Variant report

Variant	nsv887759
Chromosome Location	chr7:16642995-16686940
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1085)
CpG islands
(count:1345)
Chromatin interactive
region (count:72)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1085 , 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	ARID3A	chr7:16683713-16684264	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:16685216-16685857	K562	blood:	n/a	n/a
3	ARID3A	chr7:16684572-16684770	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:16685168-16685952	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:16686526-16686785	K562	blood:	n/a	n/a
6	ATF1	chr7:16672507-16672608	K562	blood:	n/a	n/a
7	ATF2	chr7:16685159-16685746	GM12878	blood:	n/a	n/a
8	ATF2	chr7:16685052-16685626	GM12878	blood:	n/a	n/a
9	ATF2	chr7:16659418-16660055	GM12878	blood:	n/a	n/a
10	ATF2	chr7:16659358-16660122	GM12878	blood:	n/a	n/a
11	ATF3	chr7:16685194-16685997	A549	lung:	n/a	chr7:16685766-16685774
12	BACH1	chr7:16684269-16684548	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:16683715-16684414	K562	blood:	n/a	n/a
14	BACH1	chr7:16685559-16685673	K562	blood:	n/a	n/a
15	BATF	chr7:16685035-16685490	GM12878	blood:	n/a	n/a
16	BATF	chr7:16659523-16660147	GM12878	blood:	n/a	n/a
17	BATF	chr7:16659469-16659761	GM12878	blood:	n/a	n/a
18	BATF	chr7:16685075-16685425	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:16659534-16660048	GM12878	blood:	n/a	n/a
20	BCL3	chr7:16684711-16686109	A549	lung:	n/a	n/a
21	BCLAF1	chr7:16685089-16685504	GM12878	blood:	n/a	n/a
22	BHLHE40	chr7:16684035-16686772	K562	blood:	n/a	chr7:16685403-16685419 chr7:16685997-16686013
23	BHLHE40	chr7:16659644-16659769	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:16666939-16667139	A549	lung:	n/a	n/a
25	BHLHE40	chr7:16686372-16686374	A549	lung:	n/a	n/a
26	BHLHE40	chr7:16685429-16685824	A549	lung:	n/a	n/a
27	BHLHE40	chr7:16684814-16686586	HepG2	liver:	n/a	chr7:16685403-16685419 chr7:16685997-16686013
28	BHLHE40	chr7:16685315-16685882	GM12878	blood:	n/a	chr7:16685403-16685419
29	BRCA1	chr7:16684296-16684919	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr7:16685132-16685920	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr7:16685099-16686005	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr7:16684964-16685936	HepG2	liver:	n/a	n/a
33	CBX3	chr7:16684064-16684718	K562	blood:	n/a	n/a
34	CBX3	chr7:16684943-16686041	K562	blood:	n/a	chr7:16685612-16685623
35	CBX3	chr7:16685120-16685462	K562	blood:	n/a	n/a
36	CCNT2	chr7:16684186-16684643	K562	blood:	n/a	n/a
37	CCNT2	chr7:16684925-16686572	K562	blood:	n/a	chr7:16686257-16686266
38	CEBPB	chr7:16685094-16685971	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:16684150-16684179	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:16684366-16684551	K562	blood:	n/a	n/a
41	CEBPB	chr7:16666921-16667173	A549	lung:	n/a	n/a
42	CEBPB	chr7:16666957-16667117	MCF-7	breast:	n/a	n/a
43	CEBPB	chr7:16685142-16685467	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr7:16684924-16686039	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:16666869-16667219	IMR90	lung:	n/a	n/a
46	CEBPB	chr7:16650623-16650860	HepG2	liver:	n/a	chr7:16650748-16650759
47	CEBPB	chr7:16685101-16685665	K562	blood:	n/a	n/a
48	CEBPB	chr7:16685074-16685849	K562	blood:	n/a	n/a
49	CEBPB	chr7:16666878-16667210	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr7:16684151-16686011	Hela-S3	cervix:	n/a	n/a

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16656054-16656104	SK-N-SH_RA	brain:	n/a
2	chr7:16677240-16677290	ECC-1	luminal epithelium:	n/a
3	chr7:16684752-16684802	HRE	kidney:	n/a
4	chr7:16656054-16656104	SK-N-SH_RA	brain:	n/a
5	chr7:16677240-16677290	ECC-1	luminal epithelium:	n/a
6	chr7:16684752-16684802	HRE	kidney:	n/a
7	chr7:16684504-16684554	GM12891	blood:	n/a
8	chr7:16684906-16684956	ovcar-3	ovarian:	n/a
9	chr7:16684906-16684956	SK-N-MC	brain:	n/a
10	chr7:16684906-16684956	HepG2	liver:	n/a
11	chr7:16684321-16684371	ECC-1	luminal epithelium:	n/a
12	chr7:16686311-16686361	HRE	kidney:	n/a
13	chr7:16685776-16685826	HRPEpiC	eye:	n/a
14	chr7:16684349-16684399	HIPEpiC	eye:	n/a
15	chr7:16685823-16685873	HMEC	breast:	n/a
16	chr7:16684321-16684371	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:16685769-16685819	HUVEC	blood vessel:	n/a
18	chr7:16685595-16685645	IMR90	lung:	fetal
19	chr7:16685823-16685873	HepG2	liver:	n/a
20	chr7:16685769-16685819	HMEC	breast:	n/a
21	chr7:16684906-16684956	PFSK-1	brain:	n/a
22	chr7:16686311-16686361	HRCEpiC	kidney:	n/a
23	chr7:16685680-16685730	HCPEpiC	choroid plexus:	n/a
24	chr7:16656054-16656104	A549	lung:	n/a
25	chr7:16685683-16685733	GM12891	blood:	n/a
26	chr7:16684666-16684716	HCF	heart:	n/a
27	chr7:16684666-16684716	CMK	blood:	n/a
28	chr7:16685595-16685645	MCF-7	breast:	n/a
29	chr7:16682697-16682747	ECC-1	luminal epithelium:	n/a
30	chr7:16685581-16685631	IMR90	lung:	fetal
31	chr7:16685473-16685523	AG09309	skin:	n/a
32	chr7:16685473-16685523	A549	lung:	n/a
33	chr7:16686311-16686361	ECC-1	luminal epithelium:	n/a
34	chr7:16656054-16656104	AoSMC	blood vessel:	n/a
35	chr7:16682697-16682747	HUVEC	blood vessel:	n/a
36	chr7:16684906-16684956	AG04449	skin:	fetal
37	chr7:16685473-16685523	SK-N-SH	brain:	n/a
38	chr7:16685473-16685523	U87	brain:	n/a
39	chr7:16685776-16685826	NHBE	bronchial:	n/a
40	chr7:16685595-16685645	Jurkat	blood:	n/a
41	chr7:16685683-16685733	Hela-S3	cervix:	n/a
42	chr7:16685769-16685819	SKMC	muscle:	n/a
43	chr7:16685776-16685826	HIPEpiC	eye:	n/a
44	chr7:16684752-16684802	Caco-2	colon:	n/a
45	chr7:16685646-16685696	U87	brain:	n/a
46	chr7:16685595-16685645	SK-N-MC	brain:	n/a
47	chr7:16656054-16656104	Jurkat	blood:	n/a
48	chr7:16684321-16684371	HUVEC	blood vessel:	n/a
49	chr7:16685680-16685730	HEEpiC	esophagus:	n/a
50	chr7:16685776-16685826	PANC-1	pancreas:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:2732392..2733039-chr7:16685710..16686225,2	Hela-S3	cervix:
2	chr7:16686702..16688668-chr7:16746976..16749655,2	K562	blood:
3	chr7:16644705..16646601-chr7:16684304..16687284,2	MCF-7	breast:
4	chr19:6766897..6767546-chr7:16685539..16686039,2	Hela-S3	cervix:
5	chr7:16637135..16639582-chr7:16641679..16644005,2	K562	blood:
6	chr7:16684788..16686640-chr7:16792209..16794458,2	MCF-7	breast:
7	chr7:16503769..16505524-chr7:16680989..16682822,2	K562	blood:
8	chr7:16683657..16687154-chr7:16840807..16845302,5	MCF-7	breast:
9	chr7:16685077..16688645-chr7:16790567..16794834,4	K562	blood:
10	chr7:16642756..16644444-chr7:16668487..16671282,2	K562	blood:
11	chr13:24734631..24735372-chr7:16685566..16686079,2	Hela-S3	cervix:
12	chr7:16652156..16654551-chr7:16658497..16660099,2	K562	blood:
13	chr7:16456001..16461931-chr7:16682283..16687700,6	K562	blood:
14	chr7:16684583..16687261-chr7:16726504..16728541,2	MCF-7	breast:
15	chr7:16662487..16665291-chr7:16666130..16668303,2	K562	blood:
16	chr7:16639597..16641925-chr7:16642837..16645779,2	K562	blood:
17	chr7:16307737..16311020-chr7:16684818..16687152,3	K562	blood:
18	chr7:16649613..16652124-chr7:16656843..16659640,2	K562	blood:
19	chr7:16667727..16670675-chr7:16700899..16703274,2	K562	blood:
20	chr7:16682801..16684862-chr7:16783042..16785967,2	K562	blood:
21	chr17:54991184..54991903-chr7:16685728..16686437,2	NB4	blood:
22	chr7:16647541..16650601-chr7:16652797..16655866,3	K562	blood:
23	chr7:16668784..16670369-chr7:16681708..16684420,2	MCF-7	breast:
24	chr7:16672719..16682789-chr7:16684148..16689534,15	MCF-7	breast:
25	chr1:226249205..226249806-chr7:16685776..16686578,2	Hela-S3	cervix:
26	chr13:21750495..21751436-chr7:16685207..16686307,3	NB4	blood:
27	chr7:16685826..16687639-chr7:16712666..16714460,2	MCF-7	breast:
28	chr7:16647541..16650601-chr7:16652797..16655866,3	K562	blood:
29	chr3:73160089..73160608-chr7:16685235..16685991,2	NB4	blood:
30	chr7:16685048..16687300-chr7:16700569..16704504,5	MCF-7	breast:
31	chr16:3073868..3074781-chr7:16685858..16686571,2	Hela-S3	cervix:
32	chr2:232328789..232329732-chr7:16685524..16686410,2	Hela-S3	cervix:
33	chr7:16473934..16476388-chr7:16667166..16670049,2	K562	blood:
34	chr11:9335999..9336519-chr7:16685820..16686475,2	Hela-S3	cervix:
35	chr11:62622958..62623749-chr7:16685815..16686707,2	Hela-S3	cervix:
36	chr7:16680559..16682594-chr7:16684693..16686418,2	MCF-7	breast:
37	chr7:16655192..16657272-chr7:16805854..16808580,2	MCF-7	breast:
38	chr21:40176740..40177648-chr7:16685493..16686292,2	Hela-S3	cervix:
39	chr7:16635320..16637285-chr7:16647888..16649843,2	K562	blood:
40	chr7:16649613..16652124-chr7:16656843..16659640,2	K562	blood:
41	chr7:16644986..16647948-chr7:16650301..16653215,3	K562	blood:
42	chr7:16302428..16304569-chr7:16686662..16689057,2	K562	blood:
43	chr6:90539277..90540140-chr7:16685406..16686280,2	Hela-S3	cervix:
44	chr7:16460189..16463814-chr7:16683756..16686111,3	MCF-7	breast:
45	chr1:241803156..241803874-chr7:16685787..16686722,2	Hela-S3	cervix:
46	chr7:16662487..16665291-chr7:16666130..16668303,2	K562	blood:
47	chr7:16644986..16647948-chr7:16650301..16653215,3	K562	blood:
48	chr7:16652156..16654551-chr7:16658497..16660099,2	K562	blood:
49	chr7:16646853..16650643-chr7:16684954..16687917,3	MCF-7	breast:
50	chr7:16643475..16644221-chr7:16957387..16958014,2	MCF-7	breast:

No data

Variant related genes	Relation type
ANKMY2	TF binding region
BZW2	TF binding region
ANKMY2	CpG island
BZW2	CpG island
ENSG00000054277	chromatin interactions
ENSG00000229688	chromatin interactions
ENSG00000136261	chromatin interactions
ENSG00000182957	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000255717	chromatin interactions
ENSG00000175309	chromatin interactions
ENSG00000165480	chromatin interactions
ENSG00000167977	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000115053	chromatin interactions
ENSG00000157557	chromatin interactions
ENSG00000214960	chromatin interactions
ENSG00000131652	chromatin interactions
ENSG00000125731	chromatin interactions
ENSG00000106541	chromatin interactions
ENSG00000103145	chromatin interactions
ENSG00000118412	chromatin interactions
ENSG00000106524	chromatin interactions
ENSG00000121060	chromatin interactions
ENSG00000272562	chromatin interactions
ENSG00000106537	chromatin interactions
ENSG00000173141	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000171243	chromatin interactions
ENSG00000166471	chromatin interactions
ENSG00000163041	chromatin interactions

Extended variants
information (count: 1886 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1886 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs476489	chr7:16642995-16642996	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527527362	chr7:16643002-16643003	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs184043473	chr7:16643042-16643043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187809506	chr7:16643129-16643130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532281809	chr7:16643163-16643164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117036170	chr7:16643173-16643174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189937842	chr7:16643193-16643194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535864148	chr7:16643236-16643237	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs55984610	chr7:16643281-16643282	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs55778183	chr7:16643286-16643287	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548127865	chr7:16643291-16643292	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569619360	chr7:16643301-16643302	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536920593	chr7:16643340-16643341	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1524749	chr7:16643353-16643354	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115213989	chr7:16643355-16643356	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535167137	chr7:16643369-16643370	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112327274	chr7:16643399-16643400	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138594177	chr7:16643404-16643405	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs117308433	chr7:16643418-16643419	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561370	chr7:16643467-16643468	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs561123008	chr7:16643480-16643481	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182152543	chr7:16643505-16643506	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11978049	chr7:16643566-16643567	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77219108	chr7:16643617-16643618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528678034	chr7:16643619-16643620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376636838	chr7:16643638-16643639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575237254	chr7:16643639-16643640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529748328	chr7:16643709-16643710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547900343	chr7:16643737-16643738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569276945	chr7:16643746-16643747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569517392	chr7:16643750-16643751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552049359	chr7:16643755-16643756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34141401	chr7:16643774-16643775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113943196	chr7:16643789-16643790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144068072	chr7:16643843-16643844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373479991	chr7:16643855-16643856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376428297	chr7:16643861-16643862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146939349	chr7:16643970-16643971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568479963	chr7:16644019-16644020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539666765	chr7:16644043-16644044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535906757	chr7:16644055-16644056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139919953	chr7:16644058-16644059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs67150808	chr7:16644060-16644061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557424139	chr7:16644063-16644064	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs397695851	chr7:16644064-16644065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575689904	chr7:16644088-16644089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546568604	chr7:16644101-16644102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs17169559	chr7:16644141-16644142	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs187223211	chr7:16644176-16644177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76610649	chr7:16644208-16644209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1697 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16624000-16645600	Weak transcription	Gastric	stomach
2	chr7:16627800-16654200	Weak transcription	Brain Angular Gyrus	brain
3	chr7:16630400-16643000	Weak transcription	HUVEC	blood vessel
4	chr7:16630800-16643000	Weak transcription	Thymus	Thymus
5	chr7:16632600-16643200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr7:16634200-16649600	Weak transcription	Hela-S3	cervix
7	chr7:16635600-16654800	Weak transcription	Spleen	Spleen
8	chr7:16636200-16649400	Weak transcription	Small Intestine	intestine
9	chr7:16636400-16682600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr7:16636600-16648800	Weak transcription	HMEC	breast
11	chr7:16637200-16643200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr7:16637400-16668400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr7:16637600-16644800	Strong transcription	Dnd41	blood
14	chr7:16637600-16644800	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr7:16637800-16644600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:16637800-16644600	Strong transcription	Primary T cells from cord blood	blood
17	chr7:16637800-16644600	Strong transcription	Liver	Liver
18	chr7:16637800-16644600	Strong transcription	HSMM	muscle
19	chr7:16637800-16644800	Strong transcription	Adipose Nuclei	Adipose
20	chr7:16637800-16644800	Strong transcription	Duodenum Mucosa	Duodenum
21	chr7:16637800-16644800	Strong transcription	Stomach Smooth Muscle	stomach
22	chr7:16637800-16649800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr7:16637800-16651600	Strong transcription	Fetal Muscle Leg	muscle
24	chr7:16637800-16652000	Strong transcription	Fetal Muscle Trunk	muscle
25	chr7:16637800-16654800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:16637800-16661600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr7:16637800-16664800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:16638000-16644000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr7:16638000-16644800	Strong transcription	Placenta	Placenta
30	chr7:16638000-16649000	Strong transcription	Fetal Stomach	stomach
31	chr7:16638000-16656200	Weak transcription	Brain Cingulate Gyrus	brain
32	chr7:16638000-16658800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:16638000-16660200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr7:16638000-16670800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr7:16638200-16655200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr7:16638200-16656200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:16638200-16659800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr7:16638400-16643200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr7:16638400-16647200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr7:16638400-16654800	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr7:16638400-16661600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:16638400-16670000	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr7:16638400-16670200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr7:16638800-16644800	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr7:16639000-16644000	Strong transcription	Skeletal Muscle Male	skeletal muscle
46	chr7:16639000-16644200	Strong transcription	Primary T cells fromperipheralblood	blood
47	chr7:16639000-16644600	Strong transcription	Ovary	ovary
48	chr7:16639000-16646400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr7:16639000-16654200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr7:16639000-16655000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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