Variant report

Variant	nsv832783
Chromosome Location	chr14:44059812-44218791
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	BRCA1	chr14:44213052-44213129	Hela-S3	cervix:	n/a	n/a
2	BRCA1	chr14:44214996-44215452	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr14:44143491-44143910	MCF-7	breast:	n/a	chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673
4	CEBPB	chr14:44118701-44119041	MCF-7	breast:	n/a	n/a
5	CEBPB	chr14:44073776-44073962	A549	lung:	n/a	chr14:44073863-44073874
6	CEBPB	chr14:44115978-44116204	HepG2	liver:	n/a	chr14:44116101-44116110 chr14:44116099-44116110 chr14:44116101-44116110 chr14:44116101-44116110 chr14:44116099-44116112 chr14:44116101-44116110
7	CEBPB	chr14:44143498-44143834	IMR90	lung:	n/a	chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673
8	CEBPB	chr14:44143498-44143815	A549	lung:	n/a	chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673
9	CEBPB	chr14:44198430-44198751	IMR90	lung:	n/a	chr14:44198598-44198609 chr14:44198600-44198611 chr14:44198600-44198609
10	CEBPB	chr14:44198423-44198769	HepG2	liver:	n/a	chr14:44198598-44198609 chr14:44198600-44198611 chr14:44198600-44198609
11	CEBPB	chr14:44198442-44198745	A549	lung:	n/a	chr14:44198598-44198609 chr14:44198600-44198611 chr14:44198600-44198609
12	CEBPB	chr14:44213289-44213777	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr14:44118283-44118384	A549	lung:	n/a	chr14:44118298-44118309 chr14:44118300-44118309 chr14:44118300-44118311
14	CEBPB	chr14:44143511-44143847	ECC-1	luminal epithelium:	n/a	chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673
15	CEBPB	chr14:44073820-44074020	HepG2	liver:	n/a	chr14:44073863-44073874
16	CEBPB	chr14:44205127-44205532	MCF-7	breast:	n/a	n/a
17	CEBPB	chr14:44143489-44143832	K562	blood:	n/a	chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673
18	CEBPB	chr14:44143485-44143832	HepG2	liver:	n/a	chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673
19	CEBPB	chr14:44205138-44205484	MCF-7	breast:	n/a	n/a
20	CEBPB	chr14:44118714-44119066	MCF-7	breast:	n/a	n/a
21	CEBPB	chr14:44143483-44143840	Hela-S3	cervix:	n/a	chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673
22	CEBPB	chr14:44118162-44118443	HepG2	liver:	n/a	chr14:44118298-44118309 chr14:44118300-44118309 chr14:44118300-44118311
23	CEBPB	chr14:44205087-44205862	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr14:44214897-44215477	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr14:44143512-44143840	H1-hESC	embryonic stem cell:	n/a	chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673 chr14:44143664-44143673
26	CEBPB	chr14:44194216-44194331	HepG2	liver:	n/a	chr14:44194245-44194256 chr14:44194245-44194258 chr14:44194247-44194258
27	CHD1	chr14:44086356-44086397	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr14:44116709-44116752	HepG2	liver:	n/a	n/a
29	CTCF	chr14:44166360-44166510	MCF-7	breast:	n/a	n/a
30	CTCF	chr14:44116580-44116730	BE2_C	brain:	n/a	n/a
31	CTCF	chr14:44116617-44116775	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr14:44116660-44116810	BE2_C	brain:	n/a	n/a
33	CTCF	chr14:44116560-44116710	MCF-7	breast:	n/a	n/a
34	CTCF	chr14:44166240-44166390	BE2_C	brain:	n/a	n/a
35	CTCF	chr14:44080254-44080439	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:44116640-44116790	HEK293	kidney:	n/a	n/a
37	CTCF	chr14:44116600-44116750	Caco-2	colon:	n/a	n/a
38	CTCF	chr14:44116640-44116790	AG04450	lung:	n/a	n/a
39	CTCF	chr14:44135634-44135640	MCF-7	breast:	n/a	n/a
40	CTCF	chr14:44116540-44116690	NB4	blood:	n/a	n/a
41	CTCF	chr14:44079992-44080026	GM10248	blood:	n/a	n/a
42	CTCF	chr14:44116680-44116830	HL-60	blood:	n/a	n/a
43	CTCF	chr14:44116640-44116790	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr14:44080266-44080443	MCF-7	breast:	n/a	n/a
45	CTCF	chr14:44166340-44166490	HCT-116	colon:	n/a	n/a
46	CTCF	chr14:44134480-44134630	MCF-7	breast:	n/a	n/a
47	CTCF	chr14:44116521-44116801	HepG2	liver:	n/a	n/a
48	CTCF	chr14:44166340-44166490	NB4	blood:	n/a	n/a
49	CTCF	chr14:44080240-44080390	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr14:44166320-44166470	Caco-2	colon:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:44205547..44207356-chr14:44208208..44210904,2	MCF-7	breast:
2	chr14:44116606..44118543-chr14:44247032..44249765,2	MCF-7	breast:
3	chr14:44053547..44055301-chr14:44119155..44121038,2	MCF-7	breast:
4	chr14:44178956..44181575-chr14:44181768..44183737,3	K562	blood:
5	chr14:44118983..44120802-chr14:44250661..44252811,2	MCF-7	breast:
6	chr14:44186082..44188263-chr14:44190147..44191676,2	MCF-7	breast:
7	chr14:44187135..44188917-chr14:44198793..44201549,2	MCF-7	breast:
8	chr14:44118326..44120848-chr14:44211222..44213029,2	MCF-7	breast:
9	chr14:44178956..44181575-chr14:44181768..44183737,3	K562	blood:
10	chr14:44205547..44207356-chr14:44208208..44210904,2	MCF-7	breast:
11	chr14:44118768..44119290-chr14:44370795..44371415,2	MCF-7	breast:
12	chr14:44186082..44188263-chr14:44190147..44191676,2	MCF-7	breast:
13	chr14:44196286..44198757-chr14:44200759..44202310,2	MCF-7	breast:
14	chr14:44118120..44120400-chr14:44236517..44238455,2	MCF-7	breast:
15	chr14:44077265..44078794-chr14:44085477..44087303,2	MCF-7	breast:
16	chr14:44118326..44120848-chr14:44211222..44213029,2	MCF-7	breast:
17	chr14:44083391..44085728-chr14:44088279..44090521,2	MCF-7	breast:
18	chr14:44116704..44120924-chr14:44232095..44235982,5	MCF-7	breast:
19	chr14:44118745..44119255-chr14:44233596..44234189,2	MCF-7	breast:
20	chr14:44193372..44194920-chr14:44199439..44201142,2	MCF-7	breast:
21	chr14:44093132..44094807-chr14:44105005..44106712,2	MCF-7	breast:
22	chr14:44158977..44160945-chr14:44164562..44166990,2	MCF-7	breast:
23	chr14:44118728..44122212-chr14:44202412..44204725,3	MCF-7	breast:
24	chr14:44196286..44198757-chr14:44200759..44202310,2	MCF-7	breast:
25	chr14:44093818..44096091-chr14:44098714..44101614,2	MCF-7	breast:
26	chr14:44083391..44085728-chr14:44088279..44090521,2	MCF-7	breast:
27	chr14:44193372..44194920-chr14:44199439..44201142,2	MCF-7	breast:
28	chr14:44175429..44177063-chr14:44180133..44181778,2	MCF-7	breast:
29	chr14:44159765..44161650-chr14:44161663..44164546,2	MCF-7	breast:
30	chr14:44205144..44205757-chr14:44233413..44234104,2	MCF-7	breast:
31	chr14:44118185..44120883-chr14:44261367..44263957,2	MCF-7	breast:
32	chr14:44077265..44078794-chr14:44085477..44087303,2	MCF-7	breast:
33	chr14:44086379..44089362-chr14:44231870..44234725,2	MCF-7	breast:
34	chr14:44175429..44177063-chr14:44180133..44181778,2	MCF-7	breast:
35	chr14:44187135..44188917-chr14:44198793..44201549,2	MCF-7	breast:
36	chr14:44159765..44161650-chr14:44161663..44164546,2	MCF-7	breast:
37	chr14:44118728..44122212-chr14:44202412..44204725,3	MCF-7	breast:
38	chr14:44158977..44160945-chr14:44164562..44166990,2	MCF-7	breast:
39	chr14:44118878..44120598-chr14:44261570..44263182,2	MCF-7	breast:
40	chr14:44093132..44094807-chr14:44105005..44106712,2	MCF-7	breast:
41	chr14:44093818..44096091-chr14:44098714..44101614,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-214N1.1.1-9	chr14:44086966-44087106	l_975_chr14:44046308-44077463_testes
2	lnc-RP11-214N1.1.1-8	chr14:44064339-44065886	NONHSAT036600
3	lnc-RP11-214N1.1.1-9	chr14:44077227-44077465	l_975_chr14:44046308-44077463_testes
4	lnc-RP11-214N1.1.1-9	chr14:44086691-44086961	l_975_chr14:44046308-44077463_testes
5	lnc-RP11-214N1.1.1-9	chr14:44068972-44069050	l_975_chr14:44046308-44077463_testes

Variant related genes	Relation type
ENSG00000258894	TF binding region
ENSG00000258387	TF binding region

Extended variants
information (count: 1920 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1920 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200616227	chr14:44059830-44059831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574296433	chr14:44059835-44059836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs8003814	chr14:44059838-44059839	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs189546883	chr14:44059839-44059840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182322299	chr14:44059847-44059848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187370390	chr14:44059848-44059849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs61998637	chr14:44059881-44059882	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs74048363	chr14:44059932-44059933	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs192047148	chr14:44059948-44059949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567519871	chr14:44059998-44059999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78293761	chr14:44060030-44060031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148588142	chr14:44060040-44060041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569431593	chr14:44060045-44060046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565582649	chr14:44060139-44060140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557526755	chr14:44060170-44060171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142899003	chr14:44060175-44060176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557461684	chr14:44060183-44060184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569710450	chr14:44060184-44060185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531955326	chr14:44060220-44060221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555356653	chr14:44060261-44060262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs80163796	chr14:44060276-44060277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545581561	chr14:44060309-44060310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183596651	chr14:44060337-44060338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541757546	chr14:44060340-44060341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188231826	chr14:44060346-44060347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192246502	chr14:44060378-44060379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565505670	chr14:44060396-44060397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114368903	chr14:44060415-44060416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563847431	chr14:44060450-44060451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531052292	chr14:44060455-44060456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150665540	chr14:44060458-44060459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182510281	chr14:44060508-44060509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528471385	chr14:44060524-44060525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547326054	chr14:44060550-44060551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566807799	chr14:44060635-44060636	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs187204702	chr14:44060646-44060647	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs532987754	chr14:44060684-44060685	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs551184746	chr14:44060691-44060692	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs139920371	chr14:44060712-44060713	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs61998638	chr14:44060713-44060714	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs546730346	chr14:44060717-44060718	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs555168232	chr14:44060721-44060722	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs34024253	chr14:44060723-44060724	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs142299253	chr14:44060752-44060753	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs528884527	chr14:44060778-44060779	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs567296675	chr14:44060784-44060785	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs548965612	chr14:44060785-44060786	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs143677011	chr14:44060800-44060801	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs17114268	chr14:44060888-44060889	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs117778645	chr14:44060890-44060891	Enhancers Flanking Active TSS Active TSS	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
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
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44058400-44060600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr14:44059000-44060600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr14:44059400-44060600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr14:44060600-44060800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:44060600-44061000	Active TSS	Monocytes-CD14+_RO01746	blood
6	chr14:44060600-44061200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr14:44060600-44061400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:44060600-44061800	Enhancers	Primary hematopoietic stem cells	blood
9	chr14:44060800-44061200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr14:44061000-44061200	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr14:44061000-44061200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr14:44061000-44061600	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr14:44061200-44061600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr14:44061400-44061800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr14:44061600-44064000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr14:44061600-44064600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr14:44061800-44063800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr14:44061800-44064000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr14:44063800-44064600	Enhancers	Primary hematopoietic stem cells	blood
20	chr14:44064000-44064400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr14:44064000-44067000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr14:44064400-44065000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr14:44064400-44065000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr14:44064400-44065000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr14:44064400-44065200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr14:44064400-44065200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr14:44064600-44065000	Flanking Active TSS	Primary hematopoietic stem cells	blood
28	chr14:44064600-44065200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr14:44064600-44066200	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr14:44065000-44066200	Enhancers	Primary hematopoietic stem cells	blood
31	chr14:44065000-44066800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr14:44067000-44067200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
33	chr14:44067200-44067400	Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr14:44067400-44067600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr14:44077400-44078400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr14:44077800-44078200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr14:44106000-44106400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:44108200-44108600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr14:44109000-44110200	Enhancers	Pancreas	Pancrea
40	chr14:44109800-44110200	Enhancers	Gastric	stomach
41	chr14:44109800-44110400	Enhancers	Liver	Liver
42	chr14:44109800-44110400	Enhancers	Stomach Mucosa	stomach
43	chr14:44114400-44114800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr14:44120200-44120400	Enhancers	HepG2	liver
45	chr14:44120200-44121400	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr14:44120200-44121400	Enhancers	Stomach Mucosa	stomach
47	chr14:44120400-44121000	Flanking Active TSS	HepG2	liver
48	chr14:44120600-44121000	Enhancers	Gastric	stomach
49	chr14:44120600-44121200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr14:44121000-44121200	Enhancers	HepG2	liver

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