Variant report

Variant	nsv564417
Chromosome Location	chr14:39452317-39535560
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:917)
CpG islands
(count:244)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:39486545-39486570	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:39525267-39525327	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:39503970-39504280	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:39492795-39495932	HepG2	liver:	n/a	chr14:39494126-39494142 chr14:39492999-39493015 chr14:39493063-39493079
5	ARID3A	chr14:39484605-39484978	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:39519723-39519843	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:39535349-39535507	HepG2	liver:	n/a	n/a
8	ATF2	chr14:39530043-39530474	GM12878	blood:	n/a	n/a
9	ATF2	chr14:39529946-39530545	GM12878	blood:	n/a	n/a
10	BATF	chr14:39519597-39519951	GM12878	blood:	n/a	n/a
11	BATF	chr14:39519690-39519918	GM12878	blood:	n/a	n/a
12	BATF	chr14:39515208-39515477	GM12878	blood:	n/a	chr14:39515371-39515382
13	BCL11A	chr14:39519621-39519919	GM12878	blood:	n/a	chr14:39519681-39519690
14	BCL11A	chr14:39530086-39530223	GM12878	blood:	n/a	n/a
15	BCL3	chr14:39524989-39525231	GM12878	blood:	n/a	n/a
16	BHLHE40	chr14:39495087-39495846	HepG2	liver:	n/a	n/a
17	BHLHE40	chr14:39525536-39525598	K562	blood:	n/a	n/a
18	BHLHE40	chr14:39493291-39493795	HepG2	liver:	n/a	n/a
19	BHLHE40	chr14:39515127-39515407	GM12878	blood:	n/a	n/a
20	BRCA1	chr14:39468900-39469008	GM12878	blood:	n/a	n/a
21	BRCA1	chr14:39499673-39499711	HepG2	liver:	n/a	n/a
22	CBX3	chr14:39525206-39525644	K562	blood:	n/a	n/a
23	CBX3	chr14:39525159-39525658	HCT-116	colon:	n/a	n/a
24	CBX3	chr14:39525254-39525615	K562	blood:	n/a	n/a
25	CBX3	chr14:39525191-39525717	HCT-116	colon:	n/a	n/a
26	CEBPB	chr14:39474173-39474522	K562	blood:	n/a	chr14:39474331-39474342 chr14:39474329-39474340
27	CEBPB	chr14:39469609-39469816	HepG2	liver:	n/a	chr14:39469726-39469737
28	CEBPB	chr14:39483183-39483458	HepG2	liver:	n/a	chr14:39483336-39483347
29	CEBPB	chr14:39530875-39531180	IMR90	lung:	n/a	n/a
30	CEBPB	chr14:39535508-39535763	HepG2	liver:	n/a	chr14:39535615-39535626 chr14:39535615-39535628 chr14:39535615-39535626 chr14:39535615-39535628 chr14:39535616-39535627
31	CEBPB	chr14:39485411-39485683	Hela-S3	cervix:	n/a	chr14:39485530-39485543 chr14:39485550-39485561 chr14:39485531-39485542
32	CEBPB	chr14:39495041-39495546	HepG2	liver:	n/a	chr14:39495209-39495222
33	CEBPB	chr14:39493279-39493767	HepG2	liver:	n/a	chr14:39493738-39493749 chr14:39493736-39493749 chr14:39493736-39493749
34	CEBPB	chr14:39495028-39495798	HepG2	liver:	n/a	chr14:39495209-39495222
35	CEBPB	chr14:39485372-39485723	HepG2	liver:	n/a	chr14:39485530-39485543 chr14:39485550-39485561 chr14:39485531-39485542
36	CEBPB	chr14:39472811-39472836	IMR90	lung:	n/a	n/a
37	CEBPB	chr14:39519650-39520006	IMR90	lung:	n/a	chr14:39519839-39519850
38	CEBPB	chr14:39485394-39485732	IMR90	lung:	n/a	chr14:39485530-39485543 chr14:39485550-39485561 chr14:39485531-39485542
39	CEBPB	chr14:39494953-39495547	HepG2	liver:	n/a	chr14:39495209-39495222
40	CEBPB	chr14:39474197-39474471	A549	lung:	n/a	chr14:39474331-39474342 chr14:39474329-39474340
41	CEBPB	chr14:39474213-39474432	HepG2	liver:	n/a	chr14:39474331-39474342 chr14:39474329-39474340
42	CEBPB	chr14:39493176-39493833	HepG2	liver:	n/a	chr14:39493738-39493749 chr14:39493736-39493749 chr14:39493736-39493749
43	CEBPB	chr14:39474167-39474531	IMR90	lung:	n/a	chr14:39474331-39474342 chr14:39474329-39474340
44	CEBPB	chr14:39493223-39493914	HepG2	liver:	n/a	chr14:39493738-39493749 chr14:39493736-39493749 chr14:39493736-39493749
45	CEBPB	chr14:39519702-39519969	Hela-S3	cervix:	n/a	chr14:39519839-39519850
46	CEBPB	chr14:39474158-39474513	HepG2	liver:	n/a	chr14:39474331-39474342 chr14:39474329-39474340
47	CEBPB	chr14:39519741-39519884	HepG2	liver:	n/a	chr14:39519839-39519850
48	CEBPB	chr14:39493229-39493797	HepG2	liver:	n/a	chr14:39493738-39493749 chr14:39493736-39493749 chr14:39493736-39493749
49	CEBPB	chr14:39483329-39483374	A549	lung:	n/a	chr14:39483336-39483347
50	CEBPB	chr14:39495064-39495624	HepG2	liver:	n/a	chr14:39495209-39495222

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:39474657-39474707	NHDF-neo	bronchial:	n/a
2	chr14:39519326-39519376	SK-N-MC	brain:	n/a
3	chr14:39486639-39486689	GM12891	blood:	n/a
4	chr14:39486639-39486689	HPAEpiC	pulmonary alveolar:	n/a
5	chr14:39511766-39511816	HL-60	blood:	n/a
6	chr14:39486639-39486689	ProgFib	skin:	n/a
7	chr14:39486639-39486689	Caco-2	colon:	n/a
8	chr14:39519326-39519376	NH-A	brain:	n/a
9	chr14:39511766-39511816	A549	lung:	n/a
10	chr14:39474657-39474707	SAEC	small airway:	n/a
11	chr14:39511766-39511816	AG04449	skin:	fetal
12	chr14:39486639-39486689	SK-N-MC	brain:	n/a
13	chr14:39519326-39519376	Hepatocyte	liver:	n/a
14	chr14:39511766-39511816	NB4	blood:	n/a
15	chr14:39519326-39519376	AoSMC	blood vessel:	n/a
16	chr14:39474657-39474707	K562	blood:	n/a
17	chr14:39519326-39519376	HRPEpiC	eye:	n/a
18	chr14:39519326-39519376	PANC-1	pancreas:	n/a
19	chr14:39486639-39486689	AoSMC	blood vessel:	n/a
20	chr14:39519326-39519376	SK-N-SH_RA	brain:	n/a
21	chr14:39474657-39474707	GM12878	blood:	n/a
22	chr14:39474657-39474707	PrEC	prostate:	n/a
23	chr14:39474657-39474707	AG09319	gingival:	n/a
24	chr14:39486639-39486689	HEK293	kidney:	embryo
25	chr14:39519326-39519376	LNCaP	prostate:	n/a
26	chr14:39474657-39474707	AoSMC	blood vessel:	n/a
27	chr14:39511766-39511816	HPAEpiC	pulmonary alveolar:	n/a
28	chr14:39511766-39511816	AG09309	skin:	n/a
29	chr14:39474657-39474707	PANC-1	pancreas:	n/a
30	chr14:39511766-39511816	HUVEC	blood vessel:	n/a
31	chr14:39486639-39486689	ovcar-3	ovarian:	n/a
32	chr14:39511766-39511816	GM12892	blood:	n/a
33	chr14:39486639-39486689	HCPEpiC	choroid plexus:	n/a
34	chr14:39486639-39486689	AG04450	lung:	fetal
35	chr14:39486639-39486689	GM06990	blood:	n/a
36	chr14:39519326-39519376	HCF	heart:	n/a
37	chr14:39474657-39474707	NHBE	bronchial:	n/a
38	chr14:39519326-39519376	Hela-S3	cervix:	n/a
39	chr14:39511766-39511816	ECC-1	luminal epithelium:	n/a
40	chr14:39474657-39474707	A549	lung:	n/a
41	chr14:39486639-39486689	HRCEpiC	kidney:	n/a
42	chr14:39486639-39486689	Hela-S3	cervix:	n/a
43	chr14:39486639-39486689	CMK	blood:	n/a
44	chr14:39511766-39511816	SKMC	muscle:	n/a
45	chr14:39511766-39511816	Jurkat	blood:	n/a
46	chr14:39519326-39519376	PFSK-1	brain:	n/a
47	chr14:39486639-39486689	MCF-7	breast:	n/a
48	chr14:39519326-39519376	HCT-116	colon:	n/a
49	chr14:39511766-39511816	HCF	heart:	n/a
50	chr14:39474657-39474707	BJ	skin:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:39457540..39460115-chr14:39498272..39500421,2	MCF-7	breast:
2	chr14:39469466..39471750-chr14:39473985..39476478,2	MCF-7	breast:
3	chr14:39518100..39520463-chr14:39520996..39523566,2	K562	blood:
4	chr14:39495466..39497265-chr14:39501219..39502819,2	MCF-7	breast:
5	chr14:39506080..39508862-chr14:39528355..39530994,2	K562	blood:
6	chr14:39074185..39074840-chr14:39504069..39505004,2	MCF-7	breast:
7	chr14:39513894..39516551-chr14:39652021..39654125,2	K562	blood:
8	chr14:39074650..39075215-chr14:39484283..39484824,2	MCF-7	breast:
9	chr14:39336463..39337323-chr14:39484303..39484820,2	MCF-7	breast:
10	chr14:39410789..39411608-chr14:39483894..39485313,6	MCF-7	breast:
11	chr14:39466500..39469411-chr14:39470961..39474073,3	K562	blood:
12	chr14:39486181..39486938-chr14:39503284..39504551,4	MCF-7	breast:
13	chr14:39467540..39469411-chr14:39470961..39473319,2	K562	blood:
14	chr14:39190797..39191604-chr14:39484170..39485007,2	MCF-7	breast:
15	chr14:39480586..39482188-chr14:39482483..39485186,2	MCF-7	breast:
16	chr14:39467540..39469411-chr14:39470961..39473319,2	K562	blood:
17	chr14:39480586..39482188-chr14:39482483..39485186,2	MCF-7	breast:
18	chr14:39190717..39191738-chr14:39484001..39485313,7	MCF-7	breast:
19	chr14:39506080..39508862-chr14:39528355..39530994,2	K562	blood:
20	chr14:39504261..39505866-chr14:39507926..39509842,2	K562	blood:
21	chr14:39518100..39520463-chr14:39520996..39523566,2	K562	blood:
22	chr14:39190911..39191748-chr14:39503600..39504605,4	MCF-7	breast:
23	chr14:39507492..39510436-chr14:39510983..39512776,2	MCF-7	breast:
24	chr14:39486181..39486938-chr14:39503284..39504551,4	MCF-7	breast:
25	chr14:39380747..39381570-chr14:39484361..39485038,2	K562	blood:
26	chr14:39469466..39471750-chr14:39473985..39476478,2	MCF-7	breast:
27	chr14:39507492..39510436-chr14:39510983..39512776,2	MCF-7	breast:
28	chr14:39504261..39505866-chr14:39507926..39509842,2	K562	blood:
29	chr14:39457540..39460115-chr14:39498272..39500421,2	MCF-7	breast:
30	chr14:39466500..39469411-chr14:39470961..39474073,3	K562	blood:
31	chr14:39495466..39497265-chr14:39501219..39502819,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRAPPC6B-5	chr14:39533753-39534197	NONHSAT036508

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SEC23A	hsa-miR-30a-5p	chr14:39501916-39501939
2	SEC23A	hsa-miR-93-5p	chr14:39501419-39501442
3	SEC23A	hsa-miR-30a-5p	chr14:39501558-39501579
4	SEC23A	hsa-miR-30a-5p	chr14:39501384-39501404
5	SEC23A	hsa-miR-30a-5p	chr14:39502177-39502198
6	SEC23A	hsa-miR-375	chr14:39502249-39502270
7	SEC23A	hsa-miR-30a-5p	chr14:39501221-39501242
8	SEC23A	hsa-miR-30a-5p	chr14:39501390-39501383
9	SEC23A	hsa-miR-30a-5p	chr14:39501403-39501424

Variant related genes	Relation type
ENSG00000199285	TF binding region
SEC23A	TF binding region
ENSG00000199285	CpG island
SEC23A	CpG island
ENSG00000271468	chromatin interactions

Extended variants
information (count: 3073 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3073 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4902272	chr14:39452317-39452318	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535757670	chr14:39452320-39452321	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs116114242	chr14:39452338-39452339	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs115450238	chr14:39452344-39452345	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs557271903	chr14:39452357-39452358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182268581	chr14:39452358-39452359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545592353	chr14:39452374-39452375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187887581	chr14:39452401-39452402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11628564	chr14:39452444-39452445	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs541404236	chr14:39452514-39452515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375987654	chr14:39452541-39452542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192976423	chr14:39452542-39452543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550798490	chr14:39452549-39452550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185122046	chr14:39452684-39452685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6571884	chr14:39452687-39452688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs546573452	chr14:39452783-39452784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10137988	chr14:39452827-39452828	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs572955170	chr14:39452892-39452893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540061747	chr14:39452895-39452896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs28414518	chr14:39452957-39452958	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs535042155	chr14:39453007-39453008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371046519	chr14:39453014-39453015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548585142	chr14:39453036-39453037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11848067	chr14:39453073-39453074	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs568731171	chr14:39453091-39453092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75556914	chr14:39453137-39453138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs56886394	chr14:39453173-39453174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377065076	chr14:39453185-39453186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557594969	chr14:39453200-39453201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61338087	chr14:39453205-39453206	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs539617307	chr14:39453230-39453231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141954881	chr14:39453236-39453237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371210229	chr14:39453282-39453283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566343996	chr14:39453292-39453293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71951493	chr14:39453313-39453314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114327513	chr14:39453386-39453387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192205273	chr14:39453438-39453439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75492016	chr14:39453456-39453457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375090278	chr14:39453480-39453481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145817729	chr14:39453481-39453482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145502310	chr14:39453495-39453496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs56328886	chr14:39453525-39453526	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs148858841	chr14:39453533-39453534	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs184782370	chr14:39453538-39453539	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs189560063	chr14:39453557-39453558	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs180791866	chr14:39453623-39453624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143744467	chr14:39453645-39453646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562087759	chr14:39453653-39453654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183923617	chr14:39453678-39453679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530903671	chr14:39453679-39453680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:1671 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39450000-39465000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr14:39452800-39453200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr14:39455600-39464800	Weak transcription	Psoas Muscle	Psoas
4	chr14:39455800-39465200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr14:39456600-39456800	Enhancers	Brain Substantia Nigra	brain
6	chr14:39456800-39457200	Flanking Active TSS	Brain Substantia Nigra	brain
7	chr14:39456800-39457200	Enhancers	HMEC	breast
8	chr14:39456800-39457800	Enhancers	Brain Cingulate Gyrus	brain
9	chr14:39457000-39457200	Enhancers	HUVEC	blood vessel
10	chr14:39457000-39457600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr14:39457000-39458000	Enhancers	Brain Angular Gyrus	brain
12	chr14:39457000-39458000	Enhancers	Brain Hippocampus Middle	brain
13	chr14:39457000-39458000	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr14:39457200-39457400	Enhancers	Brain Substantia Nigra	brain
15	chr14:39457400-39457600	Flanking Active TSS	Brain Substantia Nigra	brain
16	chr14:39457400-39458400	Weak transcription	HUVEC	blood vessel
17	chr14:39457600-39458000	Enhancers	Brain Anterior Caudate	brain
18	chr14:39457600-39458800	Enhancers	Brain Substantia Nigra	brain
19	chr14:39457600-39461600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr14:39457800-39463800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr14:39458000-39458400	Weak transcription	Brain Anterior Caudate	brain
22	chr14:39458000-39458800	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr14:39458000-39459400	Weak transcription	Brain Hippocampus Middle	brain
24	chr14:39458400-39459200	Enhancers	Brain Anterior Caudate	brain
25	chr14:39458400-39465000	Enhancers	HUVEC	blood vessel
26	chr14:39458600-39458800	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr14:39458600-39458800	Enhancers	Right Atrium	heart
28	chr14:39458600-39458800	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr14:39458600-39459600	Enhancers	Primary B cells from peripheral blood	blood
30	chr14:39458600-39459600	Enhancers	Small Intestine	intestine
31	chr14:39458600-39459800	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr14:39458800-39459000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr14:39458800-39459000	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr14:39458800-39459000	Enhancers	GM12878-XiMat	blood
35	chr14:39458800-39459600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr14:39458800-39459600	Active TSS	Monocytes-CD14+_RO01746	blood
37	chr14:39458800-39463800	Weak transcription	Brain Substantia Nigra	brain
38	chr14:39459000-39459400	Active TSS	Primary hematopoietic stem cells	blood
39	chr14:39459000-39459400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr14:39459000-39459400	Active TSS	Duodenum Mucosa	Duodenum
41	chr14:39459000-39459400	Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr14:39459000-39459400	Active TSS	GM12878-XiMat	blood
43	chr14:39459000-39459600	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr14:39459000-39459600	Enhancers	Stomach Mucosa	stomach
45	chr14:39459000-39463800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr14:39459000-39464800	Weak transcription	Right Atrium	heart
47	chr14:39459200-39459600	Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chr14:39459200-39463800	Weak transcription	Brain Anterior Caudate	brain
49	chr14:39459400-39459600	Enhancers	Primary hematopoietic stem cells	blood
50	chr14:39459400-39459600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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