Variant report

Variant	nsv1021234
Chromosome Location	chr9:6933222-7015397
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:469)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6955127-6955771	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6986412-6986867	HepG2	liver:	n/a	n/a
3	ATF1	chr9:7011743-7011938	K562	blood:	n/a	n/a
4	ATF2	chr9:6973706-6974207	GM12878	blood:	n/a	n/a
5	ATF2	chr9:6973498-6974318	GM12878	blood:	n/a	n/a
6	ATF2	chr9:6960665-6961260	GM12878	blood:	n/a	n/a
7	BACH1	chr9:6955248-6955617	H1-hESC	embryonic stem cell:	n/a	chr9:6955424-6955438
8	BATF	chr9:6973758-6974189	GM12878	blood:	n/a	chr9:6973978-6973989
9	BATF	chr9:6973808-6974185	GM12878	blood:	n/a	chr9:6973978-6973989
10	BCL11A	chr9:6973797-6974200	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:6973811-6974164	GM12878	blood:	n/a	n/a
12	BCLAF1	chr9:6973634-6974239	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:6955450-6955720	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:6955289-6955945	HepG2	liver:	n/a	n/a
15	BRCA1	chr9:6945537-6945561	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr9:6978200-6978538	IMR90	lung:	n/a	chr9:6978313-6978324 chr9:6978311-6978324 chr9:6978311-6978324
17	CEBPB	chr9:6977604-6977858	HepG2	liver:	n/a	chr9:6977724-6977735
18	CEBPB	chr9:6973815-6974092	IMR90	lung:	n/a	chr9:6973932-6973943
19	CEBPB	chr9:6973780-6974141	HepG2	liver:	n/a	chr9:6973932-6973943
20	CEBPB	chr9:6970250-6970503	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:6957549-6957715	HepG2	liver:	n/a	chr9:6957646-6957659 chr9:6957648-6957657 chr9:6957646-6957657
22	CEBPB	chr9:6973846-6974085	HepG2	liver:	n/a	chr9:6973932-6973943
23	CEBPB	chr9:7001595-7001907	K562	blood:	n/a	chr9:7001766-7001783 chr9:7001769-7001782
24	CEBPB	chr9:6973574-6974322	GM12878	blood:	n/a	chr9:6973932-6973943
25	CEBPB	chr9:6978304-6978492	A549	lung:	n/a	chr9:6978313-6978324 chr9:6978311-6978324 chr9:6978311-6978324
26	CEBPB	chr9:6978979-6979053	HepG2	liver:	n/a	chr9:6979013-6979024
27	CEBPB	chr9:6986475-6986845	HepG2	liver:	n/a	n/a
28	CEBPB	chr9:6978235-6978587	HepG2	liver:	n/a	chr9:6978313-6978324 chr9:6978311-6978324 chr9:6978311-6978324
29	CEBPB	chr9:7001647-7001868	IMR90	lung:	n/a	chr9:7001766-7001783 chr9:7001769-7001782
30	CEBPB	chr9:6973833-6974107	A549	lung:	n/a	chr9:6973932-6973943
31	CEBPB	chr9:6986539-6986736	HepG2	liver:	n/a	n/a
32	CEBPB	chr9:6978980-6979154	IMR90	lung:	n/a	chr9:6979013-6979024
33	CEBPB	chr9:6938525-6938902	IMR90	lung:	n/a	n/a
34	CEBPB	chr9:6944140-6944602	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr9:6973833-6974012	HepG2	liver:	n/a	chr9:6973932-6973943
36	CHD1	chr9:6955704-6955854	GM12878	blood:	n/a	n/a
37	CHD2	chr9:7006711-7006764	GM12878	blood:	n/a	n/a
38	CHD2	chr9:6955278-6955355	HepG2	liver:	n/a	n/a
39	CTCF	chr9:6944120-6944270	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr9:6985129-6985138	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr9:6944033-6944286	Medullo	brain:	n/a	n/a
42	CTCF	chr9:6985059-6985128	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr9:6943993-6944330	GM12878	blood:	n/a	n/a
44	CTCF	chr9:6944080-6944230	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr9:6944080-6944230	AG09319	gingival:	n/a	n/a
46	CTCF	chr9:6944280-6944430	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr9:6944085-6944243	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr9:6944120-6944270	HMF	breast:	n/a	n/a
49	CTCF	chr9:6944040-6944190	AG04449	skin:	n/a	n/a
50	CTCF	chr9:6944160-6944310	HEEpiC	esophagus:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6955559-6955609	HUVEC	blood vessel:	n/a
2	chr9:6955559-6955609	HRE	kidney:	n/a
3	chr9:6955559-6955609	HepG2	liver:	n/a
4	chr9:6955559-6955609	HCF	heart:	n/a
5	chr9:6955559-6955609	PANC-1	pancreas:	n/a
6	chr9:6955559-6955609	LNCaP	prostate:	n/a
7	chr9:6955559-6955609	HCM	heart:	n/a
8	chr9:6955559-6955609	SKMC	muscle:	n/a
9	chr9:6955559-6955609	HNPCEpiC	eye:	n/a
10	chr9:6955559-6955609	HRCEpiC	kidney:	n/a
11	chr9:6955559-6955609	BE2_C	brain:	n/a
12	chr9:6955559-6955609	H1-hESC	embryonic stem cell:	embryo
13	chr9:6955559-6955609	HMEC	breast:	n/a
14	chr9:6955559-6955609	PrEC	prostate:	n/a
15	chr9:6955559-6955609	Jurkat	blood:	n/a
16	chr9:6955559-6955609	AG04449	skin:	fetal
17	chr9:6955559-6955609	AG04450	lung:	fetal
18	chr9:6955559-6955609	HL-60	blood:	n/a
19	chr9:6955559-6955609	Hela-S3	cervix:	n/a
20	chr9:6955559-6955609	HCPEpiC	choroid plexus:	n/a
21	chr9:6955559-6955609	AG09319	gingival:	n/a
22	chr9:6955559-6955609	AG10803	skin:	n/a
23	chr9:6955559-6955609	A549	lung:	n/a
24	chr9:6955559-6955609	PFSK-1	brain:	n/a
25	chr9:6955559-6955609	NT2-D1	testis:	n/a
26	chr9:6955559-6955609	T-47D	breast:	n/a
27	chr9:6955559-6955609	SK-N-SH	brain:	n/a
28	chr9:6955559-6955609	SAEC	small airway:	n/a
29	chr9:6955559-6955609	GM12878	blood:	n/a
30	chr9:6955559-6955609	K562	blood:	n/a
31	chr9:6955559-6955609	Hepatocyte	liver:	n/a
32	chr9:6955559-6955609	HRPEpiC	eye:	n/a
33	chr9:6955559-6955609	U87	brain:	n/a
34	chr9:6955559-6955609	ovcar-3	ovarian:	n/a
35	chr9:6955559-6955609	AoSMC	blood vessel:	n/a
36	chr9:6955559-6955609	GM12891	blood:	n/a
37	chr9:6955559-6955609	AG09309	skin:	n/a
38	chr9:6955559-6955609	HPAEpiC	pulmonary alveolar:	n/a
39	chr9:6955559-6955609	HIPEpiC	eye:	n/a
40	chr9:6955559-6955609	HEEpiC	esophagus:	n/a
41	chr9:6955559-6955609	CMK	blood:	n/a
42	chr9:6955559-6955609	IMR90	lung:	fetal
43	chr9:6955559-6955609	RPTEC	kidney:	n/a
44	chr9:6955559-6955609	GM12892	blood:	n/a
45	chr9:6955559-6955609	ProgFib	skin:	n/a
46	chr9:6955559-6955609	GM19239	blood:	n/a
47	chr9:6955559-6955609	ECC-1	luminal epithelium:	n/a
48	chr9:6955559-6955609	SK-N-MC	brain:	n/a
49	chr9:6955559-6955609	NB4	blood:	n/a
50	chr9:6955559-6955609	MCF10A-Er-Src	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6978865..6981054-chr9:6982708..6984588,2	K562	blood:
2	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
3	chr9:6986135..6988312-chr9:6992816..6995034,2	MCF-7	breast:
4	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
5	chr9:6986135..6988312-chr9:6992816..6995034,2	MCF-7	breast:
6	chr9:6931770..6934269-chr9:6942265..6944921,2	MCF-7	breast:
7	chr9:7001163..7002731-chr9:7004777..7006309,2	K562	blood:
8	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
9	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
10	chr9:7001163..7002731-chr9:7004777..7006309,2	K562	blood:
11	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
12	chr9:6931770..6934269-chr9:6942265..6944921,2	MCF-7	breast:
13	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
14	chr9:6996659..6998506-chr9:6999056..7001855,2	K562	blood:
15	chr9:6954682..6956612-chr9:6970287..6972358,2	MCF-7	breast:
16	chr9:6928105..6930890-chr9:6932209..6935061,3	K562	blood:
17	chr9:6996659..6998506-chr9:6999056..7001855,2	K562	blood:
18	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-UHRF2-2	chr9:6978625-6978859	ENSG00000224972.1
4	lnc-UHRF2-2	chr9:6973827-6973887	ENSG00000224972.1
5	lnc-UHRF2-6	chr9:6941586-6941815	NONHSAT130166
6	lnc-UHRF2-6	chr9:6948033-6948214	NONHSAT130166

No data

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

Extended variants
information (count: 4498 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:4498 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17595877	chr9:6933222-6933223	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573994245	chr9:6933231-6933232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534768307	chr9:6933265-6933266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35855380	chr9:6933271-6933272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552915069	chr9:6933305-6933306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10975912	chr9:6933372-6933373	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs139291895	chr9:6933380-6933381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144113323	chr9:6933388-6933389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62533787	chr9:6933428-6933429	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs542222204	chr9:6933448-6933449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573378225	chr9:6933453-6933454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191491668	chr9:6933469-6933470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528778702	chr9:6933494-6933495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs201941388	chr9:6933517-6933518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565320809	chr9:6933528-6933529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532768698	chr9:6933530-6933531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550791686	chr9:6933533-6933534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552946777	chr9:6933539-6933540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568768391	chr9:6933633-6933634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569414729	chr9:6933649-6933650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569708333	chr9:6933731-6933732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530076607	chr9:6933737-6933738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs17595898	chr9:6933743-6933744	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs144132068	chr9:6933761-6933762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138463070	chr9:6933817-6933818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534628935	chr9:6933827-6933828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184856351	chr9:6933843-6933844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs199855068	chr9:6933858-6933859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113674545	chr9:6933862-6933863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181595578	chr9:6933871-6933872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148679535	chr9:6933873-6933874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141081995	chr9:6933903-6933904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs117169647	chr9:6933904-6933905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs72701484	chr9:6933931-6933932	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs554157290	chr9:6933933-6933934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185457828	chr9:6933944-6933945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190038261	chr9:6933960-6933961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565616738	chr9:6933973-6933974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs68190370	chr9:6933999-6934000	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs575837146	chr9:6934040-6934041	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113123336	chr9:6934041-6934042	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562924729	chr9:6934057-6934058	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530239225	chr9:6934062-6934063	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs151028446	chr9:6934078-6934079	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368764251	chr9:6934086-6934087	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35742224	chr9:6934102-6934103	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527716669	chr9:6934128-6934129	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112743100	chr9:6934137-6934138	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571559787	chr9:6934144-6934145	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538407250	chr9:6934154-6934155	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:1676 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

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	chr9:6903000-6938600	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr9:6906600-6938200	Weak transcription	Adipose Nuclei	Adipose
8	chr9:6908800-6942600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr9:6912400-6978400	Weak transcription	Esophagus	oesophagus
10	chr9:6921400-6934000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr9:6921600-6939200	Weak transcription	Fetal Lung	lung
12	chr9:6921600-6957600	Weak transcription	Thymus	Thymus
13	chr9:6921800-6960400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr9:6922000-6933600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr9:6922000-6941600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr9:6922200-6959000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr9:6922600-6944800	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr9:6922600-6981000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr9:6924600-6957400	Weak transcription	Fetal Thymus	thymus
20	chr9:6926800-6938600	Weak transcription	Brain Angular Gyrus	brain
21	chr9:6928400-6938400	Weak transcription	Brain Hippocampus Middle	brain
22	chr9:6928600-6941400	Weak transcription	Primary T cells from cord blood	blood
23	chr9:6929200-6933600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr9:6929600-6933800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr9:6929800-6944800	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr9:6930000-6933600	Enhancers	NHDF-Ad	bronchial
27	chr9:6930000-6939600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr9:6930800-6933600	Enhancers	A549	lung
29	chr9:6931200-6933600	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr9:6931200-6938600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:6931200-6942800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr9:6931400-6958600	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr9:6931400-6960000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr9:6932000-6933600	Enhancers	Primary B cells from peripheral blood	blood
35	chr9:6932200-6933800	Enhancers	HepG2	liver
36	chr9:6932200-6934200	Enhancers	Liver	Liver
37	chr9:6932400-6938200	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr9:6932400-6938400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr9:6932400-6943600	Weak transcription	Primary B cells from cord blood	blood
40	chr9:6932400-6944200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr9:6932400-6945400	Weak transcription	Fetal Intestine Large	intestine
42	chr9:6932600-6933400	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr9:6932600-6937800	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr9:6932600-6937800	Weak transcription	NHEK	skin
45	chr9:6932600-6938000	Weak transcription	NH-A	brain
46	chr9:6932600-6938400	Weak transcription	Brain Cingulate Gyrus	brain
47	chr9:6932600-6944200	Weak transcription	Small Intestine	intestine
48	chr9:6932600-6949600	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr9:6932800-6933600	Enhancers	K562	blood
50	chr9:6932800-6933800	Enhancers	Fetal Heart	heart

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