Variant report

Variant	esv2761483
Chromosome Location	chr9:6216925-6246144
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:238)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:238 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6238753-6239428	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6236398-6236588	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6236968-6237134	HepG2	liver:	n/a	n/a
4	BATF	chr9:6243774-6244147	GM12878	blood:	n/a	chr9:6243981-6243992
5	BATF	chr9:6243750-6244097	GM12878	blood:	n/a	chr9:6243981-6243992
6	BCL11A	chr9:6243799-6244059	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:6238901-6239586	HepG2	liver:	n/a	n/a
8	BHLHE40	chr9:6243865-6244064	GM12878	blood:	n/a	n/a
9	BRCA1	chr9:6238263-6238286	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr9:6218063-6218503	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr9:6217956-6218616	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr9:6236998-6237031	K562	blood:	n/a	n/a
13	CEBPB	chr9:6229586-6229823	A549	lung:	n/a	n/a
14	CEBPB	chr9:6236866-6237162	IMR90	lung:	n/a	chr9:6237021-6237032
15	CEBPB	chr9:6236864-6237147	A549	lung:	n/a	chr9:6237021-6237032
16	CEBPB	chr9:6236340-6237204	HepG2	liver:	n/a	chr9:6237021-6237032 chr9:6236490-6236503 chr9:6236490-6236501
17	CEBPB	chr9:6230369-6231071	Hela-S3	cervix:	n/a	chr9:6230587-6230598 chr9:6230587-6230598
18	CEBPB	chr9:6229679-6229728	HepG2	liver:	n/a	n/a
19	CEBPB	chr9:6236818-6237212	Hela-S3	cervix:	n/a	chr9:6237021-6237032
20	CEBPB	chr9:6236845-6237233	MCF-7	breast:	n/a	chr9:6237021-6237032
21	CEBPB	chr9:6218254-6218583	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr9:6218092-6218568	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr9:6218324-6218373	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr9:6238920-6239410	HepG2	liver:	n/a	n/a
25	CHD2	chr9:6218068-6218550	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr9:6230395-6230747	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr9:6236900-6237050	HCM	heart:	n/a	n/a
28	CTCF	chr9:6217478-6217518	GM20000	blood:	n/a	n/a
29	CTCF	chr9:6236880-6237030	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr9:6236753-6236882	MCF-7	breast:	n/a	n/a
31	CTCF	chr9:6224260-6224410	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr9:6236795-6236826	Fibrobl	skin:	n/a	n/a
33	CTCF	chr9:6236757-6236870	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:6236880-6237030	HVMF	connective:	n/a	n/a
35	CTCF	chr9:6236763-6236904	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr9:6239900-6240050	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr9:6236766-6236870	NHEK	skin:	n/a	n/a
38	CTCF	chr9:6236738-6236876	MCF-7	breast:	n/a	n/a
39	CTCF	chr9:6236760-6236910	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr9:6236773-6236860	MCF-7	breast:	n/a	n/a
41	CTCF	chr9:6236740-6236890	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr9:6236773-6236862	MCF-7	breast:	n/a	n/a
43	CTCF	chr9:6236680-6236830	HVMF	connective:	n/a	n/a
44	E2F4	chr9:6236958-6237169	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr9:6230482-6230871	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr9:6218304-6218586	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F6	chr9:6239046-6239521	H1-hESC	embryonic stem cell:	n/a	n/a
48	EBF1	chr9:6230396-6230676	GM12878	blood:	n/a	chr9:6230512-6230521 chr9:6230512-6230522
49	EBF1	chr9:6243842-6244103	GM12878	blood:	n/a	n/a
50	ELK4	chr9:6218190-6218527	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6241371-6241421	HCPEpiC	choroid plexus:	n/a
2	chr9:6241371-6241421	NT2-D1	testis:	n/a
3	chr9:6241371-6241421	HCM	heart:	n/a
4	chr9:6241371-6241421	NHDF-neo	bronchial:	n/a
5	chr9:6241371-6241421	AG04450	lung:	fetal
6	chr9:6241371-6241421	ProgFib	skin:	n/a
7	chr9:6241371-6241421	CMK	blood:	n/a
8	chr9:6241371-6241421	SK-N-MC	brain:	n/a
9	chr9:6241371-6241421	NB4	blood:	n/a
10	chr9:6241371-6241421	HCF	heart:	n/a
11	chr9:6241371-6241421	SKMC	muscle:	n/a
12	chr9:6241371-6241421	RPTEC	kidney:	n/a
13	chr9:6241371-6241421	HIPEpiC	eye:	n/a
14	chr9:6241371-6241421	PrEC	prostate:	n/a
15	chr9:6241371-6241421	HRE	kidney:	n/a
16	chr9:6241371-6241421	PFSK-1	brain:	n/a
17	chr9:6241371-6241421	BJ	skin:	n/a
18	chr9:6241371-6241421	SK-N-SH	brain:	n/a
19	chr9:6241371-6241421	GM19239	blood:	n/a
20	chr9:6241371-6241421	HL-60	blood:	n/a
21	chr9:6241371-6241421	HRPEpiC	eye:	n/a
22	chr9:6241371-6241421	ECC-1	luminal epithelium:	n/a
23	chr9:6241371-6241421	HepG2	liver:	n/a
24	chr9:6241371-6241421	AG10803	skin:	n/a
25	chr9:6241371-6241421	Hela-S3	cervix:	n/a
26	chr9:6241371-6241421	MCF-7	breast:	n/a
27	chr9:6241371-6241421	HEEpiC	esophagus:	n/a
28	chr9:6241371-6241421	NHBE	bronchial:	n/a
29	chr9:6241371-6241421	HNPCEpiC	eye:	n/a
30	chr9:6241371-6241421	H1-hESC	embryonic stem cell:	embryo
31	chr9:6241371-6241421	Caco-2	colon:	n/a
32	chr9:6241371-6241421	AG09319	gingival:	n/a
33	chr9:6241371-6241421	ovcar-3	ovarian:	n/a
34	chr9:6241371-6241421	MCF10A-Er-Src	breast:	n/a
35	chr9:6241371-6241421	HAEpiC	amniotic membrane:	n/a
36	chr9:6241371-6241421	HPAEpiC	pulmonary alveolar:	n/a
37	chr9:6241371-6241421	AoSMC	blood vessel:	n/a
38	chr9:6241371-6241421	T-47D	breast:	n/a
39	chr9:6241371-6241421	U87	brain:	n/a
40	chr9:6241371-6241421	K562	blood:	n/a
41	chr9:6241371-6241421	SAEC	small airway:	n/a
42	chr9:6241371-6241421	BE2_C	brain:	n/a
43	chr9:6241371-6241421	HEK293	kidney:	embryo
44	chr9:6241371-6241421	HRCEpiC	kidney:	n/a
45	chr9:6241371-6241421	AG09309	skin:	n/a
46	chr9:6241371-6241421	GM06990	blood:	n/a
47	chr9:6241371-6241421	PANC-1	pancreas:	n/a
48	chr9:6241371-6241421	Jurkat	blood:	n/a
49	chr9:6241371-6241421	Hepatocyte	liver:	n/a
50	chr9:6241371-6241421	SK-N-SH_RA	brain:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6244528..6246233-chr9:6251156..6253683,2	MCF-7	breast:
2	chr9:6234179..6236096-chr9:6238826..6241061,2	K562	blood:
3	chr9:6241308..6243910-chr9:6245192..6247268,2	MCF-7	breast:
4	chr9:6234179..6236096-chr9:6238826..6241061,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TPD52L3-1	chr9:6242192-6242734	NONHSAT130126
2	lnc-TPD52L3-1	chr9:6241693-6241785	NONHSAT130126

No data

Variant related genes	Relation type
IL33	TF binding region
IL33	CpG island
ENSG00000137033	chromatin interactions

Extended variants
information (count: 1114 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1114 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544562023	chr9:6216957-6216958	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs146033745	chr9:6216994-6216995	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs535639879	chr9:6217015-6217016	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs138374691	chr9:6217033-6217034	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs141170416	chr9:6217049-6217050	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs146956694	chr9:6217112-6217113	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs181102662	chr9:6217113-6217114	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs370409669	chr9:6217148-6217149	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs138015353	chr9:6217167-6217168	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs561450300	chr9:6217174-6217175	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs74837563	chr9:6217201-6217202	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs7850282	chr9:6217232-6217233	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs549421196	chr9:6217256-6217257	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs143592380	chr9:6217288-6217289	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs566316199	chr9:6217324-6217325	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs533649467	chr9:6217331-6217332	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs186751919	chr9:6217355-6217356	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs144060718	chr9:6217357-6217358	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs530816035	chr9:6217406-6217407	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs534982318	chr9:6217438-6217439	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs549447752	chr9:6217495-6217496	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs190743799	chr9:6217542-6217543	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs10124842	chr9:6217573-6217574	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs73639581	chr9:6217605-6217606	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs180966859	chr9:6217613-6217614	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs35277277	chr9:6217620-6217621	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs565756952	chr9:6217664-6217665	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs141331054	chr9:6217684-6217685	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs186167078	chr9:6217709-6217710	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs557171225	chr9:6217815-6217816	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs190777329	chr9:6217849-6217850	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs183326174	chr9:6217878-6217879	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs369312804	chr9:6217881-6217882	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs573382102	chr9:6217906-6217907	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs540750281	chr9:6217912-6217913	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs373760369	chr9:6217989-6217990	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs537175695	chr9:6218024-6218025	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557397122	chr9:6218056-6218057	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188204518	chr9:6218065-6218066	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191863053	chr9:6218069-6218070	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373200194	chr9:6218107-6218108	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575827864	chr9:6218111-6218112	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545638828	chr9:6218152-6218153	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs202236962	chr9:6218160-6218161	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563826355	chr9:6218324-6218325	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34194169	chr9:6218325-6218326	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373923015	chr9:6218344-6218345	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78121143	chr9:6218346-6218347	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549379767	chr9:6218414-6218415	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs182971615	chr9:6218433-6218434	Enhancers Weak transcription Active TSS Flanking Active TSS	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
Schizophrenia	23813976	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6213400-6217600	Weak transcription	HMEC	breast
2	chr9:6213400-6218000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:6213600-6217800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:6214800-6217000	Weak transcription	Stomach Mucosa	stomach
5	chr9:6215000-6217000	Weak transcription	Fetal Kidney	kidney
6	chr9:6215000-6218000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr9:6215000-6218000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr9:6215200-6217800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr9:6215400-6217000	Active TSS	Adipose Nuclei	Adipose
10	chr9:6215400-6217800	Weak transcription	Brain Anterior Caudate	brain
11	chr9:6215400-6218200	Active TSS	Fetal Brain Female	brain
12	chr9:6215400-6219600	Active TSS	Right Atrium	heart
13	chr9:6215600-6217000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr9:6215600-6217000	Active TSS	Colon Smooth Muscle	Colon
15	chr9:6215600-6217000	Active TSS	Rectal Smooth Muscle	rectum
16	chr9:6215600-6217200	Active TSS	Stomach Smooth Muscle	stomach
17	chr9:6215600-6218400	Active TSS	Brain Germinal Matrix	brain
18	chr9:6215800-6217000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
19	chr9:6215800-6217000	Weak transcription	HUVEC	blood vessel
20	chr9:6215800-6217000	Weak transcription	NHDF-Ad	bronchial
21	chr9:6215800-6217400	Active TSS	Cortex derived primary cultured neurospheres	brain
22	chr9:6215800-6217600	Weak transcription	Osteobl	bone
23	chr9:6215800-6217800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:6215800-6217800	Weak transcription	Fetal Lung	lung
25	chr9:6215800-6218400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:6215800-6218600	Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr9:6216000-6217200	Active TSS	Left Ventricle	heart
28	chr9:6216000-6217200	Active TSS	Right Ventricle	heart
29	chr9:6216000-6217800	Weak transcription	Brain Hippocampus Middle	brain
30	chr9:6216000-6217800	Weak transcription	Ovary	ovary
31	chr9:6216000-6217800	Weak transcription	NHEK	skin
32	chr9:6216000-6218000	Active TSS	Skeletal Muscle Male	skeletal muscle
33	chr9:6216000-6223800	Weak transcription	Fetal Brain Male	brain
34	chr9:6216200-6217800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr9:6216400-6217200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr9:6216400-6217400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr9:6216400-6217800	Weak transcription	Aorta	Aorta
38	chr9:6216400-6217800	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr9:6216600-6217000	Enhancers	Hela-S3	cervix
40	chr9:6216600-6217800	Weak transcription	Fetal Muscle Leg	muscle
41	chr9:6216600-6217800	Weak transcription	Fetal Stomach	stomach
42	chr9:6216800-6218000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr9:6217000-6217200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr9:6217000-6217200	Enhancers	Fetal Kidney	kidney
45	chr9:6217000-6217200	Enhancers	Stomach Mucosa	stomach
46	chr9:6217000-6217200	Flanking Active TSS	Hela-S3	cervix
47	chr9:6217000-6217400	Active TSS	Liver	Liver
48	chr9:6217000-6217400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr9:6217000-6217400	Enhancers	Rectal Smooth Muscle	rectum
50	chr9:6217000-6217600	Enhancers	HUVEC	blood vessel

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