Variant report

Variant	nsv1047166
Chromosome Location	chr9:108693810-108921872
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:619)
CpG islands
(count:122)
Chromatin interactive
region (count:81)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr9:108757348-108757506	K562	blood:	n/a	n/a
2	BATF	chr9:108737675-108737838	GM12878	blood:	n/a	n/a
3	BATF	chr9:108732016-108732206	GM12878	blood:	n/a	chr9:108732114-108732125 chr9:108732115-108732125
4	BATF	chr9:108785740-108786054	GM12878	blood:	n/a	n/a
5	BATF	chr9:108726016-108726233	GM12878	blood:	n/a	n/a
6	BATF	chr9:108785770-108786058	GM12878	blood:	n/a	n/a
7	BATF	chr9:108726019-108726216	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:108713235-108713551	GM12878	blood:	n/a	n/a
9	BHLHE40	chr9:108737735-108737932	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:108713208-108713485	GM12878	blood:	n/a	n/a
11	CEBPB	chr9:108846473-108846601	A549	lung:	n/a	n/a
12	CEBPB	chr9:108751288-108751424	H1-hESC	embryonic stem cell:	n/a	chr9:108751353-108751364 chr9:108751351-108751362
13	CEBPB	chr9:108853780-108853830	A549	lung:	n/a	n/a
14	CEBPB	chr9:108820685-108820876	HepG2	liver:	n/a	chr9:108820725-108820736
15	CEBPB	chr9:108716307-108716810	MCF-7	breast:	n/a	n/a
16	CEBPB	chr9:108860726-108860872	HepG2	liver:	n/a	n/a
17	CEBPB	chr9:108914461-108914650	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:108716426-108716719	MCF-7	breast:	n/a	n/a
19	CEBPB	chr9:108839131-108839473	MCF-7	breast:	n/a	n/a
20	CEBPB	chr9:108751265-108751465	HepG2	liver:	n/a	chr9:108751353-108751364 chr9:108751351-108751362
21	CHD2	chr9:108737634-108737889	GM12878	blood:	n/a	n/a
22	CHD2	chr9:108713302-108713522	GM12878	blood:	n/a	n/a
23	CHD2	chr9:108717006-108717071	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr9:108721040-108721190	RPTEC	kidney:	n/a	chr9:108721051-108721069
25	CTCF	chr9:108854480-108854630	HEK293	kidney:	n/a	n/a
26	CTCF	chr9:108862071-108862137	Lung_OC	lung:	n/a	n/a
27	CTCF	chr9:108721021-108721122	LNCaP	prostate:	n/a	chr9:108721051-108721069
28	CTCF	chr9:108694840-108694990	GM12871	blood:	n/a	n/a
29	CTCF	chr9:108721008-108721070	HepG2	liver:	n/a	chr9:108721051-108721069
30	CTCF	chr9:108788080-108788230	NHEK	skin:	n/a	n/a
31	CTCF	chr9:108787720-108787870	A549	lung:	n/a	n/a
32	CTCF	chr9:108721000-108721150	MCF-7	breast:	n/a	chr9:108721051-108721069
33	CTCF	chr9:108854480-108854630	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr9:108813180-108813330	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:108873400-108873550	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr9:108766297-108766326	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr9:108787760-108787910	GM12874	blood:	n/a	n/a
38	CTCF	chr9:108859981-108860038	GM10248	blood:	n/a	n/a
39	CTCF	chr9:108698509-108698556	LNCaP	prostate:	n/a	n/a
40	CTCF	chr9:108813100-108813250	NHEK	skin:	n/a	n/a
41	CTCF	chr9:108873420-108873570	NHEK	skin:	n/a	n/a
42	CTCF	chr9:108787853-108787995	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr9:108865936-108866021	GM10266	blood:	n/a	n/a
44	CTCF	chr9:108720960-108721110	HRE	kidney:	n/a	chr9:108721051-108721069
45	CTCF	chr9:108718069-108718117	GM13976	blood:	n/a	n/a
46	CTCF	chr9:108896860-108897010	GM12869	blood:	n/a	n/a
47	CTCF	chr9:108873460-108873610	HAc	cerebellar:	n/a	n/a
48	CTCF	chr9:108873420-108873570	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr9:108803460-108803610	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr9:108720974-108721135	LNCaP	prostate:	n/a	chr9:108721051-108721069

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:108800295-108800345	IMR90	lung:	fetal
2	chr9:108762462-108762512	RPTEC	kidney:	n/a
3	chr9:108762462-108762512	HMEC	breast:	n/a
4	chr9:108762462-108762512	U87	brain:	n/a
5	chr9:108762462-108762512	HRE	kidney:	n/a
6	chr9:108762462-108762512	HUVEC	blood vessel:	n/a
7	chr9:108762462-108762512	AG04450	lung:	fetal
8	chr9:108762462-108762512	Hela-S3	cervix:	n/a
9	chr9:108762462-108762512	AG09319	gingival:	n/a
10	chr9:108800295-108800345	ProgFib	skin:	n/a
11	chr9:108762462-108762512	K562	blood:	n/a
12	chr9:108762462-108762512	PrEC	prostate:	n/a
13	chr9:108800295-108800345	AG09309	skin:	n/a
14	chr9:108762462-108762512	HEEpiC	esophagus:	n/a
15	chr9:108800295-108800345	HUVEC	blood vessel:	n/a
16	chr9:108762462-108762512	GM19239	blood:	n/a
17	chr9:108762462-108762512	NB4	blood:	n/a
18	chr9:108762462-108762512	HEK293	kidney:	embryo
19	chr9:108800295-108800345	AoSMC	blood vessel:	n/a
20	chr9:108762462-108762512	A549	lung:	n/a
21	chr9:108800295-108800345	MCF-7	breast:	n/a
22	chr9:108762462-108762512	HepG2	liver:	n/a
23	chr9:108762462-108762512	ECC-1	luminal epithelium:	n/a
24	chr9:108800295-108800345	AG04449	skin:	fetal
25	chr9:108762462-108762512	GM12878	blood:	n/a
26	chr9:108762462-108762512	CMK	blood:	n/a
27	chr9:108800295-108800345	GM19239	blood:	n/a
28	chr9:108762462-108762512	HRCEpiC	kidney:	n/a
29	chr9:108762462-108762512	HIPEpiC	eye:	n/a
30	chr9:108762462-108762512	AoSMC	blood vessel:	n/a
31	chr9:108800295-108800345	PANC-1	pancreas:	n/a
32	chr9:108762462-108762512	HCF	heart:	n/a
33	chr9:108800295-108800345	BJ	skin:	n/a
34	chr9:108800295-108800345	HRE	kidney:	n/a
35	chr9:108762462-108762512	MCF-7	breast:	n/a
36	chr9:108800295-108800345	A549	lung:	n/a
37	chr9:108762462-108762512	PANC-1	pancreas:	n/a
38	chr9:108800295-108800345	NHDF-neo	bronchial:	n/a
39	chr9:108800295-108800345	LNCaP	prostate:	n/a
40	chr9:108762462-108762512	AG04449	skin:	fetal
41	chr9:108762462-108762512	GM06990	blood:	n/a
42	chr9:108800295-108800345	GM12892	blood:	n/a
43	chr9:108800295-108800345	HRCEpiC	kidney:	n/a
44	chr9:108762462-108762512	SKMC	muscle:	n/a
45	chr9:108800295-108800345	HCT-116	colon:	n/a
46	chr9:108800295-108800345	HEEpiC	esophagus:	n/a
47	chr9:108762462-108762512	AG10803	skin:	n/a
48	chr9:108800295-108800345	HMEC	breast:	n/a
49	chr9:108800295-108800345	NT2-D1	testis:	n/a
50	chr9:108762462-108762512	Caco-2	colon:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:108733704..108736486-chr9:108737620..108740615,3	K562	blood:
2	chr1:153962081..153963807-chr9:108838236..108840740,2	MCF-7	breast:
3	chr9:108818298..108821025-chr9:108821696..108823248,2	MCF-7	breast:
4	chr9:108867120..108869038-chr9:108889335..108891423,2	MCF-7	breast:
5	chr9:108743810..108745553-chr9:108748494..108750852,2	MCF-7	breast:
6	chr9:108671913..108676613-chr9:108714105..108718467,7	MCF-7	breast:
7	chr9:108664056..108664697-chr9:108716237..108717041,4	MCF-7	breast:
8	chr9:108674841..108675762-chr9:108716167..108716908,4	MCF-7	breast:
9	chr9:108739199..108741928-chr9:108744819..108747218,2	MCF-7	breast:
10	chr9:108892215..108894601-chr9:108896083..108898986,2	MCF-7	breast:
11	chr9:108735876..108737559-chr9:108746600..108748766,2	MCF-7	breast:
12	chr9:108778868..108781352-chr9:108786152..108788884,2	MCF-7	breast:
13	chr9:108746568..108749156-chr9:108749954..108752153,2	K562	blood:
14	chr9:108721151..108722856-chr9:108726087..108728070,2	K562	blood:
15	chr9:108789292..108791583-chr9:108811353..108813337,2	MCF-7	breast:
16	chr9:108859042..108861403-chr9:108867746..108869776,2	MCF-7	breast:
17	chr9:108739199..108741928-chr9:108744819..108747218,2	MCF-7	breast:
18	chr9:108811897..108815264-chr9:108817191..108819069,3	MCF-7	breast:
19	chr9:108874969..108876635-chr9:108880417..108883315,2	MCF-7	breast:
20	chr9:108764061..108766161-chr9:108771652..108773698,2	K562	blood:
21	chr9:108747334..108748914-chr9:108748996..108750788,2	MCF-7	breast:
22	chr9:108867120..108869038-chr9:108889335..108891423,2	MCF-7	breast:
23	chr9:108778868..108781352-chr9:108786152..108788884,2	MCF-7	breast:
24	chr9:108889275..108891761-chr9:108895240..108897021,2	MCF-7	breast:
25	chr9:108919400..108921084-chr9:108923657..108926656,2	K562	blood:
26	chr9:108743810..108745553-chr9:108748494..108750852,2	MCF-7	breast:
27	chr9:108812042..108815207-chr9:108821984..108824816,3	MCF-7	breast:
28	chr9:108777935..108779768-chr9:108780496..108782392,2	MCF-7	breast:
29	chr9:108758783..108761114-chr9:108762708..108764759,2	K562	blood:
30	chr9:108860723..108863185-chr9:108872500..108874726,2	MCF-7	breast:
31	chr9:108722498..108724608-chr9:108787203..108789286,2	MCF-7	breast:
32	chr9:108789292..108791583-chr9:108811353..108813337,2	MCF-7	breast:
33	chr9:108747334..108748914-chr9:108748996..108750788,2	MCF-7	breast:
34	chr17:41465705..41467813-chr9:108728033..108731013,2	K562	blood:
35	chr9:108845749..108847579-chr9:108873954..108876474,2	MCF-7	breast:
36	chr9:108735876..108737559-chr9:108746600..108748766,2	MCF-7	breast:
37	chr9:108715768..108718223-chr9:108919193..108921153,2	MCF-7	breast:
38	chr9:108730359..108732528-chr9:108735716..108738516,2	MCF-7	breast:
39	chr9:108746568..108749156-chr9:108749954..108752153,2	K562	blood:
40	chr17:41398659..41400164-chr9:108728013..108729513,2	MCF-7	breast:
41	chr9:108674585..108677315-chr9:108738998..108740830,2	MCF-7	breast:
42	chr9:108882738..108885748-chr9:108888173..108891045,3	MCF-7	breast:
43	chr9:108675540..108677148-chr9:108871397..108873655,2	MCF-7	breast:
44	chr9:108845749..108847579-chr9:108873954..108876474,2	MCF-7	breast:
45	chr9:108663816..108664349-chr9:108716067..108716712,2	MCF-7	breast:
46	chr9:108782876..108784609-chr9:108788565..108791271,2	MCF-7	breast:
47	chr9:108872411..108874776-chr9:110044815..110046368,2	MCF-7	breast:
48	chr9:108777935..108779768-chr9:108780496..108782392,2	MCF-7	breast:
49	chr9:108674706..108675762-chr9:108716067..108717001,6	MCF-7	breast:
50	chr9:108716073..108716703-chr9:109893850..109894510,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCA1-3	chr9:108826917-108827106	ENSG00000225002.2
2	lnc-ABCA1-3	chr9:108827105-108827274	XLOC_007817
3	lnc-ABCA1-3	chr9:108823635-108823900	XLOC_007817
4	lnc-TMEM38B-1	chr9:108870332-108870429	NONHSAT133833
5	lnc-TMEM38B-1	chr9:108870332-108870429	XLOC_007500
6	lnc-ABCA1-3	chr9:108823635-108823900	ENSG00000225002.2

No data

Variant related genes	Relation type
ENSG00000225002	TF binding region
ENSG00000225002	CpG island
ENSG00000188825	chromatin interactions
ENSG00000119318	chromatin interactions
ENSG00000177954	chromatin interactions
ENSG00000148143	chromatin interactions
C15orf27	miRNA target sites

Extended variants
information (count: 6454 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6454 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148246768	chr9:108693811-108693812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537000405	chr9:108693849-108693850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549273379	chr9:108693862-108693863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569647900	chr9:108693896-108693897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141870052	chr9:108693905-108693906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200031765	chr9:108693926-108693927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535239838	chr9:108693930-108693931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114339182	chr9:108693977-108693978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578113651	chr9:108694000-108694001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150638123	chr9:108694010-108694011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73508474	chr9:108694189-108694190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185126598	chr9:108694242-108694243	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs576111495	chr9:108694254-108694255	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs34235964	chr9:108694267-108694268	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs539710266	chr9:108694309-108694310	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs573880541	chr9:108694341-108694342	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs541302385	chr9:108694347-108694348	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs190733269	chr9:108694380-108694381	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs4742659	chr9:108694397-108694398	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs184226070	chr9:108694455-108694456	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs368274911	chr9:108694487-108694488	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs188679253	chr9:108694513-108694514	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs192012037	chr9:108694559-108694560	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs548935937	chr9:108694604-108694605	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs567632467	chr9:108694637-108694638	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs183082297	chr9:108694644-108694645	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs80161037	chr9:108694675-108694676	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs528820959	chr9:108694707-108694708	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs77284005	chr9:108694782-108694783	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs558679314	chr9:108694829-108694830	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs187416952	chr9:108694897-108694898	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs114544808	chr9:108694901-108694902	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs557897910	chr9:108694915-108694916	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs73668604	chr9:108694920-108694921	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs376229444	chr9:108694950-108694951	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs372230809	chr9:108694962-108694963	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs537065741	chr9:108694986-108694987	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs538201473	chr9:108695047-108695048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555102764	chr9:108695133-108695134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544326743	chr9:108695268-108695269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541011738	chr9:108695324-108695325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553184185	chr9:108695349-108695350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191791099	chr9:108695398-108695399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7470829	chr9:108697256-108697257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528917897	chr9:108697285-108697286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575101875	chr9:108697347-108697348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542141368	chr9:108697350-108697351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185447224	chr9:108697444-108697445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191132069	chr9:108697467-108697468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539944579	chr9:108697546-108697547	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:914 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108692400-108694200	Enhancers	Fetal Heart	heart
2	chr9:108693400-108694200	Enhancers	Brain Hippocampus Middle	brain
3	chr9:108693600-108694200	Enhancers	Brain Substantia Nigra	brain
4	chr9:108693600-108695200	Enhancers	Brain Cingulate Gyrus	brain
5	chr9:108693600-108695200	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr9:108693800-108694600	Weak transcription	Brain Anterior Caudate	brain
7	chr9:108693800-108695400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr9:108694200-108694400	Enhancers	Brain Angular Gyrus	brain
9	chr9:108694200-108694400	Flanking Active TSS	Brain Hippocampus Middle	brain
10	chr9:108694200-108695000	Flanking Active TSS	Brain Substantia Nigra	brain
11	chr9:108694200-108695000	Active TSS	Fetal Heart	heart
12	chr9:108694400-108694800	Active TSS	Brain Hippocampus Middle	brain
13	chr9:108694600-108695200	Enhancers	Brain Anterior Caudate	brain
14	chr9:108694800-108695000	Flanking Active TSS	Brain Hippocampus Middle	brain
15	chr9:108695000-108695200	Enhancers	Brain Substantia Nigra	brain
16	chr9:108697200-108697600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr9:108697400-108697800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:108716800-108717000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr9:108716800-108717000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr9:108716800-108717200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr9:108717000-108717200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr9:108717000-108717600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr9:108717000-108718000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr9:108717200-108717600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr9:108717200-108717800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr9:108717200-108718200	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr9:108717200-108718200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr9:108717200-108718600	Enhancers	Fetal Heart	heart
29	chr9:108717200-108721400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr9:108717400-108718200	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr9:108717400-108720000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:108717600-108717800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr9:108717600-108717800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr9:108717600-108718800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr9:108717800-108718200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr9:108717800-108719600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr9:108718000-108719000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr9:108718200-108718400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr9:108718200-108718600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr9:108718200-108720200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr9:108718200-108721800	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr9:108718400-108718600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr9:108718400-108721600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr9:108718600-108719200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr9:108718600-108719600	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr9:108718800-108719800	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr9:108719000-108719400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr9:108719200-108720200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr9:108719400-108721600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr9:108719600-108720400	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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