Variant report

Variant	nsv892185
Chromosome Location	chr9:6929053-7070962
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1103)
CpG islands
(count:122)
Chromatin interactive
region (count:34)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1103 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6986412-6986867	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6955127-6955771	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6931921-6932276	K562	blood:	n/a	n/a
4	ARID3A	chr9:6932065-6932168	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:7067058-7067598	K562	blood:	n/a	n/a
6	ARID3A	chr9:7055642-7055921	K562	blood:	n/a	n/a
7	ARID3A	chr9:7052706-7052906	K562	blood:	n/a	n/a
8	ATF1	chr9:7011743-7011938	K562	blood:	n/a	n/a
9	ATF1	chr9:7067126-7067649	K562	blood:	n/a	n/a
10	ATF1	chr9:6931877-6932320	K562	blood:	n/a	n/a
11	ATF2	chr9:7055504-7055907	GM12878	blood:	n/a	n/a
12	ATF2	chr9:6973706-6974207	GM12878	blood:	n/a	n/a
13	ATF2	chr9:6973498-6974318	GM12878	blood:	n/a	n/a
14	ATF2	chr9:6960665-6961260	GM12878	blood:	n/a	n/a
15	ATF3	chr9:6931886-6932304	K562	blood:	n/a	n/a
16	BACH1	chr9:6955248-6955617	H1-hESC	embryonic stem cell:	n/a	chr9:6955424-6955438
17	BATF	chr9:6973758-6974189	GM12878	blood:	n/a	chr9:6973978-6973989
18	BATF	chr9:6973808-6974185	GM12878	blood:	n/a	chr9:6973978-6973989
19	BATF	chr9:7055521-7055844	GM12878	blood:	n/a	n/a
20	BATF	chr9:7055473-7055753	GM12878	blood:	n/a	n/a
21	BCL11A	chr9:6973811-6974164	GM12878	blood:	n/a	n/a
22	BCL11A	chr9:6973797-6974200	GM12878	blood:	n/a	n/a
23	BCL3	chr9:7067164-7067565	K562	blood:	n/a	n/a
24	BCLAF1	chr9:6973634-6974239	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:7067212-7067556	K562	blood:	n/a	n/a
26	BHLHE40	chr9:6931869-6932449	K562	blood:	n/a	n/a
27	BHLHE40	chr9:6955289-6955945	HepG2	liver:	n/a	n/a
28	BHLHE40	chr9:6955450-6955720	GM12878	blood:	n/a	n/a
29	BRCA1	chr9:6945537-6945561	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr9:7053971-7054087	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr9:6931846-6932328	K562	blood:	n/a	n/a
32	CBX3	chr9:7052674-7052967	K562	blood:	n/a	n/a
33	CBX3	chr9:7067156-7067628	K562	blood:	n/a	n/a
34	CBX3	chr9:6931729-6932402	HCT-116	colon:	n/a	n/a
35	CCNT2	chr9:6931957-6932298	K562	blood:	n/a	chr9:6932104-6932113 chr9:6932060-6932080
36	CCNT2	chr9:7067209-7067605	K562	blood:	n/a	n/a
37	CEBPB	chr9:6944140-6944602	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr9:6931923-6932261	K562	blood:	n/a	n/a
39	CEBPB	chr9:7054868-7055092	K562	blood:	n/a	chr9:7054951-7054964
40	CEBPB	chr9:6978980-6979154	IMR90	lung:	n/a	chr9:6979013-6979024
41	CEBPB	chr9:7045420-7045680	HepG2	liver:	n/a	chr9:7045528-7045539 chr9:7045527-7045540 chr9:7045527-7045538
42	CEBPB	chr9:6931860-6932265	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr9:6986539-6986736	HepG2	liver:	n/a	n/a
44	CEBPB	chr9:7001595-7001907	K562	blood:	n/a	chr9:7001766-7001783 chr9:7001769-7001782
45	CEBPB	chr9:6957549-6957715	HepG2	liver:	n/a	chr9:6957646-6957659 chr9:6957648-6957657 chr9:6957646-6957657
46	CEBPB	chr9:6973833-6974012	HepG2	liver:	n/a	chr9:6973932-6973943
47	CEBPB	chr9:6931866-6932199	IMR90	lung:	n/a	n/a
48	CEBPB	chr9:6931045-6931122	HepG2	liver:	n/a	n/a
49	CEBPB	chr9:7067052-7067647	K562	blood:	n/a	n/a
50	CEBPB	chr9:6978235-6978587	HepG2	liver:	n/a	chr9:6978313-6978324 chr9:6978311-6978324 chr9:6978311-6978324

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6955559-6955609	Hepatocyte	liver:	n/a
2	chr9:6932042-6932092	HL-60	blood:	n/a
3	chr9:6932042-6932092	HCF	heart:	n/a
4	chr9:6955559-6955609	ovcar-3	ovarian:	n/a
5	chr9:6932042-6932092	SKMC	muscle:	n/a
6	chr9:6955559-6955609	NHBE	bronchial:	n/a
7	chr9:6955559-6955609	HCT-116	colon:	n/a
8	chr9:6932042-6932092	Hela-S3	cervix:	n/a
9	chr9:6932042-6932092	HAEpiC	amniotic membrane:	n/a
10	chr9:6932042-6932092	GM06990	blood:	n/a
11	chr9:6932042-6932092	MCF10A-Er-Src	breast:	n/a
12	chr9:6932042-6932092	RPTEC	kidney:	n/a
13	chr9:6955559-6955609	ProgFib	skin:	n/a
14	chr9:6955559-6955609	CMK	blood:	n/a
15	chr9:6955559-6955609	AG09319	gingival:	n/a
16	chr9:6932042-6932092	ProgFib	skin:	n/a
17	chr9:6955559-6955609	NB4	blood:	n/a
18	chr9:6932042-6932092	H1-hESC	embryonic stem cell:	embryo
19	chr9:6932042-6932092	HMEC	breast:	n/a
20	chr9:6932042-6932092	SK-N-SH_RA	brain:	n/a
21	chr9:6932042-6932092	HPAEpiC	pulmonary alveolar:	n/a
22	chr9:6932042-6932092	HIPEpiC	eye:	n/a
23	chr9:6932042-6932092	LNCaP	prostate:	n/a
24	chr9:6932042-6932092	HCM	heart:	n/a
25	chr9:6932042-6932092	GM12892	blood:	n/a
26	chr9:6932042-6932092	HUVEC	blood vessel:	n/a
27	chr9:6955559-6955609	HIPEpiC	eye:	n/a
28	chr9:6955559-6955609	NHDF-neo	bronchial:	n/a
29	chr9:6955559-6955609	HRE	kidney:	n/a
30	chr9:6932042-6932092	AG09309	skin:	n/a
31	chr9:6955559-6955609	SK-N-SH_RA	brain:	n/a
32	chr9:6955559-6955609	HCM	heart:	n/a
33	chr9:6932042-6932092	ECC-1	luminal epithelium:	n/a
34	chr9:6932042-6932092	HRPEpiC	eye:	n/a
35	chr9:6932042-6932092	PANC-1	pancreas:	n/a
36	chr9:6955559-6955609	GM19239	blood:	n/a
37	chr9:6932042-6932092	HCT-116	colon:	n/a
38	chr9:6932042-6932092	T-47D	breast:	n/a
39	chr9:6955559-6955609	A549	lung:	n/a
40	chr9:6955559-6955609	GM12891	blood:	n/a
41	chr9:6955559-6955609	GM06990	blood:	n/a
42	chr9:6955559-6955609	SAEC	small airway:	n/a
43	chr9:6955559-6955609	BE2_C	brain:	n/a
44	chr9:6932042-6932092	HepG2	liver:	n/a
45	chr9:6955559-6955609	GM12892	blood:	n/a
46	chr9:6955559-6955609	BJ	skin:	n/a
47	chr9:6955559-6955609	AG04450	lung:	fetal
48	chr9:6955559-6955609	PrEC	prostate:	n/a
49	chr9:6932042-6932092	IMR90	lung:	fetal
50	chr9:6955559-6955609	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
2	chr9:6996659..6998506-chr9:6999056..7001855,2	K562	blood:
3	chr9:6928105..6930890-chr9:6932209..6935061,3	K562	blood:
4	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
5	chr9:7051581..7054293-chr9:7055466..7057984,2	MCF-7	breast:
6	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
7	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
8	chr5:35003633..35004245-chr9:7020432..7021432,2	K562	blood:
9	chr9:7062837..7065514-chr9:7066672..7068819,2	MCF-7	breast:
10	chr9:7028131..7030409-chr9:7036098..7038098,2	MCF-7	breast:
11	chr9:7052337..7053367-chr9:7536144..7537120,3	MCF-7	breast:
12	chr9:7052132..7053116-chr9:7186335..7186921,2	K562	blood:
13	chr9:6954682..6956612-chr9:6970287..6972358,2	MCF-7	breast:
14	chr9:7001163..7002731-chr9:7004777..7006309,2	K562	blood:
15	chr9:6931770..6934269-chr9:6942265..6944921,2	MCF-7	breast:
16	chr9:6931770..6934269-chr9:6942265..6944921,2	MCF-7	breast:
17	chr9:7028131..7030409-chr9:7036098..7038098,2	MCF-7	breast:
18	chr9:6996659..6998506-chr9:6999056..7001855,2	K562	blood:
19	chr9:7052698..7053251-chr9:7360197..7360994,2	K562	blood:
20	chr9:6928105..6930890-chr9:6932209..6935061,3	K562	blood:
21	chr9:6978865..6981054-chr9:6982708..6984588,2	K562	blood:
22	chr9:7062837..7065514-chr9:7066672..7068819,2	MCF-7	breast:
23	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
24	chr9:7046839..7049487-chr9:7050524..7052607,2	K562	blood:
25	chr9:6986135..6988312-chr9:6992816..6995034,2	MCF-7	breast:
26	chr9:7051581..7054293-chr9:7055466..7057984,2	MCF-7	breast:
27	chr9:7052694..7053246-chr9:7259513..7260136,3	MCF-7	breast:
28	chr9:6986135..6988312-chr9:6992816..6995034,2	MCF-7	breast:
29	chr9:7070852..7073798-chr9:7075026..7077389,2	MCF-7	breast:
30	chr9:6921809..6924418-chr9:6928929..6932002,3	MCF-7	breast:
31	chr9:7052501..7053186-chr9:7233839..7234508,2	MCF-7	breast:
32	chr9:7001163..7002731-chr9:7004777..7006309,2	K562	blood:
33	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
34	chr9:6954682..6956612-chr9:6970287..6972358,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UHRF2-2	chr9:6974766-6974939	ENSG00000224972.1
2	lnc-UHRF2-6	chr9:6942460-6942634	NONHSAT130166
3	lnc-UHRF2-6	chr9:6948033-6948214	NONHSAT130166
4	lnc-UHRF2-6	chr9:6941586-6941815	NONHSAT130166
5	lnc-UHRF2-2	chr9:6978625-6978859	ENSG00000224972.1
6	lnc-UHRF2-2	chr9:6973827-6973887	ENSG00000224972.1

No data

Variant related genes	Relation type
KDM4C	TF binding region
KDM4C	CpG island
ENSG00000107077	chromatin interactions

Extended variants
information (count: 7619 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:7619 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10975906	chr9:6929053-6929054	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185767992	chr9:6929120-6929121	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190725097	chr9:6929123-6929124	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555007797	chr9:6929164-6929165	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573956351	chr9:6929223-6929224	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs182970628	chr9:6929229-6929230	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs56185621	chr9:6929244-6929245	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs188772833	chr9:6929256-6929257	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs544921815	chr9:6929345-6929346	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs370131807	chr9:6929359-6929360	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs193296036	chr9:6929390-6929391	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs10975907	chr9:6929401-6929402	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs183237880	chr9:6929404-6929405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370582325	chr9:6929421-6929422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs562923624	chr9:6929471-6929472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs367749010	chr9:6929472-6929473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79920391	chr9:6929473-6929474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560565875	chr9:6929476-6929477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528108459	chr9:6929477-6929478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs59537472	chr9:6929486-6929487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142272337	chr9:6929490-6929491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs62533764	chr9:6929492-6929493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143286274	chr9:6929498-6929499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs187267603	chr9:6929516-6929517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114790993	chr9:6929563-6929564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532727666	chr9:6929580-6929581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147540269	chr9:6929583-6929584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11789248	chr9:6929602-6929603	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs11789250	chr9:6929623-6929624	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs370248427	chr9:6929650-6929651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558184183	chr9:6929671-6929672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11794707	chr9:6929715-6929716	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs113121714	chr9:6929785-6929786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566859006	chr9:6929825-6929826	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs11794732	chr9:6929863-6929864	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs192151774	chr9:6929883-6929884	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs11788849	chr9:6929894-6929895	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs183912766	chr9:6929900-6929901	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs189953536	chr9:6929901-6929902	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs575263020	chr9:6929914-6929915	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs137888707	chr9:6929919-6929920	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs192297681	chr9:6929986-6929987	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs114623919	chr9:6930051-6930052	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184642959	chr9:6930057-6930058	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565530762	chr9:6930095-6930096	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532695658	chr9:6930108-6930109	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551128222	chr9:6930109-6930110	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74909709	chr9:6930124-6930125	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542113892	chr9:6930130-6930131	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530355557	chr9:6930224-6930225	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	21215367	CNVD

Chromatin state (count:2533 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6890000-6987200	Weak transcription	Aorta	Aorta
2	chr9:6893800-6981600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr9:6894800-6931600	Weak transcription	Dnd41	blood
4	chr9:6896200-6959000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr9:6897600-6932200	Weak transcription	Small Intestine	intestine
6	chr9:6898200-6930800	Weak transcription	HSMMtube	muscle
7	chr9:6900600-6943000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr9:6901600-6944200	Weak transcription	Duodenum Mucosa	Duodenum
9	chr9:6901800-6931600	Weak transcription	Fetal Intestine Large	intestine
10	chr9:6902800-6931000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:6903000-6938600	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr9:6906400-6933200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr9:6906600-6938200	Weak transcription	Adipose Nuclei	Adipose
14	chr9:6908800-6942600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr9:6912400-6930800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr9:6912400-6931000	Weak transcription	Right Ventricle	heart
17	chr9:6912400-6931600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr9:6912400-6932200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr9:6912400-6932200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr9:6912400-6932200	Weak transcription	Spleen	Spleen
21	chr9:6912400-6978400	Weak transcription	Esophagus	oesophagus
22	chr9:6912600-6929600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr9:6916000-6932200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr9:6920200-6930000	Weak transcription	HSMM	muscle
25	chr9:6920200-6930800	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr9:6920200-6931000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr9:6920200-6931000	Weak transcription	Fetal Muscle Leg	muscle
28	chr9:6920400-6931000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr9:6921400-6934000	Weak transcription	Primary hematopoietic stem cells	blood
30	chr9:6921600-6939200	Weak transcription	Fetal Lung	lung
31	chr9:6921600-6957600	Weak transcription	Thymus	Thymus
32	chr9:6921800-6960400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr9:6922000-6933600	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr9:6922000-6941600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr9:6922200-6959000	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr9:6922600-6944800	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr9:6922600-6981000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr9:6922800-6932000	Weak transcription	Lung	lung
39	chr9:6923000-6929200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr9:6923000-6929600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr9:6923000-6929600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr9:6923200-6930800	Weak transcription	Hela-S3	cervix
43	chr9:6923200-6930800	Weak transcription	HMEC	breast
44	chr9:6923400-6929200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr9:6924400-6929200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr9:6924600-6931000	Weak transcription	Fetal Intestine Small	intestine
47	chr9:6924600-6957400	Weak transcription	Fetal Thymus	thymus
48	chr9:6926000-6932000	Weak transcription	Brain Cingulate Gyrus	brain
49	chr9:6926200-6930800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr9:6926200-6933200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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