Variant report

Variant	nsv1020511
Chromosome Location	chr9:25724120-25864209
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:169)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:169 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr9:25830650-25830668	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr9:25742271-25742634	HepG2	liver:	n/a	chr9:25742446-25742459 chr9:25742447-25742458
3	CEBPB	chr9:25848401-25848676	HepG2	liver:	n/a	chr9:25848536-25848547
4	CEBPB	chr9:25748958-25749217	ECC-1	luminal epithelium:	n/a	chr9:25749030-25749041
5	CEBPB	chr9:25724495-25724789	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr9:25763626-25763962	IMR90	lung:	n/a	chr9:25763776-25763787
7	CEBPB	chr9:25861448-25861639	HepG2	liver:	n/a	chr9:25861567-25861578
8	CEBPB	chr9:25848385-25848609	A549	lung:	n/a	chr9:25848536-25848547
9	CEBPB	chr9:25783890-25784164	HepG2	liver:	n/a	chr9:25784053-25784064 chr9:25784055-25784064
10	CEBPB	chr9:25742346-25742582	HepG2	liver:	n/a	chr9:25742446-25742459 chr9:25742447-25742458
11	CEBPB	chr9:25783879-25784164	IMR90	lung:	n/a	chr9:25784053-25784064 chr9:25784055-25784064
12	CEBPB	chr9:25761278-25761303	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr9:25763654-25763950	A549	lung:	n/a	chr9:25763776-25763787
14	CEBPB	chr9:25742343-25742555	HepG2	liver:	n/a	chr9:25742446-25742459 chr9:25742447-25742458
15	CEBPB	chr9:25763645-25763886	H1-hESC	embryonic stem cell:	n/a	chr9:25763776-25763787
16	CEBPB	chr9:25739358-25739637	A549	lung:	n/a	chr9:25739524-25739537 chr9:25739524-25739537 chr9:25739524-25739535 chr9:25739524-25739537 chr9:25739524-25739535
17	CEBPB	chr9:25827119-25827255	HepG2	liver:	n/a	chr9:25827176-25827187
18	CEBPB	chr9:25742380-25742601	H1-hESC	embryonic stem cell:	n/a	chr9:25742446-25742459 chr9:25742447-25742458
19	CEBPB	chr9:25848391-25848698	IMR90	lung:	n/a	chr9:25848536-25848547
20	CEBPB	chr9:25763598-25763944	HepG2	liver:	n/a	chr9:25763776-25763787
21	CEBPB	chr9:25742264-25742634	HepG2	liver:	n/a	chr9:25742446-25742459 chr9:25742447-25742458
22	CEBPB	chr9:25848509-25848579	H1-hESC	embryonic stem cell:	n/a	chr9:25848536-25848547
23	CEBPB	chr9:25761129-25761425	HepG2	liver:	n/a	chr9:25761277-25761288
24	CEBPB	chr9:25724429-25724877	IMR90	lung:	n/a	n/a
25	CEBPD	chr9:25742337-25742570	HepG2	liver:	n/a	n/a
26	CTCF	chr9:25841520-25841670	AG09309	skin:	n/a	chr9:25841563-25841584
27	CTCF	chr9:25769212-25769267	GM13976	blood:	n/a	n/a
28	CTCF	chr9:25727996-25728093	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr9:25772140-25772290	GM12872	blood:	n/a	n/a
30	CTCF	chr9:25837480-25837630	HFF	foreskin:	n/a	n/a
31	CTCF	chr9:25841520-25841670	AG10803	skin:	n/a	chr9:25841563-25841584
32	CTCF	chr9:25734263-25734303	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr9:25837443-25837521	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr9:25727900-25728050	HEK293	kidney:	n/a	n/a
35	CTCF	chr9:25812187-25812230	LNCaP	prostate:	n/a	n/a
36	CTCF	chr9:25841499-25841638	ProgFib	skin:	n/a	chr9:25841563-25841584
37	CTCF	chr9:25828413-25828456	ProgFib	skin:	n/a	n/a
38	CTCF	chr9:25769883-25769937	GM13976	blood:	n/a	n/a
39	CTCF	chr9:25841521-25841616	Hela-S3	cervix:	n/a	chr9:25841563-25841584
40	E2F4	chr9:25742424-25742533	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr9:25796592-25796841	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr9:25852710-25852718	MCF10A-Er-Src	breast:	n/a	n/a
43	EBF1	chr9:25804227-25804506	GM12878	blood:	n/a	n/a
44	EP300	chr9:25742177-25742643	HepG2	liver:	n/a	n/a
45	EP300	chr9:25748755-25749311	ECC-1	luminal epithelium:	n/a	n/a
46	FAM48A	chr9:25728485-25728551	GM12878	blood:	n/a	n/a
47	FOS	chr9:25724415-25724785	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr9:25820636-25820798	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr9:25863875-25864997	HUVEC	blood vessel:	n/a	chr9:25864673-25864684
50	FOS	chr9:25724423-25724782	MCF10A-Er-Src	breast:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr9:25736248..25739126-chr9:25740036..25742643,2	MCF-7	breast:
2	chr9:25677137..25679533-chr9:25758553..25761140,2	MCF-7	breast:
3	chr9:25736248..25739126-chr9:25740036..25742643,2	MCF-7	breast:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFT74-3	chr9:25798032-25798205	XLOC_007306
2	lnc-IFT74-3	chr9:25784413-25784614	NONHSAT130503
3	lnc-IFT74-8	chr9:25770414-25770615	NONHSAT130502
4	lnc-IFT74-3	chr9:25780414-25780615	NONHSAT130503
5	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
6	lnc-IFT74-8	chr9:25770054-25770166	NONHSAT130502
7	lnc-IFT74-3	chr9:25798032-25798204	XLOC_007306
8	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
9	lnc-IFT74-8	chr9:25802619-25802963	ucscGeneNc_uc003zpy_2
10	lnc-IFT74-3	chr9:25798032-25798204	XLOC_007306
11	lnc-IFT74-8	chr9:25774413-25774560	NONHSAT130502
12	lnc-IFT74-8	chr9:25788743-25788941	ucscGeneNc_uc003zpy_2
13	lnc-IFT74-3	chr9:25812619-25812963	XLOC_007306
14	lnc-IFT74-8	chr9:25774413-25774614	ucscGeneNc_uc003zpy_2
15	lnc-IFT74-8	chr9:25770414-25770615	ucscGeneNc_uc003zpy_2
16	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
17	lnc-IFT74-3	chr9:25812619-25812942	XLOC_007306
18	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
19	lnc-IFT74-3	chr9:25780075-25780166	XLOC_007306
20	lnc-IFT74-3	chr9:25804154-25804257	XLOC_007306
21	lnc-IFT74-8	chr9:25770054-25770166	ucscGeneNc_uc003zpy_2
22	lnc-IFT74-3	chr9:25798743-25798941	NONHSAT130503
23	lnc-IFT74-3	chr9:25784413-25784560	XLOC_007306
24	lnc-IFT74-3	chr9:25812619-25812966	NONHSAT130503
25	lnc-IFT74-3	chr9:25780054-25780166	XLOC_007306
26	lnc-IFT74-3	chr9:25798032-25798204	NONHSAT130503
27	lnc-IFT74-3	chr9:25806693-25806736	XLOC_007306
28	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
29	lnc-IFT74-3	chr9:25806594-25806736	XLOC_007306
30	lnc-IFT74-8	chr9:25788032-25788204	ucscGeneNc_uc003zpy_2
31	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
32	lnc-IFT74-3	chr9:25812619-25812942	XLOC_007306
33	lnc-IFT74-3	chr9:25806594-25806736	XLOC_007306
34	lnc-IFT74-3	chr9:25802427-25802517	XLOC_007306
35	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
36	lnc-IFT74-3	chr9:25802427-25802517	XLOC_007306
37	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
38	lnc-IFT74-3	chr9:25804154-25804257	XLOC_007306
39	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
40	lnc-IFT74-3	chr9:25780075-25780166	XLOC_007306
41	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
42	lnc-IFT74-3	chr9:25780054-25780166	NONHSAT130503
43	lnc-IFT74-3	chr9:25780054-25780166	XLOC_007306

No data

Variant related genes	Relation type
ENSG00000236306	TF binding region
ENSG00000198680	chromatin interactions
RNF182	miRNA target sites
ARID5B	miRNA target sites
FBXW7	miRNA target sites
PRPF38B	miRNA target sites
PDE4D	miRNA target sites
FAM49B	miRNA target sites
DEPDC1	miRNA target sites

Extended variants
information (count: 1376 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:1376 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554351498	chr9:25724164-25724165	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs142394118	chr9:25724167-25724168	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534114332	chr9:25724174-25724175	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561027870	chr9:25724188-25724189	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150584584	chr9:25724195-25724196	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372383949	chr9:25724204-25724205	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7037917	chr9:25724234-25724235	Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs543792358	chr9:25724256-25724257	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556740545	chr9:25724258-25724259	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1231333	chr9:25724324-25724325	Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs184458313	chr9:25724338-25724339	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189238659	chr9:25724340-25724341	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139644160	chr9:25724341-25724342	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs34183586	chr9:25724344-25724345	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs60536334	chr9:25724360-25724361	Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs564714056	chr9:25724379-25724380	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182011245	chr9:25724384-25724385	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550260088	chr9:25724424-25724425	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569599348	chr9:25724472-25724473	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529741670	chr9:25724477-25724478	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547951102	chr9:25724487-25724488	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538635172	chr9:25724502-25724503	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78922205	chr9:25724509-25724510	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533811124	chr9:25724541-25724542	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558839975	chr9:25724552-25724553	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558362949	chr9:25724566-25724567	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145548161	chr9:25724570-25724571	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371704161	chr9:25724578-25724579	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538276877	chr9:25724590-25724591	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148458077	chr9:25724597-25724598	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574940925	chr9:25724613-25724614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542364799	chr9:25724656-25724657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554373207	chr9:25724679-25724680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572636466	chr9:25724717-25724718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145400175	chr9:25724725-25724726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564848459	chr9:25724726-25724727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373292962	chr9:25724769-25724770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548085454	chr9:25724773-25724774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs57033961	chr9:25724783-25724784	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs562164487	chr9:25724828-25724829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184920363	chr9:25724883-25724884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547913960	chr9:25724901-25724902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566527624	chr9:25724908-25724909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527527823	chr9:25724958-25724959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552177318	chr9:25724971-25724972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570683853	chr9:25724972-25724973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190800193	chr9:25724990-25724991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550171401	chr9:25724994-25724995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181181406	chr9:25725011-25725012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535937375	chr9:25725028-25725029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Medulloblastoma	21979893	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
Oral squamous cell carcinoma	17134496	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
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Adenoid cystic carcinoma	18332873	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Pancreatic cancer	21811587	CNVD
Bipolar disorder	19114987	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:25716800-25724400	Weak transcription	Fetal Kidney	kidney
2	chr9:25721800-25724200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:25721800-25724400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr9:25724000-25724600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr9:25724000-25724600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:25724200-25724600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr9:25724200-25724600	Enhancers	Hela-S3	cervix
8	chr9:25724200-25724600	Active TSS	HMEC	breast
9	chr9:25724200-25724600	Active TSS	NHEK	skin
10	chr9:25724200-25725600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:25724400-25724600	Enhancers	Fetal Kidney	kidney
12	chr9:25724400-25725000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:25724600-25727200	Weak transcription	Fetal Kidney	kidney
14	chr9:25726800-25727200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr9:25726800-25727400	Enhancers	Rectal Smooth Muscle	rectum
16	chr9:25727000-25727800	Enhancers	Fetal Stomach	stomach
17	chr9:25727200-25728400	Enhancers	Fetal Kidney	kidney
18	chr9:25731200-25731800	Enhancers	Gastric	stomach
19	chr9:25731200-25732800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr9:25740200-25742400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr9:25740400-25740800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr9:25740800-25741200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:25741000-25742600	Enhancers	Brain Germinal Matrix	brain
24	chr9:25741600-25743400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr9:25742200-25742600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr9:25742200-25742600	Enhancers	Fetal Lung	lung
27	chr9:25742200-25742600	Enhancers	HepG2	liver
28	chr9:25742200-25742800	Enhancers	Brain Substantia Nigra	brain
29	chr9:25742400-25742600	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr9:25742400-25742600	Enhancers	Fetal Kidney	kidney
31	chr9:25743400-25744000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr9:25747400-25747600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr9:25752000-25752200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr9:25752000-25752400	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr9:25752200-25752600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr9:25752400-25752600	Enhancers	Colon Smooth Muscle	Colon
37	chr9:25752400-25752800	Enhancers	Brain Angular Gyrus	brain
38	chr9:25752400-25752800	Active TSS	Brain Cingulate Gyrus	brain
39	chr9:25752400-25752800	Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr9:25752400-25752800	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr9:25752400-25752800	Active TSS	Ovary	ovary
42	chr9:25752600-25752800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr9:25754800-25755600	Enhancers	Fetal Stomach	stomach
44	chr9:25756200-25756800	Enhancers	Fetal Brain Male	brain
45	chr9:25758000-25758200	Enhancers	Gastric	stomach
46	chr9:25763600-25764000	ZNF genes & repeats	Pancreas	Pancrea
47	chr9:25764000-25764400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr9:25773800-25774400	Enhancers	Fetal Stomach	stomach
49	chr9:25798800-25799000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:25802400-25803400	Enhancers	Stomach Mucosa	stomach

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