Variant report

Variant	esv3338046
Chromosome Location	chr17:15466577-15467725
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	ATF1	chr17:15466756-15466960	K562	blood:	n/a	n/a
2	ATF2	chr17:15466618-15466919	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr17:15466672-15466916	GM12878	blood:	n/a	n/a
4	BRCA1	chr17:15466774-15466842	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr17:15466707-15466908	Hela-S3	cervix:	n/a	n/a
6	CEBPD	chr17:15466629-15466896	HepG2	liver:	n/a	n/a
7	CHD2	chr17:15466718-15466857	HepG2	liver:	n/a	n/a
8	CHD2	chr17:15466731-15466960	Hela-S3	cervix:	n/a	n/a
9	CREB1	chr17:15466618-15466911	A549	lung:	n/a	chr17:15466791-15466804
10	CREB1	chr17:15466726-15466879	A549	lung:	n/a	chr17:15466791-15466804
11	CTCF	chr17:15466740-15466890	SK-N-SH_RA	brain:	n/a	n/a
12	CTCF	chr17:15466789-15466813	Fibrobl	skin:	n/a	n/a
13	CTCF	chr17:15466815-15466848	Fibrobl	skin:	n/a	n/a
14	CTCF	chr17:15466562-15466636	LNCaP	prostate:	n/a	n/a
15	CTCF	chr17:15466740-15466890	AG04449	skin:	n/a	n/a
16	CTCF	chr17:15466760-15466910	Hela-S3	cervix:	n/a	n/a
17	E2F6	chr17:15466728-15466868	K562	blood:	n/a	n/a
18	EGR1	chr17:15466684-15466949	K562	blood:	n/a	n/a
19	EGR1	chr17:15466960-15467228	K562	blood:	n/a	chr17:15467046-15467060 chr17:15467017-15467031 chr17:15467002-15467016 chr17:15467204-15467214 chr17:15467041-15467063
20	EGR1	chr17:15466666-15466926	K562	blood:	n/a	n/a
21	EGR1	chr17:15467001-15467114	GM12878	blood:	n/a	chr17:15467046-15467060 chr17:15467017-15467031 chr17:15467002-15467016 chr17:15467041-15467063
22	EGR1	chr17:15466971-15467212	K562	blood:	n/a	chr17:15467046-15467060 chr17:15467017-15467031 chr17:15467002-15467016 chr17:15467041-15467063
23	EGR1	chr17:15466996-15467099	GM12878	blood:	n/a	chr17:15467046-15467060 chr17:15467017-15467031 chr17:15467002-15467016 chr17:15467041-15467063
24	ELK1	chr17:15466716-15466893	Hela-S3	cervix:	n/a	n/a
25	ETS1	chr17:15466711-15466885	K562	blood:	n/a	n/a
26	FOSL2	chr17:15466268-15467202	HepG2	liver:	n/a	chr17:15466630-15466639
27	FOSL2	chr17:15466574-15466910	HepG2	liver:	n/a	chr17:15466630-15466639
28	FOXP2	chr17:15466686-15466938	PFSK-1	brain:	n/a	n/a
29	GABPA	chr17:15466696-15466946	A549	lung:	n/a	n/a
30	GABPA	chr17:15466734-15466883	K562	blood:	n/a	n/a
31	GABPA	chr17:15466532-15466905	HepG2	liver:	n/a	chr17:15466659-15466668 chr17:15466661-15466670
32	GABPA	chr17:15466574-15466936	GM12878	blood:	n/a	chr17:15466659-15466668 chr17:15466661-15466670
33	GABPA	chr17:15466613-15466912	K562	blood:	n/a	chr17:15466659-15466668 chr17:15466661-15466670
34	GABPA	chr17:15466536-15467047	Hela-S3	cervix:	n/a	chr17:15466659-15466668 chr17:15466661-15466670
35	GABPA	chr17:15466512-15466950	GM12878	blood:	n/a	chr17:15466659-15466668 chr17:15466661-15466670
36	GABPA	chr17:15466565-15466937	Hela-S3	cervix:	n/a	chr17:15466659-15466668 chr17:15466661-15466670
37	GABPA	chr17:15466451-15466939	HepG2	liver:	n/a	chr17:15466659-15466668 chr17:15466661-15466670
38	GTF2F1	chr17:15466826-15466896	K562	blood:	n/a	n/a
39	GTF2F1	chr17:15466719-15466896	Hela-S3	cervix:	n/a	n/a
40	GTF2F1	chr17:15466713-15466900	H1-hESC	embryonic stem cell:	n/a	n/a
41	HCFC1	chr17:15466632-15467129	Hela-S3	cervix:	n/a	n/a
42	HCFC1	chr17:15466665-15466916	K562	blood:	n/a	n/a
43	HEY1	chr17:15466395-15466968	K562	blood:	n/a	n/a
44	HEY1	chr17:15464967-15466911	K562	blood:	n/a	n/a
45	HEY1	chr17:15466231-15467358	HepG2	liver:	n/a	n/a
46	HEY1	chr17:15466963-15467237	K562	blood:	n/a	n/a
47	HEY1	chr17:15467018-15467213	HepG2	liver:	n/a	n/a
48	HEY1	chr17:15466999-15467262	K562	blood:	n/a	n/a
49	HEY1	chr17:15466427-15466913	HepG2	liver:	n/a	n/a
50	IRF1	chr17:15466784-15466844	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15467447-15467497	NT2-D1	testis:	n/a
2	chr17:15467447-15467497	AG04449	skin:	fetal
3	chr17:15466921-15466971	SK-N-MC	brain:	n/a
4	chr17:15467447-15467497	NT2-D1	testis:	n/a
5	chr17:15467447-15467497	AG04449	skin:	fetal
6	chr17:15466921-15466971	SK-N-MC	brain:	n/a
7	chr17:15466718-15466768	Hela-S3	cervix:	n/a
8	chr17:15466549-15466599	NT2-D1	testis:	n/a
9	chr17:15467135-15467185	MCF10A-Er-Src	breast:	n/a
10	chr17:15466718-15466768	HCF	heart:	n/a
11	chr17:15466549-15466599	LNCaP	prostate:	n/a
12	chr17:15466718-15466768	HAEpiC	amniotic membrane:	n/a
13	chr17:15467447-15467497	AG04450	lung:	fetal
14	chr17:15467188-15467238	T-47D	breast:	n/a
15	chr17:15467135-15467185	HRPEpiC	eye:	n/a
16	chr17:15467188-15467238	NHDF-neo	bronchial:	n/a
17	chr17:15466921-15466971	GM12892	blood:	n/a
18	chr17:15466921-15466971	SK-N-SH	brain:	n/a
19	chr17:15466549-15466599	HCT-116	colon:	n/a
20	chr17:15466549-15466599	A549	lung:	n/a
21	chr17:15467188-15467238	HIPEpiC	eye:	n/a
22	chr17:15466718-15466768	HL-60	blood:	n/a
23	chr17:15466826-15466876	U87	brain:	n/a
24	chr17:15466718-15466768	Caco-2	colon:	n/a
25	chr17:15466718-15466768	SK-N-SH_RA	brain:	n/a
26	chr17:15466921-15466971	AoSMC	blood vessel:	n/a
27	chr17:15467188-15467238	ovcar-3	ovarian:	n/a
28	chr17:15467135-15467185	A549	lung:	n/a
29	chr17:15466549-15466599	HMEC	breast:	n/a
30	chr17:15467135-15467185	GM12892	blood:	n/a
31	chr17:15466549-15466599	AG09319	gingival:	n/a
32	chr17:15466549-15466599	HIPEpiC	eye:	n/a
33	chr17:15466718-15466768	A549	lung:	n/a
34	chr17:15467188-15467238	HRE	kidney:	n/a
35	chr17:15467188-15467238	PrEC	prostate:	n/a
36	chr17:15467188-15467238	HCF	heart:	n/a
37	chr17:15467135-15467185	HCT-116	colon:	n/a
38	chr17:15466921-15466971	RPTEC	kidney:	n/a
39	chr17:15466549-15466599	HAEpiC	amniotic membrane:	n/a
40	chr17:15467447-15467497	NHDF-neo	bronchial:	n/a
41	chr17:15466549-15466599	SK-N-MC	brain:	n/a
42	chr17:15466826-15466876	IMR90	lung:	fetal
43	chr17:15467188-15467238	Caco-2	colon:	n/a
44	chr17:15466921-15466971	NH-A	brain:	n/a
45	chr17:15466921-15466971	AG04450	lung:	fetal
46	chr17:15467135-15467185	AG09319	gingival:	n/a
47	chr17:15467447-15467497	HRCEpiC	kidney:	n/a
48	chr17:15466549-15466599	ECC-1	luminal epithelium:	n/a
49	chr17:15467135-15467185	BE2_C	brain:	n/a
50	chr17:15467188-15467238	HNPCEpiC	eye:	n/a

Variant related genes	Relation type
TVP23C-CDRT4	TF binding region
TVP23C	TF binding region
TVP23C-CDRT4	CpG island
TVP23C	CpG island

Extended variants
information (count: 43 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:43 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565739597	chr17:15466638-15466639	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs535281905	chr17:15466642-15466643	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs28495834	chr17:15466704-15466705	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs377288976	chr17:15466713-15466714	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs191004702	chr17:15466734-15466735	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs575245116	chr17:15466750-15466751	Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs369802859	chr17:15466756-15466757	Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs537729205	chr17:15466762-15466763	Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
9	rs557344309	chr17:15466773-15466774	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs377260184	chr17:15466783-15466784	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs370528394	chr17:15466799-15466800	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs373468170	chr17:15466803-15466804	Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs143779011	chr17:15466822-15466823	Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs184239223	chr17:15466835-15466836	Active TSS Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
15	rs572995013	chr17:15466842-15466843	Active TSS Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
16	rs540866759	chr17:15466872-15466873	Active TSS Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
17	rs186668025	chr17:15466882-15466883	Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs192020500	chr17:15466893-15466894	Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs560732350	chr17:15466916-15466917	Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs182828689	chr17:15467048-15467049	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs550070342	chr17:15467070-15467071	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs563401591	chr17:15467079-15467080	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs532142577	chr17:15467080-15467081	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs551883083	chr17:15467084-15467085	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs187087515	chr17:15467086-15467087	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs565821921	chr17:15467103-15467104	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs189527670	chr17:15467107-15467108	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs182227581	chr17:15467185-15467186	Active TSS Weak transcription Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
29	rs574272596	chr17:15467188-15467189	Active TSS Weak transcription Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
30	rs534693854	chr17:15467196-15467197	Active TSS Weak transcription Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
31	rs548829724	chr17:15467243-15467244	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs568695282	chr17:15467296-15467297	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs537215382	chr17:15467383-15467384	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs557646306	chr17:15467400-15467401	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs371562106	chr17:15467412-15467413	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs574609252	chr17:15467494-15467495	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
37	rs374665077	chr17:15467499-15467500	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs142786129	chr17:15467545-15467546	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs540207173	chr17:15467550-15467551	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs377722032	chr17:15467573-15467574	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs573033732	chr17:15467576-15467577	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs186789599	chr17:15467710-15467711	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs193090503	chr17:15467713-15467714	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:126)

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

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15463000-15466600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr17:15465200-15467400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr17:15465400-15466800	Active TSS	K562	blood
4	chr17:15465400-15467200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr17:15465400-15467400	Active TSS	HepG2	liver
6	chr17:15465400-15467600	Active TSS	Muscle Satellite Cultured Cells	--
7	chr17:15465400-15467600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr17:15465400-15467800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr17:15465600-15466800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr17:15465600-15467400	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr17:15465600-15467400	Active TSS	Hela-S3	cervix
12	chr17:15465600-15467600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr17:15465600-15467800	Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr17:15465600-15467800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr17:15465800-15467200	Active TSS	HMEC	breast
16	chr17:15465800-15467400	Active TSS	HUVEC	blood vessel
17	chr17:15465800-15467600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr17:15465800-15467600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr17:15465800-15467600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
20	chr17:15465800-15467600	Active TSS	Fetal Intestine Small	intestine
21	chr17:15466000-15466600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr17:15466000-15466800	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr17:15466000-15466800	Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr17:15466000-15466800	Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr17:15466000-15467000	Active TSS	H9 Cell Line	embryonic stem cell
26	chr17:15466000-15467000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr17:15466000-15467000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr17:15466000-15467200	Active TSS	H1 Cell Line	embryonic stem cell
29	chr17:15466000-15467200	Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr17:15466000-15467200	Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr17:15466000-15467200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr17:15466000-15467200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr17:15466000-15467200	Active TSS	Brain Angular Gyrus	brain
34	chr17:15466000-15467200	Active TSS	Brain Cingulate Gyrus	brain
35	chr17:15466000-15467200	Active TSS	Dnd41	blood
36	chr17:15466000-15467200	Active TSS	HSMM	muscle
37	chr17:15466000-15467200	Active TSS	HSMMtube	muscle
38	chr17:15466000-15467200	Active TSS	NHDF-Ad	bronchial
39	chr17:15466000-15467400	Active TSS	HUES64 Cell Line	embryonic stem cell
40	chr17:15466000-15467400	Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr17:15466000-15467400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr17:15466000-15467400	Active TSS	Brain Germinal Matrix	brain
43	chr17:15466000-15467400	Active TSS	Fetal Intestine Large	intestine
44	chr17:15466000-15467400	Active TSS	Fetal Muscle Trunk	muscle
45	chr17:15466000-15467400	Active TSS	Fetal Stomach	stomach
46	chr17:15466000-15467400	Active TSS	A549	lung
47	chr17:15466000-15467400	Active TSS	Monocytes-CD14+_RO01746	blood
48	chr17:15466000-15467400	Active TSS	NH-A	brain
49	chr17:15466000-15467400	Active TSS	NHEK	skin
50	chr17:15466000-15467600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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