Variant report

Variant	nsv615116
Chromosome Location	chr9:108468129-108546438
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:108480761-108481267	K562	blood:	n/a	n/a
2	ATF1	chr9:108480887-108481087	K562	blood:	n/a	n/a
3	ATF3	chr9:108522343-108522623	K562	blood:	n/a	n/a
4	CBX3	chr9:108497568-108498142	K562	blood:	n/a	n/a
5	CBX3	chr9:108497567-108498134	HCT-116	colon:	n/a	n/a
6	CBX3	chr9:108497622-108498078	K562	blood:	n/a	n/a
7	CEBPB	chr9:108522452-108522537	HepG2	liver:	n/a	chr9:108522506-108522517
8	CEBPB	chr9:108474608-108474905	A549	lung:	n/a	chr9:108474760-108474771
9	CEBPB	chr9:108514934-108515205	IMR90	lung:	n/a	chr9:108515051-108515062
10	CEBPB	chr9:108519804-108520152	Hela-S3	cervix:	n/a	chr9:108519932-108519943 chr9:108519931-108519942 chr9:108519948-108519959
11	CEBPB	chr9:108487467-108487961	K562	blood:	n/a	n/a
12	CEBPB	chr9:108522383-108522621	IMR90	lung:	n/a	chr9:108522506-108522517
13	CEBPB	chr9:108514918-108515219	A549	lung:	n/a	chr9:108515051-108515062
14	CEBPB	chr9:108522362-108522652	Hela-S3	cervix:	n/a	chr9:108522506-108522517
15	CEBPB	chr9:108474679-108474806	HepG2	liver:	n/a	chr9:108474760-108474771
16	CEBPB	chr9:108487662-108487823	A549	lung:	n/a	n/a
17	CEBPB	chr9:108519827-108520134	HepG2	liver:	n/a	chr9:108519932-108519943 chr9:108519931-108519942 chr9:108519948-108519959
18	CEBPB	chr9:108522355-108522675	K562	blood:	n/a	chr9:108522506-108522517
19	CEBPB	chr9:108474581-108474948	HepG2	liver:	n/a	chr9:108474760-108474771
20	CEBPB	chr9:108514878-108515199	HepG2	liver:	n/a	chr9:108515051-108515062
21	CEBPB	chr9:108514922-108515122	Hela-S3	cervix:	n/a	chr9:108515051-108515062
22	CEBPB	chr9:108519856-108520066	K562	blood:	n/a	chr9:108519932-108519943 chr9:108519931-108519942 chr9:108519948-108519959
23	CEBPB	chr9:108519810-108520088	IMR90	lung:	n/a	chr9:108519932-108519943 chr9:108519931-108519942 chr9:108519948-108519959
24	CEBPB	chr9:108519835-108520126	A549	lung:	n/a	chr9:108519932-108519943 chr9:108519931-108519942 chr9:108519948-108519959
25	CEBPB	chr9:108474612-108474962	A549	lung:	n/a	chr9:108474760-108474771
26	CEBPB	chr9:108514906-108515223	K562	blood:	n/a	chr9:108515051-108515062
27	CEBPB	chr9:108522343-108522655	A549	lung:	n/a	chr9:108522506-108522517
28	CEBPB	chr9:108474587-108474952	IMR90	lung:	n/a	chr9:108474760-108474771
29	CEBPB	chr9:108513468-108513735	HepG2	liver:	n/a	chr9:108513604-108513615
30	CEBPB	chr9:108474594-108474935	K562	blood:	n/a	chr9:108474760-108474771
31	CEBPB	chr9:108487592-108487858	K562	blood:	n/a	n/a
32	CEBPB	chr9:108522333-108522696	K562	blood:	n/a	chr9:108522506-108522517
33	CEBPB	chr9:108474619-108474912	A549	lung:	n/a	chr9:108474760-108474771
34	CTCF	chr9:108481620-108481770	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr9:108480860-108481010	HMEC	breast:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939
36	CTCF	chr9:108480840-108480990	HEK293	kidney:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939
37	CTCF	chr9:108480802-108481056	Hela-S3	cervix:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939
38	CTCF	chr9:108480880-108481030	A549	lung:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939
39	CTCF	chr9:108480820-108480970	WERI-Rb-1	eye:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939
40	CTCF	chr9:108480880-108481030	GM06990	blood:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939
41	CTCF	chr9:108480701-108481110	HepG2	liver:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939
42	CTCF	chr9:108484560-108484710	GM12864	blood:	n/a	n/a
43	CTCF	chr9:108480784-108481059	K562	blood:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939
44	CTCF	chr9:108481320-108481470	HCM	heart:	n/a	n/a
45	CTCF	chr9:108480846-108481013	GM10266	blood:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939
46	CTCF	chr9:108484440-108484590	BE2_C	brain:	n/a	n/a
47	CTCF	chr9:108480940-108481090	HCT-116	colon:	n/a	n/a
48	CTCF	chr9:108480840-108480990	BJ	skin:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939
49	CTCF	chr9:108480860-108481010	HEEpiC	esophagus:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939
50	CTCF	chr9:108480820-108480970	AG09309	skin:	n/a	chr9:108480925-108480938 chr9:108480923-108480941 chr9:108480924-108480940 chr9:108480918-108480939

No.	Distal block	Cell Line	Cell type
1	chr9:108399961..108400729-chr9:108480607..108481430,3	MCF-7	breast:
2	chr9:108456694..108458530-chr9:108468137..108470116,2	MCF-7	breast:
3	chr9:108455793..108458148-chr9:108533070..108535920,2	K562	blood:
4	chr9:108532137..108533710-chr9:108537549..108539905,2	K562	blood:
5	chr9:108469613..108472169-chr9:108477924..108480274,2	K562	blood:
6	chr9:108469613..108472169-chr9:108477924..108480274,2	K562	blood:
7	chr9:108456301..108459785-chr9:108473235..108475830,3	MCF-7	breast:
8	chr9:108526044..108528062-chr9:108534104..108535847,2	MCF-7	breast:
9	chr9:108471863..108473966-chr9:108475296..108477111,2	K562	blood:
10	chr9:108417995..108418590-chr9:108480446..108481418,3	K562	blood:
11	chr9:108465735..108468384-chr9:108469174..108471784,2	K562	blood:
12	chr9:108526044..108528062-chr9:108534104..108535847,2	MCF-7	breast:
13	chr9:108399430..108400714-chr9:108479607..108481929,7	MCF-7	breast:
14	chr9:108370952..108371979-chr9:108480070..108481346,6	K562	blood:
15	chr9:108530827..108532419-chr9:108534650..108537088,2	K562	blood:
16	chr9:108532137..108533710-chr9:108537549..108539905,2	K562	blood:
17	chr9:108410737..108412265-chr9:108498939..108500477,2	K562	blood:
18	chr9:108474643..108476985-chr9:108479080..108480662,2	MCF-7	breast:
19	chr9:108530827..108532419-chr9:108534650..108537088,2	K562	blood:
20	chr9:108459267..108461864-chr9:108470911..108472758,2	K562	blood:
21	chr9:108371365..108371976-chr9:108480471..108481581,4	MCF-7	breast:
22	chr9:108207677..108209988-chr9:108545420..108547936,2	K562	blood:
23	chr9:108455042..108457950-chr9:108472079..108474194,2	K562	blood:
24	chr9:108474643..108476985-chr9:108479080..108480662,2	MCF-7	breast:
25	chr9:108456785..108458481-chr9:108485454..108487475,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAL2-2	chr9:108474971-108475041	NONHSAT133824
2	lnc-TAL2-2	chr9:108504611-108504764	NONHSAT133826
3	lnc-TAL2-2	chr9:108474971-108475041	ucscGeneNc_uc004bcy_1
4	lnc-TAL2-2	chr9:108468659-108469824	NONHSAT133824
5	lnc-TAL2-3	chr9:108520651-108523036	NONHSAT133827
6	lnc-TAL2-4	chr9:108530807-108535529	NONHSAT133828
7	lnc-TAL2-2	chr9:108499910-108500246	NONHSAT133826
8	lnc-TAL2-2	chr9:108474971-108475041	NONHSAT133826
9	lnc-TAL2-2	chr9:108468659-108469824	ucscGeneNc_uc004bcy_1
10	lnc-TAL2-2	chr9:108481660-108481900	ucscGeneNc_uc004bcy_1
11	lnc-TAL2-3	chr9:108520445-108520492	NONHSAT133827
12	lnc-TAL2-2	chr9:108481660-108481900	NONHSAT133824

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TMEM38B	hsa-miR-98-5p	chr9:108536391-108536413

Variant related genes	Relation type
TMEM38B	TF binding region
ENSG00000232486	TF binding region
ENSG00000228366	TF binding region
ENSG00000228366	chromatin interactions
ENSG00000095209	chromatin interactions

Extended variants
information (count: 3215 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3215 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3817141	chr9:108468129-108468130	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560624490	chr9:108468155-108468156	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs565068755	chr9:108468170-108468171	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs199874260	chr9:108468180-108468181	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370270920	chr9:108468184-108468185	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs75220376	chr9:108468197-108468198	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs184339791	chr9:108468230-108468231	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7030040	chr9:108468269-108468270	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs570726930	chr9:108468271-108468272	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs139487717	chr9:108468296-108468297	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs550480157	chr9:108468300-108468301	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190809628	chr9:108468325-108468326	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs116949535	chr9:108468328-108468329	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568797248	chr9:108468329-108468330	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536051682	chr9:108468338-108468339	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs145289337	chr9:108468353-108468354	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182044022	chr9:108468378-108468379	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs572610801	chr9:108468432-108468433	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs147646173	chr9:108468486-108468487	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs558641489	chr9:108468515-108468516	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs576732838	chr9:108468636-108468637	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs543842324	chr9:108468639-108468640	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs562423275	chr9:108468648-108468649	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs574441493	chr9:108468654-108468655	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs79309572	chr9:108468745-108468746	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs112986889	chr9:108468754-108468755	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs3126471	chr9:108468784-108468785	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs115974277	chr9:108468785-108468786	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs564638042	chr9:108468828-108468829	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs114698987	chr9:108468844-108468845	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs550244624	chr9:108468869-108468870	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs10118720	chr9:108468886-108468887	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs536116994	chr9:108468889-108468890	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs78812828	chr9:108468902-108468903	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs184651803	chr9:108468915-108468916	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs540041831	chr9:108468945-108468946	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs371771815	chr9:108468956-108468957	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs566379176	chr9:108468966-108468967	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs558357142	chr9:108468969-108468970	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs570243671	chr9:108468973-108468974	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs377177833	chr9:108468983-108468984	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs537446368	chr9:108468994-108468995	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs555697334	chr9:108469007-108469008	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs116393355	chr9:108469008-108469009	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs541689829	chr9:108469060-108469061	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs374800335	chr9:108469069-108469070	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs539414420	chr9:108469073-108469074	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs369170833	chr9:108469094-108469095	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs116759407	chr9:108469122-108469123	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs572131874	chr9:108469133-108469134	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Chordoma	18071362	CNVD
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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	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
Leukemia	18688285	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
Acute promyelocytic leukemia	19109227	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:880 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108457800-108472800	Weak transcription	Spleen	Spleen
2	chr9:108457800-108476200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:108457800-108492200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr9:108458000-108468400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr9:108458000-108472400	Weak transcription	HSMM	muscle
6	chr9:108458000-108473000	Weak transcription	Left Ventricle	heart
7	chr9:108458000-108475200	Weak transcription	Fetal Thymus	thymus
8	chr9:108458000-108475600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr9:108458000-108475600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr9:108458000-108475600	Weak transcription	Thymus	Thymus
11	chr9:108458000-108476000	Weak transcription	Ovary	ovary
12	chr9:108458000-108479200	Weak transcription	Fetal Brain Male	brain
13	chr9:108458000-108497800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr9:108458200-108468400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr9:108458200-108468600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr9:108458200-108470600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr9:108458200-108476400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr9:108458200-108478800	Weak transcription	Brain Hippocampus Middle	brain
19	chr9:108458200-108480800	Weak transcription	Brain Angular Gyrus	brain
20	chr9:108458200-108491400	Weak transcription	HSMMtube	muscle
21	chr9:108458200-108491600	Weak transcription	Brain Anterior Caudate	brain
22	chr9:108458200-108495400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr9:108458200-108497000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr9:108458400-108470200	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr9:108458400-108470400	Weak transcription	Liver	Liver
26	chr9:108458600-108472600	Weak transcription	Duodenum Mucosa	Duodenum
27	chr9:108458800-108470600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr9:108459000-108468200	Weak transcription	Fetal Muscle Leg	muscle
29	chr9:108459000-108476000	Weak transcription	Fetal Brain Female	brain
30	chr9:108459200-108468600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr9:108459200-108472400	Weak transcription	Dnd41	blood
32	chr9:108459200-108489400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr9:108459600-108470200	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr9:108462600-108472600	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr9:108463200-108478400	Weak transcription	Hela-S3	cervix
36	chr9:108463200-108496800	Weak transcription	HepG2	liver
37	chr9:108463400-108487600	Weak transcription	Primary B cells from cord blood	blood
38	chr9:108463800-108470600	Weak transcription	Primary hematopoietic stem cells	blood
39	chr9:108463800-108472400	Weak transcription	K562	blood
40	chr9:108464000-108468400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr9:108464000-108468400	Weak transcription	Small Intestine	intestine
42	chr9:108464000-108474800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr9:108464200-108468400	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr9:108464200-108474800	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr9:108464400-108468600	Weak transcription	Fetal Intestine Large	intestine
46	chr9:108464400-108471800	Weak transcription	Psoas Muscle	Psoas
47	chr9:108464400-108476000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr9:108464800-108468400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr9:108465000-108496600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr9:108465200-108470600	Weak transcription	Primary monocytes fromperipheralblood	blood

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