47285438-47285439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370587974	chr14:47285465-47285466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190245582	chr14:47285475-47285476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181427101	chr14:47285517-47285518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373694856	chr14:47285604-47285605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76327256	chr14:47285640-47285641	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	19907438	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:145 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:47272400-47273400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:47285200-47285400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr14:47285200-47288400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr14:47285400-47285800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr14:47285800-47286200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr14:47286200-47287600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr14:47286200-47287600	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr14:47286800-47288000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:47286800-47288400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr14:47286800-47288600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
11	chr14:47287000-47288200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr14:47287600-47287800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr14:47287600-47287800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr14:47287600-47288000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr14:47287600-47288400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr14:47287600-47288400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr14:47287800-47288000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr14:47287800-47288200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr14:47287800-47288600	Enhancers	H1 Cell Line	embryonic stem cell
20	chr14:47288000-47288400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
21	chr14:47288200-47288400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr14:47288200-47288600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
23	chr14:47289400-47289600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
24	chr14:47289400-47290000	Enhancers	Placenta	Placenta
25	chr14:47289600-47290000	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr14:47292800-47294600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr14:47293200-47293600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr14:47293600-47294000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr14:47294000-47294200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr14:47294200-47298600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr14:47294600-47298600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr14:47298600-47299000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr14:47298600-47299000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr14:47302800-47303000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr14:47305400-47306600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr14:47307600-47307800	Enhancers	Brain Germinal Matrix	brain
37	chr14:47307800-47309200	Weak transcription	Brain Germinal Matrix	brain
38	chr14:47309200-47310400	Enhancers	Brain Germinal Matrix	brain
39	chr14:47309600-47310000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr14:47309600-47310000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr14:47309800-47310000	Enhancers	Brain Anterior Caudate	brain
42	chr14:47309800-47311200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr14:47309800-47311600	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr14:47310000-47310200	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr14:47310000-47310200	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr14:47310000-47310400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr14:47310000-47310400	Active TSS	Brain Hippocampus Middle	brain
48	chr14:47310000-47310600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr14:47310000-47310600	Active TSS	Brain Cingulate Gyrus	brain
50	chr14:47310000-47310800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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