Variant report

Variant	nsv615239
Chromosome Location	chr9:116984070-116999628
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:231)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:231 , 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	ATF3	chr9:116986229-116986445	K562	blood:	n/a	n/a
2	BACH1	chr9:116986542-116986815	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr9:116986245-116986445	HepG2	liver:	n/a	n/a
4	BHLHE40	chr9:116986739-116986747	K562	blood:	n/a	n/a
5	BRCA1	chr9:116991752-116991761	HepG2	liver:	n/a	n/a
6	CCNT2	chr9:116986206-116986428	K562	blood:	n/a	n/a
7	CEBPB	chr9:116986143-116986476	HepG2	liver:	n/a	n/a
8	CEBPB	chr9:116986123-116986513	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:116986077-116986834	A549	lung:	n/a	n/a
10	CEBPB	chr9:116986147-116986480	IMR90	lung:	n/a	n/a
11	CTCF	chr9:116986600-116986750	AG09319	gingival:	n/a	n/a
12	CTCF	chr9:116998660-116998810	NHDF-neo	bronchial:	n/a	n/a
13	CTCF	chr9:116989420-116989570	HepG2	liver:	n/a	n/a
14	CTCF	chr9:116996280-116996430	BJ	skin:	n/a	n/a
15	CTCF	chr9:116989480-116989630	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr9:116998560-116998710	HMF	breast:	n/a	n/a
17	CTCF	chr9:116996260-116996410	HMF	breast:	n/a	n/a
18	CTCF	chr9:116998740-116998890	AG09319	gingival:	n/a	n/a
19	CTCF	chr9:116997620-116997770	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr9:116996220-116996370	NHDF-neo	bronchial:	n/a	n/a
21	CTCF	chr9:116996120-116996270	AG09319	gingival:	n/a	n/a
22	CTCF	chr9:116996220-116996370	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr9:116996200-116996350	HPF	lung:	n/a	n/a
24	CTCF	chr9:116996280-116996430	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr9:116989464-116989503	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr9:116989420-116989570	HEK293	kidney:	n/a	n/a
27	EP300	chr9:116986163-116986462	Hela-S3	cervix:	n/a	n/a
28	EP300	chr9:116993455-116993724	SK-N-SH_RA	brain:	n/a	chr9:116993675-116993682
29	EP300	chr9:116986199-116986421	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr9:116995989-116996022	K562	blood:	n/a	n/a
31	FOS	chr9:116987781-116988104	MCF10A-Er-Src	breast:	n/a	chr9:116987921-116987931 chr9:116987867-116987881 chr9:116987920-116987931 chr9:116987921-116987931 chr9:116987922-116987931 chr9:116987921-116987931 chr9:116987921-116987931
32	FOS	chr9:116987681-116988273	HUVEC	blood vessel:	n/a	chr9:116987921-116987931 chr9:116987867-116987881 chr9:116987920-116987931 chr9:116987921-116987931 chr9:116987922-116987931 chr9:116987921-116987931 chr9:116987921-116987931
33	FOS	chr9:116986167-116986527	MCF10A-Er-Src	breast:	n/a	chr9:116986343-116986354
34	FOS	chr9:116986146-116986955	MCF10A-Er-Src	breast:	n/a	chr9:116986343-116986354
35	FOS	chr9:116986157-116986534	MCF10A-Er-Src	breast:	n/a	chr9:116986343-116986354
36	FOS	chr9:116987768-116988106	MCF10A-Er-Src	breast:	n/a	chr9:116987921-116987931 chr9:116987867-116987881 chr9:116987920-116987931 chr9:116987921-116987931 chr9:116987922-116987931 chr9:116987921-116987931 chr9:116987921-116987931
37	FOS	chr9:116983798-116984404	HUVEC	blood vessel:	n/a	chr9:116984131-116984142
38	FOS	chr9:116986117-116986963	MCF10A-Er-Src	breast:	n/a	chr9:116986343-116986354
39	FOS	chr9:116985880-116987067	HUVEC	blood vessel:	n/a	chr9:116986343-116986354
40	FOSL1	chr9:116985994-116986760	HCT-116	colon:	n/a	n/a
41	FOSL1	chr9:116985959-116987020	HCT-116	colon:	n/a	n/a
42	FOSL2	chr9:116986055-116986577	MCF-7	breast:	n/a	chr9:116986344-116986355
43	FOSL2	chr9:116986173-116986568	HepG2	liver:	n/a	chr9:116986344-116986355
44	FOSL2	chr9:116986615-116986886	HepG2	liver:	n/a	n/a
45	FOSL2	chr9:116986120-116986576	A549	lung:	n/a	chr9:116986344-116986355
46	FOSL2	chr9:116985900-116987015	A549	lung:	n/a	chr9:116986344-116986355
47	FOSL2	chr9:116986148-116986521	HepG2	liver:	n/a	chr9:116986344-116986355
48	FOSL2	chr9:116986027-116986999	SK-N-SH	brain:	n/a	chr9:116986344-116986355
49	FOSL2	chr9:116997356-116997689	HepG2	liver:	n/a	n/a
50	FOXA1	chr9:116986551-116986893	HepG2	liver:	n/a	chr9:116986767-116986782

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:116990636-116990686	AG09309	skin:	n/a
2	chr9:116990636-116990686	NH-A	brain:	n/a
3	chr9:116990636-116990686	PrEC	prostate:	n/a
4	chr9:116990636-116990686	Hela-S3	cervix:	n/a
5	chr9:116990636-116990686	HUVEC	blood vessel:	n/a
6	chr9:116990636-116990686	LNCaP	prostate:	n/a
7	chr9:116990636-116990686	HMEC	breast:	n/a
8	chr9:116990636-116990686	AG10803	skin:	n/a
9	chr9:116990636-116990686	HAEpiC	amniotic membrane:	n/a
10	chr9:116990636-116990686	SK-N-SH_RA	brain:	n/a
11	chr9:116990636-116990686	ovcar-3	ovarian:	n/a
12	chr9:116990636-116990686	GM12891	blood:	n/a
13	chr9:116990636-116990686	RPTEC	kidney:	n/a
14	chr9:116990636-116990686	Hepatocyte	liver:	n/a
15	chr9:116990636-116990686	HCPEpiC	choroid plexus:	n/a
16	chr9:116990636-116990686	BJ	skin:	n/a
17	chr9:116990636-116990686	U87	brain:	n/a
18	chr9:116990636-116990686	HIPEpiC	eye:	n/a
19	chr9:116990636-116990686	ECC-1	luminal epithelium:	n/a
20	chr9:116990636-116990686	BE2_C	brain:	n/a
21	chr9:116990636-116990686	IMR90	lung:	fetal
22	chr9:116990636-116990686	SK-N-SH	brain:	n/a
23	chr9:116990636-116990686	SKMC	muscle:	n/a
24	chr9:116990636-116990686	SK-N-MC	brain:	n/a
25	chr9:116990636-116990686	CMK	blood:	n/a
26	chr9:116990636-116990686	HRE	kidney:	n/a
27	chr9:116990636-116990686	ProgFib	skin:	n/a
28	chr9:116990636-116990686	PFSK-1	brain:	n/a
29	chr9:116990636-116990686	NT2-D1	testis:	n/a
30	chr9:116990636-116990686	Caco-2	colon:	n/a
31	chr9:116990636-116990686	HCT-116	colon:	n/a
32	chr9:116990636-116990686	GM12878	blood:	n/a
33	chr9:116990636-116990686	HL-60	blood:	n/a
34	chr9:116990636-116990686	GM12892	blood:	n/a
35	chr9:116990636-116990686	AG09319	gingival:	n/a
36	chr9:116990636-116990686	MCF10A-Er-Src	breast:	n/a
37	chr9:116990636-116990686	HPAEpiC	pulmonary alveolar:	n/a
38	chr9:116990636-116990686	AG04449	skin:	fetal
39	chr9:116990636-116990686	GM19239	blood:	n/a
40	chr9:116990636-116990686	HCF	heart:	n/a
41	chr9:116990636-116990686	NB4	blood:	n/a
42	chr9:116990636-116990686	HCM	heart:	n/a
43	chr9:116990636-116990686	HNPCEpiC	eye:	n/a
44	chr9:116990636-116990686	GM06990	blood:	n/a
45	chr9:116990636-116990686	Jurkat	blood:	n/a
46	chr9:116990636-116990686	HepG2	liver:	n/a
47	chr9:116990636-116990686	MCF-7	breast:	n/a
48	chr9:116990636-116990686	AG04450	lung:	fetal
49	chr9:116990636-116990686	HRPEpiC	eye:	n/a
50	chr9:116990636-116990686	HEEpiC	esophagus:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:116989029..116991616-chr9:116992422..116994544,2	MCF-7	breast:
2	chr9:116997510..116999400-chr9:117003425..117005684,2	MCF-7	breast:
3	chr9:116984201..116985813-chr9:116998426..117000350,2	MCF-7	breast:
4	chr9:116981540..116984031-chr9:116988688..116990296,2	MCF-7	breast:
5	chr9:116993047..116995452-chr9:116997006..116999883,2	MCF-7	breast:
6	chr9:116993047..116995452-chr9:116997006..116999883,2	MCF-7	breast:
7	chr9:116984500..116987071-chr9:116987461..116989631,3	MCF-7	breast:
8	chr9:116986241..116988764-chr9:116994069..116996364,2	K562	blood:
9	chr9:116979624..116983135-chr9:116986711..116989467,3	MCF-7	breast:
10	chr9:116990174..116993027-chr9:116994971..116997028,2	K562	blood:
11	chr9:116986815..116989169-chr9:116992019..116993746,2	K562	blood:
12	chr9:116984500..116987071-chr9:116987461..116989631,3	MCF-7	breast:
13	chr20:45958971..45959830-chr9:116998602..116999464,2	MCF-7	breast:
14	chr9:116967299..116969937-chr9:116982841..116985605,2	K562	blood:
15	chr9:116989029..116991616-chr9:116992422..116994544,2	MCF-7	breast:
16	chr9:116990174..116993027-chr9:116994971..116997028,2	K562	blood:
17	chr9:116986815..116989169-chr9:116992019..116993746,2	K562	blood:
18	chr9:116984201..116985813-chr9:116998426..117000350,2	MCF-7	breast:
19	chr9:116943873..116946561-chr9:116991422..116993679,2	MCF-7	breast:
20	chr9:116986241..116988764-chr9:116994069..116996364,2	K562	blood:

No data

Variant related genes	Relation type
COL27A1	TF binding region
COL27A1	CpG island

Extended variants
information (count: 660 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:660 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7019849	chr9:116984070-116984071	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185205380	chr9:116984100-116984101	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538977722	chr9:116984151-116984152	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200870872	chr9:116984165-116984166	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201382877	chr9:116984173-116984174	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189908495	chr9:116984182-116984183	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143255944	chr9:116984206-116984207	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539020693	chr9:116984222-116984223	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551358168	chr9:116984225-116984226	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555163241	chr9:116984231-116984232	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574991693	chr9:116984267-116984268	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111978084	chr9:116984280-116984281	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs58707713	chr9:116984306-116984307	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs560303245	chr9:116984351-116984352	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577154661	chr9:116984352-116984353	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545003671	chr9:116984353-116984354	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565183646	chr9:116984435-116984436	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372772490	chr9:116984450-116984451	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377387408	chr9:116984508-116984509	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370987097	chr9:116984516-116984517	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200237175	chr9:116984523-116984524	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143813724	chr9:116984524-116984525	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373679558	chr9:116984542-116984543	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374540360	chr9:116984557-116984558	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs72762630	chr9:116984562-116984563	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560701950	chr9:116984597-116984598	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529759495	chr9:116984600-116984601	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546639157	chr9:116984609-116984610	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566378318	chr9:116984678-116984679	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141401194	chr9:116984707-116984708	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183317345	chr9:116984724-116984725	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34092206	chr9:116984755-116984756	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569521261	chr9:116984847-116984848	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150852575	chr9:116984878-116984879	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555226366	chr9:116984903-116984904	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs367821680	chr9:116984905-116984906	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs575054718	chr9:116984910-116984911	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534325834	chr9:116984919-116984920	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554219141	chr9:116984941-116984942	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577216218	chr9:116984980-116984981	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546169694	chr9:116985012-116985013	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556775410	chr9:116985065-116985066	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545898181	chr9:116985074-116985075	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186522799	chr9:116985122-116985123	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138357168	chr9:116985127-116985128	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556322644	chr9:116985154-116985155	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529822592	chr9:116985244-116985245	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539979849	chr9:116985256-116985257	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191563677	chr9:116985292-116985293	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs73562580	chr9:116985293-116985294	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Melanoma	17363583	CNVD
Retinoblastoma	19183342	CNVD

Chromatin state (count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116952400-116986600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr9:116953400-116985800	Weak transcription	A549	lung
3	chr9:116954600-116986000	Weak transcription	Hela-S3	cervix
4	chr9:116967800-116986000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr9:116968600-116985600	Strong transcription	HepG2	liver
6	chr9:116969800-116986000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr9:116969800-116986000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr9:116969800-116993400	Weak transcription	Stomach Mucosa	stomach
9	chr9:116970000-116987400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr9:116970400-116985800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr9:116973400-116987600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr9:116973400-117047000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr9:116974000-116987400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr9:116975400-116986200	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr9:116976400-116986000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr9:116977000-116987400	Weak transcription	Fetal Brain Male	brain
17	chr9:116977400-116986200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr9:116978400-116991600	Weak transcription	Aorta	Aorta
19	chr9:116978600-116986000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr9:116978600-116988600	Weak transcription	Brain Anterior Caudate	brain
21	chr9:116978600-117011800	Weak transcription	Lung	lung
22	chr9:116978600-117041200	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr9:116978800-116986200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr9:116978800-116986200	Weak transcription	Pancreas	Pancrea
25	chr9:116978800-116986600	Weak transcription	Brain Substantia Nigra	brain
26	chr9:116978800-116987600	Weak transcription	Adipose Nuclei	Adipose
27	chr9:116978800-116998400	Weak transcription	Left Ventricle	heart
28	chr9:116978800-117027600	Weak transcription	Esophagus	oesophagus
29	chr9:116978800-117027600	Weak transcription	Gastric	stomach
30	chr9:116979000-116984600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr9:116979000-116986200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr9:116979000-116988000	Weak transcription	Right Ventricle	heart
33	chr9:116980000-116985600	Strong transcription	Fetal Muscle Leg	muscle
34	chr9:116980000-116986000	Strong transcription	Fetal Muscle Trunk	muscle
35	chr9:116980800-116984200	Genic enhancers	Fetal Intestine Small	intestine
36	chr9:116980800-116984200	Enhancers	NHLF	lung
37	chr9:116981400-116985800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr9:116981600-116985600	Weak transcription	NHDF-Ad	bronchial
39	chr9:116981600-116985800	Weak transcription	Osteobl	bone
40	chr9:116982000-116985600	Strong transcription	Liver	Liver
41	chr9:116982200-116986200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr9:116982400-116985800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr9:116982600-116984200	Weak transcription	Placenta	Placenta
44	chr9:116982600-116986400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr9:116982600-116987400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr9:116982800-116984800	Weak transcription	Fetal Lung	lung
47	chr9:116982800-116985600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr9:116982800-116985600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr9:116982800-116985800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:116982800-116987400	Weak transcription	H9 Cell Line	embryonic stem cell

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