Variant report

Variant	nsv892658
Chromosome Location	chr9:17041557-17532840
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2521)
CpG islands
(count:428)
Chromatin interactive
region (count:30)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2521 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:17531669-17532065	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:17171685-17171982	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:17137735-17137782	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:17531774-17531980	K562	blood:	n/a	n/a
5	ARID3A	chr9:17138550-17138914	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:17057789-17058149	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:17116377-17116869	HepG2	liver:	n/a	n/a
8	BACH1	chr9:17134393-17135230	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:17469243-17469263	K562	blood:	n/a	n/a
10	BATF	chr9:17057808-17058032	GM12878	blood:	n/a	n/a
11	BCL3	chr9:17134706-17135204	A549	lung:	n/a	n/a
12	BHLHE40	chr9:17493831-17493973	K562	blood:	n/a	n/a
13	BHLHE40	chr9:17462961-17463213	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:17057793-17058031	HepG2	liver:	n/a	n/a
15	BRCA1	chr9:17134759-17135091	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr9:17135427-17135902	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr9:17134617-17135090	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr9:17396862-17396940	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr9:17110915-17111000	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:17089787-17090042	HepG2	liver:	n/a	chr9:17089927-17089938
21	CEBPB	chr9:17526758-17527072	MCF-7	breast:	n/a	chr9:17526931-17526942
22	CEBPB	chr9:17457566-17457746	HepG2	liver:	n/a	chr9:17457686-17457697
23	CEBPB	chr9:17526868-17527080	HepG2	liver:	n/a	chr9:17526931-17526942
24	CEBPB	chr9:17103234-17103434	HepG2	liver:	n/a	chr9:17103349-17103360
25	CEBPB	chr9:17440906-17441152	IMR90	lung:	n/a	chr9:17441002-17441013
26	CEBPB	chr9:17104175-17104375	A549	lung:	n/a	n/a
27	CEBPB	chr9:17464930-17465234	A549	lung:	n/a	n/a
28	CEBPB	chr9:17342525-17342788	IMR90	lung:	n/a	chr9:17342605-17342616 chr9:17342604-17342617 chr9:17342604-17342615 chr9:17342604-17342617 chr9:17342604-17342617
29	CEBPB	chr9:17494858-17494998	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr9:17134379-17135487	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr9:17359924-17360128	HepG2	liver:	n/a	chr9:17360064-17360075 chr9:17360018-17360029
32	CEBPB	chr9:17138347-17138844	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:17130336-17130640	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr9:17440917-17441132	HepG2	liver:	n/a	chr9:17441002-17441013
35	CEBPB	chr9:17531450-17531951	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr9:17180013-17180198	IMR90	lung:	n/a	chr9:17180087-17180098
37	CEBPB	chr9:17377365-17377657	Hela-S3	cervix:	n/a	chr9:17377489-17377500
38	CEBPB	chr9:17377353-17377651	IMR90	lung:	n/a	chr9:17377489-17377500
39	CEBPB	chr9:17464897-17465248	IMR90	lung:	n/a	n/a
40	CEBPB	chr9:17531531-17531857	A549	lung:	n/a	n/a
41	CEBPB	chr9:17377353-17377652	H1-hESC	embryonic stem cell:	n/a	chr9:17377489-17377500
42	CEBPB	chr9:17464977-17465153	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr9:17377317-17377640	A549	lung:	n/a	chr9:17377489-17377500
44	CEBPB	chr9:17103254-17103425	A549	lung:	n/a	chr9:17103349-17103360
45	CEBPB	chr9:17130849-17131069	H1-hESC	embryonic stem cell:	n/a	chr9:17130907-17130918
46	CEBPB	chr9:17134697-17135085	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr9:17526883-17527024	Hela-S3	cervix:	n/a	chr9:17526931-17526942
48	CEBPB	chr9:17280466-17280824	IMR90	lung:	n/a	n/a
49	CEBPB	chr9:17458729-17459037	IMR90	lung:	n/a	chr9:17458858-17458869 chr9:17458860-17458869 chr9:17458858-17458871 chr9:17458859-17458870
50	CEBPB	chr9:17406822-17407056	A549	lung:	n/a	chr9:17406919-17406930 chr9:17406918-17406931

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17134842-17134892	A549	lung:	n/a
2	chr9:17134842-17134892	A549	lung:	n/a
3	chr9:17137020-17137070	AG04450	lung:	fetal
4	chr9:17134842-17134892	IMR90	lung:	fetal
5	chr9:17137020-17137070	SK-N-MC	brain:	n/a
6	chr9:17134842-17134892	AG04449	skin:	fetal
7	chr9:17135705-17135755	ProgFib	skin:	n/a
8	chr9:17132989-17133039	U87	brain:	n/a
9	chr9:17134569-17134619	HEK293	kidney:	embryo
10	chr9:17134569-17134619	HRE	kidney:	n/a
11	chr9:17503269-17503319	HCT-116	colon:	n/a
12	chr9:17135705-17135755	IMR90	lung:	fetal
13	chr9:17135705-17135755	SKMC	muscle:	n/a
14	chr9:17503269-17503319	NH-A	brain:	n/a
15	chr9:17134842-17134892	NB4	blood:	n/a
16	chr9:17135705-17135755	PANC-1	pancreas:	n/a
17	chr9:17132989-17133039	HIPEpiC	eye:	n/a
18	chr9:17354129-17354179	SK-N-SH_RA	brain:	n/a
19	chr9:17354129-17354179	RPTEC	kidney:	n/a
20	chr9:17137020-17137070	GM06990	blood:	n/a
21	chr9:17132989-17133039	GM12878	blood:	n/a
22	chr9:17134569-17134619	HCPEpiC	choroid plexus:	n/a
23	chr9:17134569-17134619	HRPEpiC	eye:	n/a
24	chr9:17135705-17135755	T-47D	breast:	n/a
25	chr9:17137020-17137070	PANC-1	pancreas:	n/a
26	chr9:17134569-17134619	AG09309	skin:	n/a
27	chr9:17137020-17137070	NH-A	brain:	n/a
28	chr9:17503269-17503319	AG04449	skin:	fetal
29	chr9:17503269-17503319	HL-60	blood:	n/a
30	chr9:17137020-17137070	HMEC	breast:	n/a
31	chr9:17132989-17133039	SK-N-MC	brain:	n/a
32	chr9:17132989-17133039	HUVEC	blood vessel:	n/a
33	chr9:17132989-17133039	BE2_C	brain:	n/a
34	chr9:17132989-17133039	RPTEC	kidney:	n/a
35	chr9:17503269-17503319	AG04450	lung:	fetal
36	chr9:17503269-17503319	MCF10A-Er-Src	breast:	n/a
37	chr9:17134842-17134892	HRPEpiC	eye:	n/a
38	chr9:17137020-17137070	ovcar-3	ovarian:	n/a
39	chr9:17135705-17135755	HPAEpiC	pulmonary alveolar:	n/a
40	chr9:17134569-17134619	HCT-116	colon:	n/a
41	chr9:17503269-17503319	PANC-1	pancreas:	n/a
42	chr9:17132989-17133039	IMR90	lung:	fetal
43	chr9:17132989-17133039	LNCaP	prostate:	n/a
44	chr9:17134569-17134619	HIPEpiC	eye:	n/a
45	chr9:17134569-17134619	HRCEpiC	kidney:	n/a
46	chr9:17354129-17354179	NB4	blood:	n/a
47	chr9:17135705-17135755	HIPEpiC	eye:	n/a
48	chr9:17135705-17135755	HNPCEpiC	eye:	n/a
49	chr9:17503269-17503319	NT2-D1	testis:	n/a
50	chr9:17134569-17134619	GM06990	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:17219375..17219930-chr9:17402045..17403347,3	MCF-7	breast:
2	chr1:11969364..11970234-chr9:17134620..17135236,2	Hela-S3	cervix:
3	chr9:17531372..17532326-chr9:17801979..17802845,5	MCF-7	breast:
4	chr9:17219375..17219930-chr9:17402045..17403347,3	MCF-7	breast:
5	chr9:17531792..17532337-chr9:17794326..17794832,2	MCF-7	breast:
6	chr9:17116081..17117141-chr9:17402172..17402905,3	MCF-7	breast:
7	chr9:17531556..17532244-chr9:17793906..17794864,2	MCF-7	breast:
8	chr5:34498444..34499344-chr9:17525014..17525908,2	MCF-7	breast:
9	chr9:17317781..17319396-chr9:17320003..17322475,2	MCF-7	breast:
10	chr9:17063303..17064146-chr9:17462547..17463504,3	MCF-7	breast:
11	chr9:17116081..17117141-chr9:17402172..17402905,3	MCF-7	breast:
12	chr9:17219155..17220052-chr9:17401883..17402825,5	MCF-7	breast:
13	chr9:17219155..17220052-chr9:17401883..17402825,5	MCF-7	breast:
14	chr15:23810837..23811461-chr9:17134816..17135417,2	NB4	blood:
15	chr9:17317781..17319396-chr9:17320003..17322475,2	MCF-7	breast:
16	chr9:17116233..17116835-chr9:17462927..17463473,2	MCF-7	breast:
17	chr9:17116046..17116795-chr9:17462771..17463533,2	MCF-7	breast:
18	chr9:17528626..17529303-chr9:17802052..17802868,3	MCF-7	breast:
19	chr6:692813..693544-chr9:17134998..17135501,2	NB4	blood:
20	chr9:17063303..17064146-chr9:17462547..17463504,3	MCF-7	breast:
21	chr9:17116233..17116835-chr9:17462927..17463473,2	MCF-7	breast:
22	chr9:17219048..17219921-chr9:17462587..17463121,2	MCF-7	breast:
23	chr9:17531221..17532407-chr9:17801949..17802935,11	MCF-7	breast:
24	chr13:49549584..49550165-chr9:17134587..17135235,2	NB4	blood:
25	chr17:59651978..59652576-chr9:17247861..17248361,2	MCF-7	breast:
26	chr9:17531412..17532247-chr9:18212958..18213842,2	MCF-7	breast:
27	chr5:43121428..43122109-chr9:17134722..17135406,2	Hela-S3	cervix:
28	chr9:17219048..17219921-chr9:17462587..17463121,2	MCF-7	breast:
29	chr9:17528534..17529118-chr9:18207797..18208372,2	MCF-7	breast:
30	chr9:17116046..17116795-chr9:17462771..17463533,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3GL2-2	chr9:17415964-17416187	NONHSAT130301
2	lnc-CNTLN-1	chr9:17048917-17049039	ENSG00000237153.1
3	lnc-CNTLN-4	chr9:17053899-17054200	NONHSAT130298
4	lnc-SH3GL2-3	chr9:17322212-17322433	uc_253_+
5	lnc-SH3GL2-2	chr9:17415816-17415879	NONHSAT130301
6	lnc-BNC2-4	chr9:17447143-17448541	NONHSAT130303
7	lnc-SH3GL2-1	chr9:17435732-17437445	NONHSAT130302
8	lnc-SH3GL2-2	chr9:17457522-17457626	NONHSAT130301
9	lnc-SH3GL2-2	chr9:17462914-17462982	NONHSAT130301
10	lnc-SH3GL2-2	chr9:17444195-17444244	NONHSAT130301
11	lnc-BNC2-3	chr9:17322212-17322433	uc_253_-
12	lnc-CNTLN-1	chr9:17112271-17112813	ENSG00000237153.1
13	lnc-BNC2-2	chr9:17108302-17108602	NONHSAT130300

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CNTLN	hsa-miR-26b-5p	chr9:17503103-17503123

Variant related genes	Relation type
ENSG00000226470	TF binding region
ENSG00000237083	TF binding region
RN7SL720P	TF binding region
ENSG00000237153	TF binding region
ENSG00000224488	TF binding region
CNTLN	TF binding region
ENSG00000226470	CpG island
ENSG00000237083	CpG island
RN7SL720P	CpG island
ENSG00000237153	CpG island
ENSG00000224488	CpG island
CNTLN	CpG island
ENSG00000112685	chromatin interactions
ENSG00000102531	chromatin interactions
ENSG00000201801	chromatin interactions
ENSG00000179455	chromatin interactions
ENSG00000172262	chromatin interactions

Extended variants
information (count: 20454 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:20454 , 50 per page) page: 1 2 3 4 5 6 7 ... 410

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs193206955	chr9:17042240-17042241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560854701	chr9:17042248-17042249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7020057	chr9:17042290-17042291	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs538854357	chr9:17042307-17042308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184898706	chr9:17042320-17042321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566137366	chr9:17042334-17042335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113731921	chr9:17042340-17042341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536789515	chr9:17042388-17042389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188049685	chr9:17042414-17042415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576408043	chr9:17042425-17042426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34411620	chr9:17042520-17042521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149157313	chr9:17042522-17042523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2694058	chr9:17042544-17042545	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs577964442	chr9:17042589-17042590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs75690228	chr9:17042623-17042624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148288551	chr9:17042635-17042636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572130088	chr9:17042636-17042637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542734189	chr9:17042691-17042692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142990395	chr9:17042697-17042698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531353471	chr9:17042733-17042734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369748889	chr9:17042791-17042792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549322514	chr9:17042846-17042847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565237708	chr9:17042855-17042856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2632544	chr9:17042893-17042894	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs547672935	chr9:17042908-17042909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566293484	chr9:17042924-17042925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs80047243	chr9:17042933-17042934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs56284864	chr9:17042974-17042975	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs375127394	chr9:17043024-17043025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191369175	chr9:17043036-17043037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564696013	chr9:17043037-17043038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147048747	chr9:17043052-17043053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183894366	chr9:17043070-17043071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138187025	chr9:17043092-17043093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189739928	chr9:17043100-17043101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201715562	chr9:17043101-17043102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146346917	chr9:17043102-17043103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377730168	chr9:17043103-17043104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151304452	chr9:17043155-17043156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71933946	chr9:17043156-17043157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143769265	chr9:17043163-17043164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113896359	chr9:17043165-17043166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs56132921	chr9:17043169-17043170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561047812	chr9:17043198-17043199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181335452	chr9:17043253-17043254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543107788	chr9:17043258-17043259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564577711	chr9:17043274-17043275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73416311	chr9:17043283-17043284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs185127976	chr9:17043291-17043292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559763805	chr9:17043299-17043300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:2480 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17042200-17043000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr9:17043000-17044800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr9:17044800-17045600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr9:17052800-17053200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:17053200-17062600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:17057400-17058400	Enhancers	Fetal Intestine Large	intestine
7	chr9:17057600-17058200	Enhancers	Duodenum Mucosa	Duodenum
8	chr9:17057600-17058200	Enhancers	Fetal Intestine Small	intestine
9	chr9:17057600-17058200	Enhancers	HepG2	liver
10	chr9:17058000-17058400	Enhancers	Stomach Mucosa	stomach
11	chr9:17058400-17062200	Weak transcription	Fetal Intestine Large	intestine
12	chr9:17059800-17060400	Enhancers	Adipose Nuclei	Adipose
13	chr9:17060200-17061000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:17062200-17062800	Enhancers	Fetal Intestine Small	intestine
15	chr9:17062200-17063200	Enhancers	Fetal Intestine Large	intestine
16	chr9:17062600-17062800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:17064400-17065200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:17064600-17064800	Enhancers	A549	lung
19	chr9:17064600-17066200	Enhancers	HUVEC	blood vessel
20	chr9:17064800-17065000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr9:17064800-17065400	Enhancers	Liver	Liver
22	chr9:17065000-17065400	Enhancers	Osteobl	bone
23	chr9:17065000-17078200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr9:17065200-17065400	Enhancers	Fetal Intestine Large	intestine
25	chr9:17068600-17069000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr9:17075000-17075800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr9:17075600-17076000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr9:17075600-17076800	Enhancers	Fetal Kidney	kidney
29	chr9:17076000-17076600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr9:17076600-17081600	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr9:17076800-17081800	Weak transcription	Fetal Kidney	kidney
32	chr9:17078200-17078400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr9:17078400-17078800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr9:17078800-17079000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr9:17079000-17081800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr9:17081200-17081600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:17081200-17082800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr9:17081400-17081800	Enhancers	Fetal Lung	lung
39	chr9:17081400-17082800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr9:17081400-17083000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr9:17081600-17082600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr9:17081600-17083000	Enhancers	H1 Cell Line	embryonic stem cell
43	chr9:17081600-17083000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr9:17081600-17083000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr9:17081600-17083400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr9:17081600-17083400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr9:17081600-17083400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr9:17081800-17082000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr9:17081800-17082200	Weak transcription	Fetal Lung	lung
50	chr9:17081800-17082800	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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