Variant report

Variant	nsv540171
Chromosome Location	chr9:94500213-94639367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1503)
CpG islands
(count:613)
Chromatin interactive
region (count:157)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1503 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:94509263-94509593	K562	blood:	n/a	n/a
2	ATF3	chr9:94594636-94594885	K562	blood:	n/a	n/a
3	BACH1	chr9:94509326-94509472	K562	blood:	n/a	n/a
4	BACH1	chr9:94537719-94537974	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:94518197-94518397	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr9:94520885-94521133	GM12878	blood:	n/a	chr9:94521028-94521037 chr9:94520955-94520962
7	BCL11A	chr9:94560694-94560892	GM12878	blood:	n/a	n/a
8	BCL3	chr9:94571805-94572046	GM12878	blood:	n/a	chr9:94571924-94571933
9	BHLHE40	chr9:94543502-94543538	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:94562799-94563091	K562	blood:	n/a	n/a
11	BHLHE40	chr9:94594687-94594884	K562	blood:	n/a	n/a
12	BHLHE40	chr9:94520748-94521291	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:94558018-94558354	K562	blood:	n/a	n/a
14	BHLHE40	chr9:94605121-94605334	GM12878	blood:	n/a	chr9:94605241-94605254
15	BHLHE40	chr9:94600505-94600832	K562	blood:	n/a	n/a
16	BHLHE40	chr9:94509152-94509632	K562	blood:	n/a	n/a
17	BHLHE40	chr9:94539172-94539470	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:94512785-94512905	K562	blood:	n/a	n/a
19	BHLHE40	chr9:94602447-94602630	GM12878	blood:	n/a	n/a
20	BHLHE40	chr9:94537775-94538055	K562	blood:	n/a	n/a
21	BHLHE40	chr9:94520787-94521016	K562	blood:	n/a	n/a
22	BHLHE40	chr9:94537821-94538068	GM12878	blood:	n/a	n/a
23	CBX3	chr9:94559904-94560500	K562	blood:	n/a	n/a
24	CBX3	chr9:94550185-94550700	K562	blood:	n/a	n/a
25	CBX3	chr9:94558815-94559856	K562	blood:	n/a	n/a
26	CBX3	chr9:94509158-94509614	K562	blood:	n/a	n/a
27	CBX3	chr9:94526946-94527316	K562	blood:	n/a	n/a
28	CCNT2	chr9:94560735-94560874	K562	blood:	n/a	n/a
29	CCNT2	chr9:94558828-94559160	K562	blood:	n/a	n/a
30	CCNT2	chr9:94548714-94548984	K562	blood:	n/a	n/a
31	CEBPB	chr9:94533294-94533576	A549	lung:	n/a	chr9:94533410-94533421
32	CEBPB	chr9:94570240-94570401	K562	blood:	n/a	n/a
33	CEBPB	chr9:94630121-94630432	K562	blood:	n/a	chr9:94630261-94630272
34	CEBPB	chr9:94533401-94533435	Hela-S3	cervix:	n/a	chr9:94533410-94533421
35	CEBPB	chr9:94630124-94630438	IMR90	lung:	n/a	chr9:94630261-94630272
36	CEBPB	chr9:94539753-94540073	A549	lung:	n/a	chr9:94539892-94539903
37	CEBPB	chr9:94525971-94526183	A549	lung:	n/a	chr9:94526057-94526068
38	CEBPB	chr9:94533222-94533541	MCF-7	breast:	n/a	chr9:94533410-94533421
39	CEBPB	chr9:94541856-94542045	HepG2	liver:	n/a	chr9:94541976-94541989 chr9:94541977-94541988
40	CEBPB	chr9:94570167-94570484	IMR90	lung:	n/a	n/a
41	CEBPB	chr9:94630119-94630407	K562	blood:	n/a	chr9:94630261-94630272
42	CEBPB	chr9:94540454-94540589	A549	lung:	n/a	chr9:94540509-94540520 chr9:94540508-94540521
43	CEBPB	chr9:94533228-94533780	IMR90	lung:	n/a	chr9:94533623-94533636 chr9:94533410-94533421
44	CEBPB	chr9:94580333-94580670	Hela-S3	cervix:	n/a	chr9:94580640-94580653
45	CEBPB	chr9:94539741-94540092	K562	blood:	n/a	chr9:94539892-94539903
46	CEBPB	chr9:94583523-94583811	IMR90	lung:	n/a	chr9:94583647-94583658 chr9:94583649-94583660 chr9:94583647-94583660 chr9:94583649-94583660
47	CEBPB	chr9:94541885-94542128	IMR90	lung:	n/a	chr9:94541976-94541989 chr9:94541977-94541988
48	CEBPB	chr9:94540387-94540564	Hela-S3	cervix:	n/a	chr9:94540509-94540520 chr9:94540508-94540521
49	CEBPB	chr9:94630243-94630289	Hela-S3	cervix:	n/a	chr9:94630261-94630272
50	CEBPB	chr9:94580239-94580769	IMR90	lung:	n/a	chr9:94580640-94580653

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:94565110-94565160	ovcar-3	ovarian:	n/a
2	chr9:94520862-94520912	IMR90	lung:	fetal
3	chr9:94540286-94540336	NH-A	brain:	n/a
4	chr9:94565110-94565160	ovcar-3	ovarian:	n/a
5	chr9:94520862-94520912	IMR90	lung:	fetal
6	chr9:94540286-94540336	NH-A	brain:	n/a
7	chr9:94533180-94533230	CMK	blood:	n/a
8	chr9:94540286-94540336	BJ	skin:	n/a
9	chr9:94606638-94606688	MCF10A-Er-Src	breast:	n/a
10	chr9:94572995-94573045	H1-hESC	embryonic stem cell:	embryo
11	chr9:94520862-94520912	NT2-D1	testis:	n/a
12	chr9:94561075-94561125	MCF-7	breast:	n/a
13	chr9:94533180-94533230	K562	blood:	n/a
14	chr9:94533180-94533230	A549	lung:	n/a
15	chr9:94520862-94520912	AoSMC	blood vessel:	n/a
16	chr9:94606638-94606688	RPTEC	kidney:	n/a
17	chr9:94533180-94533230	AG09319	gingival:	n/a
18	chr9:94606638-94606688	GM12892	blood:	n/a
19	chr9:94606638-94606688	HCT-116	colon:	n/a
20	chr9:94561075-94561125	HIPEpiC	eye:	n/a
21	chr9:94579826-94579876	T-47D	breast:	n/a
22	chr9:94565110-94565160	HPAEpiC	pulmonary alveolar:	n/a
23	chr9:94572995-94573045	BJ	skin:	n/a
24	chr9:94565110-94565160	SKMC	muscle:	n/a
25	chr9:94565110-94565160	HUVEC	blood vessel:	n/a
26	chr9:94565110-94565160	HL-60	blood:	n/a
27	chr9:94577112-94577162	PANC-1	pancreas:	n/a
28	chr9:94577112-94577162	K562	blood:	n/a
29	chr9:94577112-94577162	PFSK-1	brain:	n/a
30	chr9:94619684-94619734	AoSMC	blood vessel:	n/a
31	chr9:94577112-94577162	SKMC	muscle:	n/a
32	chr9:94579826-94579876	HRCEpiC	kidney:	n/a
33	chr9:94572995-94573045	NHDF-neo	bronchial:	n/a
34	chr9:94619684-94619734	HPAEpiC	pulmonary alveolar:	n/a
35	chr9:94565110-94565160	LNCaP	prostate:	n/a
36	chr9:94577112-94577162	HCPEpiC	choroid plexus:	n/a
37	chr9:94565110-94565160	HRCEpiC	kidney:	n/a
38	chr9:94577112-94577162	MCF10A-Er-Src	breast:	n/a
39	chr9:94572995-94573045	HL-60	blood:	n/a
40	chr9:94561075-94561125	NT2-D1	testis:	n/a
41	chr9:94619684-94619734	HCM	heart:	n/a
42	chr9:94606638-94606688	SK-N-SH	brain:	n/a
43	chr9:94577112-94577162	Jurkat	blood:	n/a
44	chr9:94540286-94540336	HRCEpiC	kidney:	n/a
45	chr9:94572995-94573045	HAEpiC	amniotic membrane:	n/a
46	chr9:94579826-94579876	SK-N-MC	brain:	n/a
47	chr9:94561075-94561125	GM06990	blood:	n/a
48	chr9:94606638-94606688	HRCEpiC	kidney:	n/a
49	chr9:94533180-94533230	HepG2	liver:	n/a
50	chr9:94540286-94540336	LNCaP	prostate:	n/a

(count:157 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr9:94614773..94617225-chr9:94629164..94630767,2	K562	blood:
2	chr9:94591392..94592961-chr9:94594858..94596367,2	K562	blood:
3	chr9:94569574..94571873-chr9:94577542..94579809,2	K562	blood:
4	chr9:94547554..94551405-chr9:94555591..94559410,4	K562	blood:
5	chr9:94534777..94536619-chr9:94540454..94542317,2	MCF-7	breast:
6	chr9:94516080..94518691-chr9:94519626..94521518,2	MCF-7	breast:
7	chr9:94520499..94521292-chr9:94533176..94533953,2	MCF-7	breast:
8	chr9:94530728..94533133-chr9:94548212..94550355,2	K562	blood:
9	chr9:94597146..94598805-chr9:94600443..94602240,2	K562	blood:
10	chr9:94570310..94572963-chr9:94575340..94577393,3	K562	blood:
11	chr9:94626758..94629803-chr9:94629808..94631771,3	K562	blood:
12	chr9:94538158..94540180-chr9:94661146..94663275,2	K562	blood:
13	chr9:94626760..94629171-chr9:94633039..94635717,3	K562	blood:
14	chr9:94599805..94602377-chr9:94607458..94609463,2	K562	blood:
15	chr9:94572281..94574995-chr9:94578094..94579689,2	MCF-7	breast:
16	chr9:94596679..94601637-chr9:94602257..94606458,6	K562	blood:
17	chr9:94626760..94629171-chr9:94633039..94635717,3	K562	blood:
18	chr9:94509113..94511832-chr9:94540924..94543887,2	K562	blood:
19	chr9:94508551..94510877-chr9:94514167..94515784,2	MCF-7	breast:
20	chr9:94559930..94562957-chr9:94564256..94567376,4	K562	blood:
21	chr9:94545257..94548150-chr9:94554695..94556652,2	K562	blood:
22	chr9:94511870..94513759-chr9:94524409..94527120,2	MCF-7	breast:
23	chr9:94560025..94562581-chr9:94709584..94711088,2	K562	blood:
24	chr9:94579358..94582251-chr9:94586460..94588565,3	MCF-7	breast:
25	chr9:94602829..94604983-chr9:94613867..94616038,2	K562	blood:
26	chr9:94538204..94538891-chr9:94644905..94645570,2	MCF-7	breast:
27	chr9:94516080..94518691-chr9:94519626..94521518,2	MCF-7	breast:
28	chr10:131265189..131266009-chr9:94537721..94538470,2	HCT-116	colon:
29	chr9:94549725..94552292-chr9:94608057..94610041,2	K562	blood:
30	chr9:94603914..94606181-chr9:94621038..94623335,2	MCF-7	breast:
31	chr9:94619022..94622671-chr9:94625624..94629747,5	K562	blood:
32	chr9:94597584..94599500-chr9:94607793..94610758,2	K562	blood:
33	chr9:94497979..94500430-chr9:94500591..94503129,2	K562	blood:
34	chr9:94566439..94568761-chr9:94577681..94581250,3	MCF-7	breast:
35	chr9:94520440..94521332-chr9:94712111..94713033,4	K562	blood:
36	chr9:94513749..94516669-chr9:94667565..94670057,2	K562	blood:
37	chr9:94626758..94629803-chr9:94629808..94631771,3	K562	blood:
38	chr9:94537447..94538880-chr9:94712081..94713098,9	MCF-7	breast:
39	chr9:94562652..94565421-chr9:94572696..94575201,2	K562	blood:
40	chr9:94497979..94500430-chr9:94500591..94503129,2	K562	blood:
41	chr9:94520495..94521314-chr9:94740802..94741704,2	MCF-7	breast:
42	chr9:94579358..94582251-chr9:94586460..94588565,3	MCF-7	breast:
43	chr9:94527497..94529105-chr9:94533152..94535517,2	K562	blood:
44	chr9:94541932..94544615-chr9:94547110..94550430,3	MCF-7	breast:
45	chr9:94560147..94563596-chr9:94565851..94569196,3	MCF-7	breast:
46	chr9:94580430..94582585-chr9:94584118..94590050,5	K562	blood:
47	chr9:94603914..94606181-chr9:94621038..94623335,2	MCF-7	breast:
48	chr9:94631306..94632967-chr9:94636056..94637975,2	K562	blood:
49	chr9:94554175..94556375-chr9:94562019..94564292,2	MCF-7	breast:
50	chr9:94566439..94568761-chr9:94577681..94581250,3	MCF-7	breast:

No data

Variant related genes	Relation type
ROR2	TF binding region
ROR2	CpG island
ENSG00000167103	chromatin interactions
ENSG00000169071	chromatin interactions
ENSG00000170430	chromatin interactions

Extended variants
information (count: 5701 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:5701 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533568975	chr9:94500244-94500245	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552001162	chr9:94500253-94500254	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547665823	chr9:94500264-94500265	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142273393	chr9:94500282-94500283	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150177767	chr9:94500309-94500310	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78798148	chr9:94500347-94500348	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529996118	chr9:94500348-94500349	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138373796	chr9:94500353-94500354	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188129250	chr9:94500365-94500366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149252681	chr9:94500372-94500373	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550410386	chr9:94500451-94500452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568563504	chr9:94500482-94500483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539291070	chr9:94500510-94500511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191585486	chr9:94500524-94500525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572830664	chr9:94500691-94500692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533859046	chr9:94500693-94500694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555603387	chr9:94500738-94500739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143457425	chr9:94500743-94500744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185541956	chr9:94500767-94500768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9409652	chr9:94500776-94500777	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs578137019	chr9:94500784-94500785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545652164	chr9:94500857-94500858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560646070	chr9:94500894-94500895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs137917949	chr9:94500917-94500918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563409498	chr9:94500932-94500933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532362960	chr9:94500938-94500939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190747391	chr9:94500943-94500944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561585982	chr9:94500970-94500971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565808613	chr9:94500997-94500998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528882784	chr9:94501007-94501008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550544419	chr9:94501008-94501009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10117385	chr9:94501080-94501081	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs181672860	chr9:94501111-94501112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142465325	chr9:94501172-94501173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376730513	chr9:94501202-94501203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566347482	chr9:94501278-94501279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146107953	chr9:94501288-94501289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186834365	chr9:94501289-94501290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138987180	chr9:94501290-94501291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73504500	chr9:94501355-94501356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556505059	chr9:94501395-94501396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141569627	chr9:94501407-94501408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370232128	chr9:94501408-94501409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534704564	chr9:94501412-94501413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28630390	chr9:94501468-94501469	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs189015783	chr9:94501470-94501471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181035032	chr9:94501486-94501487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185493252	chr9:94501507-94501508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548257959	chr9:94501508-94501509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34926722	chr9:94501519-94501520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Melanoma	18172304	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
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
overgrowth syndrome	16570072	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2478 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94477200-94533000	Weak transcription	Fetal Kidney	kidney
2	chr9:94483400-94501600	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr9:94483600-94504000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr9:94483600-94519400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr9:94486200-94521000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:94486800-94517400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:94487000-94502200	Weak transcription	Esophagus	oesophagus
8	chr9:94487000-94535400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr9:94489000-94508800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr9:94490400-94521000	Weak transcription	Right Atrium	heart
11	chr9:94491600-94501000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr9:94493200-94517400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr9:94495000-94501800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:94497200-94502400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:94497200-94502400	Weak transcription	Spleen	Spleen
16	chr9:94497200-94502600	Strong transcription	Fetal Stomach	stomach
17	chr9:94497400-94503000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr9:94497600-94503000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr9:94498400-94500400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr9:94499400-94509400	Weak transcription	Fetal Intestine Large	intestine
21	chr9:94499600-94500400	Enhancers	Rectal Smooth Muscle	rectum
22	chr9:94499600-94517200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr9:94499800-94502200	Weak transcription	Fetal Intestine Small	intestine
24	chr9:94499800-94502200	Weak transcription	Fetal Lung	lung
25	chr9:94499800-94502400	Weak transcription	Ovary	ovary
26	chr9:94499800-94503000	Weak transcription	Fetal Muscle Leg	muscle
27	chr9:94499800-94503000	Weak transcription	Stomach Smooth Muscle	stomach
28	chr9:94499800-94503200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr9:94499800-94503200	Weak transcription	Colon Smooth Muscle	Colon
30	chr9:94499800-94508800	Weak transcription	K562	blood
31	chr9:94499800-94517000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr9:94499800-94520400	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr9:94499800-94522800	Weak transcription	Gastric	stomach
34	chr9:94499800-94523200	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr9:94500400-94505600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr9:94501000-94515800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr9:94502200-94502400	Enhancers	Esophagus	oesophagus
38	chr9:94502200-94502800	Strong transcription	Fetal Intestine Small	intestine
39	chr9:94502200-94503200	Enhancers	Fetal Lung	lung
40	chr9:94502200-94503400	Enhancers	Fetal Brain Male	brain
41	chr9:94502200-94503400	Enhancers	Fetal Muscle Trunk	muscle
42	chr9:94502200-94504400	Enhancers	Rectal Smooth Muscle	rectum
43	chr9:94502400-94503200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr9:94502400-94503400	Enhancers	Ovary	ovary
45	chr9:94502600-94508400	Weak transcription	Fetal Stomach	stomach
46	chr9:94502800-94516600	Weak transcription	Fetal Intestine Small	intestine
47	chr9:94503000-94503200	Enhancers	Fetal Muscle Leg	muscle
48	chr9:94503000-94503200	Active TSS	Stomach Smooth Muscle	stomach
49	chr9:94503000-94504400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr9:94503000-94504600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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