Variant report

Variant	nsv575933
Chromosome Location	chr17:67153386-67215712
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:433)
CpG islands
(count:62)
Chromatin interactive
region (count:26)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:67167697-67167955	K562	blood:	n/a	n/a
2	ARID3A	chr17:67171664-67172397	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:67171301-67172388	K562	blood:	n/a	n/a
4	ARID3A	chr17:67194522-67194736	K562	blood:	n/a	n/a
5	ATF1	chr17:67194476-67194801	K562	blood:	n/a	n/a
6	ATF1	chr17:67171921-67172466	K562	blood:	n/a	n/a
7	ATF1	chr17:67166565-67167142	K562	blood:	n/a	n/a
8	ATF3	chr17:67194490-67194700	K562	blood:	n/a	n/a
9	ATF3	chr17:67171634-67172355	HCT-116	colon:	n/a	n/a
10	ATF3	chr17:67171867-67172250	K562	blood:	n/a	n/a
11	ATF3	chr17:67171733-67172352	HCT-116	colon:	n/a	n/a
12	BHLHE40	chr17:67194360-67195239	K562	blood:	n/a	n/a
13	BRCA1	chr17:67213899-67213921	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr17:67171794-67172397	HCT-116	colon:	n/a	n/a
15	CCNT2	chr17:67171822-67172433	K562	blood:	n/a	n/a
16	CEBPB	chr17:67203340-67203670	K562	blood:	n/a	n/a
17	CEBPB	chr17:67171502-67172374	Hela-S3	cervix:	n/a	chr17:67172082-67172093
18	CEBPB	chr17:67175717-67176039	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr17:67171926-67172256	HepG2	liver:	n/a	chr17:67172082-67172093
20	CEBPB	chr17:67171882-67172240	IMR90	lung:	n/a	chr17:67172082-67172093
21	CEBPB	chr17:67171957-67172119	K562	blood:	n/a	chr17:67172082-67172093
22	CEBPB	chr17:67161272-67161630	Hela-S3	cervix:	n/a	chr17:67161439-67161452 chr17:67161439-67161450 chr17:67161440-67161451 chr17:67161439-67161450
23	CEBPB	chr17:67171853-67172235	MCF-7	breast:	n/a	chr17:67172082-67172093
24	CEBPB	chr17:67171901-67172261	K562	blood:	n/a	chr17:67172082-67172093
25	CEBPB	chr17:67171613-67172347	A549	lung:	n/a	chr17:67172082-67172093
26	CEBPB	chr17:67188810-67189154	K562	blood:	n/a	chr17:67188955-67188966
27	CEBPB	chr17:67171592-67172262	A549	lung:	n/a	chr17:67172082-67172093
28	CEBPB	chr17:67155608-67155909	HepG2	liver:	n/a	n/a
29	CEBPB	chr17:67171853-67172250	K562	blood:	n/a	chr17:67172082-67172093
30	CEBPB	chr17:67171571-67172581	HCT-116	colon:	n/a	chr17:67172082-67172093
31	CEBPB	chr17:67171937-67172105	HepG2	liver:	n/a	chr17:67172082-67172093
32	CEBPB	chr17:67194405-67194763	K562	blood:	n/a	n/a
33	CEBPB	chr17:67161311-67161616	HepG2	liver:	n/a	chr17:67161439-67161452 chr17:67161439-67161450 chr17:67161440-67161451 chr17:67161439-67161450
34	CEBPB	chr17:67166605-67166870	K562	blood:	n/a	n/a
35	CEBPB	chr17:67171736-67172473	HCT-116	colon:	n/a	chr17:67172082-67172093
36	CEBPB	chr17:67172699-67172868	HepG2	liver:	n/a	chr17:67172804-67172815
37	CEBPB	chr17:67188786-67189065	HepG2	liver:	n/a	chr17:67188955-67188966
38	CEBPB	chr17:67171822-67172308	A549	lung:	n/a	chr17:67172082-67172093
39	CEBPB	chr17:67188873-67189055	A549	lung:	n/a	chr17:67188955-67188966
40	CEBPB	chr17:67155676-67155813	K562	blood:	n/a	n/a
41	CEBPB	chr17:67171875-67172274	MCF-7	breast:	n/a	chr17:67172082-67172093
42	CEBPB	chr17:67170560-67170563	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr17:67179741-67179747	K562	blood:	n/a	n/a
44	CTCF	chr17:67169329-67169579	K562	blood:	n/a	n/a
45	CTCF	chr17:67209300-67209384	MCF-7	breast:	n/a	n/a
46	CTCF	chr17:67209278-67209422	K562	blood:	n/a	n/a
47	CTCF	chr17:67209279-67209441	MCF-7	breast:	n/a	n/a
48	CTCF	chr17:67209087-67209569	K562	blood:	n/a	n/a
49	CTCF	chr17:67209300-67209450	GM12874	blood:	n/a	n/a
50	CTCF	chr17:67209280-67209430	HBMEC	blood vessel:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:67192236-67192286	HRPEpiC	eye:	n/a
2	chr17:67192236-67192286	HRPEpiC	eye:	n/a
3	chr17:67192236-67192286	HEEpiC	esophagus:	n/a
4	chr17:67192236-67192286	HCT-116	colon:	n/a
5	chr17:67192236-67192286	AG09309	skin:	n/a
6	chr17:67192236-67192286	GM19239	blood:	n/a
7	chr17:67192236-67192286	SKMC	muscle:	n/a
8	chr17:67192236-67192286	NHDF-neo	bronchial:	n/a
9	chr17:67192236-67192286	MCF-7	breast:	n/a
10	chr17:67192236-67192286	PANC-1	pancreas:	n/a
11	chr17:67192236-67192286	Caco-2	colon:	n/a
12	chr17:67192236-67192286	HMEC	breast:	n/a
13	chr17:67192236-67192286	CMK	blood:	n/a
14	chr17:67192236-67192286	ECC-1	luminal epithelium:	n/a
15	chr17:67192236-67192286	HAEpiC	amniotic membrane:	n/a
16	chr17:67192236-67192286	GM12891	blood:	n/a
17	chr17:67192236-67192286	HCM	heart:	n/a
18	chr17:67192236-67192286	HNPCEpiC	eye:	n/a
19	chr17:67192236-67192286	SK-N-MC	brain:	n/a
20	chr17:67192236-67192286	PFSK-1	brain:	n/a
21	chr17:67192236-67192286	T-47D	breast:	n/a
22	chr17:67192236-67192286	A549	lung:	n/a
23	chr17:67192236-67192286	AG10803	skin:	n/a
24	chr17:67192236-67192286	RPTEC	kidney:	n/a
25	chr17:67192236-67192286	U87	brain:	n/a
26	chr17:67192236-67192286	AG09319	gingival:	n/a
27	chr17:67192236-67192286	GM12878	blood:	n/a
28	chr17:67192236-67192286	HRE	kidney:	n/a
29	chr17:67192236-67192286	IMR90	lung:	fetal
30	chr17:67192236-67192286	LNCaP	prostate:	n/a
31	chr17:67192236-67192286	SK-N-SH	brain:	n/a
32	chr17:67192236-67192286	HRCEpiC	kidney:	n/a
33	chr17:67192236-67192286	GM12892	blood:	n/a
34	chr17:67192236-67192286	BE2_C	brain:	n/a
35	chr17:67192236-67192286	SK-N-SH_RA	brain:	n/a
36	chr17:67192236-67192286	PrEC	prostate:	n/a
37	chr17:67192236-67192286	Hepatocyte	liver:	n/a
38	chr17:67192236-67192286	HPAEpiC	pulmonary alveolar:	n/a
39	chr17:67192236-67192286	BJ	skin:	n/a
40	chr17:67192236-67192286	ProgFib	skin:	n/a
41	chr17:67192236-67192286	GM06990	blood:	n/a
42	chr17:67192236-67192286	HepG2	liver:	n/a
43	chr17:67192236-67192286	HUVEC	blood vessel:	n/a
44	chr17:67192236-67192286	ovcar-3	ovarian:	n/a
45	chr17:67192236-67192286	MCF10A-Er-Src	breast:	n/a
46	chr17:67192236-67192286	Hela-S3	cervix:	n/a
47	chr17:67192236-67192286	HCPEpiC	choroid plexus:	n/a
48	chr17:67192236-67192286	NH-A	brain:	n/a
49	chr17:67192236-67192286	NB4	blood:	n/a
50	chr17:67192236-67192286	AG04449	skin:	fetal

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:59858450..59859069-chr17:67181632..67182584,2	MCF-7	breast:
2	chr17:66956572..66959212-chr17:67192982..67195972,2	K562	blood:
3	chr11:113089423..113090210-chr17:67209041..67209729,2	MCF-7	breast:
4	chr17:67210361..67212344-chr17:67215371..67216914,2	K562	blood:
5	chr17:67187941..67190345-chr17:67199208..67201903,2	K562	blood:
6	chr17:67171865..67173735-chr17:67181917..67184586,2	MCF-7	breast:
7	chr17:67158951..67162432-chr17:67165135..67168064,3	MCF-7	breast:
8	chr17:67186049..67188636-chr17:67189493..67191063,2	K562	blood:
9	chr17:67176922..67179514-chr17:67180251..67183069,4	K562	blood:
10	chr17:67176730..67179192-chr17:67186322..67188052,2	K562	blood:
11	chr17:67196658..67197255-chr4:86998915..86999454,2	HCT-116	colon:
12	chr17:67176922..67179514-chr17:67180251..67183069,4	K562	blood:
13	chr17:67186049..67188636-chr17:67189493..67191063,2	K562	blood:
14	chr17:67158951..67162432-chr17:67165135..67168064,3	MCF-7	breast:
15	chr17:67164157..67165944-chr17:67167753..67170464,2	K562	blood:
16	chr17:67177313..67180145-chr17:67180462..67183327,2	K562	blood:
17	chr17:67145912..67148693-chr17:67151700..67153677,2	K562	blood:
18	chr17:67171044..67172569-chr17:67176750..67178997,2	K562	blood:
19	chr17:67176730..67179192-chr17:67186322..67188052,2	K562	blood:
20	chr17:67164157..67165944-chr17:67167753..67170464,2	K562	blood:
21	chr17:67210361..67212344-chr17:67215371..67216914,2	K562	blood:
22	chr17:67088212..67090645-chr17:67172453..67175365,2	K562	blood:
23	chr17:67187941..67190345-chr17:67199208..67201903,2	K562	blood:
24	chr17:67177313..67180145-chr17:67180462..67183327,2	K562	blood:
25	chr17:67215225..67217068-chr17:67219332..67222293,2	K562	blood:
26	chr17:67149952..67151489-chr17:67155682..67158035,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAP2K6-8	chr17:67209853-67210159	NONHSAT055573
2	lnc-MAP2K6-8	chr17:67209847-67210173	NONHSAT055572

No data

Variant related genes	Relation type
ABCA10	TF binding region
ABCA10	CpG island
ENSG00000154263	chromatin interactions

Extended variants
information (count: 2416 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2416 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8071611	chr17:67153386-67153387	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371644891	chr17:67153389-67153390	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575046662	chr17:67153405-67153406	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs542163704	chr17:67153437-67153438	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs16973672	chr17:67153450-67153451	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs183306729	chr17:67153453-67153454	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs148813419	chr17:67153570-67153571	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs187795231	chr17:67153669-67153670	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564120842	chr17:67153685-67153686	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs79889734	chr17:67153701-67153702	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs115928518	chr17:67153734-67153735	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs548889333	chr17:67153777-67153778	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs566370428	chr17:67153821-67153822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs193269239	chr17:67153835-67153836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548069995	chr17:67153876-67153877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563633002	chr17:67153924-67153925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185012995	chr17:67153956-67153957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552172163	chr17:67153962-67153963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570428014	chr17:67153969-67153970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188676205	chr17:67153978-67153979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546672733	chr17:67153998-67153999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568159861	chr17:67154040-67154041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536088886	chr17:67154056-67154057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145897708	chr17:67154101-67154102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116232229	chr17:67154129-67154130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553266101	chr17:67154131-67154132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192702672	chr17:67154152-67154153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184109195	chr17:67154252-67154253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74001828	chr17:67154319-67154320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188063265	chr17:67154329-67154330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116816755	chr17:67154336-67154337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9889366	chr17:67154396-67154397	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs542035322	chr17:67154413-67154414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563310008	chr17:67154471-67154472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191166802	chr17:67154483-67154484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552459562	chr17:67154516-67154517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564074567	chr17:67154532-67154533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528140093	chr17:67154578-67154579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546611377	chr17:67154597-67154598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183659711	chr17:67154615-67154616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368393521	chr17:67154655-67154656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190213796	chr17:67154692-67154693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569320573	chr17:67154696-67154697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28629345	chr17:67154697-67154698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138463695	chr17:67154728-67154729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573188388	chr17:67154784-67154785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557135176	chr17:67154822-67154823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141358635	chr17:67155023-67155024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555319286	chr17:67155045-67155046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528030429	chr17:67155111-67155112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Neuroblastoma	18923191	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
Chordoma	18071362	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	21523713	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21858162	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Cancer	21129771	CNVD
Congenital generalized hypertrichosis terminalis	19463983	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Gingival hyperplasia	19463983	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neuroblastoma	20406844	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Breast cancer	21045282	CNVD
Epilepsy	22083797	CNVD
Sezary syndrome	18413736	CNVD
Honadal dysgenesis	21408189	CNVD
Basal cell lymphoma	17053054	CNVD
Acute monocytic leukemia	16498392	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:67114600-67162800	Weak transcription	Brain Angular Gyrus	brain
2	chr17:67138000-67154000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr17:67138600-67155400	Weak transcription	Brain Anterior Caudate	brain
4	chr17:67138800-67162800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr17:67138800-67182000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr17:67140200-67154000	Weak transcription	Fetal Lung	lung
7	chr17:67141600-67155400	Weak transcription	Colon Smooth Muscle	Colon
8	chr17:67141800-67171800	Weak transcription	GM12878-XiMat	blood
9	chr17:67143800-67154200	Weak transcription	Right Ventricle	heart
10	chr17:67144000-67163200	Weak transcription	Left Ventricle	heart
11	chr17:67144000-67175800	Weak transcription	Gastric	stomach
12	chr17:67144000-67236000	Weak transcription	Psoas Muscle	Psoas
13	chr17:67148400-67171600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr17:67148600-67175600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr17:67148800-67190200	Weak transcription	Fetal Muscle Trunk	muscle
16	chr17:67149600-67153600	Weak transcription	Pancreas	Pancrea
17	chr17:67150200-67174400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr17:67150600-67166800	Weak transcription	Adipose Nuclei	Adipose
19	chr17:67150800-67153400	Weak transcription	Ovary	ovary
20	chr17:67150800-67192400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr17:67150800-67193200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr17:67151400-67169200	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr17:67151600-67178000	Weak transcription	Liver	Liver
24	chr17:67153400-67153800	Strong transcription	Ovary	ovary
25	chr17:67153600-67153800	ZNF genes & repeats	Pancreas	Pancrea
26	chr17:67153800-67154200	Weak transcription	Pancreas	Pancrea
27	chr17:67153800-67163000	Weak transcription	Ovary	ovary
28	chr17:67158000-67158600	Enhancers	Hela-S3	cervix
29	chr17:67160600-67220000	Weak transcription	Fetal Lung	lung
30	chr17:67162800-67163000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr17:67162800-67163000	Enhancers	Brain Angular Gyrus	brain
32	chr17:67163000-67163400	Strong transcription	Ovary	ovary
33	chr17:67163000-67169200	Weak transcription	Brain Angular Gyrus	brain
34	chr17:67163200-67163400	Enhancers	Left Ventricle	heart
35	chr17:67163200-67163400	Enhancers	Right Atrium	heart
36	chr17:67163400-67174200	Weak transcription	Ovary	ovary
37	chr17:67163400-67181200	Weak transcription	Left Ventricle	heart
38	chr17:67165800-67166600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr17:67166000-67166200	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr17:67166000-67167000	Enhancers	Primary hematopoietic stem cells	blood
41	chr17:67166000-67167600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr17:67166000-67168600	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr17:67166000-67169600	Enhancers	K562	blood
44	chr17:67166200-67167200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr17:67166200-67167400	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr17:67166400-67167000	Enhancers	HUVEC	blood vessel
47	chr17:67166400-67167200	Enhancers	Primary B cells from cord blood	blood
48	chr17:67166600-67167200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr17:67166800-67167200	Enhancers	Adipose Nuclei	Adipose
50	chr17:67167000-67171400	Weak transcription	HUVEC	blood vessel

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