Variant report

Variant	nsv433034
Chromosome Location	chr7:17021242-17135544
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1521)
CpG islands
(count:184)
Chromatin interactive
region (count:60)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1521 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:17022256-17022689	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:17059850-17060284	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:17126123-17126528	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:17056009-17056632	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:17029437-17030037	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:17102713-17102938	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:17060687-17061303	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:17124870-17125152	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:17048886-17048952	K562	blood:	n/a	n/a
10	ATF1	chr7:17081104-17081304	K562	blood:	n/a	n/a
11	ATF1	chr7:17078025-17078124	K562	blood:	n/a	n/a
12	ATF1	chr7:17025470-17025636	K562	blood:	n/a	n/a
13	ATF2	chr7:17109742-17110279	GM12878	blood:	n/a	n/a
14	ATF2	chr7:17111460-17111967	GM12878	blood:	n/a	n/a
15	ATF2	chr7:17111490-17111921	GM12878	blood:	n/a	n/a
16	ATF2	chr7:17109647-17110319	GM12878	blood:	n/a	n/a
17	ATF3	chr7:17029447-17030026	A549	lung:	n/a	n/a
18	ATF3	chr7:17029365-17029942	A549	lung:	n/a	n/a
19	BATF	chr7:17111530-17111902	GM12878	blood:	n/a	n/a
20	BATF	chr7:17108761-17109164	GM12878	blood:	n/a	chr7:17108972-17108983
21	BATF	chr7:17098268-17098529	GM12878	blood:	n/a	chr7:17098354-17098365 chr7:17098355-17098365
22	BATF	chr7:17098279-17098524	GM12878	blood:	n/a	chr7:17098354-17098365 chr7:17098355-17098365
23	BATF	chr7:17062519-17062729	GM12878	blood:	n/a	n/a
24	BATF	chr7:17111485-17111873	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:17111507-17111882	GM12878	blood:	n/a	chr7:17111753-17111762
26	BCL3	chr7:17108755-17109162	GM12878	blood:	n/a	n/a
27	BCL3	chr7:17029345-17030062	A549	lung:	n/a	n/a
28	BCL3	chr7:17029246-17030035	A549	lung:	n/a	n/a
29	BCLAF1	chr7:17111458-17111890	GM12878	blood:	n/a	chr7:17111753-17111762
30	BCLAF1	chr7:17022216-17022582	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:17111784-17111876	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:17109582-17110082	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:17108919-17109119	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:17029520-17029978	HepG2	liver:	n/a	n/a
35	BRCA1	chr7:17048757-17048831	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr7:17081999-17082268	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr7:17080965-17081277	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr7:17022293-17022592	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr7:17029517-17029912	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr7:17134375-17135095	Hela-S3	cervix:	n/a	n/a
41	CCNT2	chr7:17059330-17059498	K562	blood:	n/a	n/a
42	CEBPB	chr7:17034532-17035264	A549	lung:	n/a	chr7:17034680-17034691 chr7:17035115-17035126
43	CEBPB	chr7:17029392-17030006	A549	lung:	n/a	n/a
44	CEBPB	chr7:17081016-17081269	A549	lung:	n/a	n/a
45	CEBPB	chr7:17082629-17082912	A549	lung:	n/a	n/a
46	CEBPB	chr7:17130491-17130731	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:17067095-17067292	HepG2	liver:	n/a	chr7:17067206-17067217
48	CEBPB	chr7:17088207-17088473	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:17110210-17110278	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:17080984-17081208	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:17029795-17029845	MCF-7	breast:	n/a
2	chr7:17029795-17029845	MCF-7	breast:	n/a
3	chr7:17029795-17029845	HEEpiC	esophagus:	n/a
4	chr7:17081421-17081471	HEK293	kidney:	embryo
5	chr7:17055230-17055280	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:17029795-17029845	A549	lung:	n/a
7	chr7:17055230-17055280	AG10803	skin:	n/a
8	chr7:17029795-17029845	PANC-1	pancreas:	n/a
9	chr7:17029795-17029845	GM19239	blood:	n/a
10	chr7:17055230-17055280	HepG2	liver:	n/a
11	chr7:17029795-17029845	HAEpiC	amniotic membrane:	n/a
12	chr7:17081421-17081471	NT2-D1	testis:	n/a
13	chr7:17081421-17081471	GM06990	blood:	n/a
14	chr7:17081421-17081471	GM19239	blood:	n/a
15	chr7:17029795-17029845	ProgFib	skin:	n/a
16	chr7:17081421-17081471	HNPCEpiC	eye:	n/a
17	chr7:17029795-17029845	NHBE	bronchial:	n/a
18	chr7:17029795-17029845	AG09319	gingival:	n/a
19	chr7:17081421-17081471	HL-60	blood:	n/a
20	chr7:17081421-17081471	A549	lung:	n/a
21	chr7:17055230-17055280	GM06990	blood:	n/a
22	chr7:17029795-17029845	HIPEpiC	eye:	n/a
23	chr7:17081421-17081471	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:17055230-17055280	NHDF-neo	bronchial:	n/a
25	chr7:17055230-17055280	A549	lung:	n/a
26	chr7:17081421-17081471	Jurkat	blood:	n/a
27	chr7:17081421-17081471	ECC-1	luminal epithelium:	n/a
28	chr7:17081421-17081471	HCM	heart:	n/a
29	chr7:17055230-17055280	NH-A	brain:	n/a
30	chr7:17055230-17055280	Hepatocyte	liver:	n/a
31	chr7:17055230-17055280	MCF-7	breast:	n/a
32	chr7:17029795-17029845	Jurkat	blood:	n/a
33	chr7:17055230-17055280	Jurkat	blood:	n/a
34	chr7:17055230-17055280	HCF	heart:	n/a
35	chr7:17029795-17029845	GM12878	blood:	n/a
36	chr7:17055230-17055280	AG09319	gingival:	n/a
37	chr7:17029795-17029845	AG04449	skin:	fetal
38	chr7:17029795-17029845	BE2_C	brain:	n/a
39	chr7:17055230-17055280	NHBE	bronchial:	n/a
40	chr7:17081421-17081471	HIPEpiC	eye:	n/a
41	chr7:17029795-17029845	HRPEpiC	eye:	n/a
42	chr7:17029795-17029845	HCT-116	colon:	n/a
43	chr7:17029795-17029845	HMEC	breast:	n/a
44	chr7:17029795-17029845	NHDF-neo	bronchial:	n/a
45	chr7:17081421-17081471	HCF	heart:	n/a
46	chr7:17055230-17055280	HRE	kidney:	n/a
47	chr7:17029795-17029845	SAEC	small airway:	n/a
48	chr7:17081421-17081471	BE2_C	brain:	n/a
49	chr7:17081421-17081471	NB4	blood:	n/a
50	chr7:17081421-17081471	MCF10A-Er-Src	breast:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:16973446..16975003-chr7:17029206..17031058,2	MCF-7	breast:
2	chr7:17031300..17033743-chr7:17037382..17039290,2	MCF-7	breast:
3	chr7:17100496..17103422-chr7:17133231..17136201,2	MCF-7	breast:
4	chr7:17132686..17134514-chr7:17337406..17339797,2	MCF-7	breast:
5	chr7:17028983..17030992-chr7:17046440..17048706,2	MCF-7	breast:
6	chr7:17074027..17076854-chr7:17079702..17081342,2	K562	blood:
7	chr7:17117134..17118847-chr7:17125152..17127998,2	MCF-7	breast:
8	chr7:17095846..17098605-chr7:17101734..17104493,2	MCF-7	breast:
9	chr7:17022288..17022890-chr7:17340797..17341678,2	MCF-7	breast:
10	chr7:17040567..17043366-chr7:17054083..17055908,2	K562	blood:
11	chr7:17028907..17031240-chr7:17033861..17036771,2	MCF-7	breast:
12	chr7:17102519..17103019-chr7:17570516..17571366,2	MCF-7	breast:
13	chr7:17115671..17117289-chr7:17121951..17124476,2	K562	blood:
14	chr7:17079412..17081235-chr7:17083345..17084902,2	K562	blood:
15	chr7:17019593..17021865-chr7:17036928..17039185,2	MCF-7	breast:
16	chr7:17101013..17102818-chr7:17107864..17110439,2	MCF-7	breast:
17	chr7:17108384..17110452-chr7:17112989..17115073,2	MCF-7	breast:
18	chr7:17112512..17114354-chr7:17120399..17122441,2	MCF-7	breast:
19	chr7:17048460..17049301-chr7:17197592..17198341,2	MCF-7	breast:
20	chr7:17048036..17050899-chr7:17337557..17339706,3	MCF-7	breast:
21	chr7:17101013..17102818-chr7:17107864..17110439,2	MCF-7	breast:
22	chr7:17082436..17084513-chr7:17337542..17339848,2	MCF-7	breast:
23	chr7:17017060..17018874-chr7:17032172..17033946,2	K562	blood:
24	chr7:17115671..17117289-chr7:17121951..17124476,2	K562	blood:
25	chr7:17060484..17062454-chr7:17134581..17136153,2	MCF-7	breast:
26	chr7:17050581..17052320-chr7:17054806..17056954,2	MCF-7	breast:
27	chr7:17028983..17030992-chr7:17046440..17048706,2	MCF-7	breast:
28	chr7:17043705..17046242-chr7:17047852..17050297,2	K562	blood:
29	chr7:17031300..17033743-chr7:17037382..17039290,2	MCF-7	breast:
30	chr7:17059828..17063648-chr7:17339289..17342084,4	MCF-7	breast:
31	chr7:17022497..17024169-chr7:17337462..17339700,2	MCF-7	breast:
32	chr7:17021642..17024426-chr7:17028854..17030510,2	MCF-7	breast:
33	chr7:17108384..17110452-chr7:17112989..17115073,2	MCF-7	breast:
34	chr7:17019593..17021865-chr7:17036928..17039185,2	MCF-7	breast:
35	chr7:17022004..17022890-chr7:17197303..17198260,4	MCF-7	breast:
36	chr7:17043705..17046242-chr7:17047852..17050297,2	K562	blood:
37	chr7:17102437..17103359-chr7:17340354..17341360,3	MCF-7	breast:
38	chr7:17112512..17114354-chr7:17120399..17122441,2	MCF-7	breast:
39	chr7:17117134..17118847-chr7:17125152..17127998,2	MCF-7	breast:
40	chr7:17079412..17081235-chr7:17083345..17084902,2	K562	blood:
41	chr7:17095846..17098605-chr7:17101734..17104493,2	MCF-7	breast:
42	chr7:17022402..17022926-chr7:17341282..17342277,2	MCF-7	breast:
43	chr7:17022092..17022805-chr7:17340854..17341791,2	K562	blood:
44	chr7:17082649..17084895-chr7:17336676..17339527,2	MCF-7	breast:
45	chr7:17101748..17103793-chr7:17132668..17134988,2	MCF-7	breast:
46	chr7:17032617..17034774-chr7:17337906..17339660,2	MCF-7	breast:
47	chr7:17069681..17071851-chr7:17337146..17339702,2	MCF-7	breast:
48	chr7:17100496..17103422-chr7:17133231..17136201,2	MCF-7	breast:
49	chr7:17101748..17103793-chr7:17132668..17134988,2	MCF-7	breast:
50	chr7:17024574..17026803-chr7:17338054..17340044,3	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN13-3	chr7:17060974-17061188	NONHSAT119311
2	lnc-AGR3-4	chr7:17072713-17073102	NONHSAT119313
3	lnc-TSPAN13-3	chr7:17060901-17061251	NONHSAT119312
4	lnc-TSPAN13-3	chr7:17059892-17060086	NONHSAT119311
5	lnc-AHR-5	chr7:17120222-17122197	NONHSAT119316
6	lnc-AHR-6	chr7:17092504-17093105	NONHSAT119314
7	lnc-AHR-2	chr7:17105864-17105946	XLOC_005997
8	lnc-TSPAN13-3	chr7:17059793-17060635	NONHSAT119312
9	lnc-AHR-2	chr7:17133141-17133395	XLOC_005997
10	lnc-TSPAN13-3	chr7:17029804-17030051	NONHSAT119311

No data

Variant related genes	Relation type
ENSG00000232841	TF binding region
ENSG00000232841	CpG island
ENSG00000237773	chromatin interactions
ENSG00000106546	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000228675	chromatin interactions

Extended variants
information (count: 4622 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4622 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs847436	chr7:17021242-17021243	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75553570	chr7:17021258-17021259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371634895	chr7:17021274-17021275	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs182350810	chr7:17021313-17021314	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548946475	chr7:17021314-17021315	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567359609	chr7:17021321-17021322	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530847204	chr7:17021358-17021359	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs556287409	chr7:17021389-17021390	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs571652003	chr7:17021390-17021391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs847435	chr7:17021434-17021435	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs557680492	chr7:17021438-17021439	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573061057	chr7:17021469-17021470	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs548888897	chr7:17021502-17021503	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540560533	chr7:17021516-17021517	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs555385918	chr7:17021573-17021574	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs568497198	chr7:17021621-17021622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573719466	chr7:17021657-17021658	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544319338	chr7:17021713-17021714	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs186926104	chr7:17021722-17021723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191351838	chr7:17021810-17021811	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369966769	chr7:17021841-17021842	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs141680323	chr7:17021857-17021858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs146011437	chr7:17021866-17021867	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs527974232	chr7:17021880-17021881	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112054007	chr7:17021909-17021910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567320487	chr7:17021928-17021929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531553827	chr7:17021947-17021948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549770181	chr7:17021994-17021995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10260321	chr7:17021999-17022000	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs547442112	chr7:17022002-17022003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570948534	chr7:17022012-17022013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539502929	chr7:17022015-17022016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538776258	chr7:17022035-17022036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs74782575	chr7:17022040-17022041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568702811	chr7:17022057-17022058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116231696	chr7:17022088-17022089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183462126	chr7:17022169-17022170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537796241	chr7:17022182-17022183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10081310	chr7:17022212-17022213	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs187952383	chr7:17022242-17022243	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs847434	chr7:17022243-17022244	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs577645633	chr7:17022266-17022267	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs847433	chr7:17022268-17022269	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs193165905	chr7:17022329-17022330	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs199556662	chr7:17022357-17022358	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs148272508	chr7:17022358-17022359	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs73681964	chr7:17022359-17022360	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs34235705	chr7:17022360-17022361	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs10577279	chr7:17022382-17022383	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs34752167	chr7:17022410-17022411	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:1194 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17001400-17025600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:17016400-17021800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr7:17018600-17022200	Weak transcription	NHEK	skin
4	chr7:17018600-17025600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:17018800-17022000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr7:17019000-17022000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr7:17019000-17022200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:17019000-17022200	Weak transcription	Duodenum Mucosa	Duodenum
9	chr7:17019000-17022400	Weak transcription	Aorta	Aorta
10	chr7:17019000-17022600	Weak transcription	Fetal Lung	lung
11	chr7:17019000-17022800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:17019200-17022000	Weak transcription	Osteobl	bone
13	chr7:17019200-17022400	Weak transcription	HepG2	liver
14	chr7:17019200-17022600	Weak transcription	Adipose Nuclei	Adipose
15	chr7:17019200-17022600	Weak transcription	Small Intestine	intestine
16	chr7:17019200-17029400	Weak transcription	NH-A	brain
17	chr7:17019400-17021800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:17019600-17021800	Weak transcription	HSMM	muscle
19	chr7:17019800-17021600	Weak transcription	Stomach Mucosa	stomach
20	chr7:17019800-17021800	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr7:17019800-17021800	Weak transcription	Hela-S3	cervix
22	chr7:17019800-17022000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:17019800-17022200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr7:17019800-17022200	Weak transcription	HUVEC	blood vessel
25	chr7:17019800-17022600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr7:17019800-17023000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr7:17019800-17029600	Weak transcription	Gastric	stomach
28	chr7:17020000-17022000	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr7:17020000-17022000	Weak transcription	NHDF-Ad	bronchial
30	chr7:17020000-17028400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr7:17020800-17033000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:17021600-17021800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr7:17021600-17022000	Enhancers	Stomach Mucosa	stomach
34	chr7:17021800-17022000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:17021800-17022000	Enhancers	HSMM	muscle
36	chr7:17021800-17022400	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr7:17021800-17022800	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr7:17021800-17023000	Enhancers	Hela-S3	cervix
39	chr7:17022000-17022200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:17022000-17022200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:17022000-17022200	Enhancers	Colon Smooth Muscle	Colon
42	chr7:17022000-17022400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr7:17022000-17022600	Enhancers	Muscle Satellite Cultured Cells	--
44	chr7:17022000-17022800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr7:17022000-17023000	Enhancers	Liver	Liver
46	chr7:17022000-17023000	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr7:17022000-17023000	Enhancers	Osteobl	bone
48	chr7:17022000-17023200	Enhancers	A549	lung
49	chr7:17022000-17023400	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr7:17022000-17023600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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