Variant report

Variant	esv1802470
Chromosome Location	chr17:15976558-16004368
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:190)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:190 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr17:15995089-15995466	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr17:15995090-15995456	K562	blood:	n/a	n/a
3	BATF	chr17:15990257-15990528	GM12878	blood:	n/a	n/a
4	BHLHE40	chr17:15990365-15990449	GM12878	blood:	n/a	n/a
5	CBX3	chr17:15995175-15995382	K562	blood:	n/a	n/a
6	CBX3	chr17:15984887-15985173	K562	blood:	n/a	n/a
7	CCNT2	chr17:15992643-15992843	K562	blood:	n/a	n/a
8	CEBPB	chr17:15979277-15979646	HepG2	liver:	n/a	chr17:15979463-15979474
9	CEBPB	chr17:15979288-15979647	IMR90	lung:	n/a	chr17:15979463-15979474
10	CEBPB	chr17:15991998-15992145	A549	lung:	n/a	n/a
11	CEBPB	chr17:15979290-15979645	Hela-S3	cervix:	n/a	chr17:15979463-15979474
12	CEBPB	chr17:15979276-15979642	A549	lung:	n/a	chr17:15979463-15979474
13	CEBPB	chr17:15979148-15979711	A549	lung:	n/a	chr17:15979463-15979474
14	CEBPB	chr17:15979293-15979632	H1-hESC	embryonic stem cell:	n/a	chr17:15979463-15979474
15	CEBPB	chr17:15988407-15988944	IMR90	lung:	n/a	n/a
16	CEBPB	chr17:15979281-15979649	K562	blood:	n/a	chr17:15979463-15979474
17	CHD2	chr17:15990452-15990454	GM12878	blood:	n/a	n/a
18	CTCF	chr17:16004171-16004363	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr17:16004140-16004290	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr17:16004200-16004350	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr17:16004160-16004310	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr17:16004180-16004330	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr17:16004140-16004290	HCT-116	colon:	n/a	n/a
24	CTCF	chr17:16004260-16004410	BJ	skin:	n/a	n/a
25	CTCF	chr17:16004180-16004330	AG09309	skin:	n/a	n/a
26	CTCF	chr17:16004140-16004290	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr17:16004220-16004370	HCM	heart:	n/a	n/a
28	CTCF	chr17:16004176-16004290	MCF-7	breast:	n/a	n/a
29	CTCF	chr17:16004161-16004303	HepG2	liver:	n/a	n/a
30	CTCF	chr17:16004137-16004393	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr17:16004200-16004244	GM19238	blood:	n/a	n/a
32	CTCF	chr17:16004186-16004252	GM12891	blood:	n/a	n/a
33	CTCF	chr17:16004183-16004258	MCF-7	breast:	n/a	n/a
34	CTCF	chr17:16004171-16004341	GM12878	blood:	n/a	n/a
35	CTCF	chr17:16004200-16004350	HCFaa	heart:	n/a	n/a
36	CTCF	chr17:16004137-16004338	Gliobla	brain:	n/a	n/a
37	CTCF	chr17:16004140-16004290	AG04450	lung:	n/a	n/a
38	CTCF	chr17:16004140-16004290	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr17:16004140-16004290	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr17:16004100-16004250	HVMF	connective:	n/a	n/a
41	CTCF	chr17:16004220-16004370	HVMF	connective:	n/a	n/a
42	CTCF	chr17:16004120-16004270	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr17:16004200-16004350	GM12873	blood:	n/a	n/a
44	CTCF	chr17:16004160-16004310	HepG2	liver:	n/a	n/a
45	CTCF	chr17:16004140-16004290	AG04449	skin:	n/a	n/a
46	CTCF	chr17:16004180-16004330	AG04450	lung:	n/a	n/a
47	CTCF	chr17:16004260-16004410	NHEK	skin:	n/a	n/a
48	CTCF	chr17:16004160-16004310	BE2_C	brain:	n/a	n/a
49	CTCF	chr17:16004257-16004277	GM13977	blood:	n/a	n/a
50	CTCF	chr17:16004140-16004290	AG10803	skin:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:15978459..15981234-chr17:15984249..15986179,2	K562	blood:
2	chr17:15978459..15981234-chr17:15984249..15986179,2	K562	blood:
3	chr17:15976524..15978868-chr17:15991864..15993766,2	K562	blood:
4	chr17:15976524..15978868-chr17:15991864..15993766,2	K562	blood:
5	chr17:15987048..15989365-chr17:16117375..16120147,2	MCF-7	breast:
6	chr17:15972800..15974994-chr17:15979206..15981179,2	MCF-7	breast:
7	chr17:15979525..15982244-chr17:16118246..16120149,2	K562	blood:
8	chr17:15968719..15971375-chr17:15978183..15980041,2	K562	blood:
9	chr17:15992643..15994988-chr17:16118980..16121101,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC19-1	chr17:15987356-15987695	NONHSAT145891

No data

Variant related genes	Relation type
NCOR1	TF binding region
RNU6-314P	TF binding region
ENSG00000233979	TF binding region
ENSG00000141027	chromatin interactions
ENSG00000108474	chromatin interactions

Extended variants
information (count: 975 )
Associated
traits (count: 170 )

Variant overlapped rSNPs/rCNVs (count:975 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9891379	chr17:15976558-15976559	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544949973	chr17:15976595-15976596	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564666943	chr17:15976644-15976645	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117087658	chr17:15976696-15976697	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375947365	chr17:15976705-15976706	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181571624	chr17:15976715-15976716	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201608686	chr17:15976718-15976719	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560337998	chr17:15976735-15976736	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143500271	chr17:15976750-15976751	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150518868	chr17:15976755-15976756	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146528543	chr17:15976776-15976777	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200471424	chr17:15976786-15976787	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369440540	chr17:15976793-15976794	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372678215	chr17:15976814-15976815	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140879242	chr17:15976822-15976823	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375656232	chr17:15976830-15976831	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139458532	chr17:15976868-15976869	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs199584699	chr17:15976876-15976877	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370039161	chr17:15976887-15976888	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373502975	chr17:15976892-15976893	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201847462	chr17:15976915-15976916	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539204015	chr17:15976916-15976917	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186298264	chr17:15976923-15976924	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs201596454	chr17:15976924-15976925	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535573750	chr17:15976962-15976963	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11078330	chr17:15977005-15977006	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs527646053	chr17:15977019-15977020	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9896441	chr17:15977043-15977044	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs59543390	chr17:15977107-15977108	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs9898313	chr17:15977132-15977133	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs540801775	chr17:15977138-15977139	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191262092	chr17:15977162-15977163	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs118023219	chr17:15977214-15977215	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73981436	chr17:15977238-15977239	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs150140541	chr17:15977291-15977292	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145543067	chr17:15977304-15977305	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556362684	chr17:15977319-15977320	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556689731	chr17:15977323-15977324	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs117942956	chr17:15977399-15977400	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11655793	chr17:15977411-15977412	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564014554	chr17:15977433-15977434	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12946478	chr17:15977444-15977445	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377147116	chr17:15977479-15977480	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148958626	chr17:15977480-15977481	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182672188	chr17:15977559-15977560	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566688411	chr17:15977580-15977581	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541846289	chr17:15977622-15977623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372437398	chr17:15977630-15977631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370264745	chr17:15977631-15977632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562109476	chr17:15977657-15977658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:170)

Disease	PMID	Source
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
Melanoma	18172304	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
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
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD

Chromatin state (count:1128 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15905200-15986400	Strong transcription	Primary T helper cells fromperipheralblood	blood
2	chr17:15913800-15990800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr17:15915400-15998000	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr17:15921000-15991000	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr17:15921000-15991200	Strong transcription	Primary B cells from peripheral blood	blood
6	chr17:15923800-15998000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr17:15926800-15985400	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr17:15926800-15987600	Strong transcription	Rectal Mucosa Donor 29	rectum
9	chr17:15927800-15987800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr17:15931800-15988800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr17:15940000-15980600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr17:15942000-15985000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr17:15944800-15991000	Strong transcription	Fetal Intestine Large	intestine
14	chr17:15948200-15978800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr17:15953800-15988400	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr17:15954000-15986000	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr17:15954200-15985400	Strong transcription	Duodenum Mucosa	Duodenum
18	chr17:15955800-15982200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr17:15955800-15985400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr17:15955800-15985400	Strong transcription	Primary B cells from cord blood	blood
21	chr17:15955800-15985600	Strong transcription	Dnd41	blood
22	chr17:15955800-15990600	Strong transcription	Fetal Thymus	thymus
23	chr17:15956200-15985400	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr17:15956400-15984000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr17:15956400-15985600	Strong transcription	Adipose Nuclei	Adipose
26	chr17:15956400-15990800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr17:15956800-15979600	Strong transcription	Primary hematopoietic stem cells	blood
28	chr17:15957000-15985400	Strong transcription	Liver	Liver
29	chr17:15957400-15988200	Strong transcription	Primary T cells from cord blood	blood
30	chr17:15957400-15990600	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr17:15957600-15979200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr17:15957600-15980600	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr17:15957600-15986400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr17:15957600-15988400	Strong transcription	A549	lung
35	chr17:15958000-15984000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr17:15958000-15991000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr17:15958200-15988000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr17:15958400-15985000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr17:15958400-15985600	Strong transcription	GM12878-XiMat	blood
40	chr17:15958800-15985800	Strong transcription	Osteobl	bone
41	chr17:15959200-15981400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr17:15959200-15984800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr17:15960000-15985400	Strong transcription	NH-A	brain
44	chr17:15960200-15979400	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr17:15961600-15995000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr17:15962800-15984000	Strong transcription	HepG2	liver
47	chr17:15963000-15985200	Strong transcription	HUES48 Cell Line	embryonic stem cell
48	chr17:15963000-15985400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr17:15964200-15984000	Strong transcription	Skeletal Muscle Female	skeletal muscle
50	chr17:15964400-15984000	Strong transcription	H1 Cell Line	embryonic stem cell

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