Variant report

Variant	nsv564901
Chromosome Location	chr14:63778748-63852177
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	ATF2	chr14:63850463-63850949	GM12878	blood:	n/a	n/a
2	BATF	chr14:63837850-63838032	GM12878	blood:	n/a	n/a
3	BATF	chr14:63837832-63838034	GM12878	blood:	n/a	n/a
4	BATF	chr14:63850478-63850694	GM12878	blood:	n/a	n/a
5	BCL3	chr14:63829151-63829554	GM12878	blood:	n/a	n/a
6	BCL3	chr14:63827695-63827949	GM12878	blood:	n/a	n/a
7	BCL3	chr14:63829154-63829566	GM12878	blood:	n/a	n/a
8	BRCA1	chr14:63782321-63782360	GM12878	blood:	n/a	n/a
9	CEBPB	chr14:63820978-63821201	HepG2	liver:	n/a	chr14:63821071-63821082
10	CEBPB	chr14:63842517-63842730	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
11	CEBPB	chr14:63782893-63783093	A549	lung:	n/a	n/a
12	CEBPB	chr14:63842444-63843021	IMR90	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
13	CEBPB	chr14:63809186-63809476	A549	lung:	n/a	n/a
14	CEBPB	chr14:63842449-63843004	HepG2	liver:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
15	CEBPB	chr14:63798403-63798684	IMR90	lung:	n/a	n/a
16	CEBPB	chr14:63835079-63835317	HepG2	liver:	n/a	chr14:63835165-63835176
17	CEBPB	chr14:63842470-63842926	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
18	CEBPB	chr14:63842570-63842689	HepG2	liver:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
19	CEBPB	chr14:63798468-63798578	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr14:63798489-63798718	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:63842418-63842898	MCF-7	breast:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
22	CEBPB	chr14:63834999-63835300	A549	lung:	n/a	chr14:63835165-63835176
23	CEBPB	chr14:63790310-63790386	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:63845972-63846129	MCF-7	breast:	n/a	chr14:63846045-63846056
25	CEBPB	chr14:63842579-63842902	K562	blood:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
26	CEBPB	chr14:63846009-63846069	HepG2	liver:	n/a	chr14:63846045-63846056
27	CEBPB	chr14:63842462-63842947	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
28	CEBPB	chr14:63842433-63843010	Hela-S3	cervix:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
29	CEBPB	chr14:63842540-63842810	H1-hESC	embryonic stem cell:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
30	CEBPB	chr14:63842544-63842804	MCF-7	breast:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
31	CEBPB	chr14:63835037-63835278	K562	blood:	n/a	chr14:63835165-63835176
32	CEBPB	chr14:63826972-63827278	HepG2	liver:	n/a	n/a
33	CEBPB	chr14:63798372-63798717	A549	lung:	n/a	n/a
34	CEBPB	chr14:63835034-63835323	IMR90	lung:	n/a	chr14:63835165-63835176
35	CEBPB	chr14:63809144-63809428	HepG2	liver:	n/a	n/a
36	CHD2	chr14:63842557-63842804	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr14:63810023-63810048	HepG2	liver:	n/a	n/a
38	CTCF	chr14:63834540-63834690	SAEC	small airway:	n/a	n/a
39	CTCF	chr14:63834560-63834710	HCT-116	colon:	n/a	n/a
40	CTCF	chr14:63838440-63838590	AG10803	skin:	n/a	n/a
41	CTCF	chr14:63828620-63828770	Hela-S3	cervix:	n/a	chr14:63828705-63828723 chr14:63828710-63828718 chr14:63828707-63828728
42	CTCF	chr14:63834540-63834690	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:63838447-63838625	LNCaP	prostate:	n/a	n/a
44	CTCF	chr14:63828660-63828810	GM12873	blood:	n/a	chr14:63828705-63828723 chr14:63828710-63828718 chr14:63828707-63828728
45	CTCF	chr14:63834520-63834670	AG10803	skin:	n/a	n/a
46	CTCF	chr14:63834540-63834690	AG09309	skin:	n/a	n/a
47	CTCF	chr14:63834620-63834770	NHEK	skin:	n/a	n/a
48	CTCF	chr14:63834580-63834730	AG10803	skin:	n/a	n/a
49	CTCF	chr14:63838340-63838490	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr14:63838400-63838550	HPAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:63781994-63782044	AG04449	skin:	fetal
2	chr14:63781994-63782044	HL-60	blood:	n/a
3	chr14:63785523-63785573	Hela-S3	cervix:	n/a
4	chr14:63785287-63785337	NHDF-neo	bronchial:	n/a
5	chr14:63784394-63784444	Hela-S3	cervix:	n/a
6	chr14:63785287-63785337	NB4	blood:	n/a
7	chr14:63785287-63785337	HepG2	liver:	n/a
8	chr14:63784394-63784444	GM12891	blood:	n/a
9	chr14:63785287-63785337	NT2-D1	testis:	n/a
10	chr14:63781994-63782044	SK-N-SH	brain:	n/a
11	chr14:63784394-63784444	HRPEpiC	eye:	n/a
12	chr14:63785287-63785337	HRPEpiC	eye:	n/a
13	chr14:63781994-63782044	HMEC	breast:	n/a
14	chr14:63779694-63779744	Jurkat	blood:	n/a
15	chr14:63781994-63782044	GM06990	blood:	n/a
16	chr14:63784574-63784624	HCPEpiC	choroid plexus:	n/a
17	chr14:63784394-63784444	HL-60	blood:	n/a
18	chr14:63781994-63782044	HCPEpiC	choroid plexus:	n/a
19	chr14:63779694-63779744	ECC-1	luminal epithelium:	n/a
20	chr14:63785287-63785337	SK-N-SH_RA	brain:	n/a
21	chr14:63785287-63785337	ECC-1	luminal epithelium:	n/a
22	chr14:63785334-63785384	U87	brain:	n/a
23	chr14:63785287-63785337	HNPCEpiC	eye:	n/a
24	chr14:63784574-63784624	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:63785523-63785573	AG10803	skin:	n/a
26	chr14:63784394-63784444	ProgFib	skin:	n/a
27	chr14:63784574-63784624	NH-A	brain:	n/a
28	chr14:63784394-63784444	Hepatocyte	liver:	n/a
29	chr14:63785287-63785337	HEEpiC	esophagus:	n/a
30	chr14:63779694-63779744	ProgFib	skin:	n/a
31	chr14:63784574-63784624	HAEpiC	amniotic membrane:	n/a
32	chr14:63784394-63784444	NT2-D1	testis:	n/a
33	chr14:63785523-63785573	NH-A	brain:	n/a
34	chr14:63784394-63784444	GM06990	blood:	n/a
35	chr14:63785287-63785337	LNCaP	prostate:	n/a
36	chr14:63779694-63779744	GM06990	blood:	n/a
37	chr14:63784394-63784444	HUVEC	blood vessel:	n/a
38	chr14:63784574-63784624	SK-N-MC	brain:	n/a
39	chr14:63784394-63784444	GM19239	blood:	n/a
40	chr14:63781994-63782044	NB4	blood:	n/a
41	chr14:63784394-63784444	AG10803	skin:	n/a
42	chr14:63784394-63784444	HMEC	breast:	n/a
43	chr14:63784574-63784624	PFSK-1	brain:	n/a
44	chr14:63779694-63779744	HRCEpiC	kidney:	n/a
45	chr14:63785334-63785384	GM12878	blood:	n/a
46	chr14:63784574-63784624	GM06990	blood:	n/a
47	chr14:63784394-63784444	GM12892	blood:	n/a
48	chr14:63781994-63782044	HRCEpiC	kidney:	n/a
49	chr14:63785334-63785384	AG09319	gingival:	n/a
50	chr14:63785287-63785337	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:63823098..63825061-chr14:63826857..63829778,2	MCF-7	breast:
2	chr14:63816228..63817986-chr14:63819817..63821976,2	MCF-7	breast:
3	chr14:63816228..63817986-chr14:63819817..63821976,2	MCF-7	breast:
4	chr14:63833848..63836637-chr14:63841701..63844309,2	MCF-7	breast:
5	chr14:63784531..63787249-chr14:63793902..63795892,2	MCF-7	breast:
6	chr14:63837297..63838980-chr14:63840657..63842212,2	MCF-7	breast:
7	chr14:63792244..63793991-chr14:63822346..63825319,2	MCF-7	breast:
8	chr14:63830891..63833406-chr14:63833743..63835753,2	K562	blood:
9	chr14:63807896..63809809-chr14:63818163..63820932,2	MCF-7	breast:
10	chr14:63823098..63825061-chr14:63826857..63829778,2	MCF-7	breast:
11	chr14:63792244..63793991-chr14:63822346..63825319,2	MCF-7	breast:
12	chr14:63837297..63838980-chr14:63840657..63842212,2	MCF-7	breast:
13	chr14:63836099..63836920-chr6:128541621..128542384,2	MCF-7	breast:
14	chr14:63833848..63836637-chr14:63841701..63844309,2	MCF-7	breast:
15	chr14:63830891..63833406-chr14:63833743..63835753,2	K562	blood:
16	chr14:63807896..63809809-chr14:63818163..63820932,2	MCF-7	breast:
17	chr14:63848595..63851169-chr14:64107183..64109145,2	K562	blood:

Variant related genes	Relation type
GPHB5	TF binding region
GPHB5	CpG island
ENSG00000140006	chromatin interactions
ENSG00000179600	chromatin interactions

Extended variants
information (count: 1947 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1947 , 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	rs1255577	chr14:63778748-63778749	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150983110	chr14:63778789-63778790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570007014	chr14:63778898-63778899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35766106	chr14:63778973-63778974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs67506653	chr14:63778975-63778976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539043637	chr14:63778996-63778997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569921410	chr14:63779605-63779606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577992104	chr14:63779661-63779662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138605177	chr14:63779662-63779663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs118004333	chr14:63779665-63779666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371551605	chr14:63779684-63779685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534120208	chr14:63779690-63779691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547664197	chr14:63779703-63779704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540479788	chr14:63779705-63779706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567399169	chr14:63779733-63779734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369482608	chr14:63779763-63779764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140208070	chr14:63779773-63779774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376425106	chr14:63779774-63779775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs202152731	chr14:63779790-63779791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575761660	chr14:63779791-63779792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538332945	chr14:63779796-63779797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369232899	chr14:63779805-63779806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201745048	chr14:63779813-63779814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558172699	chr14:63779815-63779816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs5809192	chr14:63779846-63779847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs397710669	chr14:63779849-63779850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74954403	chr14:63779850-63779851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571706279	chr14:63779866-63779867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184467105	chr14:63779883-63779884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372594947	chr14:63779897-63779898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561637291	chr14:63779901-63779902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574998580	chr14:63779912-63779913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544017477	chr14:63779928-63779929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563849574	chr14:63779929-63779930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558934783	chr14:63779952-63779953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7142587	chr14:63779983-63779984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs115732439	chr14:63780016-63780017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs8006976	chr14:63780103-63780104	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs117653833	chr14:63780147-63780148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531064813	chr14:63780188-63780189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1739037	chr14:63780193-63780194	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs528495438	chr14:63780199-63780200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548256634	chr14:63780219-63780220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145253208	chr14:63780264-63780265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs9635248	chr14:63780317-63780318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549983878	chr14:63780351-63780352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs58737358	chr14:63780352-63780353	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs137904236	chr14:63780354-63780355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558234096	chr14:63780355-63780356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs55948827	chr14:63780368-63780369	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Leukemia	18688285	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22737080	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63777200-63779000	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr14:63779600-63780400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:63779800-63780000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chr14:63779800-63780200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr14:63780000-63780400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr14:63784200-63784600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:63789000-63790800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr14:63789200-63790200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr14:63789200-63790400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr14:63789400-63790200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr14:63789400-63790200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr14:63789600-63790000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr14:63789800-63790400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr14:63790000-63790400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr14:63790000-63790400	Enhancers	Fetal Muscle Leg	muscle
16	chr14:63790000-63790600	Enhancers	Fetal Brain Male	brain
17	chr14:63793400-63794400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr14:63795000-63797200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:63797200-63799600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr14:63799600-63799800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:63799800-63800000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr14:63800000-63800200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr14:63800200-63800600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr14:63800200-63801000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:63801000-63801400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:63801400-63801600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr14:63801600-63801800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr14:63801800-63802000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr14:63802000-63802600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr14:63806800-63807400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr14:63808800-63809400	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr14:63809000-63809600	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr14:63809000-63809600	Enhancers	A549	lung
34	chr14:63809000-63809800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr14:63809000-63811600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr14:63809400-63809600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr14:63809400-63809800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr14:63809400-63810000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr14:63809800-63812000	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr14:63810000-63811000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr14:63810200-63811400	Enhancers	HUVEC	blood vessel
42	chr14:63810600-63811400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr14:63811000-63811400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr14:63811200-63811600	Enhancers	Fetal Muscle Leg	muscle
45	chr14:63811600-63811800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:63811800-63812000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr14:63812000-63812200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr14:63812000-63813200	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr14:63812200-63813000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr14:63813000-63813200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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