Variant report

Variant	nsv960117
Chromosome Location	chr17:45257797-45260714
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:152)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:152 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr17:45258767-45259157	K562	blood:	n/a	n/a
2	BCL3	chr17:45258765-45259050	GM12878	blood:	n/a	n/a
3	BHLHE40	chr17:45258767-45259159	K562	blood:	n/a	n/a
4	BRCA1	chr17:45258767-45259155	GM12878	blood:	n/a	n/a
5	CEBPB	chr17:45258766-45259309	K562	blood:	n/a	n/a
6	CHD2	chr17:45258767-45259156	K562	blood:	n/a	n/a
7	CHD2	chr17:45258764-45259152	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr17:45258957-45258997	Kidney_OC	kidney:	n/a	n/a
9	CTCF	chr17:45258840-45258990	HRPEpiC	eye:	n/a	n/a
10	CTCF	chr17:45258920-45259070	K562	blood:	n/a	n/a
11	CTCF	chr17:45258820-45258970	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr17:45258820-45258970	BJ	skin:	n/a	n/a
13	CTCF	chr17:45258840-45258990	GM12865	blood:	n/a	n/a
14	CTCF	chr17:45258880-45259030	HMF	breast:	n/a	n/a
15	CTCF	chr17:45258920-45259070	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr17:45258960-45259110	AG09319	gingival:	n/a	n/a
17	CTCF	chr17:45258920-45259070	AG09319	gingival:	n/a	n/a
18	CTCF	chr17:45258900-45259050	AG04449	skin:	n/a	n/a
19	CTCF	chr17:45258895-45259070	Fibrobl	skin:	n/a	n/a
20	CTCF	chr17:45258940-45259090	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr17:45258911-45259036	MCF-7	breast:	n/a	n/a
22	CTCF	chr17:45258820-45258970	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr17:45258860-45259010	WI-38	lung:	n/a	n/a
24	CTCF	chr17:45258860-45259010	GM12868	blood:	n/a	n/a
25	CTCF	chr17:45258932-45259065	GM12892	blood:	n/a	n/a
26	CTCF	chr17:45258860-45259010	GM12869	blood:	n/a	n/a
27	CTCF	chr17:45258887-45259100	MCF-7	breast:	n/a	n/a
28	CTCF	chr17:45258820-45258970	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr17:45258907-45258997	GM20000	blood:	n/a	n/a
30	CTCF	chr17:45258860-45259010	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr17:45258900-45259050	GM12869	blood:	n/a	n/a
32	CTCF	chr17:45258860-45259010	GM12866	blood:	n/a	n/a
33	CTCF	chr17:45258900-45259050	HEK293	kidney:	n/a	n/a
34	CTCF	chr17:45258933-45259039	GM19240	blood:	n/a	n/a
35	CTCF	chr17:45258840-45258990	GM12875	blood:	n/a	n/a
36	CTCF	chr17:45258840-45258990	HCFaa	heart:	n/a	n/a
37	CTCF	chr17:45258880-45259030	RPTEC	kidney:	n/a	n/a
38	CTCF	chr17:45258820-45258970	GM12875	blood:	n/a	n/a
39	CTCF	chr17:45258900-45259050	HL-60	blood:	n/a	n/a
40	CTCF	chr17:45258947-45258986	GM10248	blood:	n/a	n/a
41	CTCF	chr17:45258932-45259071	GM12891	blood:	n/a	n/a
42	CTCF	chr17:45258846-45259098	ProgFib	skin:	n/a	n/a
43	CTCF	chr17:45258860-45259010	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr17:45258860-45259010	GM12871	blood:	n/a	n/a
45	CTCF	chr17:45258930-45259002	GM13976	blood:	n/a	n/a
46	CTCF	chr17:45258860-45259010	GM12870	blood:	n/a	n/a
47	CTCF	chr17:45258840-45258990	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr17:45258951-45258973	GM13977	blood:	n/a	n/a
49	CTCF	chr17:45258920-45259052	Gliobla	brain:	n/a	n/a
50	CTCF	chr17:45258860-45259010	AG04450	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45258206-45258256	Jurkat	blood:	n/a
2	chr17:45258206-45258256	PANC-1	pancreas:	n/a
3	chr17:45258206-45258256	AG09319	gingival:	n/a
4	chr17:45258206-45258256	HepG2	liver:	n/a
5	chr17:45258206-45258256	HCT-116	colon:	n/a
6	chr17:45258206-45258256	ECC-1	luminal epithelium:	n/a
7	chr17:45258206-45258256	HRCEpiC	kidney:	n/a
8	chr17:45258206-45258256	MCF10A-Er-Src	breast:	n/a
9	chr17:45258206-45258256	GM12891	blood:	n/a
10	chr17:45258206-45258256	HRE	kidney:	n/a
11	chr17:45258206-45258256	LNCaP	prostate:	n/a
12	chr17:45258206-45258256	Caco-2	colon:	n/a
13	chr17:45258206-45258256	NHDF-neo	bronchial:	n/a
14	chr17:45258206-45258256	HCM	heart:	n/a
15	chr17:45258206-45258256	BE2_C	brain:	n/a
16	chr17:45258206-45258256	AoSMC	blood vessel:	n/a
17	chr17:45258206-45258256	GM19239	blood:	n/a
18	chr17:45258206-45258256	ovcar-3	ovarian:	n/a
19	chr17:45258206-45258256	PrEC	prostate:	n/a
20	chr17:45258206-45258256	HL-60	blood:	n/a
21	chr17:45258206-45258256	HAEpiC	amniotic membrane:	n/a
22	chr17:45258206-45258256	SAEC	small airway:	n/a
23	chr17:45258206-45258256	K562	blood:	n/a
24	chr17:45258206-45258256	HPAEpiC	pulmonary alveolar:	n/a
25	chr17:45258206-45258256	ProgFib	skin:	n/a
26	chr17:45258206-45258256	BJ	skin:	n/a
27	chr17:45258206-45258256	HEK293	kidney:	embryo
28	chr17:45258206-45258256	NT2-D1	testis:	n/a
29	chr17:45258206-45258256	HMEC	breast:	n/a
30	chr17:45258206-45258256	GM12892	blood:	n/a
31	chr17:45258206-45258256	A549	lung:	n/a
32	chr17:45258206-45258256	NHBE	bronchial:	n/a
33	chr17:45258206-45258256	Hepatocyte	liver:	n/a
34	chr17:45258206-45258256	SK-N-SH	brain:	n/a
35	chr17:45258206-45258256	NB4	blood:	n/a
36	chr17:45258206-45258256	PFSK-1	brain:	n/a
37	chr17:45258206-45258256	CMK	blood:	n/a
38	chr17:45258206-45258256	T-47D	breast:	n/a
39	chr17:45258206-45258256	NH-A	brain:	n/a
40	chr17:45258206-45258256	GM12878	blood:	n/a
41	chr17:45258206-45258256	SK-N-MC	brain:	n/a
42	chr17:45258206-45258256	SKMC	muscle:	n/a
43	chr17:45258206-45258256	IMR90	lung:	fetal
44	chr17:45258206-45258256	Hela-S3	cervix:	n/a
45	chr17:45258206-45258256	HIPEpiC	eye:	n/a
46	chr17:45258206-45258256	GM06990	blood:	n/a
47	chr17:45258206-45258256	AG09309	skin:	n/a
48	chr17:45258206-45258256	U87	brain:	n/a
49	chr17:45258206-45258256	MCF-7	breast:	n/a
50	chr17:45258206-45258256	HUVEC	blood vessel:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45257003..45258810-chr17:45262193..45263942,2	MCF-7	breast:
2	chr17:45230648..45232405-chr17:45259040..45262576,3	K562	blood:
3	chr17:45259720..45263817-chr17:45399412..45402337,5	K562	blood:
4	chr17:45256968..45259015-chr17:45265544..45267226,2	MCF-7	breast:
5	chr17:45260373..45262889-chr17:45263866..45266203,2	MCF-7	breast:
6	chr17:45213650..45214313-chr17:45258453..45258970,2	MCF-7	breast:
7	chr17:45257479..45260473-chr2:133018355..133021074,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPRML-7	chr17:45258648-45259003	NONHSAT054290

No data

Variant related genes	Relation type
CDC27	TF binding region
CDC27	CpG island
ENSG00000004897	chromatin interactions
ENSG00000233786	chromatin interactions
ENSG00000178852	chromatin interactions
ENSG00000263293	chromatin interactions

Extended variants
information (count: 116 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:116 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533284293	chr17:45257815-45257816	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs78095535	chr17:45257845-45257846	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs546975079	chr17:45257882-45257883	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs183086580	chr17:45257965-45257966	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs536153857	chr17:45258006-45258007	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs574238352	chr17:45258051-45258052	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138623180	chr17:45258057-45258058	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs569328695	chr17:45258058-45258059	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs149334649	chr17:45258081-45258082	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs558083460	chr17:45258115-45258116	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs60574276	chr17:45258128-45258129	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs61502164	chr17:45258146-45258147	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs144545702	chr17:45258237-45258238	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs34350181	chr17:45258266-45258267	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs117745151	chr17:45258278-45258279	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs186256637	chr17:45258279-45258280	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs58151287	chr17:45258283-45258284	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs9904549	chr17:45258309-45258310	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs34061862	chr17:45258311-45258312	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs137988196	chr17:45258312-45258313	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs201397588	chr17:45258336-45258337	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs9905595	chr17:45258337-45258338	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs572543432	chr17:45258353-45258354	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs148462470	chr17:45258393-45258394	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs71375397	chr17:45258398-45258399	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs190374473	chr17:45258420-45258421	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs530738805	chr17:45258435-45258436	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs71375398	chr17:45258449-45258450	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs71375399	chr17:45258451-45258452	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs542120720	chr17:45258455-45258456	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs11871023	chr17:45258481-45258482	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs544364019	chr17:45258531-45258532	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs2905371	chr17:45258554-45258555	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs12936578	chr17:45258572-45258573	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs544698743	chr17:45258580-45258581	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs552740004	chr17:45258621-45258622	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs34104273	chr17:45258652-45258653	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs368926843	chr17:45258660-45258661	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs372949976	chr17:45258663-45258664	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs370953694	chr17:45258670-45258671	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs71365050	chr17:45258672-45258673	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs575218423	chr17:45258677-45258678	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs545508313	chr17:45258718-45258719	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs376297134	chr17:45258723-45258724	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs183810492	chr17:45258738-45258739	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs376119729	chr17:45258764-45258765	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs9909538	chr17:45258781-45258782	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs9909569	chr17:45258818-45258819	ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Enhancers Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs11570463	chr17:45258867-45258868	ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Enhancers Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs368256588	chr17:45258880-45258881	ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Enhancers Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	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
Breast cancer	21858162	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
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	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
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	17142309	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45249600-45258400	Weak transcription	Left Ventricle	heart
2	chr17:45249600-45258400	Strong transcription	Dnd41	blood
3	chr17:45249600-45258800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr17:45249600-45258800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr17:45249600-45258800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr17:45249600-45258800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr17:45249600-45258800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr17:45249600-45258800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr17:45249600-45258800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr17:45249600-45258800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr17:45249600-45258800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr17:45249600-45258800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr17:45249600-45258800	Weak transcription	Aorta	Aorta
14	chr17:45249600-45258800	Weak transcription	Brain Cingulate Gyrus	brain
15	chr17:45249600-45258800	Weak transcription	Brain Hippocampus Middle	brain
16	chr17:45249600-45258800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr17:45249600-45258800	Weak transcription	Brain Substantia Nigra	brain
18	chr17:45249600-45258800	Weak transcription	Colonic Mucosa	Colon
19	chr17:45249600-45258800	Weak transcription	Esophagus	oesophagus
20	chr17:45249600-45258800	Weak transcription	Fetal Brain Male	brain
21	chr17:45249600-45258800	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr17:45249600-45258800	Weak transcription	Gastric	stomach
23	chr17:45249600-45258800	Weak transcription	Pancreas	Pancrea
24	chr17:45249600-45258800	Weak transcription	Psoas Muscle	Psoas
25	chr17:45249600-45258800	Weak transcription	Right Atrium	heart
26	chr17:45249600-45258800	Weak transcription	Small Intestine	intestine
27	chr17:45249600-45258800	Weak transcription	Stomach Mucosa	stomach
28	chr17:45249800-45258800	Strong transcription	Fetal Thymus	thymus
29	chr17:45250000-45258800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr17:45250200-45258200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr17:45250200-45258400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr17:45250200-45258800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr17:45250400-45258400	Strong transcription	A549	lung
34	chr17:45250400-45258800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr17:45250400-45258800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr17:45250800-45258400	Strong transcription	HSMM	muscle
37	chr17:45251000-45258200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr17:45251000-45258400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr17:45251000-45258400	Strong transcription	Muscle Satellite Cultured Cells	--
40	chr17:45251200-45257800	Strong transcription	Adipose Nuclei	Adipose
41	chr17:45251200-45258000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr17:45251200-45258800	Strong transcription	Fetal Stomach	stomach
43	chr17:45251200-45259200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr17:45251200-45260600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr17:45251400-45257800	Strong transcription	Liver	Liver
46	chr17:45251600-45258800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr17:45251800-45258800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr17:45252400-45258000	Strong transcription	HUES64 Cell Line	embryonic stem cell
49	chr17:45252400-45258000	Strong transcription	Fetal Muscle Trunk	muscle
50	chr17:45252400-45258200	Strong transcription	NHDF-Ad	bronchial

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