Variant report

Variant	nsv902121
Chromosome Location	chr14:82075469-82146538
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	chr14:82122168-82122570	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:82129357-82129431	HepG2	liver:	n/a	n/a
3	BACH1	chr14:82113851-82113910	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr14:82121750-82122172	K562	blood:	n/a	chr14:82121842-82121853
5	CEBPB	chr14:82121788-82122026	H1-hESC	embryonic stem cell:	n/a	chr14:82121842-82121853
6	CEBPB	chr14:82121662-82122593	HepG2	liver:	n/a	chr14:82121842-82121853
7	CEBPB	chr14:82098524-82098859	HepG2	liver:	n/a	n/a
8	CEBPB	chr14:82098523-82098885	HepG2	liver:	n/a	n/a
9	CEBPB	chr14:82121675-82122026	IMR90	lung:	n/a	chr14:82121842-82121853
10	CEBPB	chr14:82121682-82122013	A549	lung:	n/a	chr14:82121842-82121853
11	CEBPB	chr14:82108922-82109159	HepG2	liver:	n/a	n/a
12	CTCF	chr14:82085170-82085353	Pancreas_OC	pancreas:	n/a	n/a
13	CTCF	chr14:82091429-82092105	GM12878	blood:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
14	CTCF	chr14:82092352-82092425	GM10266	blood:	n/a	n/a
15	CTCF	chr14:82091820-82091970	HEEpiC	esophagus:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
16	CTCF	chr14:82091737-82091983	HepG2	liver:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
17	CTCF	chr14:82091740-82091890	GM12864	blood:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091872-82091888
18	CTCF	chr14:82091560-82091710	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr14:82091800-82091950	Caco-2	colon:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
20	CTCF	chr14:82091920-82092070	HCM	heart:	n/a	n/a
21	CTCF	chr14:82135955-82136046	GM20000	blood:	n/a	n/a
22	CTCF	chr14:82091781-82091981	SK-N-SH_RA	brain:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
23	CTCF	chr14:82091760-82091910	MCF-7	breast:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
24	CTCF	chr14:82091840-82091990	SK-N-SH_RA	brain:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
25	CTCF	chr14:82140393-82140510	MCF-7	breast:	n/a	n/a
26	CTCF	chr14:82089315-82089377	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr14:82091763-82092007	Medullo	brain:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
28	CTCF	chr14:82091740-82091890	SAEC	small airway:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091872-82091888
29	CTCF	chr14:82091760-82091910	GM12878	blood:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
30	CTCF	chr14:82091800-82091950	GM12864	blood:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
31	CTCF	chr14:82091797-82091932	HepG2	liver:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
32	CTCF	chr14:82091340-82091490	GM12868	blood:	n/a	n/a
33	CTCF	chr14:82091720-82091870	NB4	blood:	n/a	n/a
34	CTCF	chr14:82091832-82091896	GM13976	blood:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
35	CTCF	chr14:82091860-82092010	HPAF	blood vessel:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
36	CTCF	chr14:82091440-82091590	GM06990	blood:	n/a	n/a
37	CTCF	chr14:82091740-82091890	HRE	kidney:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091872-82091888
38	CTCF	chr14:82091762-82091991	Spleen_OC	spleen:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
39	CTCF	chr14:82091780-82091990	Hela-S3	cervix:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
40	CTCF	chr14:82085238-82085299	LNCaP	prostate:	n/a	n/a
41	CTCF	chr14:82091780-82091930	HL-60	blood:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
42	CTCF	chr14:82091760-82091910	GM12865	blood:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
43	CTCF	chr14:82136416-82136418	GM10248	blood:	n/a	n/a
44	CTCF	chr14:82091800-82091950	HepG2	liver:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
45	CTCF	chr14:82108960-82109110	GM12866	blood:	n/a	n/a
46	CTCF	chr14:82091820-82091970	GM12878	blood:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
47	CTCF	chr14:82091777-82092017	GM12878	blood:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
48	CTCF	chr14:82135469-82135487	ProgFib	skin:	n/a	n/a
49	CTCF	chr14:82091780-82091930	NHDF-neo	bronchial:	n/a	chr14:82091871-82091889 chr14:82091876-82091884 chr14:82091873-82091894 chr14:82091872-82091888
50	CTCF	chr14:82096800-82096950	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:82135353-82135403	A549	lung:	n/a
2	chr14:82135353-82135403	SK-N-MC	brain:	n/a
3	chr14:82089415-82089465	GM19239	blood:	n/a
4	chr14:82135353-82135403	MCF10A-Er-Src	breast:	n/a
5	chr14:82086140-82086190	PFSK-1	brain:	n/a
6	chr14:82090632-82090682	NH-A	brain:	n/a
7	chr14:82090632-82090682	GM12878	blood:	n/a
8	chr14:82135353-82135403	HEK293	kidney:	embryo
9	chr14:82090632-82090682	H1-hESC	embryonic stem cell:	embryo
10	chr14:82124963-82125013	LNCaP	prostate:	n/a
11	chr14:82135353-82135403	HIPEpiC	eye:	n/a
12	chr14:82135353-82135403	PFSK-1	brain:	n/a
13	chr14:82090632-82090682	Hela-S3	cervix:	n/a
14	chr14:82090632-82090682	PrEC	prostate:	n/a
15	chr14:82135353-82135403	ECC-1	luminal epithelium:	n/a
16	chr14:82089415-82089465	SAEC	small airway:	n/a
17	chr14:82135353-82135403	H1-hESC	embryonic stem cell:	embryo
18	chr14:82124963-82125013	HEK293	kidney:	embryo
19	chr14:82086140-82086190	AG10803	skin:	n/a
20	chr14:82135353-82135403	Hepatocyte	liver:	n/a
21	chr14:82124963-82125013	NHDF-neo	bronchial:	n/a
22	chr14:82086140-82086190	HNPCEpiC	eye:	n/a
23	chr14:82086140-82086190	GM12891	blood:	n/a
24	chr14:82135353-82135403	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:82089415-82089465	HMEC	breast:	n/a
26	chr14:82124963-82125013	GM12878	blood:	n/a
27	chr14:82124963-82125013	RPTEC	kidney:	n/a
28	chr14:82089415-82089465	Hepatocyte	liver:	n/a
29	chr14:82090632-82090682	PANC-1	pancreas:	n/a
30	chr14:82089415-82089465	BE2_C	brain:	n/a
31	chr14:82135353-82135403	HRE	kidney:	n/a
32	chr14:82090632-82090682	PFSK-1	brain:	n/a
33	chr14:82086140-82086190	Caco-2	colon:	n/a
34	chr14:82089415-82089465	SK-N-MC	brain:	n/a
35	chr14:82086140-82086190	SK-N-SH	brain:	n/a
36	chr14:82089415-82089465	AG04450	lung:	fetal
37	chr14:82124963-82125013	T-47D	breast:	n/a
38	chr14:82089415-82089465	HCF	heart:	n/a
39	chr14:82090632-82090682	NHDF-neo	bronchial:	n/a
40	chr14:82089415-82089465	HL-60	blood:	n/a
41	chr14:82089415-82089465	HRCEpiC	kidney:	n/a
42	chr14:82086140-82086190	GM12892	blood:	n/a
43	chr14:82090632-82090682	ovcar-3	ovarian:	n/a
44	chr14:82089415-82089465	PrEC	prostate:	n/a
45	chr14:82089415-82089465	U87	brain:	n/a
46	chr14:82135353-82135403	HAEpiC	amniotic membrane:	n/a
47	chr14:82089415-82089465	GM12878	blood:	n/a
48	chr14:82090632-82090682	HEEpiC	esophagus:	n/a
49	chr14:82089415-82089465	A549	lung:	n/a
50	chr14:82090632-82090682	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:82091384..82092373-chr14:82204011..82204637,3	MCF-7	breast:
2	chr14:82134770..82137572-chr20:47128262..47129981,2	MCF-7	breast:
3	chr14:82091438..82092213-chr14:87112845..87113730,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEL1L-1	chr14:82085504-82085672	XLOC_011088
2	lnc-SEL1L-1	chr14:82085504-82085611	XLOC_011088
3	lnc-SEL1L-1	chr14:82088997-82089405	XLOC_011088
4	lnc-SEL1L-1	chr14:82089038-82089424	NONHSAT038068

Variant related genes	Relation type
ENSG00000258977	TF binding region
ENSG00000258841	TF binding region
ENSG00000258977	CpG island
ENSG00000258841	CpG island

Extended variants
information (count: 2307 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2307 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1957535	chr14:82075469-82075470	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189276973	chr14:82075470-82075471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544915745	chr14:82075489-82075490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371572621	chr14:82075492-82075493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569168433	chr14:82075506-82075507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182029508	chr14:82075536-82075537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145452500	chr14:82075555-82075556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542686438	chr14:82075558-82075559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4573871	chr14:82075590-82075591	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs371757979	chr14:82075595-82075596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186268656	chr14:82075619-82075620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs17642779	chr14:82075638-82075639	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs565477358	chr14:82075673-82075674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189290057	chr14:82075683-82075684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547701279	chr14:82075747-82075748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74066225	chr14:82075761-82075762	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs527397017	chr14:82075781-82075782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549058258	chr14:82075782-82075783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376160208	chr14:82075819-82075820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531911236	chr14:82075895-82075896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567273756	chr14:82075900-82075901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148701563	chr14:82075901-82075902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556115980	chr14:82075932-82075933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs180915410	chr14:82075943-82075944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186427475	chr14:82075977-82075978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539695035	chr14:82075989-82075990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370895484	chr14:82076000-82076001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563376108	chr14:82076006-82076007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553707873	chr14:82076040-82076041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11849976	chr14:82076065-82076066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11846133	chr14:82076075-82076076	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs554599239	chr14:82076085-82076086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576116526	chr14:82076086-82076087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543484188	chr14:82076090-82076091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139118691	chr14:82076091-82076092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75627090	chr14:82076148-82076149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191327519	chr14:82076149-82076150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559997511	chr14:82076156-82076157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs3918539	chr14:82076186-82076187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183631053	chr14:82076207-82076208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548797165	chr14:82076209-82076210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569797356	chr14:82076221-82076222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567410183	chr14:82076222-82076223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373741723	chr14:82076240-82076241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111438301	chr14:82076248-82076249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs58372121	chr14:82076249-82076250	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs369855286	chr14:82076275-82076276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538574861	chr14:82076293-82076294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553996374	chr14:82076298-82076299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565543768	chr14:82076336-82076337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:82068000-82076400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:82076400-82079200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr14:82078600-82079400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:82079200-82080800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:82079600-82080400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr14:82079800-82080200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr14:82079800-82080200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr14:82079800-82080600	Enhancers	H1 Cell Line	embryonic stem cell
9	chr14:82080000-82080400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr14:82080800-82086600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr14:82084800-82088000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr14:82085600-82086800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr14:82085800-82086800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr14:82085800-82086800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr14:82086000-82086400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr14:82086000-82086600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr14:82086200-82086800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr14:82087800-82088200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr14:82088000-82088400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr14:82088200-82088600	Enhancers	Fetal Stomach	stomach
21	chr14:82088200-82091000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr14:82088400-82095600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr14:82091000-82091600	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr14:82091000-82091600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr14:82092800-82093800	Enhancers	Brain Hippocampus Middle	brain
26	chr14:82093000-82093600	Enhancers	Brain Cingulate Gyrus	brain
27	chr14:82093000-82094600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr14:82093200-82093600	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr14:82093400-82093800	Enhancers	Brain Substantia Nigra	brain
30	chr14:82099000-82099200	Enhancers	Fetal Intestine Large	intestine
31	chr14:82099600-82100200	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr14:82099600-82100200	Enhancers	Pancreas	Pancrea
33	chr14:82100200-82105600	Weak transcription	Pancreas	Pancrea
34	chr14:82100600-82100800	Enhancers	Small Intestine	intestine
35	chr14:82104000-82104600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr14:82104200-82105000	Enhancers	Ovary	ovary
37	chr14:82104600-82106600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr14:82105000-82105400	Weak transcription	Ovary	ovary
39	chr14:82105200-82105800	Enhancers	Brain Hippocampus Middle	brain
40	chr14:82105400-82105800	Enhancers	Brain Germinal Matrix	brain
41	chr14:82105400-82106000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr14:82105400-82106200	Enhancers	Ovary	ovary
43	chr14:82105600-82105800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr14:82105600-82106000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr14:82105600-82106000	Enhancers	Pancreas	Pancrea
46	chr14:82105600-82106000	Enhancers	Right Atrium	heart
47	chr14:82105800-82106800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr14:82106600-82107000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr14:82106600-82107200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr14:82106600-82107200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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