Variant report

Variant	esv2761298
Chromosome Location	chr9:6505897-6544766
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:308)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6542871-6542968	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6530270-6530987	HepG2	liver:	n/a	n/a
3	BRCA1	chr9:6513565-6513758	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr9:6532209-6532495	HepG2	liver:	n/a	n/a
5	CEBPB	chr9:6530246-6530475	A549	lung:	n/a	chr9:6530420-6530437
6	CEBPB	chr9:6513131-6513433	A549	lung:	n/a	n/a
7	CEBPB	chr9:6513123-6513392	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr9:6525314-6525712	IMR90	lung:	n/a	n/a
9	CEBPB	chr9:6538666-6538916	A549	lung:	n/a	n/a
10	CEBPB	chr9:6530218-6530841	HepG2	liver:	n/a	chr9:6530420-6530437
11	CEBPB	chr9:6534938-6534957	HepG2	liver:	n/a	chr9:6534938-6534949
12	CEBPB	chr9:6513160-6513387	K562	blood:	n/a	n/a
13	CEBPB	chr9:6532217-6532441	IMR90	lung:	n/a	n/a
14	CEBPB	chr9:6513096-6513454	IMR90	lung:	n/a	n/a
15	CEBPB	chr9:6513102-6513433	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:6538579-6539119	IMR90	lung:	n/a	n/a
17	CHD2	chr9:6530536-6530903	HepG2	liver:	n/a	n/a
18	CTCF	chr9:6512080-6512230	GM06990	blood:	n/a	n/a
19	CTCF	chr9:6519980-6520130	GM12865	blood:	n/a	n/a
20	CTCF	chr9:6527080-6527230	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr9:6542578-6542618	GM20000	blood:	n/a	n/a
22	ELF1	chr9:6530590-6530770	HepG2	liver:	n/a	n/a
23	ELK1	chr9:6527262-6527307	GM12878	blood:	n/a	n/a
24	EP300	chr9:6511963-6512817	SK-N-SH	brain:	n/a	chr9:6512211-6512225
25	EP300	chr9:6530323-6530931	HepG2	liver:	n/a	n/a
26	EP300	chr9:6506341-6506859	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr9:6530277-6530876	HepG2	liver:	n/a	n/a
28	EP300	chr9:6530230-6530926	HepG2	liver:	n/a	n/a
29	EP300	chr9:6538652-6539025	SK-N-SH_RA	brain:	n/a	chr9:6538978-6538991
30	EP300	chr9:6538588-6539040	SK-N-SH_RA	brain:	n/a	chr9:6538978-6538991
31	EP300	chr9:6506535-6506834	SK-N-SH_RA	brain:	n/a	n/a
32	FOS	chr9:6530302-6530632	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr9:6540893-6540901	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr9:6538822-6539110	MCF10A-Er-Src	breast:	n/a	chr9:6538985-6538994
35	FOS	chr9:6538221-6538459	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr9:6538653-6539165	MCF10A-Er-Src	breast:	n/a	chr9:6538985-6538994
37	FOS	chr9:6538650-6539169	MCF10A-Er-Src	breast:	n/a	chr9:6538985-6538994
38	FOS	chr9:6530242-6530752	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr9:6506643-6506654	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr9:6538287-6538419	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr9:6530277-6530583	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr9:6530391-6530575	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr9:6506786-6506839	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr9:6538746-6539163	HUVEC	blood vessel:	n/a	chr9:6538985-6538994
45	FOS	chr9:6538821-6539140	MCF10A-Er-Src	breast:	n/a	chr9:6538985-6538994
46	FOSL2	chr9:6512266-6512762	SK-N-SH	brain:	n/a	n/a
47	FOSL2	chr9:6530237-6531052	HepG2	liver:	n/a	n/a
48	FOSL2	chr9:6511742-6512064	HepG2	liver:	n/a	n/a
49	FOSL2	chr9:6506611-6506989	SK-N-SH	brain:	n/a	n/a
50	FOXA1	chr9:6530269-6530824	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6532828-6532878	GM19239	blood:	n/a
2	chr9:6532828-6532878	NHBE	bronchial:	n/a
3	chr9:6532828-6532878	HCF	heart:	n/a
4	chr9:6532828-6532878	HIPEpiC	eye:	n/a
5	chr9:6532828-6532878	SKMC	muscle:	n/a
6	chr9:6532828-6532878	HRE	kidney:	n/a
7	chr9:6532828-6532878	AG10803	skin:	n/a
8	chr9:6532828-6532878	HMEC	breast:	n/a
9	chr9:6532828-6532878	ovcar-3	ovarian:	n/a
10	chr9:6532828-6532878	GM12878	blood:	n/a
11	chr9:6532828-6532878	HRCEpiC	kidney:	n/a
12	chr9:6532828-6532878	GM12891	blood:	n/a
13	chr9:6532828-6532878	HCM	heart:	n/a
14	chr9:6532828-6532878	AoSMC	blood vessel:	n/a
15	chr9:6532828-6532878	HCT-116	colon:	n/a
16	chr9:6532828-6532878	HEK293	kidney:	embryo
17	chr9:6532828-6532878	HAEpiC	amniotic membrane:	n/a
18	chr9:6532828-6532878	PrEC	prostate:	n/a
19	chr9:6532828-6532878	HRPEpiC	eye:	n/a
20	chr9:6532828-6532878	T-47D	breast:	n/a
21	chr9:6532828-6532878	HPAEpiC	pulmonary alveolar:	n/a
22	chr9:6532828-6532878	Hela-S3	cervix:	n/a
23	chr9:6532828-6532878	GM12892	blood:	n/a
24	chr9:6532828-6532878	Caco-2	colon:	n/a
25	chr9:6532828-6532878	K562	blood:	n/a
26	chr9:6532828-6532878	CMK	blood:	n/a
27	chr9:6532828-6532878	BJ	skin:	n/a
28	chr9:6532828-6532878	A549	lung:	n/a
29	chr9:6532828-6532878	NB4	blood:	n/a
30	chr9:6532828-6532878	HepG2	liver:	n/a
31	chr9:6532828-6532878	SK-N-SH_RA	brain:	n/a
32	chr9:6532828-6532878	MCF-7	breast:	n/a
33	chr9:6532828-6532878	Hepatocyte	liver:	n/a
34	chr9:6532828-6532878	HL-60	blood:	n/a
35	chr9:6532828-6532878	SAEC	small airway:	n/a
36	chr9:6532828-6532878	MCF10A-Er-Src	breast:	n/a
37	chr9:6532828-6532878	BE2_C	brain:	n/a
38	chr9:6532828-6532878	AG09309	skin:	n/a
39	chr9:6532828-6532878	ProgFib	skin:	n/a
40	chr9:6532828-6532878	GM06990	blood:	n/a
41	chr9:6532828-6532878	HEEpiC	esophagus:	n/a
42	chr9:6532828-6532878	Jurkat	blood:	n/a
43	chr9:6532828-6532878	H1-hESC	embryonic stem cell:	embryo
44	chr9:6532828-6532878	PFSK-1	brain:	n/a
45	chr9:6532828-6532878	ECC-1	luminal epithelium:	n/a
46	chr9:6532828-6532878	U87	brain:	n/a
47	chr9:6532828-6532878	SK-N-MC	brain:	n/a
48	chr9:6532828-6532878	NT2-D1	testis:	n/a
49	chr9:6532828-6532878	HNPCEpiC	eye:	n/a
50	chr9:6532828-6532878	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:6516849..6518888-chr9:6521453..6523458,2	K562	blood:
2	chr9:6533272..6535800-chr9:6681069..6683891,2	K562	blood:
3	chr9:6523722..6524445-chr9:6667595..6668159,2	K562	blood:
4	chr9:6516849..6518888-chr9:6521453..6523458,2	K562	blood:
5	chr6:26305236..26306818-chr9:6510894..6512414,2	K562	blood:
6	chr9:6504123..6506541-chr9:6507327..6509655,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UHRF2-3	chr9:6529539-6529917	NONHSAT130138
2	lnc-UHRF2-4	chr9:6542094-6542350	NONHSAT130139

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	UHRF2	hsa-let-7a-5p	chr9:6506445-6506465
2	UHRF2	hsa-let-7a-5p	chr9:6506458-6506465

Variant related genes	Relation type
RN7SL25P	TF binding region
GLDC	TF binding region
RN7SL25P	CpG island
GLDC	CpG island
ENSG00000147854	chromatin interactions

Extended variants
information (count: 2043 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2043 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547615987	chr9:6505903-6505904	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566350738	chr9:6505906-6505907	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148011842	chr9:6505983-6505984	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373728296	chr9:6505997-6505998	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112064627	chr9:6505999-6506000	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs41281767	chr9:6506001-6506002	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376126514	chr9:6506011-6506012	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs33962342	chr9:6506038-6506039	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs530766938	chr9:6506071-6506072	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200374753	chr9:6506072-6506073	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141724018	chr9:6506101-6506102	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368093815	chr9:6506118-6506119	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537452113	chr9:6506140-6506141	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555863329	chr9:6506141-6506142	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs371648083	chr9:6506175-6506176	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200169545	chr9:6506184-6506185	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574203639	chr9:6506192-6506193	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368378792	chr9:6506198-6506199	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113880101	chr9:6506212-6506213	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542023700	chr9:6506261-6506262	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560122844	chr9:6506269-6506270	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189404525	chr9:6506298-6506299	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545824934	chr9:6506309-6506310	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564407937	chr9:6506391-6506392	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553798790	chr9:6506405-6506406	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181822683	chr9:6506430-6506431	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs527850862	chr9:6506477-6506478	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200113974	chr9:6506504-6506505	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547931799	chr9:6506514-6506515	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549378971	chr9:6506553-6506554	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561427178	chr9:6506609-6506610	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs528992181	chr9:6506639-6506640	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs547577858	chr9:6506653-6506654	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs566190681	chr9:6506657-6506658	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs533576563	chr9:6506671-6506672	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs572247579	chr9:6506697-6506698	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs369521468	chr9:6506704-6506705	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs551748449	chr9:6506765-6506766	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs565701948	chr9:6506768-6506769	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs539393196	chr9:6506811-6506812	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186508441	chr9:6506892-6506893	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142519970	chr9:6506893-6506894	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549854331	chr9:6506896-6506897	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555826371	chr9:6506961-6506962	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190450804	chr9:6506964-6506965	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567746533	chr9:6507003-6507004	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1044642	chr9:6507006-6507007	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535163217	chr9:6507009-6507010	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs36108024	chr9:6507024-6507025	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570908282	chr9:6507094-6507095	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	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
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Dyslexia	22102821	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
early-passage human iPS cells	21368824	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:622 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6463600-6518400	Weak transcription	Fetal Brain Male	brain
2	chr9:6472200-6508200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:6473800-6506200	Weak transcription	Small Intestine	intestine
4	chr9:6475400-6508200	Strong transcription	Primary T helper cells fromperipheralblood	blood
5	chr9:6475400-6508400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
6	chr9:6475400-6508800	Strong transcription	Primary B cells from peripheral blood	blood
7	chr9:6475400-6508800	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr9:6475800-6509000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr9:6475800-6510800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr9:6476000-6509400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr9:6477600-6507800	Strong transcription	Primary T helper cells PMA-I stimulated	--
12	chr9:6477800-6511000	Weak transcription	Fetal Heart	heart
13	chr9:6480200-6508400	Weak transcription	Stomach Mucosa	stomach
14	chr9:6487600-6510600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr9:6492800-6508800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr9:6493000-6509000	Strong transcription	Adipose Nuclei	Adipose
17	chr9:6493400-6508400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr9:6493600-6507400	Strong transcription	Duodenum Smooth Muscle	Duodenum
19	chr9:6493800-6506000	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr9:6493800-6508200	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr9:6494000-6508800	Strong transcription	GM12878-XiMat	blood
22	chr9:6495000-6506400	Strong transcription	HepG2	liver
23	chr9:6495000-6508400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
24	chr9:6495200-6510800	Strong transcription	Fetal Thymus	thymus
25	chr9:6495400-6510200	Strong transcription	HUVEC	blood vessel
26	chr9:6495400-6510600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr9:6495400-6511400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr9:6496400-6508200	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr9:6496800-6508400	Strong transcription	Sigmoid Colon	Sigmoid Colon
30	chr9:6498800-6507800	Weak transcription	Psoas Muscle	Psoas
31	chr9:6498800-6554400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr9:6499000-6506000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr9:6499000-6506600	Weak transcription	K562	blood
34	chr9:6499000-6511400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr9:6499000-6528400	Weak transcription	Pancreas	Pancrea
36	chr9:6499200-6506600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr9:6499600-6506200	Strong transcription	NHDF-Ad	bronchial
38	chr9:6499600-6507200	Strong transcription	HSMM	muscle
39	chr9:6500200-6506600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr9:6500400-6506000	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr9:6500800-6510200	Weak transcription	Colonic Mucosa	Colon
42	chr9:6500800-6517400	Weak transcription	Esophagus	oesophagus
43	chr9:6501800-6510400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr9:6502000-6506000	Weak transcription	Brain Anterior Caudate	brain
45	chr9:6502200-6506000	Weak transcription	Fetal Kidney	kidney
46	chr9:6502200-6508200	Strong transcription	Fetal Stomach	stomach
47	chr9:6502200-6513600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr9:6502600-6512200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr9:6502600-6512400	Weak transcription	Aorta	Aorta
50	chr9:6503000-6509800	Strong transcription	A549	lung

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