Variant report

Variant	nsv442411
Chromosome Location	chr17:15677001-15694785
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:87)
CpG islands
(count:796)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:87 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr17:15687864-15688082	A549	lung:	n/a	chr17:15687996-15688009 chr17:15687996-15688007 chr17:15687998-15688009
2	CEBPB	chr17:15687871-15688095	IMR90	lung:	n/a	chr17:15687996-15688009 chr17:15687996-15688007 chr17:15687998-15688009
3	CEBPB	chr17:15687884-15688101	HepG2	liver:	n/a	chr17:15687996-15688009 chr17:15687996-15688007 chr17:15687998-15688009
4	CTCF	chr17:15686215-15686295	Pancreas_OC	pancreas:	n/a	n/a
5	CTCF	chr17:15682280-15682430	GM12870	blood:	n/a	n/a
6	CTCF	chr17:15686201-15686306	Lung_OC	lung:	n/a	n/a
7	CTCF	chr17:15689399-15689488	Kidney_OC	kidney:	n/a	n/a
8	CTCF	chr17:15686160-15686310	BJ	skin:	n/a	n/a
9	CTCF	chr17:15677252-15677352	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr17:15686140-15686290	HCM	heart:	n/a	n/a
11	CTCF	chr17:15686120-15686270	HUVEC	blood vessel:	n/a	n/a
12	CTCF	chr17:15677202-15677291	GM20000	blood:	n/a	n/a
13	CTCF	chr17:15686120-15686270	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr17:15686160-15686310	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr17:15690268-15690448	A549	lung:	n/a	n/a
16	CTCF	chr17:15686120-15686270	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr17:15686180-15686330	HCFaa	heart:	n/a	n/a
18	CTCF	chr17:15686180-15686330	HA-sp	spinal cord:	n/a	n/a
19	CTCF	chr17:15686140-15686290	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr17:15686298-15686301	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr17:15686180-15686330	HRE	kidney:	n/a	n/a
22	FOS	chr17:15685180-15685458	MCF10A-Er-Src	breast:	n/a	chr17:15685313-15685324
23	FOS	chr17:15685044-15685394	HUVEC	blood vessel:	n/a	chr17:15685313-15685324
24	FOXA2	chr17:15689329-15689568	A549	lung:	n/a	n/a
25	GABPA	chr17:15689256-15689571	A549	lung:	n/a	n/a
26	GABPA	chr17:15689362-15689578	SK-N-SH	brain:	n/a	n/a
27	GABPA	chr17:15689256-15689526	A549	lung:	n/a	n/a
28	JUND	chr17:15692380-15692446	HepG2	liver:	n/a	chr17:15692412-15692421
29	KAP1	chr17:15682334-15682836	HEK293	kidney:	n/a	n/a
30	MYC	chr17:15689876-15690057	MCF-7	breast:	n/a	n/a
31	MYC	chr17:15689356-15689483	HUVEC	blood vessel:	n/a	n/a
32	MYC	chr17:15690213-15690264	MCF-7	breast:	n/a	n/a
33	POLR2A	chr17:15689325-15690090	MCF-7	breast:	n/a	n/a
34	POLR2A	chr17:15690620-15690696	MCF-7	breast:	n/a	n/a
35	POLR2A	chr17:15690264-15690301	A549	lung:	n/a	n/a
36	POLR2A	chr17:15689892-15689902	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr17:15690168-15690285	MCF-7	breast:	n/a	n/a
38	POLR2A	chr17:15686968-15687180	HUVEC	blood vessel:	n/a	n/a
39	POLR2A	chr17:15690760-15690791	MCF-7	breast:	n/a	n/a
40	POLR2A	chr17:15680298-15680312	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr17:15686275-15686384	A549	lung:	n/a	n/a
42	POLR2A	chr17:15689845-15690072	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr17:15689398-15689745	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr17:15690338-15690343	Gliobla	brain:	n/a	n/a
45	POLR2A	chr17:15685052-15685252	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr17:15686579-15686613	HUVEC	blood vessel:	n/a	n/a
47	POLR2A	chr17:15690388-15690423	A549	lung:	n/a	n/a
48	POLR2A	chr17:15690794-15690842	MCF-7	breast:	n/a	n/a
49	POLR2A	chr17:15689298-15689539	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr17:15689432-15689552	Gliobla	brain:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15687603-15687653	Hepatocyte	liver:	n/a
2	chr17:15689920-15689970	SAEC	small airway:	n/a
3	chr17:15686438-15686488	HCT-116	colon:	n/a
4	chr17:15687603-15687653	Hepatocyte	liver:	n/a
5	chr17:15689920-15689970	SAEC	small airway:	n/a
6	chr17:15686438-15686488	HCT-116	colon:	n/a
7	chr17:15689957-15690007	HL-60	blood:	n/a
8	chr17:15686473-15686523	PrEC	prostate:	n/a
9	chr17:15692425-15692475	SK-N-SH	brain:	n/a
10	chr17:15686294-15686344	SAEC	small airway:	n/a
11	chr17:15689957-15690007	HNPCEpiC	eye:	n/a
12	chr17:15690132-15690182	HCPEpiC	choroid plexus:	n/a
13	chr17:15690713-15690763	SK-N-SH	brain:	n/a
14	chr17:15690132-15690182	AG04449	skin:	fetal
15	chr17:15686309-15686359	Jurkat	blood:	n/a
16	chr17:15686473-15686523	HEK293	kidney:	embryo
17	chr17:15690713-15690763	SK-N-SH_RA	brain:	n/a
18	chr17:15690132-15690182	Hepatocyte	liver:	n/a
19	chr17:15689091-15689141	Caco-2	colon:	n/a
20	chr17:15686294-15686344	HNPCEpiC	eye:	n/a
21	chr17:15686438-15686488	AG10803	skin:	n/a
22	chr17:15689920-15689970	PFSK-1	brain:	n/a
23	chr17:15689957-15690007	K562	blood:	n/a
24	chr17:15690181-15690231	LNCaP	prostate:	n/a
25	chr17:15689957-15690007	A549	lung:	n/a
26	chr17:15686473-15686523	HRPEpiC	eye:	n/a
27	chr17:15686438-15686488	SK-N-SH	brain:	n/a
28	chr17:15689920-15689970	HUVEC	blood vessel:	n/a
29	chr17:15689920-15689970	H1-hESC	embryonic stem cell:	embryo
30	chr17:15690181-15690231	HRPEpiC	eye:	n/a
31	chr17:15686294-15686344	MCF-7	breast:	n/a
32	chr17:15686438-15686488	GM19239	blood:	n/a
33	chr17:15683060-15683110	HCT-116	colon:	n/a
34	chr17:15689091-15689141	A549	lung:	n/a
35	chr17:15683060-15683110	PANC-1	pancreas:	n/a
36	chr17:15686438-15686488	ovcar-3	ovarian:	n/a
37	chr17:15683060-15683110	MCF10A-Er-Src	breast:	n/a
38	chr17:15686438-15686488	RPTEC	kidney:	n/a
39	chr17:15686309-15686359	GM06990	blood:	n/a
40	chr17:15686309-15686359	BE2_C	brain:	n/a
41	chr17:15690132-15690182	T-47D	breast:	n/a
42	chr17:15683060-15683110	HCM	heart:	n/a
43	chr17:15689920-15689970	GM19239	blood:	n/a
44	chr17:15686309-15686359	PANC-1	pancreas:	n/a
45	chr17:15686438-15686488	K562	blood:	n/a
46	chr17:15687603-15687653	GM12891	blood:	n/a
47	chr17:15689920-15689970	A549	lung:	n/a
48	chr17:15689957-15690007	HRPEpiC	eye:	n/a
49	chr17:15686309-15686359	A549	lung:	n/a
50	chr17:15689091-15689141	ProgFib	skin:	n/a

No data

Variant related genes	Relation type
ZSWIM5P1	TF binding region
RNA5SP436	TF binding region
MEIS3P1	TF binding region
ENSG00000265519	TF binding region
IL6STP1	TF binding region
ENSG00000233090	TF binding region
ZSWIM5P1	CpG island
RNA5SP436	CpG island
MEIS3P1	CpG island
ENSG00000265519	CpG island
IL6STP1	CpG island
ENSG00000233090	CpG island

Extended variants
information (count: 503 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4286144	chr17:15677203-15677204	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs386795817	chr17:15677219-15677220	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs200158628	chr17:15677220-15677221	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs370735725	chr17:15677235-15677236	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs8068317	chr17:15677245-15677246	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs577905288	chr17:15677274-15677275	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs543084027	chr17:15677287-15677288	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs143822919	chr17:15677323-15677324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs151292112	chr17:15677324-15677325	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs538082231	chr17:15679117-15679118	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs34172152	chr17:15679166-15679167	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs536899575	chr17:15679172-15679173	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs142768420	chr17:15679173-15679174	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs553883616	chr17:15679207-15679208	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs181851006	chr17:15680656-15680657	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs35111349	chr17:15680657-15680658	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs372110062	chr17:15680658-15680659	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs3062358	chr17:15680671-15680672	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs374806898	chr17:15680731-15680732	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs1561956	chr17:15680743-15680744	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs114964862	chr17:15680753-15680754	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs567771162	chr17:15680761-15680762	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs536219465	chr17:15680787-15680788	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs556609671	chr17:15680847-15680848	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs1822412	chr17:15680855-15680856	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs1822413	chr17:15680900-15680901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556817469	chr17:15680909-15680910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575565400	chr17:15680924-15680925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4561504	chr17:15680937-15680938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538132813	chr17:15680957-15680958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185273047	chr17:15681097-15681098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577744940	chr17:15681168-15681169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545316060	chr17:15681267-15681268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540447334	chr17:15681269-15681270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559962604	chr17:15681295-15681296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536476335	chr17:15681305-15681306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542175548	chr17:15681329-15681330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562147770	chr17:15681344-15681345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531247205	chr17:15681345-15681346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551643322	chr17:15681370-15681371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565600496	chr17:15681385-15681386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141199545	chr17:15681476-15681477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547986840	chr17:15681496-15681497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145043760	chr17:15681546-15681547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4614768	chr17:15681562-15681563	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs572048129	chr17:15681572-15681573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550348313	chr17:15681576-15681577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570053552	chr17:15681628-15681629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188475796	chr17:15681636-15681637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181242489	chr17:15681661-15681662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:128)

Disease	PMID	Source
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	19435819	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Hepatocellular carcinoma	18803288	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Multiple myeloma	16616336	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	21811587	CNVD
Autism	17322880	CNVD
Hereditary neuropathy with liability to pressure palsy	19521722	CNVD
Schizophrenia	19571808	CNVD
Schizophrenia	19955444	CNVD
Charcot-marie-tooth disease	18787571	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Peripheral neuropathy	21193943	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	20844748	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15680600-15682400	Weak transcription	Aorta	Aorta
2	chr17:15682200-15682600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr17:15682400-15682600	ZNF genes & repeats	Aorta	Aorta
4	chr17:15682600-15686200	Weak transcription	Aorta	Aorta
5	chr17:15683400-15683600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr17:15683600-15685400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr17:15685400-15686000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr17:15685600-15685800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
9	chr17:15685600-15685800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
10	chr17:15685600-15685800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
11	chr17:15685600-15685800	Enhancers	Ovary	ovary
12	chr17:15685600-15686000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr17:15685600-15686200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr17:15685600-15686200	Bivalent/Poised TSS	Brain Angular Gyrus	brain
15	chr17:15685600-15686200	Enhancers	Right Ventricle	heart
16	chr17:15685600-15686400	Enhancers	Fetal Lung	lung
17	chr17:15685600-15687200	Enhancers	Colon Smooth Muscle	Colon
18	chr17:15685800-15686000	Enhancers	Fetal Brain Male	brain
19	chr17:15685800-15686200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
20	chr17:15685800-15686200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr17:15685800-15686200	Enhancers	Primary hematopoietic stem cells	blood
22	chr17:15685800-15686200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
23	chr17:15685800-15686200	Enhancers	Fetal Muscle Leg	muscle
24	chr17:15685800-15686200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
25	chr17:15685800-15686400	Active TSS	Ovary	ovary
26	chr17:15685800-15686400	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr17:15685800-15686400	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr17:15685800-15686600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr17:15685800-15686600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr17:15685800-15686600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr17:15685800-15686800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr17:15686000-15686200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr17:15686000-15686200	Bivalent Enhancer	Fetal Stomach	stomach
34	chr17:15686000-15686400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr17:15686000-15686400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr17:15686000-15686600	Active TSS	Adipose Nuclei	Adipose
37	chr17:15686000-15686600	Active TSS	Fetal Muscle Trunk	muscle
38	chr17:15686000-15686600	Enhancers	Placenta	Placenta
39	chr17:15686000-15686600	Active TSS	Left Ventricle	heart
40	chr17:15686000-15686600	Active TSS	Right Atrium	heart
41	chr17:15686000-15686800	Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr17:15686000-15686800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr17:15686200-15686400	Flanking Active TSS	Primary hematopoietic stem cells	blood
44	chr17:15686200-15686400	Active TSS	Muscle Satellite Cultured Cells	--
45	chr17:15686200-15686400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr17:15686200-15686400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr17:15686200-15686400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
48	chr17:15686200-15686400	Bivalent/Poised TSS	Fetal Stomach	stomach
49	chr17:15686200-15686400	Active TSS	HMEC	breast
50	chr17:15686200-15686400	Bivalent/Poised TSS	NHEK	skin

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