Variant report

Variant	nsv892190
Chromosome Location	chr9:7094860-7186074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:706)
CpG islands
(count:183)
Chromatin interactive
region (count:34)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:706 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:7166084-7166596	K562	blood:	n/a	n/a
2	ATF2	chr9:7117972-7118647	GM12878	blood:	n/a	n/a
3	ATF2	chr9:7129409-7129746	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr9:7121088-7121548	GM12878	blood:	n/a	n/a
5	ATF2	chr9:7117915-7118904	GM12878	blood:	n/a	n/a
6	BACH1	chr9:7118189-7118393	K562	blood:	n/a	chr9:7118319-7118333
7	BACH1	chr9:7171429-7171690	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:7115951-7116002	K562	blood:	n/a	n/a
9	BACH1	chr9:7118151-7118560	H1-hESC	embryonic stem cell:	n/a	chr9:7118319-7118333
10	BATF	chr9:7118732-7118985	GM12878	blood:	n/a	n/a
11	BATF	chr9:7121046-7121340	GM12878	blood:	n/a	n/a
12	BATF	chr9:7118578-7118990	GM12878	blood:	n/a	n/a
13	BATF	chr9:7118096-7118519	GM12878	blood:	n/a	chr9:7118319-7118329 chr9:7118318-7118329
14	BATF	chr9:7118109-7118568	GM12878	blood:	n/a	chr9:7118319-7118329 chr9:7118318-7118329
15	BCL11A	chr9:7118085-7118517	GM12878	blood:	n/a	chr9:7118322-7118331 chr9:7118321-7118330
16	BCL11A	chr9:7118214-7118499	GM12878	blood:	n/a	chr9:7118322-7118331 chr9:7118321-7118330
17	BCL3	chr9:7118006-7118488	GM12878	blood:	n/a	chr9:7118322-7118331 chr9:7118321-7118330
18	BHLHE40	chr9:7117926-7118784	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:7165773-7166538	K562	blood:	n/a	n/a
20	BHLHE40	chr9:7121030-7121536	K562	blood:	n/a	n/a
21	CEBPB	chr9:7114912-7115164	HepG2	liver:	n/a	chr9:7115029-7115040
22	CEBPB	chr9:7145686-7146202	IMR90	lung:	n/a	n/a
23	CEBPB	chr9:7137393-7137583	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:7137385-7137629	A549	lung:	n/a	n/a
25	CEBPB	chr9:7103761-7104150	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:7166066-7166446	K562	blood:	n/a	n/a
27	CEBPB	chr9:7105154-7105496	HepG2	liver:	n/a	chr9:7105312-7105323
28	CEBPB	chr9:7105156-7105475	IMR90	lung:	n/a	chr9:7105312-7105323
29	CEBPB	chr9:7103804-7104189	A549	lung:	n/a	n/a
30	CEBPB	chr9:7185673-7186002	ECC-1	luminal epithelium:	n/a	chr9:7185769-7185786 chr9:7185774-7185785
31	CEBPB	chr9:7118259-7118459	A549	lung:	n/a	n/a
32	CEBPB	chr9:7166038-7166427	K562	blood:	n/a	n/a
33	CEBPB	chr9:7137135-7137652	IMR90	lung:	n/a	n/a
34	CEBPB	chr9:7129438-7129817	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr9:7103480-7103684	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr9:7114880-7115114	A549	lung:	n/a	chr9:7115029-7115040
37	CEBPB	chr9:7114904-7115107	K562	blood:	n/a	chr9:7115029-7115040
38	CEBPB	chr9:7185507-7186100	A549	lung:	n/a	chr9:7185769-7185786 chr9:7185774-7185785
39	CEBPB	chr9:7114878-7115178	MCF-7	breast:	n/a	chr9:7115029-7115040
40	CEBPB	chr9:7114896-7115164	IMR90	lung:	n/a	chr9:7115029-7115040
41	CEBPB	chr9:7185655-7186046	A549	lung:	n/a	chr9:7185769-7185786 chr9:7185774-7185785
42	CEBPB	chr9:7105151-7105467	K562	blood:	n/a	chr9:7105312-7105323
43	CEBPB	chr9:7185589-7186022	Hela-S3	cervix:	n/a	chr9:7185769-7185786 chr9:7185774-7185785
44	CEBPB	chr9:7105213-7105435	MCF-7	breast:	n/a	chr9:7105312-7105323
45	CEBPB	chr9:7185473-7186006	IMR90	lung:	n/a	chr9:7185769-7185786 chr9:7185774-7185785
46	CEBPD	chr9:7166121-7166481	K562	blood:	n/a	n/a
47	CEBPD	chr9:7166009-7166524	K562	blood:	n/a	n/a
48	CHD2	chr9:7176232-7176274	HepG2	liver:	n/a	n/a
49	CHD2	chr9:7118139-7118888	GM12878	blood:	n/a	n/a
50	CREB1	chr9:7185710-7185923	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:7172362-7172412	NH-A	brain:	n/a
2	chr9:7172362-7172412	GM19239	blood:	n/a
3	chr9:7103479-7103529	RPTEC	kidney:	n/a
4	chr9:7172362-7172412	HCT-116	colon:	n/a
5	chr9:7148129-7148179	HAEpiC	amniotic membrane:	n/a
6	chr9:7148129-7148179	SK-N-SH_RA	brain:	n/a
7	chr9:7103479-7103529	AoSMC	blood vessel:	n/a
8	chr9:7172362-7172412	Caco-2	colon:	n/a
9	chr9:7103479-7103529	HIPEpiC	eye:	n/a
10	chr9:7103479-7103529	HRE	kidney:	n/a
11	chr9:7103479-7103529	PrEC	prostate:	n/a
12	chr9:7103479-7103529	K562	blood:	n/a
13	chr9:7172362-7172412	HepG2	liver:	n/a
14	chr9:7148129-7148179	NHBE	bronchial:	n/a
15	chr9:7103479-7103529	NH-A	brain:	n/a
16	chr9:7148129-7148179	BE2_C	brain:	n/a
17	chr9:7172362-7172412	ECC-1	luminal epithelium:	n/a
18	chr9:7148129-7148179	T-47D	breast:	n/a
19	chr9:7172362-7172412	HUVEC	blood vessel:	n/a
20	chr9:7148129-7148179	U87	brain:	n/a
21	chr9:7103479-7103529	HAEpiC	amniotic membrane:	n/a
22	chr9:7148129-7148179	HEK293	kidney:	embryo
23	chr9:7103479-7103529	ECC-1	luminal epithelium:	n/a
24	chr9:7103479-7103529	HNPCEpiC	eye:	n/a
25	chr9:7172362-7172412	Jurkat	blood:	n/a
26	chr9:7103479-7103529	SKMC	muscle:	n/a
27	chr9:7148129-7148179	SK-N-SH	brain:	n/a
28	chr9:7148129-7148179	NHDF-neo	bronchial:	n/a
29	chr9:7103479-7103529	BJ	skin:	n/a
30	chr9:7172362-7172412	K562	blood:	n/a
31	chr9:7103479-7103529	U87	brain:	n/a
32	chr9:7103479-7103529	MCF10A-Er-Src	breast:	n/a
33	chr9:7148129-7148179	BJ	skin:	n/a
34	chr9:7148129-7148179	AG10803	skin:	n/a
35	chr9:7172362-7172412	HAEpiC	amniotic membrane:	n/a
36	chr9:7172362-7172412	Hepatocyte	liver:	n/a
37	chr9:7148129-7148179	HepG2	liver:	n/a
38	chr9:7172362-7172412	HL-60	blood:	n/a
39	chr9:7103479-7103529	HUVEC	blood vessel:	n/a
40	chr9:7148129-7148179	Hepatocyte	liver:	n/a
41	chr9:7148129-7148179	AoSMC	blood vessel:	n/a
42	chr9:7172362-7172412	NT2-D1	testis:	n/a
43	chr9:7172362-7172412	HRCEpiC	kidney:	n/a
44	chr9:7103479-7103529	SAEC	small airway:	n/a
45	chr9:7148129-7148179	NB4	blood:	n/a
46	chr9:7172362-7172412	HCPEpiC	choroid plexus:	n/a
47	chr9:7172362-7172412	HMEC	breast:	n/a
48	chr9:7103479-7103529	HCM	heart:	n/a
49	chr9:7148129-7148179	HCF	heart:	n/a
50	chr9:7103479-7103529	SK-N-MC	brain:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:7116711..7118405-chr9:7121180..7122819,2	K562	blood:
2	chr9:7169706..7171250-chr9:7171522..7173272,2	K562	blood:
3	chr9:7148888..7150780-chr9:7164097..7166257,2	K562	blood:
4	chr9:7169706..7171250-chr9:7171522..7173272,2	K562	blood:
5	chr9:7149048..7151328-chr9:7152979..7155533,2	K562	blood:
6	chr9:7148888..7150780-chr9:7164097..7166257,2	K562	blood:
7	chr9:7168923..7170527-chr9:7184801..7187324,2	MCF-7	breast:
8	chr9:7133804..7136423-chr9:7140653..7143572,2	K562	blood:
9	chr9:7163757..7166355-chr9:7173278..7174995,2	MCF-7	breast:
10	chr9:7126745..7128307-chr9:7132756..7134893,2	K562	blood:
11	chr9:7168923..7170527-chr9:7184801..7187324,2	MCF-7	breast:
12	chr9:7112692..7114873-chr9:7119931..7121625,2	K562	blood:
13	chr9:7144039..7145587-chr9:7147490..7149036,2	MCF-7	breast:
14	chr9:7139809..7142579-chr9:7145353..7147881,3	MCF-7	breast:
15	chr9:6920289..6921801-chr9:7142294..7145025,2	K562	blood:
16	chr9:7128721..7131684-chr9:7133933..7136070,2	K562	blood:
17	chr9:7166311..7168822-chr9:7171544..7173706,2	K562	blood:
18	chr9:7133804..7136423-chr9:7140653..7143572,2	K562	blood:
19	chr9:7166311..7168822-chr9:7171544..7173706,2	K562	blood:
20	chr9:7128721..7131684-chr9:7133933..7136070,2	K562	blood:
21	chr9:7091442..7093437-chr9:7097777..7099418,2	K562	blood:
22	chr9:7149048..7151328-chr9:7152979..7155533,2	K562	blood:
23	chr9:7134161..7136244-chr9:7147456..7149239,2	K562	blood:
24	chr9:7131849..7134386-chr9:7150388..7153232,2	K562	blood:
25	chr9:7163757..7166355-chr9:7173278..7174995,2	MCF-7	breast:
26	chr9:7139809..7142579-chr9:7145353..7147881,3	MCF-7	breast:
27	chr9:7131849..7134386-chr9:7150388..7153232,2	K562	blood:
28	chr9:7112692..7114873-chr9:7119931..7121625,2	K562	blood:
29	chr9:7116711..7118405-chr9:7121180..7122819,2	K562	blood:
30	chr12:40495673..40496364-chr9:7098775..7099598,2	K562	blood:
31	chr9:7108240..7110187-chr9:7110966..7112955,2	K562	blood:
32	chr9:7134161..7136244-chr9:7147456..7149239,2	K562	blood:
33	chr9:7144039..7145587-chr9:7147490..7149036,2	MCF-7	breast:
34	chr9:7108240..7110187-chr9:7110966..7112955,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-3	chr9:7177838-7178166	XLOC_007276
2	lnc-KDM4C-3	chr9:7177450-7178166	XLOC_007276
3	lnc-KDM4C-3	chr9:7178524-7178549	XLOC_007276

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KDM4C	hsa-miR-335-5p	chr9:7175374-7175381
2	KDM4C	hsa-miR-335-5p	chr9:7175359-7175381

Variant related genes	Relation type
KDM4C	TF binding region
KDM4C	CpG island
ENSG00000107077	chromatin interactions
LASS2	miRNA target sites

Extended variants
information (count: 4513 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:4513 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7849812	chr9:7094860-7094861	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541006998	chr9:7094868-7094869	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558965029	chr9:7094903-7094904	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149073551	chr9:7094937-7094938	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371471620	chr9:7094957-7094958	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs16925332	chr9:7094970-7094971	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs533783245	chr9:7094982-7094983	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531102979	chr9:7094990-7094991	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549335312	chr9:7095012-7095013	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143136533	chr9:7095015-7095016	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528609672	chr9:7095018-7095019	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532675336	chr9:7095025-7095026	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547004177	chr9:7095037-7095038	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117449385	chr9:7095039-7095040	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539037578	chr9:7095058-7095059	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551660638	chr9:7095094-7095095	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12347341	chr9:7095098-7095099	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs537220457	chr9:7095100-7095101	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555308773	chr9:7095103-7095104	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567346469	chr9:7095108-7095109	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534466210	chr9:7095110-7095111	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552653252	chr9:7095156-7095157	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7469735	chr9:7095169-7095170	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148265389	chr9:7095174-7095175	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576565251	chr9:7095203-7095204	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562788477	chr9:7095206-7095207	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78112105	chr9:7095232-7095233	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73407474	chr9:7095242-7095243	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs543188928	chr9:7095243-7095244	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189171382	chr9:7095269-7095270	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4271022	chr9:7095278-7095279	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540681791	chr9:7095286-7095287	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565387627	chr9:7095292-7095293	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192532038	chr9:7095295-7095296	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551015332	chr9:7095307-7095308	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146333383	chr9:7095366-7095367	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555957847	chr9:7095431-7095432	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530754325	chr9:7095474-7095475	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201222689	chr9:7095485-7095486	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201957774	chr9:7095518-7095519	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs59318739	chr9:7095529-7095530	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550009076	chr9:7095530-7095531	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575994619	chr9:7095536-7095537	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541423663	chr9:7095554-7095555	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12115780	chr9:7095588-7095589	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs143105049	chr9:7095593-7095594	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184386958	chr9:7095598-7095599	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552618388	chr9:7095599-7095600	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571035058	chr9:7095623-7095624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531632431	chr9:7095634-7095635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Chordoma	21215367	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:2055 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7012200-7111200	Weak transcription	Colonic Mucosa	Colon
2	chr9:7034000-7103600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr9:7043400-7103600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr9:7051600-7103200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr9:7053200-7099200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr9:7061200-7104600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr9:7061600-7103600	Weak transcription	Spleen	Spleen
8	chr9:7062800-7096400	Weak transcription	Fetal Intestine Small	intestine
9	chr9:7066200-7096200	Weak transcription	Stomach Mucosa	stomach
10	chr9:7067200-7103600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:7068400-7103600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr9:7073600-7099200	Weak transcription	NHEK	skin
13	chr9:7075000-7097800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr9:7075600-7105800	Weak transcription	NHLF	lung
15	chr9:7076600-7103600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr9:7077000-7098000	Weak transcription	Colon Smooth Muscle	Colon
17	chr9:7077800-7103200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr9:7077800-7103200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr9:7077800-7103600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr9:7077800-7103600	Weak transcription	Brain Angular Gyrus	brain
21	chr9:7077800-7103600	Weak transcription	HMEC	breast
22	chr9:7077800-7103600	Weak transcription	K562	blood
23	chr9:7077800-7103800	Weak transcription	HSMM	muscle
24	chr9:7078000-7103600	Weak transcription	Dnd41	blood
25	chr9:7078200-7103800	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr9:7079400-7103200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr9:7079600-7103600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr9:7081600-7097000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:7082800-7103600	Weak transcription	Pancreas	Pancrea
30	chr9:7085400-7096000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr9:7085400-7103600	Weak transcription	Brain Anterior Caudate	brain
32	chr9:7086600-7105600	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr9:7087000-7096400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr9:7087000-7096400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr9:7087000-7096600	Weak transcription	Thymus	Thymus
36	chr9:7087000-7096800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr9:7087000-7097000	Weak transcription	Esophagus	oesophagus
38	chr9:7087000-7097800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr9:7087000-7099000	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr9:7087000-7099400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr9:7087000-7099400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr9:7087000-7099400	Weak transcription	Adipose Nuclei	Adipose
43	chr9:7087000-7099400	Weak transcription	Liver	Liver
44	chr9:7087000-7099400	Weak transcription	Duodenum Mucosa	Duodenum
45	chr9:7087000-7099600	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr9:7087000-7103400	Weak transcription	Fetal Stomach	stomach
47	chr9:7087000-7103400	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr9:7087000-7103600	Weak transcription	Aorta	Aorta
49	chr9:7087000-7103600	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr9:7087000-7103600	Weak transcription	Fetal Intestine Large	intestine

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