Variant report

Variant	nsv887739
Chromosome Location	chr7:16216494-16284139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:221)
CpG islands
(count:122)
Chromatin interactive
region (count:36)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:16249884-16249963	K562	blood:	n/a	n/a
2	ARID3A	chr7:16252388-16252536	K562	blood:	n/a	n/a
3	ATF1	chr7:16266719-16266733	K562	blood:	n/a	n/a
4	ATF1	chr7:16230945-16230986	K562	blood:	n/a	n/a
5	BACH1	chr7:16243269-16243380	K562	blood:	n/a	n/a
6	BHLHE40	chr7:16242216-16242218	K562	blood:	n/a	n/a
7	CBX3	chr7:16240929-16241356	K562	blood:	n/a	n/a
8	CBX3	chr7:16269828-16270194	K562	blood:	n/a	n/a
9	CBX3	chr7:16271850-16272277	K562	blood:	n/a	n/a
10	CBX3	chr7:16269898-16270150	K562	blood:	n/a	n/a
11	CCNT2	chr7:16254761-16254970	K562	blood:	n/a	n/a
12	CEBPB	chr7:16246794-16247066	K562	blood:	n/a	n/a
13	CEBPB	chr7:16246860-16247062	A549	lung:	n/a	n/a
14	CEBPB	chr7:16216852-16216879	K562	blood:	n/a	n/a
15	CEBPB	chr7:16221312-16221339	K562	blood:	n/a	n/a
16	CEBPB	chr7:16220104-16220262	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:16228989-16229268	IMR90	lung:	n/a	chr7:16229185-16229197
18	CEBPB	chr7:16274104-16274388	K562	blood:	n/a	n/a
19	CEBPB	chr7:16229080-16229110	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:16251244-16251545	K562	blood:	n/a	n/a
21	CEBPB	chr7:16240258-16240479	IMR90	lung:	n/a	chr7:16240358-16240369 chr7:16240357-16240370
22	CEBPB	chr7:16240297-16240490	A549	lung:	n/a	chr7:16240358-16240369 chr7:16240357-16240370
23	CEBPB	chr7:16251340-16251603	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:16234605-16234660	K562	blood:	n/a	chr7:16234630-16234641
25	CEBPB	chr7:16240270-16240516	HepG2	liver:	n/a	chr7:16240358-16240369 chr7:16240357-16240370
26	CEBPB	chr7:16234751-16234761	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:16251298-16251575	K562	blood:	n/a	n/a
28	CEBPB	chr7:16234545-16234739	HepG2	liver:	n/a	chr7:16234630-16234641
29	CEBPB	chr7:16279656-16279856	HepG2	liver:	n/a	chr7:16279790-16279801
30	CEBPB	chr7:16216843-16216912	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPZ	chr7:16247712-16247786	HepG2	liver:	n/a	n/a
32	CTCF	chr7:16276880-16277030	NHEK	skin:	n/a	n/a
33	CTCF	chr7:16276820-16276970	HMEC	breast:	n/a	n/a
34	CTCF	chr7:16276820-16276970	HVMF	connective:	n/a	n/a
35	CTCF	chr7:16276800-16276950	AG10803	skin:	n/a	n/a
36	CTCF	chr7:16237499-16237527	GM13977	blood:	n/a	n/a
37	CTCF	chr7:16276740-16276890	BE2_C	brain:	n/a	n/a
38	CTCF	chr7:16276780-16276930	HMEC	breast:	n/a	n/a
39	CTCF	chr7:16276680-16276830	NHEK	skin:	n/a	n/a
40	CTCF	chr7:16275900-16276050	BE2_C	brain:	n/a	n/a
41	CUX1	chr7:16275242-16275395	K562	blood:	n/a	n/a
42	EGR1	chr7:16249857-16250173	K562	blood:	n/a	n/a
43	EGR1	chr7:16249834-16250068	K562	blood:	n/a	n/a
44	EP300	chr7:16272631-16273009	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr7:16243136-16243590	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr7:16274175-16276342	SK-N-SH	brain:	n/a	chr7:16274619-16274633 chr7:16274240-16274254
47	EP300	chr7:16217710-16218057	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr7:16232674-16232687	GM12878	blood:	n/a	n/a
49	EP300	chr7:16273080-16273457	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr7:16217701-16218033	SK-N-SH_RA	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16223374-16223424	SAEC	small airway:	n/a
2	chr7:16223374-16223424	GM12892	blood:	n/a
3	chr7:16223374-16223424	NHBE	bronchial:	n/a
4	chr7:16223374-16223424	Hela-S3	cervix:	n/a
5	chr7:16254882-16254932	BJ	skin:	n/a
6	chr7:16254882-16254932	NHDF-neo	bronchial:	n/a
7	chr7:16223374-16223424	HIPEpiC	eye:	n/a
8	chr7:16254882-16254932	HIPEpiC	eye:	n/a
9	chr7:16223374-16223424	HRE	kidney:	n/a
10	chr7:16223374-16223424	HAEpiC	amniotic membrane:	n/a
11	chr7:16254882-16254932	HRCEpiC	kidney:	n/a
12	chr7:16223374-16223424	Caco-2	colon:	n/a
13	chr7:16254882-16254932	HPAEpiC	pulmonary alveolar:	n/a
14	chr7:16254882-16254932	HRE	kidney:	n/a
15	chr7:16254882-16254932	HMEC	breast:	n/a
16	chr7:16223374-16223424	BJ	skin:	n/a
17	chr7:16223374-16223424	PFSK-1	brain:	n/a
18	chr7:16254882-16254932	CMK	blood:	n/a
19	chr7:16254882-16254932	AG09309	skin:	n/a
20	chr7:16223374-16223424	SK-N-MC	brain:	n/a
21	chr7:16254882-16254932	AG09319	gingival:	n/a
22	chr7:16223374-16223424	RPTEC	kidney:	n/a
23	chr7:16223374-16223424	AG04449	skin:	fetal
24	chr7:16254882-16254932	PANC-1	pancreas:	n/a
25	chr7:16254882-16254932	A549	lung:	n/a
26	chr7:16223374-16223424	HRPEpiC	eye:	n/a
27	chr7:16223374-16223424	HRCEpiC	kidney:	n/a
28	chr7:16223374-16223424	GM12891	blood:	n/a
29	chr7:16223374-16223424	HNPCEpiC	eye:	n/a
30	chr7:16254882-16254932	NB4	blood:	n/a
31	chr7:16223374-16223424	GM19239	blood:	n/a
32	chr7:16223374-16223424	T-47D	breast:	n/a
33	chr7:16223374-16223424	NB4	blood:	n/a
34	chr7:16254882-16254932	HAEpiC	amniotic membrane:	n/a
35	chr7:16254882-16254932	HNPCEpiC	eye:	n/a
36	chr7:16254882-16254932	GM12878	blood:	n/a
37	chr7:16223374-16223424	HCM	heart:	n/a
38	chr7:16223374-16223424	CMK	blood:	n/a
39	chr7:16223374-16223424	ECC-1	luminal epithelium:	n/a
40	chr7:16254882-16254932	Jurkat	blood:	n/a
41	chr7:16223374-16223424	PrEC	prostate:	n/a
42	chr7:16223374-16223424	NH-A	brain:	n/a
43	chr7:16254882-16254932	ovcar-3	ovarian:	n/a
44	chr7:16254882-16254932	NHBE	bronchial:	n/a
45	chr7:16223374-16223424	MCF-7	breast:	n/a
46	chr7:16254882-16254932	SK-N-SH_RA	brain:	n/a
47	chr7:16223374-16223424	LNCaP	prostate:	n/a
48	chr7:16223374-16223424	NT2-D1	testis:	n/a
49	chr7:16254882-16254932	ECC-1	luminal epithelium:	n/a
50	chr7:16223374-16223424	Hepatocyte	liver:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:16271837..16274588-chr7:16275186..16279473,3	K562	blood:
2	chr7:16217459..16219153-chr7:16224658..16227242,2	K562	blood:
3	chr7:16271837..16274588-chr7:16275186..16279473,3	K562	blood:
4	chr7:16272248..16275452-chr7:16305157..16308165,4	K562	blood:
5	chr7:16262958..16265861-chr7:16270760..16273242,2	K562	blood:
6	chr7:16262958..16265861-chr7:16270760..16273242,2	K562	blood:
7	chr7:16275733..16277560-chr7:16684679..16686192,2	K562	blood:
8	chr7:16217459..16219153-chr7:16224658..16227242,2	K562	blood:
9	chr7:16237727..16240035-chr7:16245292..16248267,2	K562	blood:
10	chr7:16247118..16249897-chr7:16251885..16253666,2	K562	blood:
11	chr7:16272248..16274869-chr7:16305157..16307096,2	K562	blood:
12	chr7:16217013..16219760-chr7:16220726..16222323,2	K562	blood:
13	chr7:16271772..16276074-chr7:16279630..16282231,4	K562	blood:
14	chr7:16277063..16278861-chr7:16280781..16282424,2	K562	blood:
15	chr7:16277063..16278675-chr7:16280781..16282945,2	K562	blood:
16	chr7:16226388..16229084-chr7:16230552..16232417,2	K562	blood:
17	chr7:16225600..16227633-chr7:16239698..16241301,2	K562	blood:
18	chr7:16274806..16276431-chr7:16298235..16300903,2	K562	blood:
19	chr7:16213039..16215303-chr7:16232402..16234352,2	K562	blood:
20	chr7:16237727..16240035-chr7:16245292..16248267,2	K562	blood:
21	chr7:16195841..16198251-chr7:16237665..16240574,2	K562	blood:
22	chr7:16221967..16224628-chr7:16306153..16308389,2	K562	blood:
23	chr7:16263097..16266771-chr7:16270720..16274586,3	K562	blood:
24	chr7:16211386..16214233-chr7:16216618..16219049,2	MCF-7	breast:
25	chr7:16232287..16234085-chr7:16683259..16685789,2	K562	blood:
26	chr7:16277063..16278675-chr7:16280781..16282945,2	K562	blood:
27	chr7:16225600..16227633-chr7:16239698..16241301,2	K562	blood:
28	chr7:16277063..16278861-chr7:16280781..16282424,2	K562	blood:
29	chr7:16217013..16219760-chr7:16220726..16222323,2	K562	blood:
30	chr7:16242935..16245142-chr7:16460996..16462500,2	MCF-7	breast:
31	chr7:16271772..16276074-chr7:16279630..16282231,4	K562	blood:
32	chr7:16207885..16209563-chr7:16230892..16233884,2	K562	blood:
33	chr7:16226388..16229084-chr7:16230552..16232417,2	K562	blood:
34	chr7:16242380..16245309-chr7:16338722..16341323,2	K562	blood:
35	chr7:16216050..16218726-chr7:16604270..16606079,2	K562	blood:
36	chr7:16263097..16266771-chr7:16270720..16274586,3	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006035.2-1	chr7:16275527-16275604	NONHSAT119295
2	lnc-AC006035.2-1	chr7:16276934-16276977	NONHSAT119292
3	lnc-AC006035.2-1	chr7:16272377-16272461	ucscGeneNc_uc003stf_2
4	lnc-AC006035.2-1	chr7:16250132-16250228	ENSG00000229688.3
5	lnc-AC006035.2-1	chr7:16275007-16276752	ucscGeneNc_uc003stf_2
6	lnc-AC006035.2-1	chr7:16276934-16277035	ENSG00000229688.3
7	lnc-AC006035.2-1	chr7:16268049-16268246	ucscGeneNc_uc003stf_2
8	lnc-AC006035.2-1	chr7:16276934-16277031	ENSG00000229688.3
9	lnc-AC006035.2-1	chr7:16243459-16243563	ucscGeneNc_uc003stf_2
10	lnc-AC006035.2-1	chr7:16250118-16250228	NONHSAT119294
11	lnc-AC006035.2-1	chr7:16276934-16277038	NONHSAT119293
12	lnc-AC006035.2-1	chr7:16250130-16250228	NONHSAT119296
13	lnc-AC006035.2-1	chr7:16250169-16250228	ENSG00000229688
14	lnc-AC006035.2-1	chr7:16216643-16216753	ucscGeneNc_uc003stf_2
15	lnc-AC006035.2-1	chr7:16276934-16276977	ENSG00000229688
16	lnc-AC006035.2-1	chr7:16250111-16250228	NONHSAT119293
17	lnc-AC006035.2-6	chr7:16248570-16248890	NONHSAT119291
18	lnc-AC006035.2-1	chr7:16276934-16277035	NONHSAT119295
19	lnc-AC006035.2-1	chr7:16276934-16277038	ENSG00000229688
20	lnc-AC006035.2-1	chr7:16250111-16250228	NONHSAT119292
21	lnc-AC006035.2-1	chr7:16276934-16277038	NONHSAT119294
22	lnc-AC006035.2-1	chr7:16255958-16256194	ENSG00000229688.3
23	lnc-AC006035.2-1	chr7:16250130-16250228	NONHSAT119295
24	lnc-AC006035.2-1	chr7:16275527-16275604	ENSG00000229688
25	lnc-AC006035.2-1	chr7:16250167-16250228	ENSG00000229688.3
26	lnc-AC006035.2-1	chr7:16256009-16256194	ENSG00000229688.3
27	lnc-AC006035.2-1	chr7:16250113-16250228	ENSG00000229688
28	lnc-AC006035.2-1	chr7:16275527-16275604	NONHSAT119292

No data

Variant related genes	Relation type
RPL36AP29	TF binding region
ISPD-AS1	TF binding region
RPL36AP29	CpG island
ISPD-AS1	CpG island
ENSG00000214960	chromatin interactions
ENSG00000136261	chromatin interactions
ENSG00000106524	chromatin interactions
ENSG00000224683	chromatin interactions
HAS3	miRNA target sites
ERCC4	miRNA target sites
DIS3L	miRNA target sites
RANBP9	miRNA target sites
CDKN1B	miRNA target sites

Extended variants
information (count: 2172 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2172 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10266491	chr7:16216645-16216646	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552937153	chr7:16216677-16216678	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs574537672	chr7:16216678-16216679	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs57824034	chr7:16216683-16216684	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs557668632	chr7:16216690-16216691	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs575863018	chr7:16216700-16216701	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs546350714	chr7:16216713-16216714	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs564527512	chr7:16216719-16216720	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs377425096	chr7:16216736-16216737	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs541174088	chr7:16216737-16216738	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs559370651	chr7:16216739-16216740	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs550923671	chr7:16222415-16222416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376340854	chr7:16222420-16222421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185246953	chr7:16222455-16222456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563596641	chr7:16222489-16222490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7789183	chr7:16222528-16222529	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531541819	chr7:16222573-16222574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536126320	chr7:16222605-16222606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188155924	chr7:16222622-16222623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569549990	chr7:16222657-16222658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181120771	chr7:16222662-16222663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368286528	chr7:16222828-16222829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548033061	chr7:16222876-16222877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373676149	chr7:16222987-16222988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531546546	chr7:16226421-16226422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181872351	chr7:16226424-16226425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34850559	chr7:16226434-16226435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200746319	chr7:16226435-16226436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200297292	chr7:16226437-16226438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149756686	chr7:16226498-16226499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185910791	chr7:16226509-16226510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190675267	chr7:16226518-16226519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572473008	chr7:16226528-16226529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536602587	chr7:16226532-16226533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375569023	chr7:16226591-16226592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12699772	chr7:16226615-16226616	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs543753080	chr7:16226646-16226647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371027079	chr7:16226775-16226776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370787879	chr7:16226797-16226798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75464412	chr7:16226799-16226800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554917748	chr7:16226801-16226802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541249033	chr7:16226820-16226821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560144402	chr7:16226830-16226831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527401946	chr7:16226841-16226842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs557114515	chr7:16226901-16226902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548952903	chr7:16226954-16226955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573959843	chr7:16226982-16226983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560767567	chr7:16226993-16226994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145623839	chr7:16227021-16227022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4721478	chr7:16227094-16227095	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:90)

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
Colorectal cancer	16272173	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	19492091	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	19805367	CNVD
Autism	20808228	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16222400-16223000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:16226400-16227200	Enhancers	Muscle Satellite Cultured Cells	--
3	chr7:16226800-16227200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr7:16228600-16229800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:16228800-16229200	Enhancers	HSMMtube	muscle
6	chr7:16228800-16229400	Enhancers	Fetal Brain Female	brain
7	chr7:16228800-16230200	Weak transcription	Left Ventricle	heart
8	chr7:16233200-16234000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr7:16233200-16234400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr7:16233200-16234400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:16233400-16233800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:16233600-16234000	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr7:16233600-16234000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr7:16233800-16234000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:16233800-16234200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr7:16234000-16235000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:16234000-16235000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr7:16234000-16236200	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr7:16234000-16238400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr7:16234200-16234600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr7:16234400-16238400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr7:16234400-16238600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:16234600-16234800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:16234800-16244000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr7:16235000-16235200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr7:16235000-16235400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:16235200-16236600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr7:16236200-16237000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr7:16237000-16238200	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr7:16238200-16239000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:16238400-16239000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr7:16238400-16239800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr7:16238600-16238800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr7:16238600-16239000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr7:16238800-16239000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr7:16238800-16241200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr7:16239000-16240800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr7:16239000-16244000	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr7:16239800-16244200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr7:16240200-16240800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr7:16240200-16242200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr7:16240400-16240600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr7:16240600-16242000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:16240800-16241200	Weak transcription	Left Ventricle	heart
45	chr7:16240800-16241400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
46	chr7:16240800-16241400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr7:16241200-16241400	Enhancers	Left Ventricle	heart
48	chr7:16241200-16241600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr7:16241200-16243200	Enhancers	HUVEC	blood vessel
50	chr7:16241400-16244000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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