Variant report

Variant	nsv887826
Chromosome Location	chr7:19816240-20033899
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1052)
CpG islands
(count:122)
Chromatin interactive
region (count:21)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1052 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:19995174-19995307	K562	blood:	n/a	n/a
2	ATF2	chr7:19967799-19968231	GM12878	blood:	n/a	n/a
3	ATF2	chr7:19967840-19968308	GM12878	blood:	n/a	n/a
4	ATF3	chr7:19997847-19998517	A549	lung:	n/a	n/a
5	ATF3	chr7:20009609-20010216	A549	lung:	n/a	n/a
6	ATF3	chr7:19939093-19939558	A549	lung:	n/a	n/a
7	ATF3	chr7:19997844-19998453	A549	lung:	n/a	n/a
8	ATF3	chr7:20009647-20010236	A549	lung:	n/a	n/a
9	BACH1	chr7:19852637-19852680	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:19818509-19818513	K562	blood:	n/a	n/a
11	BATF	chr7:19967879-19968267	GM12878	blood:	n/a	chr7:19968083-19968094 chr7:19968122-19968130
12	BATF	chr7:19955665-19955957	GM12878	blood:	n/a	chr7:19955794-19955804
13	BATF	chr7:19967871-19968233	GM12878	blood:	n/a	chr7:19968083-19968094 chr7:19968122-19968130
14	BATF	chr7:19955619-19955990	GM12878	blood:	n/a	chr7:19955794-19955804
15	BATF	chr7:19967522-19967794	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:19955737-19955878	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:19955612-19955973	GM12878	blood:	n/a	n/a
18	BCL3	chr7:19939130-19939601	A549	lung:	n/a	n/a
19	BCL3	chr7:20009573-20010231	A549	lung:	n/a	n/a
20	BCL3	chr7:19938976-19939578	A549	lung:	n/a	n/a
21	BCL3	chr7:19997828-19998541	A549	lung:	n/a	n/a
22	BCL3	chr7:19997858-19998418	A549	lung:	n/a	n/a
23	BCL3	chr7:19874216-19874751	A549	lung:	n/a	n/a
24	BCL3	chr7:20009545-20010519	A549	lung:	n/a	n/a
25	BRCA1	chr7:19855858-19855879	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr7:19997916-19998507	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr7:20009570-20010247	HCT-116	colon:	n/a	n/a
28	CBX3	chr7:19997709-19998597	HCT-116	colon:	n/a	n/a
29	CBX3	chr7:19975754-19976112	HCT-116	colon:	n/a	n/a
30	CBX3	chr7:20009652-20010197	HCT-116	colon:	n/a	n/a
31	CBX3	chr7:19997627-19998566	HCT-116	colon:	n/a	n/a
32	CBX3	chr7:19955600-19956120	HCT-116	colon:	n/a	n/a
33	CBX3	chr7:19984175-19984867	HCT-116	colon:	n/a	n/a
34	CEBPB	chr7:19997178-19997671	MCF-7	breast:	n/a	n/a
35	CEBPB	chr7:20008416-20008876	A549	lung:	n/a	chr7:20008461-20008472
36	CEBPB	chr7:20009696-20010222	A549	lung:	n/a	n/a
37	CEBPB	chr7:20029827-20030094	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr7:19997780-19998523	A549	lung:	n/a	chr7:19998274-19998287 chr7:19998274-19998285 chr7:19998275-19998286
39	CEBPB	chr7:19950695-19951007	A549	lung:	n/a	chr7:19950830-19950841
40	CEBPB	chr7:20003373-20003488	A549	lung:	n/a	n/a
41	CEBPB	chr7:20009788-20010209	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr7:19997391-19998671	A549	lung:	n/a	chr7:19998274-19998287 chr7:19998274-19998285 chr7:19998275-19998286
43	CEBPB	chr7:20007265-20007500	HepG2	liver:	n/a	chr7:20007380-20007391
44	CEBPB	chr7:19939220-19939589	A549	lung:	n/a	n/a
45	CEBPB	chr7:19997819-19998658	MCF-7	breast:	n/a	chr7:19998274-19998287 chr7:19998274-19998285 chr7:19998275-19998286
46	CEBPB	chr7:20018965-20019235	HepG2	liver:	n/a	chr7:20019063-20019074
47	CEBPB	chr7:20018964-20019154	A549	lung:	n/a	chr7:20019063-20019074
48	CEBPB	chr7:20029798-20030091	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:19950735-19950984	HepG2	liver:	n/a	chr7:19950830-19950841
50	CEBPB	chr7:19880808-19880960	HepG2	liver:	n/a	chr7:19880896-19880907

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:19961027-19961077	SKMC	muscle:	n/a
2	chr7:19961027-19961077	H1-hESC	embryonic stem cell:	embryo
3	chr7:19961027-19961077	HepG2	liver:	n/a
4	chr7:19961027-19961077	RPTEC	kidney:	n/a
5	chr7:20010777-20010827	AG04449	skin:	fetal
6	chr7:20010777-20010827	AG09309	skin:	n/a
7	chr7:20010777-20010827	Hela-S3	cervix:	n/a
8	chr7:19961027-19961077	NH-A	brain:	n/a
9	chr7:19961027-19961077	HCM	heart:	n/a
10	chr7:19961027-19961077	NHBE	bronchial:	n/a
11	chr7:20010777-20010827	HRPEpiC	eye:	n/a
12	chr7:20010777-20010827	PANC-1	pancreas:	n/a
13	chr7:20010777-20010827	NT2-D1	testis:	n/a
14	chr7:20010777-20010827	Jurkat	blood:	n/a
15	chr7:19961027-19961077	ProgFib	skin:	n/a
16	chr7:19961027-19961077	MCF-7	breast:	n/a
17	chr7:20010777-20010827	PFSK-1	brain:	n/a
18	chr7:19961027-19961077	SK-N-SH_RA	brain:	n/a
19	chr7:19961027-19961077	HIPEpiC	eye:	n/a
20	chr7:20010777-20010827	AoSMC	blood vessel:	n/a
21	chr7:20010777-20010827	U87	brain:	n/a
22	chr7:20010777-20010827	HPAEpiC	pulmonary alveolar:	n/a
23	chr7:19961027-19961077	SK-N-SH	brain:	n/a
24	chr7:19961027-19961077	BJ	skin:	n/a
25	chr7:19961027-19961077	Jurkat	blood:	n/a
26	chr7:20010777-20010827	RPTEC	kidney:	n/a
27	chr7:20010777-20010827	HRE	kidney:	n/a
28	chr7:19961027-19961077	AG09319	gingival:	n/a
29	chr7:20010777-20010827	AG10803	skin:	n/a
30	chr7:19961027-19961077	Hepatocyte	liver:	n/a
31	chr7:20010777-20010827	SKMC	muscle:	n/a
32	chr7:20010777-20010827	GM12878	blood:	n/a
33	chr7:20010777-20010827	BE2_C	brain:	n/a
34	chr7:19961027-19961077	GM06990	blood:	n/a
35	chr7:19961027-19961077	LNCaP	prostate:	n/a
36	chr7:20010777-20010827	A549	lung:	n/a
37	chr7:19961027-19961077	HRE	kidney:	n/a
38	chr7:19961027-19961077	NT2-D1	testis:	n/a
39	chr7:19961027-19961077	U87	brain:	n/a
40	chr7:19961027-19961077	Hela-S3	cervix:	n/a
41	chr7:20010777-20010827	NHBE	bronchial:	n/a
42	chr7:19961027-19961077	GM19239	blood:	n/a
43	chr7:19961027-19961077	SK-N-MC	brain:	n/a
44	chr7:19961027-19961077	ovcar-3	ovarian:	n/a
45	chr7:20010777-20010827	GM12891	blood:	n/a
46	chr7:19961027-19961077	PANC-1	pancreas:	n/a
47	chr7:19961027-19961077	AoSMC	blood vessel:	n/a
48	chr7:19961027-19961077	NB4	blood:	n/a
49	chr7:20010777-20010827	MCF-7	breast:	n/a
50	chr7:19961027-19961077	HRPEpiC	eye:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:19899612..19901422-chr7:19904101..19906352,2	MCF-7	breast:
2	chr7:19873630..19875873-chr7:19878314..19880296,2	K562	blood:
3	chr7:20022231..20022930-chr7:20212481..20213023,2	MCF-7	breast:
4	chr7:19996523..19999289-chr7:20000423..20003780,3	MCF-7	breast:
5	chr7:19953806..19956698-chr7:19965814..19968012,2	K562	blood:
6	chr7:19880470..19882183-chr7:19884471..19887080,2	K562	blood:
7	chr7:19996523..19999289-chr7:20000423..20003780,3	MCF-7	breast:
8	chr7:20007265..20009765-chr7:20010945..20013296,2	K562	blood:
9	chr7:19873630..19875873-chr7:19878314..19880296,2	K562	blood:
10	chr7:19973391..19975123-chr7:19986550..19989057,2	MCF-7	breast:
11	chr7:19814760..19817027-chr7:19818630..19820862,2	K562	blood:
12	chr7:19900301..19903128-chr7:19903366..19905836,3	MCF-7	breast:
13	chr7:19899734..19901908-chr7:19902300..19904189,2	K562	blood:
14	chr7:19814760..19817027-chr7:19818630..19820862,2	K562	blood:
15	chr7:19900301..19903128-chr7:19903366..19905836,3	MCF-7	breast:
16	chr3:63777404..63778151-chr7:19886673..19887328,2	MCF-7	breast:
17	chr7:19973391..19975123-chr7:19986550..19989057,2	MCF-7	breast:
18	chr7:19899734..19901908-chr7:19902300..19904189,2	K562	blood:
19	chr7:19880470..19882183-chr7:19884471..19887080,2	K562	blood:
20	chr7:19899612..19901422-chr7:19904101..19906352,2	MCF-7	breast:
21	chr7:19953806..19956698-chr7:19965814..19968012,2	K562	blood:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM196-1	chr7:19853308-19853347	XLOC_006365
2	lnc-MACC1-1	chr7:20000545-20000617	NONHSAT119395
3	lnc-MACC1-1	chr7:19958604-19958883	NR_110114
4	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1
5	lnc-MACC1-1	chr7:20007760-20008018	ENSG00000243004.1
6	lnc-TMEM196-1	chr7:19857580-19857713	XLOC_006365
7	lnc-MACC1-1	chr7:20007760-20008018	NONHSAT119395
8	lnc-MACC1-1	chr7:19959489-19959600	ENSG00000243004.1
9	lnc-TMEM196-1	chr7:19855826-19855937	ENSG00000237921
10	lnc-MACC1-1	chr7:20000545-20000617	NR_110114
11	lnc-MACC1-1	chr7:19958602-19958883	NONHSAT119395
12	lnc-MACC1-1	chr7:19958823-19958883	ENSG00000243004.1
13	lnc-MACC1-1	chr7:19982842-19983111	ENSG00000243004.1
14	lnc-MACC1-1	chr7:19970876-19970921	NONHSAT119395
15	lnc-TMEM196-1	chr7:19857580-19857713	ENSG00000237921
16	lnc-MACC1-1	chr7:19959489-19960253	NONHSAT119395
17	lnc-TMEM196-1	chr7:19871002-19871039	XLOC_006365
18	lnc-TMEM196-2	chr7:19824105-19824238	NONHSAT119391
19	lnc-TMEM196-1	chr7:19853308-19853347	ENSG00000237921
20	lnc-MACC1-1	chr7:19970694-19970921	ENSG00000243004.1
21	lnc-MACC1-1	chr7:19958615-19958883	ENSG00000243004.1
22	lnc-TMEM196-1	chr7:19855826-19855937	XLOC_006365
23	lnc-MACC1-1	chr7:19938142-19938370	NONHSAT119395
24	lnc-TMEM196-2	chr7:19823372-19823454	NONHSAT119391
25	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1
26	lnc-MACC1-1	chr7:20007760-20008018	ENSG00000243004.1
27	lnc-TMEM196-2	chr7:19822351-19822462	NONHSAT119391
28	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1
29	lnc-MACC1-1	chr7:20007760-20008018	ENSG00000243004.1
30	lnc-TMEM196-2	chr7:19837527-19837564	NONHSAT119391
31	lnc-TMEM196-1	chr7:19867978-19868096	XLOC_006365
32	lnc-TMEM196-1	chr7:19856847-19856929	XLOC_006365
33	lnc-TMEM196-2	chr7:19819833-19819872	NONHSAT119391
34	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1
35	lnc-TMEM196-2	chr7:19834503-19834621	NONHSAT119391
36	lnc-MACC1-1	chr7:19958604-19958883	ENSG00000243004.1
37	lnc-MACC1-1	chr7:20007777-20008018	ENSG00000243004.1
38	lnc-TMEM196-1	chr7:19856847-19856929	ENSG00000237921
39	lnc-TMEM196-2	chr7:19834235-19834363	NONHSAT119391
40	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1
41	lnc-MACC1-1	chr7:20007760-20007860	ENSG00000243004.1
42	lnc-MACC1-1	chr7:19970876-19970921	ENSG00000243004.1
43	lnc-TMEM196-1	chr7:19867710-19867838	XLOC_006365
44	lnc-MACC1-1	chr7:20007760-20008018	NR_110114
45	lnc-MACC1-1	chr7:20007777-20008018	ENSG00000243004.1
46	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1

No data

Variant related genes	Relation type
TMEM196	TF binding region
ENSG00000243004	TF binding region
ENSG00000237921	TF binding region
TMEM196	CpG island
ENSG00000243004	CpG island
ENSG00000237921	CpG island
ENSG00000243004	chromatin interactions
NID2	miRNA target sites
C13orf34	miRNA target sites
PDHX	miRNA target sites
ARID3B	miRNA target sites
BCL2	miRNA target sites
PGAM4	miRNA target sites
CD46	miRNA target sites

Extended variants
information (count: 5595 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:5595 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73680520	chr7:19819860-19819861	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79407523	chr7:19822353-19822354	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs191767126	chr7:19822354-19822355	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs573660918	chr7:19822368-19822369	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs555392704	chr7:19822373-19822374	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs377567575	chr7:19822374-19822375	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs557632495	chr7:19822381-19822382	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs10252965	chr7:19822385-19822386	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs560651800	chr7:19822386-19822387	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs564785172	chr7:19822389-19822390	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs373119198	chr7:19822450-19822451	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs4719584	chr7:19823388-19823389	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs4721825	chr7:19823427-19823428	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534427912	chr7:19824126-19824127	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs555739550	chr7:19824148-19824149	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs60323090	chr7:19824149-19824150	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs78121794	chr7:19824168-19824169	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs144343029	chr7:19824170-19824171	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs181301191	chr7:19824178-19824179	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs577691992	chr7:19824180-19824181	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs148758456	chr7:19824182-19824183	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs554258180	chr7:19824198-19824199	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs572121433	chr7:19824225-19824226	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs186172188	chr7:19827817-19827818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546919060	chr7:19827834-19827835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562866121	chr7:19827849-19827850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558443135	chr7:19827961-19827962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75317497	chr7:19827966-19827967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140874253	chr7:19827981-19827982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555430059	chr7:19828016-19828017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573842676	chr7:19828039-19828040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17142012	chr7:19828054-19828055	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs562376231	chr7:19828059-19828060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191845674	chr7:19828060-19828061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs17142014	chr7:19828099-19828100	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs181905389	chr7:19828136-19828137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17142015	chr7:19828138-19828139	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs549005941	chr7:19828149-19828150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185683565	chr7:19828167-19828168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4719587	chr7:19828174-19828175	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs547057526	chr7:19828194-19828195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550209300	chr7:19834253-19834254	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs571690893	chr7:19834267-19834268	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs554904182	chr7:19834508-19834509	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs186586701	chr7:19834535-19834536	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs190413132	chr7:19834545-19834546	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs558614772	chr7:19834556-19834557	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs148015087	chr7:19834561-19834562	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs545181175	chr7:19834566-19834567	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs539521857	chr7:19837549-19837550	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
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
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19827800-19828200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:19842600-19843800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr7:19842800-19843000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr7:19842800-19843400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr7:19852800-19853200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr7:19852800-19853200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr7:19852800-19853200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:19873200-19873800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr7:19873800-19874000	Enhancers	A549	lung
10	chr7:19873800-19874400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr7:19873800-19874800	Enhancers	NHEK	skin
12	chr7:19874000-19874400	Flanking Active TSS	A549	lung
13	chr7:19874200-19875000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:19874400-19874600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:19874400-19875200	Enhancers	A549	lung
16	chr7:19874800-19875200	Enhancers	HMEC	breast
17	chr7:19880600-19881200	ZNF genes & repeats	Small Intestine	intestine
18	chr7:19881000-19881200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:19887600-19888000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr7:19889800-19890000	Enhancers	Pancreas	Pancrea
21	chr7:19890000-19891200	Weak transcription	Pancreas	Pancrea
22	chr7:19890800-19891000	Enhancers	A549	lung
23	chr7:19891000-19891400	Flanking Active TSS	A549	lung
24	chr7:19891200-19891400	ZNF genes & repeats	Pancreas	Pancrea
25	chr7:19891400-19891600	Weak transcription	Pancreas	Pancrea
26	chr7:19891600-19892000	Enhancers	Pancreas	Pancrea
27	chr7:19896000-19896400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr7:19904000-19904600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr7:19914000-19914200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:19915400-19916000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:19916600-19917000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:19916600-19917000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
33	chr7:19929000-19929600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr7:19938200-19938400	Enhancers	Colon Smooth Muscle	Colon
35	chr7:19938200-19938600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
36	chr7:19938400-19939200	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr7:19938600-19939600	Enhancers	A549	lung
38	chr7:19939000-19939200	Enhancers	Colon Smooth Muscle	Colon
39	chr7:19939000-19939400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr7:19939000-19939800	Enhancers	NHDF-Ad	bronchial
41	chr7:19939000-19940000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:19939000-19940000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr7:19939000-19940000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:19939200-19939400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr7:19939200-19939600	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr7:19939400-19955400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr7:19939600-19940000	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr7:19939600-19940000	Flanking Active TSS	A549	lung
49	chr7:19945200-19947000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
50	chr7:19945400-19946400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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