Variant report

Variant	nsv892186
Chromosome Location	chr9:6942605-7075305
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:7067058-7067598	K562	blood:	n/a	n/a
2	ARID3A	chr9:6986412-6986867	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:7052706-7052906	K562	blood:	n/a	n/a
4	ARID3A	chr9:7055642-7055921	K562	blood:	n/a	n/a
5	ARID3A	chr9:6955127-6955771	HepG2	liver:	n/a	n/a
6	ATF1	chr9:7067126-7067649	K562	blood:	n/a	n/a
7	ATF1	chr9:7011743-7011938	K562	blood:	n/a	n/a
8	ATF2	chr9:6973706-6974207	GM12878	blood:	n/a	n/a
9	ATF2	chr9:6973498-6974318	GM12878	blood:	n/a	n/a
10	ATF2	chr9:6960665-6961260	GM12878	blood:	n/a	n/a
11	ATF2	chr9:7055504-7055907	GM12878	blood:	n/a	n/a
12	BACH1	chr9:6955248-6955617	H1-hESC	embryonic stem cell:	n/a	chr9:6955424-6955438
13	BATF	chr9:7055473-7055753	GM12878	blood:	n/a	n/a
14	BATF	chr9:6973808-6974185	GM12878	blood:	n/a	chr9:6973978-6973989
15	BATF	chr9:7055521-7055844	GM12878	blood:	n/a	n/a
16	BATF	chr9:6973758-6974189	GM12878	blood:	n/a	chr9:6973978-6973989
17	BCL11A	chr9:6973811-6974164	GM12878	blood:	n/a	n/a
18	BCL11A	chr9:6973797-6974200	GM12878	blood:	n/a	n/a
19	BCL3	chr9:7067164-7067565	K562	blood:	n/a	n/a
20	BCLAF1	chr9:6973634-6974239	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:6955289-6955945	HepG2	liver:	n/a	n/a
22	BHLHE40	chr9:7067212-7067556	K562	blood:	n/a	n/a
23	BHLHE40	chr9:6955450-6955720	GM12878	blood:	n/a	n/a
24	BRCA1	chr9:7053971-7054087	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr9:6945537-6945561	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr9:7067156-7067628	K562	blood:	n/a	n/a
27	CBX3	chr9:7052674-7052967	K562	blood:	n/a	n/a
28	CCNT2	chr9:7067209-7067605	K562	blood:	n/a	n/a
29	CEBPB	chr9:7056868-7057207	IMR90	lung:	n/a	n/a
30	CEBPB	chr9:6986475-6986845	HepG2	liver:	n/a	n/a
31	CEBPB	chr9:6973815-6974092	IMR90	lung:	n/a	chr9:6973932-6973943
32	CEBPB	chr9:7056874-7057147	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:7042168-7042550	HepG2	liver:	n/a	chr9:7042358-7042367 chr9:7042356-7042367 chr9:7042356-7042369 chr9:7042358-7042367 chr9:7042358-7042367 chr9:7042356-7042369
34	CEBPB	chr9:7054868-7055092	K562	blood:	n/a	chr9:7054951-7054964
35	CEBPB	chr9:7042178-7042526	H1-hESC	embryonic stem cell:	n/a	chr9:7042358-7042367 chr9:7042356-7042367 chr9:7042356-7042369 chr9:7042358-7042367 chr9:7042358-7042367 chr9:7042356-7042369
36	CEBPB	chr9:6978304-6978492	A549	lung:	n/a	chr9:6978313-6978324 chr9:6978311-6978324 chr9:6978311-6978324
37	CEBPB	chr9:6986539-6986736	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:7042171-7042626	K562	blood:	n/a	chr9:7042358-7042367 chr9:7042356-7042367 chr9:7042356-7042369 chr9:7042358-7042367 chr9:7042358-7042367 chr9:7042356-7042369
39	CEBPB	chr9:7042244-7042559	ECC-1	luminal epithelium:	n/a	chr9:7042358-7042367 chr9:7042356-7042367 chr9:7042356-7042369 chr9:7042358-7042367 chr9:7042358-7042367 chr9:7042356-7042369
40	CEBPB	chr9:7042175-7042483	MCF-7	breast:	n/a	chr9:7042358-7042367 chr9:7042356-7042367 chr9:7042356-7042369 chr9:7042358-7042367 chr9:7042358-7042367 chr9:7042356-7042369
41	CEBPB	chr9:7042060-7042598	A549	lung:	n/a	chr9:7042358-7042367 chr9:7042356-7042367 chr9:7042356-7042369 chr9:7042358-7042367 chr9:7042358-7042367 chr9:7042356-7042369
42	CEBPB	chr9:6977604-6977858	HepG2	liver:	n/a	chr9:6977724-6977735
43	CEBPB	chr9:7045376-7045704	IMR90	lung:	n/a	chr9:7045528-7045539 chr9:7045527-7045540 chr9:7045527-7045538
44	CEBPB	chr9:7052708-7052881	K562	blood:	n/a	n/a
45	CEBPB	chr9:6973833-6974107	A549	lung:	n/a	chr9:6973932-6973943
46	CEBPB	chr9:6944140-6944602	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr9:6978979-6979053	HepG2	liver:	n/a	chr9:6979013-6979024
48	CEBPB	chr9:6973846-6974085	HepG2	liver:	n/a	chr9:6973932-6973943
49	CEBPB	chr9:6970250-6970503	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:7042160-7042593	MCF-7	breast:	n/a	chr9:7042358-7042367 chr9:7042356-7042367 chr9:7042356-7042369 chr9:7042358-7042367 chr9:7042358-7042367 chr9:7042356-7042369

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6955559-6955609	NHDF-neo	bronchial:	n/a
2	chr9:6955559-6955609	HRE	kidney:	n/a
3	chr9:6955559-6955609	Caco-2	colon:	n/a
4	chr9:6955559-6955609	IMR90	lung:	fetal
5	chr9:6955559-6955609	HRCEpiC	kidney:	n/a
6	chr9:6955559-6955609	GM12878	blood:	n/a
7	chr9:6955559-6955609	HL-60	blood:	n/a
8	chr9:6955559-6955609	T-47D	breast:	n/a
9	chr9:6955559-6955609	NT2-D1	testis:	n/a
10	chr9:6955559-6955609	HepG2	liver:	n/a
11	chr9:6955559-6955609	AG04450	lung:	fetal
12	chr9:6955559-6955609	PrEC	prostate:	n/a
13	chr9:6955559-6955609	HIPEpiC	eye:	n/a
14	chr9:6955559-6955609	PANC-1	pancreas:	n/a
15	chr9:6955559-6955609	BJ	skin:	n/a
16	chr9:6955559-6955609	HAEpiC	amniotic membrane:	n/a
17	chr9:6955559-6955609	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:6955559-6955609	SKMC	muscle:	n/a
19	chr9:6955559-6955609	HCM	heart:	n/a
20	chr9:6955559-6955609	U87	brain:	n/a
21	chr9:6955559-6955609	ProgFib	skin:	n/a
22	chr9:6955559-6955609	HEK293	kidney:	embryo
23	chr9:6955559-6955609	ECC-1	luminal epithelium:	n/a
24	chr9:6955559-6955609	SK-N-SH_RA	brain:	n/a
25	chr9:6955559-6955609	Hepatocyte	liver:	n/a
26	chr9:6955559-6955609	BE2_C	brain:	n/a
27	chr9:6955559-6955609	AG10803	skin:	n/a
28	chr9:6955559-6955609	PFSK-1	brain:	n/a
29	chr9:6955559-6955609	MCF-7	breast:	n/a
30	chr9:6955559-6955609	AG09319	gingival:	n/a
31	chr9:6955559-6955609	AoSMC	blood vessel:	n/a
32	chr9:6955559-6955609	HCPEpiC	choroid plexus:	n/a
33	chr9:6955559-6955609	Jurkat	blood:	n/a
34	chr9:6955559-6955609	SAEC	small airway:	n/a
35	chr9:6955559-6955609	HEEpiC	esophagus:	n/a
36	chr9:6955559-6955609	ovcar-3	ovarian:	n/a
37	chr9:6955559-6955609	LNCaP	prostate:	n/a
38	chr9:6955559-6955609	RPTEC	kidney:	n/a
39	chr9:6955559-6955609	HMEC	breast:	n/a
40	chr9:6955559-6955609	GM12891	blood:	n/a
41	chr9:6955559-6955609	SK-N-SH	brain:	n/a
42	chr9:6955559-6955609	HUVEC	blood vessel:	n/a
43	chr9:6955559-6955609	A549	lung:	n/a
44	chr9:6955559-6955609	NHBE	bronchial:	n/a
45	chr9:6955559-6955609	H1-hESC	embryonic stem cell:	embryo
46	chr9:6955559-6955609	HCT-116	colon:	n/a
47	chr9:6955559-6955609	SK-N-MC	brain:	n/a
48	chr9:6955559-6955609	GM12892	blood:	n/a
49	chr9:6955559-6955609	MCF10A-Er-Src	breast:	n/a
50	chr9:6955559-6955609	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
2	chr9:6996659..6998506-chr9:6999056..7001855,2	K562	blood:
3	chr9:7052698..7053251-chr9:7360197..7360994,2	K562	blood:
4	chr9:6978865..6981054-chr9:6982708..6984588,2	K562	blood:
5	chr5:35003633..35004245-chr9:7020432..7021432,2	K562	blood:
6	chr9:6954682..6956612-chr9:6970287..6972358,2	MCF-7	breast:
7	chr9:7028131..7030409-chr9:7036098..7038098,2	MCF-7	breast:
8	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
9	chr9:7074844..7076869-chr9:7078894..7081188,2	K562	blood:
10	chr9:7051581..7054293-chr9:7055466..7057984,2	MCF-7	breast:
11	chr9:7070852..7073798-chr9:7075026..7077389,2	MCF-7	breast:
12	chr9:6954682..6956612-chr9:6970287..6972358,2	MCF-7	breast:
13	chr9:7001163..7002731-chr9:7004777..7006309,2	K562	blood:
14	chr9:7062837..7065514-chr9:7066672..7068819,2	MCF-7	breast:
15	chr9:6986135..6988312-chr9:6992816..6995034,2	MCF-7	breast:
16	chr9:7052694..7053246-chr9:7259513..7260136,3	MCF-7	breast:
17	chr9:6931770..6934269-chr9:6942265..6944921,2	MCF-7	breast:
18	chr9:7070852..7073798-chr9:7075026..7077389,2	MCF-7	breast:
19	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
20	chr9:7028131..7030409-chr9:7036098..7038098,2	MCF-7	breast:
21	chr9:7052501..7053186-chr9:7233839..7234508,2	MCF-7	breast:
22	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
23	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
24	chr9:7051581..7054293-chr9:7055466..7057984,2	MCF-7	breast:
25	chr9:6996659..6998506-chr9:6999056..7001855,2	K562	blood:
26	chr9:6986135..6988312-chr9:6992816..6995034,2	MCF-7	breast:
27	chr9:7046839..7049487-chr9:7050524..7052607,2	K562	blood:
28	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
29	chr9:7052337..7053367-chr9:7536144..7537120,3	MCF-7	breast:
30	chr9:7001163..7002731-chr9:7004777..7006309,2	K562	blood:
31	chr9:7052132..7053116-chr9:7186335..7186921,2	K562	blood:
32	chr9:7062837..7065514-chr9:7066672..7068819,2	MCF-7	breast:

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

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

Extended variants
information (count: 7057 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:7057 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12342436	chr9:6942605-6942606	Weak transcription Enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567444442	chr9:6942610-6942611	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs534552917	chr9:6942612-6942613	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs146411507	chr9:6942623-6942624	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs182749396	chr9:6942628-6942629	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs11791950	chr9:6942643-6942644	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs368122476	chr9:6942656-6942657	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140739496	chr9:6942748-6942749	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577260306	chr9:6942756-6942757	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189011284	chr9:6942786-6942787	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193017889	chr9:6942792-6942793	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568796316	chr9:6942812-6942813	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572697787	chr9:6942822-6942823	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372042165	chr9:6942864-6942865	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150108436	chr9:6942867-6942868	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7850286	chr9:6942877-6942878	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184060098	chr9:6942881-6942882	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs386732169	chr9:6942890-6942891	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78600476	chr9:6942892-6942893	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372978021	chr9:6942906-6942907	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35433789	chr9:6942910-6942911	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs544408098	chr9:6942914-6942915	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7037266	chr9:6942940-6942941	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
24	rs530079436	chr9:6942944-6942945	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6477129	chr9:6942951-6942952	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs376204963	chr9:6942974-6942975	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138556494	chr9:6942982-6942983	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528229270	chr9:6942993-6942994	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546402414	chr9:6943000-6943001	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570978302	chr9:6943001-6943002	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187275305	chr9:6943013-6943014	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148873892	chr9:6943025-6943026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568834241	chr9:6943026-6943027	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541700920	chr9:6943048-6943049	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192159281	chr9:6943068-6943069	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555205354	chr9:6943129-6943130	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183922045	chr9:6943168-6943169	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559900018	chr9:6943172-6943173	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544951679	chr9:6943179-6943180	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs111698998	chr9:6943192-6943193	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534362442	chr9:6943209-6943210	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559173619	chr9:6943239-6943240	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188658841	chr9:6943265-6943266	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544683174	chr9:6943324-6943325	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs60170601	chr9:6943341-6943342	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs551887843	chr9:6943350-6943351	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7025865	chr9:6943374-6943375	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs35043731	chr9:6943390-6943391	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560813348	chr9:6943395-6943396	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6477130	chr9:6943467-6943468	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	21215367	CNVD

Chromatin state (count:2268 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

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	chr9:6896200-6959000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr9:6900600-6943000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr9:6901600-6944200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr9:6912400-6978400	Weak transcription	Esophagus	oesophagus
7	chr9:6921600-6957600	Weak transcription	Thymus	Thymus
8	chr9:6921800-6960400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr9:6922200-6959000	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr9:6922600-6944800	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr9:6922600-6981000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr9:6924600-6957400	Weak transcription	Fetal Thymus	thymus
13	chr9:6929800-6944800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr9:6931200-6942800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr9:6931400-6958600	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr9:6931400-6960000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr9:6932400-6943600	Weak transcription	Primary B cells from cord blood	blood
18	chr9:6932400-6944200	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr9:6932400-6945400	Weak transcription	Fetal Intestine Large	intestine
20	chr9:6932600-6944200	Weak transcription	Small Intestine	intestine
21	chr9:6932600-6949600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr9:6932800-6943400	Weak transcription	Left Ventricle	heart
23	chr9:6932800-6944200	Weak transcription	Psoas Muscle	Psoas
24	chr9:6932800-6944800	Weak transcription	Gastric	stomach
25	chr9:6932800-6955000	Weak transcription	Right Atrium	heart
26	chr9:6932800-6985000	Weak transcription	Spleen	Spleen
27	chr9:6933400-6944000	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr9:6933600-6944600	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr9:6933800-6943200	Weak transcription	HepG2	liver
30	chr9:6936800-6965200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr9:6937000-6943600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr9:6938800-6960400	Weak transcription	Adipose Nuclei	Adipose
33	chr9:6939000-6943000	Weak transcription	HUVEC	blood vessel
34	chr9:6939200-6943600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr9:6939200-6943600	Weak transcription	Brain Hippocampus Middle	brain
36	chr9:6939200-6943800	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr9:6939200-6943800	Weak transcription	NHEK	skin
38	chr9:6939200-6944200	Weak transcription	Brain Angular Gyrus	brain
39	chr9:6939200-6944200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr9:6939200-6944200	Weak transcription	HSMMtube	muscle
41	chr9:6939200-6944400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr9:6939200-6945600	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr9:6939400-6942800	Weak transcription	Fetal Intestine Small	intestine
44	chr9:6939400-6943400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr9:6939400-6943400	Weak transcription	Osteobl	bone
46	chr9:6939400-6943600	Weak transcription	Placenta	Placenta
47	chr9:6939400-6943800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr9:6939400-6943800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr9:6939400-6943800	Weak transcription	HMEC	breast
50	chr9:6939400-6944000	Weak transcription	HSMM	muscle

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