Variant report

Variant	nsv892605
Chromosome Location	chr9:14585052-14709151
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1286)
CpG islands
(count:550)
Chromatin interactive
region (count:41)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14652772-14653234	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:14661451-14661789	K562	blood:	n/a	n/a
3	ARID3A	chr9:14616366-14616729	K562	blood:	n/a	n/a
4	ARID3A	chr9:14616384-14616695	HepG2	liver:	n/a	n/a
5	ATF1	chr9:14661502-14661775	K562	blood:	n/a	n/a
6	ATF2	chr9:14693237-14693620	GM12878	blood:	n/a	n/a
7	ATF2	chr9:14688075-14688638	GM12878	blood:	n/a	n/a
8	ATF2	chr9:14585524-14586203	GM12878	blood:	n/a	n/a
9	ATF2	chr9:14585562-14586344	GM12878	blood:	n/a	n/a
10	BACH1	chr9:14693258-14693548	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr9:14585675-14586118	GM12878	blood:	n/a	n/a
12	BCL11A	chr9:14585612-14586175	GM12878	blood:	n/a	chr9:14585907-14585916
13	BCL11A	chr9:14585726-14586068	GM12878	blood:	n/a	chr9:14585907-14585916
14	BCL3	chr9:14585642-14586081	GM12878	blood:	n/a	chr9:14585907-14585916
15	BCLAF1	chr9:14688097-14688460	GM12878	blood:	n/a	chr9:14688341-14688350
16	BCLAF1	chr9:14693175-14693606	GM12878	blood:	n/a	n/a
17	BCLAF1	chr9:14693199-14693708	GM12878	blood:	n/a	n/a
18	BCLAF1	chr9:14585603-14586186	GM12878	blood:	n/a	chr9:14585907-14585916
19	BHLHE40	chr9:14616435-14616720	GM12878	blood:	n/a	n/a
20	BHLHE40	chr9:14688140-14688529	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:14689247-14689350	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:14692950-14693814	GM12878	blood:	n/a	chr9:14693117-14693133
23	BHLHE40	chr9:14585516-14586154	GM12878	blood:	n/a	n/a
24	BRCA1	chr9:14652862-14653081	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr9:14654938-14655346	K562	blood:	n/a	n/a
26	CBX3	chr9:14654942-14655330	K562	blood:	n/a	n/a
27	CBX3	chr9:14593377-14593719	K562	blood:	n/a	n/a
28	CBX3	chr9:14654909-14655424	HCT-116	colon:	n/a	n/a
29	CBX3	chr9:14654902-14655428	HCT-116	colon:	n/a	n/a
30	CCNT2	chr9:14693300-14693572	K562	blood:	n/a	n/a
31	CEBPB	chr9:14640433-14640716	A549	lung:	n/a	n/a
32	CEBPB	chr9:14620535-14620536	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:14593410-14593662	K562	blood:	n/a	n/a
34	CEBPB	chr9:14626442-14626622	HepG2	liver:	n/a	chr9:14626550-14626561 chr9:14626549-14626562 chr9:14626549-14626560 chr9:14626549-14626562 chr9:14626549-14626562 chr9:14626549-14626560
35	CEBPB	chr9:14593561-14593669	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:14661506-14661801	K562	blood:	n/a	n/a
37	CEBPB	chr9:14687100-14687489	IMR90	lung:	n/a	n/a
38	CHD1	chr9:14688156-14688623	GM12878	blood:	n/a	n/a
39	CHD1	chr9:14693269-14693945	GM12878	blood:	n/a	n/a
40	CHD1	chr9:14693268-14693369	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr9:14692666-14692698	HepG2	liver:	n/a	n/a
42	CHD2	chr9:14693310-14693896	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr9:14616421-14616609	GM12878	blood:	n/a	n/a
44	CHD2	chr9:14692865-14693793	GM12878	blood:	n/a	chr9:14693027-14693037
45	CREB1	chr9:14693169-14693584	A549	lung:	n/a	n/a
46	CREB1	chr9:14652817-14653056	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr9:14693141-14693720	HepG2	liver:	n/a	n/a
48	CTBP2	chr9:14693233-14693890	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr9:14652827-14653077	K562	blood:	n/a	n/a
50	CTCF	chr9:14661580-14661730	AG09319	gingival:	n/a	chr9:14661642-14661663

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14693648-14693698	PFSK-1	brain:	n/a
2	chr9:14693648-14693698	PFSK-1	brain:	n/a
3	chr9:14690531-14690581	IMR90	lung:	fetal
4	chr9:14693538-14693588	HNPCEpiC	eye:	n/a
5	chr9:14691289-14691339	PANC-1	pancreas:	n/a
6	chr9:14693538-14693588	SK-N-SH	brain:	n/a
7	chr9:14693888-14693938	Hepatocyte	liver:	n/a
8	chr9:14693888-14693938	NH-A	brain:	n/a
9	chr9:14693648-14693698	HAEpiC	amniotic membrane:	n/a
10	chr9:14693648-14693698	HL-60	blood:	n/a
11	chr9:14693648-14693698	SAEC	small airway:	n/a
12	chr9:14690531-14690581	HRCEpiC	kidney:	n/a
13	chr9:14643897-14643947	Caco-2	colon:	n/a
14	chr9:14693648-14693698	SKMC	muscle:	n/a
15	chr9:14693648-14693698	NB4	blood:	n/a
16	chr9:14643897-14643947	HAEpiC	amniotic membrane:	n/a
17	chr9:14643897-14643947	SK-N-SH	brain:	n/a
18	chr9:14693888-14693938	HCF	heart:	n/a
19	chr9:14693082-14693132	GM12892	blood:	n/a
20	chr9:14690531-14690581	AG09309	skin:	n/a
21	chr9:14692931-14692981	AG10803	skin:	n/a
22	chr9:14693648-14693698	Caco-2	colon:	n/a
23	chr9:14693082-14693132	AG10803	skin:	n/a
24	chr9:14691289-14691339	U87	brain:	n/a
25	chr9:14693648-14693698	AG04450	lung:	fetal
26	chr9:14693648-14693698	AG10803	skin:	n/a
27	chr9:14693888-14693938	HMEC	breast:	n/a
28	chr9:14693082-14693132	PFSK-1	brain:	n/a
29	chr9:14693538-14693588	GM19239	blood:	n/a
30	chr9:14693504-14693554	AG04450	lung:	fetal
31	chr9:14692931-14692981	PrEC	prostate:	n/a
32	chr9:14693504-14693554	GM12878	blood:	n/a
33	chr9:14690531-14690581	NT2-D1	testis:	n/a
34	chr9:14693082-14693132	MCF10A-Er-Src	breast:	n/a
35	chr9:14690531-14690581	HPAEpiC	pulmonary alveolar:	n/a
36	chr9:14693888-14693938	MCF-7	breast:	n/a
37	chr9:14693538-14693588	SAEC	small airway:	n/a
38	chr9:14693888-14693938	SK-N-SH_RA	brain:	n/a
39	chr9:14693082-14693132	SK-N-SH	brain:	n/a
40	chr9:14643897-14643947	MCF10A-Er-Src	breast:	n/a
41	chr9:14692931-14692981	U87	brain:	n/a
42	chr9:14690531-14690581	SK-N-MC	brain:	n/a
43	chr9:14693504-14693554	SK-N-SH	brain:	n/a
44	chr9:14693504-14693554	HCPEpiC	choroid plexus:	n/a
45	chr9:14692931-14692981	ProgFib	skin:	n/a
46	chr9:14693538-14693588	PrEC	prostate:	n/a
47	chr9:14643897-14643947	A549	lung:	n/a
48	chr9:14693082-14693132	Hepatocyte	liver:	n/a
49	chr9:14693538-14693588	HepG2	liver:	n/a
50	chr9:14643897-14643947	SK-N-SH_RA	brain:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:14676498..14678344-chr9:14692478..14694843,2	MCF-7	breast:
2	chr9:14616153..14617361-chr9:14660905..14661912,4	MCF-7	breast:
3	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
4	chr9:14671286..14673264-chr9:14676237..14678702,2	K562	blood:
5	chr9:14652918..14654762-chr9:14661773..14663664,2	MCF-7	breast:
6	chr9:14652918..14654762-chr9:14661773..14663664,2	MCF-7	breast:
7	chr9:14442114..14442886-chr9:14652552..14653366,4	MCF-7	breast:
8	chr9:14700452..14703179-chr9:14705217..14707235,2	MCF-7	breast:
9	chr10:61799790..61802033-chr9:14680041..14681542,2	MCF-7	breast:
10	chr9:14692215..14694584-chr9:14703998..14706013,2	MCF-7	breast:
11	chr9:14464938..14465658-chr9:14661578..14662250,2	MCF-7	breast:
12	chr9:14616185..14616937-chr9:14768483..14769168,4	MCF-7	breast:
13	chr9:14607657..14609554-chr9:14615392..14617575,2	K562	blood:
14	chr9:14607657..14609554-chr9:14615392..14617575,2	K562	blood:
15	chr9:14690708..14693231-chr9:14713433..14715842,2	MCF-7	breast:
16	chr9:14677358..14679032-chr9:14729314..14731148,2	MCF-7	breast:
17	chr9:14650294..14652492-chr9:14659969..14661655,2	K562	blood:
18	chr9:14655200..14658776-chr9:14658922..14661546,4	K562	blood:
19	chr9:14691643..14693414-chr9:14700745..14703153,2	K562	blood:
20	chr9:14594819..14596399-chr9:14599180..14601861,2	K562	blood:
21	chr9:14616153..14617361-chr9:14660905..14661912,4	MCF-7	breast:
22	chr9:14594819..14596399-chr9:14599180..14601861,2	K562	blood:
23	chr9:14678774..14681640-chr9:14758881..14761517,2	MCF-7	breast:
24	chr9:14693520..14695525-chr9:14717829..14719510,2	MCF-7	breast:
25	chr9:14700452..14703179-chr9:14705217..14707235,2	MCF-7	breast:
26	chr9:14607927..14609572-chr9:14611159..14613571,2	MCF-7	breast:
27	chr9:14655200..14658177-chr9:14659364..14661546,3	K562	blood:
28	chr9:14686674..14691236-chr9:14691548..14694778,7	MCF-7	breast:
29	chr9:14465217..14466121-chr9:14652305..14653436,3	K562	blood:
30	chr9:14594419..14596910-chr9:14651251..14653446,2	K562	blood:
31	chr9:14655200..14658177-chr9:14659364..14661546,3	K562	blood:
32	chr9:14671286..14673264-chr9:14676237..14678702,2	K562	blood:
33	chr9:14465253..14465899-chr9:14652688..14653342,2	MCF-7	breast:
34	chr9:14673551..14675387-chr9:14691158..14693433,2	MCF-7	breast:
35	chr9:14627684..14629345-chr9:14693335..14694855,2	MCF-7	breast:
36	chr9:14655200..14658776-chr9:14658922..14661546,4	K562	blood:
37	chr9:14594419..14596910-chr9:14651251..14653446,2	K562	blood:
38	chr9:14607927..14609572-chr9:14611159..14613571,2	MCF-7	breast:
39	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
40	chr9:14650294..14652492-chr9:14659969..14661655,2	K562	blood:
41	chr9:14442256..14442845-chr9:14661275..14662107,4	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf146-7	chr9:14588795-14589277	NONHSAT130249
2	lnc-ZDHHC21-4	chr9:14586767-14587324	ENSG00000273399.1
3	lnc-ZDHHC21-2	chr9:14606167-14606546	NONHSAT130251
4	lnc-CER1-1	chr9:14683569-14683727	NONHSAT130254
5	lnc-CER1-1	chr9:14677364-14677470	NONHSAT130254
6	lnc-ZDHHC21-3	chr9:14588795-14590063	ENSG00000272871.1
7	lnc-C9orf146-8	chr9:14593575-14594198	NONHSAT130250
8	lnc-ZDHHC21-2	chr9:14609848-14609996	NONHSAT130251
9	lnc-CER1-1	chr9:14693227-14693263	NONHSAT130254
10	lnc-ZDHHC21-1	chr9:14611070-14614754	NONHSAT130252
11	lnc-CER1-1	chr9:14690335-14690383	NONHSAT130254
12	lnc-C9orf146-7	chr9:14588065-14588629	NONHSAT130249
13	lnc-CER1-1	chr9:14680031-14680160	NONHSAT130254
14	lnc-C9orf146-7	chr9:14586764-14587315	NONHSAT130249

No data

Variant related genes	Relation type
ENSG00000229029	TF binding region
ZDHHC21	TF binding region
ENSG00000272871	TF binding region
ENSG00000273399	TF binding region
ENSG00000229029	CpG island
ZDHHC21	CpG island
ENSG00000272871	CpG island
ENSG00000273399	CpG island
ENSG00000175893	chromatin interactions

Extended variants
information (count: 5947 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5947 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7029906	chr9:14585052-14585053	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74429567	chr9:14585057-14585058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144058445	chr9:14585062-14585063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370981283	chr9:14585089-14585090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577729961	chr9:14585095-14585096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536769660	chr9:14585140-14585141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10961598	chr9:14585160-14585161	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs145804693	chr9:14585182-14585183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542264824	chr9:14585183-14585184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559258138	chr9:14585242-14585243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572662044	chr9:14585254-14585255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541676742	chr9:14585257-14585258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189494165	chr9:14585265-14585266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181722123	chr9:14585291-14585292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186769072	chr9:14585296-14585297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550383215	chr9:14585297-14585298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533988156	chr9:14585343-14585344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377296120	chr9:14585356-14585357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563811758	chr9:14585398-14585399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376549112	chr9:14585408-14585409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529401719	chr9:14585425-14585426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114428956	chr9:14585463-14585464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148991611	chr9:14585482-14585483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78679721	chr9:14585530-14585531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560642211	chr9:14585533-14585534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571427657	chr9:14585539-14585540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143816625	chr9:14585572-14585573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556735719	chr9:14585575-14585576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs118012422	chr9:14585603-14585604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs151103278	chr9:14585646-14585647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs367830204	chr9:14585652-14585653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs117552839	chr9:14585693-14585694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142646069	chr9:14585794-14585795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190015410	chr9:14585796-14585797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111374068	chr9:14585799-14585800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558464787	chr9:14585812-14585813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs578247377	chr9:14585829-14585830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs146304880	chr9:14585840-14585841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371805314	chr9:14585843-14585844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529529456	chr9:14585844-14585845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139057620	chr9:14585846-14585847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543071132	chr9:14585856-14585857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559507194	chr9:14585863-14585864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10961599	chr9:14585866-14585867	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs556054549	chr9:14585898-14585899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551467909	chr9:14585908-14585909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181141422	chr9:14585925-14585926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs55688346	chr9:14585930-14585931	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs550372638	chr9:14585931-14585932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376167081	chr9:14585935-14585936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
early-passage human iPS cells	21368824	CNVD
Glioblastoma multiforme	18628472	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:1721 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14577400-14597200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:14577600-14596200	Weak transcription	Pancreas	Pancrea
3	chr9:14582400-14596200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:14584800-14585200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr9:14585200-14586200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr9:14585200-14587200	Enhancers	GM12878-XiMat	blood
7	chr9:14585200-14589000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:14585400-14586200	Enhancers	Primary B cells from peripheral blood	blood
9	chr9:14585400-14586200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr9:14585400-14586200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr9:14585400-14586400	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr9:14585400-14586400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr9:14585400-14586400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr9:14585400-14586800	Enhancers	Primary T cells from cord blood	blood
15	chr9:14585600-14586000	Enhancers	Primary T cells fromperipheralblood	blood
16	chr9:14585600-14586000	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr9:14585600-14586000	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr9:14585600-14586400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr9:14585800-14586000	Enhancers	Lung	lung
20	chr9:14585800-14586200	Enhancers	Dnd41	blood
21	chr9:14585800-14586400	Enhancers	Brain Germinal Matrix	brain
22	chr9:14585800-14586800	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr9:14585800-14598000	Weak transcription	Right Ventricle	heart
24	chr9:14586000-14586200	Enhancers	Fetal Brain Female	brain
25	chr9:14586000-14592000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr9:14586000-14596200	Weak transcription	Lung	lung
27	chr9:14586000-14597000	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr9:14586200-14595200	Weak transcription	Primary B cells from peripheral blood	blood
29	chr9:14586400-14586600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr9:14586400-14587800	Weak transcription	Aorta	Aorta
31	chr9:14586400-14595800	Weak transcription	Brain Germinal Matrix	brain
32	chr9:14586600-14595200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr9:14586800-14587000	Enhancers	Fetal Brain Female	brain
34	chr9:14586800-14593400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr9:14586800-14629800	Weak transcription	Primary T cells from cord blood	blood
36	chr9:14587200-14591600	Weak transcription	GM12878-XiMat	blood
37	chr9:14587400-14595800	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr9:14587600-14595600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr9:14587600-14596200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr9:14587600-14596200	Weak transcription	Left Ventricle	heart
41	chr9:14587600-14599600	Weak transcription	Placenta	Placenta
42	chr9:14587800-14588000	Enhancers	Brain Cingulate Gyrus	brain
43	chr9:14587800-14588200	Strong transcription	Aorta	Aorta
44	chr9:14587800-14618400	Weak transcription	HUVEC	blood vessel
45	chr9:14588000-14596000	Weak transcription	Brain Cingulate Gyrus	brain
46	chr9:14588200-14589000	Weak transcription	Aorta	Aorta
47	chr9:14588200-14591200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr9:14588200-14618800	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr9:14588800-14595800	Weak transcription	Liver	Liver
50	chr9:14588800-14595800	Weak transcription	Duodenum Mucosa	Duodenum

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