Variant report

Variant	nsv887738
Chromosome Location	chr7:16211553-16284139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:233)
CpG islands
(count:122)
Chromatin interactive
region (count:39)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:233 , 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	chr7:16252388-16252536	K562	blood:	n/a	n/a
2	ARID3A	chr7:16249884-16249963	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	chr7:16271850-16272277	K562	blood:	n/a	n/a
8	CBX3	chr7:16269828-16270194	K562	blood:	n/a	n/a
9	CBX3	chr7:16240929-16241356	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	chr7:16251298-16251575	K562	blood:	n/a	n/a
13	CEBPB	chr7:16240270-16240516	HepG2	liver:	n/a	chr7:16240358-16240369 chr7:16240357-16240370
14	CEBPB	chr7:16246860-16247062	A549	lung:	n/a	n/a
15	CEBPB	chr7:16220104-16220262	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:16216852-16216879	K562	blood:	n/a	n/a
17	CEBPB	chr7:16228989-16229268	IMR90	lung:	n/a	chr7:16229185-16229197
18	CEBPB	chr7:16246794-16247066	K562	blood:	n/a	n/a
19	CEBPB	chr7:16234605-16234660	K562	blood:	n/a	chr7:16234630-16234641
20	CEBPB	chr7:16279656-16279856	HepG2	liver:	n/a	chr7:16279790-16279801
21	CEBPB	chr7:16216843-16216912	H1-hESC	embryonic stem cell:	n/a	n/a
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	chr7:16221312-16221339	K562	blood:	n/a	n/a
25	CEBPB	chr7:16229080-16229110	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:16234751-16234761	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:16274104-16274388	K562	blood:	n/a	n/a
28	CEBPB	chr7:16240258-16240479	IMR90	lung:	n/a	chr7:16240358-16240369 chr7:16240357-16240370
29	CEBPB	chr7:16251244-16251545	K562	blood:	n/a	n/a
30	CEBPB	chr7:16234545-16234739	HepG2	liver:	n/a	chr7:16234630-16234641
31	CEBPZ	chr7:16247712-16247786	HepG2	liver:	n/a	n/a
32	CTCF	chr7:16276820-16276970	HVMF	connective:	n/a	n/a
33	CTCF	chr7:16276680-16276830	NHEK	skin:	n/a	n/a
34	CTCF	chr7:16276880-16277030	NHEK	skin:	n/a	n/a
35	CTCF	chr7:16276800-16276950	AG10803	skin:	n/a	n/a
36	CTCF	chr7:16276740-16276890	BE2_C	brain:	n/a	n/a
37	CTCF	chr7:16276780-16276930	HMEC	breast:	n/a	n/a
38	CTCF	chr7:16275900-16276050	BE2_C	brain:	n/a	n/a
39	CTCF	chr7:16237499-16237527	GM13977	blood:	n/a	n/a
40	CTCF	chr7:16276820-16276970	HMEC	breast:	n/a	n/a
41	CUX1	chr7:16275242-16275395	K562	blood:	n/a	n/a
42	E2F4	chr7:16214093-16214275	MCF10A-Er-Src	breast:	n/a	n/a
43	EGR1	chr7:16249834-16250068	K562	blood:	n/a	n/a
44	EGR1	chr7:16249857-16250173	K562	blood:	n/a	n/a
45	EP300	chr7:16243136-16243590	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr7:16275313-16275866	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr7:16273131-16273555	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr7:16272631-16273009	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr7:16243815-16244147	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr7:16217710-16218057	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	chr7:16254882-16254932	NHBE	bronchial:	n/a
2	chr7:16254882-16254932	PFSK-1	brain:	n/a
3	chr7:16223374-16223424	Jurkat	blood:	n/a
4	chr7:16254882-16254932	HAEpiC	amniotic membrane:	n/a
5	chr7:16223374-16223424	PFSK-1	brain:	n/a
6	chr7:16223374-16223424	HIPEpiC	eye:	n/a
7	chr7:16223374-16223424	PANC-1	pancreas:	n/a
8	chr7:16254882-16254932	IMR90	lung:	fetal
9	chr7:16254882-16254932	HCPEpiC	choroid plexus:	n/a
10	chr7:16223374-16223424	AG04450	lung:	fetal
11	chr7:16223374-16223424	AG09309	skin:	n/a
12	chr7:16223374-16223424	BJ	skin:	n/a
13	chr7:16254882-16254932	GM19239	blood:	n/a
14	chr7:16223374-16223424	NT2-D1	testis:	n/a
15	chr7:16254882-16254932	GM12892	blood:	n/a
16	chr7:16223374-16223424	BE2_C	brain:	n/a
17	chr7:16223374-16223424	AoSMC	blood vessel:	n/a
18	chr7:16254882-16254932	Hela-S3	cervix:	n/a
19	chr7:16254882-16254932	Hepatocyte	liver:	n/a
20	chr7:16254882-16254932	HNPCEpiC	eye:	n/a
21	chr7:16254882-16254932	MCF-7	breast:	n/a
22	chr7:16223374-16223424	HRE	kidney:	n/a
23	chr7:16223374-16223424	NHBE	bronchial:	n/a
24	chr7:16254882-16254932	HEK293	kidney:	embryo
25	chr7:16223374-16223424	AG04449	skin:	fetal
26	chr7:16254882-16254932	PANC-1	pancreas:	n/a
27	chr7:16223374-16223424	HEEpiC	esophagus:	n/a
28	chr7:16223374-16223424	K562	blood:	n/a
29	chr7:16254882-16254932	GM12891	blood:	n/a
30	chr7:16254882-16254932	HEEpiC	esophagus:	n/a
31	chr7:16223374-16223424	HUVEC	blood vessel:	n/a
32	chr7:16254882-16254932	HCF	heart:	n/a
33	chr7:16254882-16254932	AG09309	skin:	n/a
34	chr7:16223374-16223424	HPAEpiC	pulmonary alveolar:	n/a
35	chr7:16223374-16223424	RPTEC	kidney:	n/a
36	chr7:16223374-16223424	LNCaP	prostate:	n/a
37	chr7:16223374-16223424	HAEpiC	amniotic membrane:	n/a
38	chr7:16254882-16254932	Jurkat	blood:	n/a
39	chr7:16254882-16254932	ProgFib	skin:	n/a
40	chr7:16223374-16223424	HepG2	liver:	n/a
41	chr7:16223374-16223424	Hela-S3	cervix:	n/a
42	chr7:16254882-16254932	AG10803	skin:	n/a
43	chr7:16254882-16254932	BE2_C	brain:	n/a
44	chr7:16223374-16223424	HCF	heart:	n/a
45	chr7:16223374-16223424	U87	brain:	n/a
46	chr7:16254882-16254932	U87	brain:	n/a
47	chr7:16254882-16254932	LNCaP	prostate:	n/a
48	chr7:16254882-16254932	SK-N-MC	brain:	n/a
49	chr7:16254882-16254932	A549	lung:	n/a
50	chr7:16223374-16223424	T-47D	breast:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:16247118..16249897-chr7:16251885..16253666,2	K562	blood:
2	chr7:16217013..16219760-chr7:16220726..16222323,2	K562	blood:
3	chr7:16242935..16245142-chr7:16460996..16462500,2	MCF-7	breast:
4	chr7:16211386..16214233-chr7:16216618..16219049,2	MCF-7	breast:
5	chr7:16221967..16224628-chr7:16306153..16308389,2	K562	blood:
6	chr7:16195841..16198251-chr7:16237665..16240574,2	K562	blood:
7	chr7:16277063..16278675-chr7:16280781..16282945,2	K562	blood:
8	chr7:16211386..16214233-chr7:16216618..16219049,2	MCF-7	breast:
9	chr7:16262958..16265861-chr7:16270760..16273242,2	K562	blood:
10	chr7:16226388..16229084-chr7:16230552..16232417,2	K562	blood:
11	chr7:16192281..16194569-chr7:16210731..16212589,2	K562	blood:
12	chr7:16225600..16227633-chr7:16239698..16241301,2	K562	blood:
13	chr7:16271837..16274588-chr7:16275186..16279473,3	K562	blood:
14	chr7:16237727..16240035-chr7:16245292..16248267,2	K562	blood:
15	chr7:16277063..16278861-chr7:16280781..16282424,2	K562	blood:
16	chr7:16232287..16234085-chr7:16683259..16685789,2	K562	blood:
17	chr7:16213039..16215303-chr7:16232402..16234352,2	K562	blood:
18	chr7:16272248..16274869-chr7:16305157..16307096,2	K562	blood:
19	chr7:16213039..16215303-chr7:16232402..16234352,2	K562	blood:
20	chr7:16275733..16277560-chr7:16684679..16686192,2	K562	blood:
21	chr7:16263097..16266771-chr7:16270720..16274586,3	K562	blood:
22	chr7:16237727..16240035-chr7:16245292..16248267,2	K562	blood:
23	chr7:16262958..16265861-chr7:16270760..16273242,2	K562	blood:
24	chr7:16274806..16276431-chr7:16298235..16300903,2	K562	blood:
25	chr7:16277063..16278675-chr7:16280781..16282945,2	K562	blood:
26	chr7:16225600..16227633-chr7:16239698..16241301,2	K562	blood:
27	chr7:16271772..16276074-chr7:16279630..16282231,4	K562	blood:
28	chr7:16271837..16274588-chr7:16275186..16279473,3	K562	blood:
29	chr7:16272248..16275452-chr7:16305157..16308165,4	K562	blood:
30	chr7:16226388..16229084-chr7:16230552..16232417,2	K562	blood:
31	chr7:16271772..16276074-chr7:16279630..16282231,4	K562	blood:
32	chr7:16217459..16219153-chr7:16224658..16227242,2	K562	blood:
33	chr7:16217459..16219153-chr7:16224658..16227242,2	K562	blood:
34	chr7:16217013..16219760-chr7:16220726..16222323,2	K562	blood:
35	chr7:16277063..16278861-chr7:16280781..16282424,2	K562	blood:
36	chr7:16242380..16245309-chr7:16338722..16341323,2	K562	blood:
37	chr7:16216050..16218726-chr7:16604270..16606079,2	K562	blood:
38	chr7:16207885..16209563-chr7:16230892..16233884,2	K562	blood:
39	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	chr7:16250111-16250228	NONHSAT119293
2	lnc-AC006035.2-1	chr7:16272377-16272461	ucscGeneNc_uc003stf_2
3	lnc-AC006035.2-1	chr7:16255958-16256194	ENSG00000229688.3
4	lnc-AC006035.2-1	chr7:16276934-16277035	NONHSAT119295
5	lnc-AC006035.2-1	chr7:16250169-16250228	ENSG00000229688
6	lnc-AC006035.2-1	chr7:16275007-16276752	ucscGeneNc_uc003stf_2
7	lnc-AC006035.2-6	chr7:16248570-16248890	NONHSAT119291
8	lnc-AC006035.2-1	chr7:16275527-16275604	NONHSAT119292
9	lnc-AC006035.2-1	chr7:16250130-16250228	NONHSAT119296
10	lnc-AC006035.2-1	chr7:16275527-16275604	NONHSAT119295
11	lnc-AC006035.2-1	chr7:16250167-16250228	ENSG00000229688.3
12	lnc-AC006035.2-1	chr7:16276934-16277038	NONHSAT119294
13	lnc-AC006035.2-1	chr7:16276934-16277038	NONHSAT119293
14	lnc-AC006035.2-1	chr7:16250132-16250228	ENSG00000229688.3
15	lnc-AC006035.2-1	chr7:16250111-16250228	NONHSAT119292
16	lnc-AC006035.2-1	chr7:16256009-16256194	ENSG00000229688.3
17	lnc-AC006035.2-1	chr7:16243459-16243563	ucscGeneNc_uc003stf_2
18	lnc-AC006035.2-1	chr7:16216643-16216753	ucscGeneNc_uc003stf_2
19	lnc-AC006035.2-1	chr7:16276934-16276977	ENSG00000229688
20	lnc-AC006035.2-1	chr7:16276934-16277035	ENSG00000229688.3
21	lnc-AC006035.2-1	chr7:16250113-16250228	ENSG00000229688
22	lnc-AC006035.2-1	chr7:16250118-16250228	NONHSAT119294
23	lnc-AC006035.2-1	chr7:16275527-16275604	ENSG00000229688
24	lnc-AC006035.2-1	chr7:16276934-16277038	ENSG00000229688
25	lnc-AC006035.2-1	chr7:16276934-16277031	ENSG00000229688.3
26	lnc-AC006035.2-1	chr7:16276934-16276977	NONHSAT119292
27	lnc-AC006035.2-1	chr7:16250130-16250228	NONHSAT119295
28	lnc-AC006035.2-1	chr7:16268049-16268246	ucscGeneNc_uc003stf_2

No data

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

Extended variants
information (count: 2209 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2209 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1012401	chr7:16211553-16211554	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562272770	chr7:16211554-16211555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529776611	chr7:16211569-16211570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74518396	chr7:16211590-16211591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74442255	chr7:16211591-16211592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78689801	chr7:16211592-16211593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139740970	chr7:16211598-16211599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563272480	chr7:16211603-16211604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530547566	chr7:16211605-16211606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552169382	chr7:16211624-16211625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564369233	chr7:16211627-16211628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528395307	chr7:16211631-16211632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143190976	chr7:16211661-16211662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146674323	chr7:16211683-16211684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201540751	chr7:16211758-16211759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535543511	chr7:16211791-16211792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1012402	chr7:16211816-16211817	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs568896834	chr7:16211820-16211821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs74718519	chr7:16211822-16211823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190699685	chr7:16211831-16211832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573438300	chr7:16211873-16211874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550530246	chr7:16211897-16211898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62440374	chr7:16211915-16211916	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs369738483	chr7:16211937-16211938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182992152	chr7:16211946-16211947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574333601	chr7:16211952-16211953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368434886	chr7:16212001-16212002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1034960	chr7:16212032-16212033	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs148399231	chr7:16212033-16212034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs17169301	chr7:16212054-16212055	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs545753027	chr7:16212062-16212063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10452774	chr7:16212070-16212071	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs546529497	chr7:16212071-16212072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150957420	chr7:16212073-16212074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529080233	chr7:16212083-16212084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116359916	chr7:16212104-16212105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534446721	chr7:16212132-16212133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10266491	chr7:16216645-16216646	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs552937153	chr7:16216677-16216678	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs574537672	chr7:16216678-16216679	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs57824034	chr7:16216683-16216684	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs557668632	chr7:16216690-16216691	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs575863018	chr7:16216700-16216701	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs546350714	chr7:16216713-16216714	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs564527512	chr7:16216719-16216720	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs377425096	chr7:16216736-16216737	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs541174088	chr7:16216737-16216738	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs559370651	chr7:16216739-16216740	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs550923671	chr7:16222415-16222416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376340854	chr7:16222420-16222421	Enhancers	n/a	n/a	Overlapped CNVs	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:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16211400-16211800	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr7:16211400-16212200	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr7:16211600-16212000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr7:16222400-16223000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:16226400-16227200	Enhancers	Muscle Satellite Cultured Cells	--
6	chr7:16226800-16227200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr7:16228600-16229800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:16228800-16229200	Enhancers	HSMMtube	muscle
9	chr7:16228800-16229400	Enhancers	Fetal Brain Female	brain
10	chr7:16228800-16230200	Weak transcription	Left Ventricle	heart
11	chr7:16233200-16234000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr7:16233200-16234400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr7:16233200-16234400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:16233400-16233800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:16233600-16234000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr7:16233600-16234000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr7:16233800-16234000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:16233800-16234200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr7:16234000-16235000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:16234000-16235000	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr7:16234000-16236200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr7:16234000-16238400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr7:16234200-16234600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:16234400-16238400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr7:16234400-16238600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:16234600-16234800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr7:16234800-16244000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr7:16235000-16235200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr7:16235000-16235400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:16235200-16236600	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr7:16236200-16237000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr7:16237000-16238200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr7:16238200-16239000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr7:16238400-16239000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr7:16238400-16239800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr7:16238600-16238800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr7:16238600-16239000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:16238800-16239000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr7:16238800-16241200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr7:16239000-16240800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr7:16239000-16244000	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr7:16239800-16244200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr7:16240200-16240800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr7:16240200-16242200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr7:16240400-16240600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:16240600-16242000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr7:16240800-16241200	Weak transcription	Left Ventricle	heart
48	chr7:16240800-16241400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
49	chr7:16240800-16241400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr7:16241200-16241400	Enhancers	Left Ventricle	heart

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