Variant report

Variant	nsv1038709
Chromosome Location	chr12:11165117-11283834
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:496)
CpG islands
(count:796)
Chromatin interactive
region (count:11)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:11224069-11224255	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:11168444-11168649	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:11176072-11176303	HepG2	liver:	n/a	n/a
4	ATF2	chr12:11237956-11238445	GM12878	blood:	n/a	n/a
5	ATF2	chr12:11238009-11238486	GM12878	blood:	n/a	n/a
6	BATF	chr12:11186631-11186911	GM12878	blood:	n/a	n/a
7	BATF	chr12:11238012-11238373	GM12878	blood:	n/a	n/a
8	BATF	chr12:11263799-11264109	GM12878	blood:	n/a	n/a
9	BATF	chr12:11228218-11228560	GM12878	blood:	n/a	n/a
10	BATF	chr12:11238084-11238352	GM12878	blood:	n/a	n/a
11	BATF	chr12:11216721-11217010	GM12878	blood:	n/a	n/a
12	BATF	chr12:11263857-11264113	GM12878	blood:	n/a	n/a
13	BATF	chr12:11225254-11225547	GM12878	blood:	n/a	n/a
14	BATF	chr12:11247547-11247827	GM12878	blood:	n/a	n/a
15	BATF	chr12:11247482-11247799	GM12878	blood:	n/a	n/a
16	BATF	chr12:11186566-11186883	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:11247500-11247829	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:11186584-11186913	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:11228248-11228517	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:11238061-11238356	GM12878	blood:	n/a	chr12:11238263-11238272
21	BCL11A	chr12:11263900-11264159	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:11228293-11228667	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:11168360-11168714	HepG2	liver:	n/a	n/a
24	BRCA1	chr12:11168480-11168660	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:11170024-11170162	HepG2	liver:	n/a	chr12:11170139-11170150
26	CEBPB	chr12:11226186-11226481	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:11167458-11167736	HepG2	liver:	n/a	chr12:11167582-11167593
28	CEBPB	chr12:11222658-11222813	HepG2	liver:	n/a	n/a
29	CEBPB	chr12:11260954-11260970	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:11223987-11224332	HepG2	liver:	n/a	n/a
31	CHD2	chr12:11238132-11238304	GM12878	blood:	n/a	n/a
32	CTCF	chr12:11178840-11178990	HepG2	liver:	n/a	n/a
33	CTCF	chr12:11281056-11281182	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr12:11178862-11178967	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr12:11178860-11179010	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr12:11265530-11265560	GM13976	blood:	n/a	n/a
37	CTCF	chr12:11178872-11178912	GM12891	blood:	n/a	n/a
38	CTCF	chr12:11187719-11187757	GM13976	blood:	n/a	n/a
39	CTCF	chr12:11248748-11248798	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr12:11178902-11178949	HepG2	liver:	n/a	n/a
41	CTCF	chr12:11281909-11281930	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr12:11209740-11209890	HepG2	liver:	n/a	n/a
43	CTCF	chr12:11178800-11178950	AG09309	skin:	n/a	n/a
44	CTCF	chr12:11169080-11169230	RPTEC	kidney:	n/a	n/a
45	CTCF	chr12:11178800-11178950	AG04450	lung:	n/a	n/a
46	CTCF	chr12:11178920-11179070	GM12868	blood:	n/a	n/a
47	CTCF	chr12:11178800-11178950	HFF	foreskin:	n/a	n/a
48	CTCF	chr12:11209820-11209970	HEK293	kidney:	n/a	n/a
49	CTCF	chr12:11178880-11179030	BJ	skin:	n/a	n/a
50	CTCF	chr12:11178780-11178930	RPTEC	kidney:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11244899-11244949	HMEC	breast:	n/a
2	chr12:11216351-11216401	PFSK-1	brain:	n/a
3	chr12:11185058-11185108	GM12878	blood:	n/a
4	chr12:11244899-11244949	HMEC	breast:	n/a
5	chr12:11216351-11216401	PFSK-1	brain:	n/a
6	chr12:11185058-11185108	GM12878	blood:	n/a
7	chr12:11176574-11176624	Caco-2	colon:	n/a
8	chr12:11244899-11244949	HCT-116	colon:	n/a
9	chr12:11185058-11185108	CMK	blood:	n/a
10	chr12:11174898-11174948	HUVEC	blood vessel:	n/a
11	chr12:11184005-11184055	MCF-7	breast:	n/a
12	chr12:11184005-11184055	SK-N-MC	brain:	n/a
13	chr12:11184037-11184087	BJ	skin:	n/a
14	chr12:11215083-11215133	ProgFib	skin:	n/a
15	chr12:11176574-11176624	AG10803	skin:	n/a
16	chr12:11184347-11184397	AG04449	skin:	fetal
17	chr12:11174898-11174948	ECC-1	luminal epithelium:	n/a
18	chr12:11176386-11176436	HCPEpiC	choroid plexus:	n/a
19	chr12:11215083-11215133	SK-N-MC	brain:	n/a
20	chr12:11176386-11176436	GM19239	blood:	n/a
21	chr12:11216351-11216401	PrEC	prostate:	n/a
22	chr12:11184347-11184397	HCF	heart:	n/a
23	chr12:11184005-11184055	HL-60	blood:	n/a
24	chr12:11174898-11174948	A549	lung:	n/a
25	chr12:11184037-11184087	AG10803	skin:	n/a
26	chr12:11216351-11216401	NH-A	brain:	n/a
27	chr12:11184037-11184087	Caco-2	colon:	n/a
28	chr12:11184037-11184087	Jurkat	blood:	n/a
29	chr12:11184149-11184199	LNCaP	prostate:	n/a
30	chr12:11184347-11184397	U87	brain:	n/a
31	chr12:11174898-11174948	NB4	blood:	n/a
32	chr12:11244899-11244949	NB4	blood:	n/a
33	chr12:11244899-11244949	SK-N-SH_RA	brain:	n/a
34	chr12:11216351-11216401	HCPEpiC	choroid plexus:	n/a
35	chr12:11184415-11184465	NB4	blood:	n/a
36	chr12:11184037-11184087	GM12878	blood:	n/a
37	chr12:11184037-11184087	NT2-D1	testis:	n/a
38	chr12:11184415-11184465	H1-hESC	embryonic stem cell:	embryo
39	chr12:11185058-11185108	MCF10A-Er-Src	breast:	n/a
40	chr12:11184149-11184199	HMEC	breast:	n/a
41	chr12:11176386-11176436	Hela-S3	cervix:	n/a
42	chr12:11215083-11215133	HNPCEpiC	eye:	n/a
43	chr12:11184347-11184397	HUVEC	blood vessel:	n/a
44	chr12:11184347-11184397	BE2_C	brain:	n/a
45	chr12:11184149-11184199	H1-hESC	embryonic stem cell:	embryo
46	chr12:11184149-11184199	NT2-D1	testis:	n/a
47	chr12:11184347-11184397	HL-60	blood:	n/a
48	chr12:11184347-11184397	HEEpiC	esophagus:	n/a
49	chr12:11184415-11184465	HAEpiC	amniotic membrane:	n/a
50	chr12:11244899-11244949	ovcar-3	ovarian:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
2	chr12:11271454..11274346-chr12:11279643..11282306,2	MCF-7	breast:
3	chr12:11169301..11171201-chr12:11322573..11325255,2	MCF-7	breast:
4	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
5	chr12:11157746..11159406-chr12:11165545..11167423,2	K562	blood:
6	chr12:11009323..11011109-chr12:11168207..11170860,2	K562	blood:
7	chr12:11158423..11160257-chr12:11164352..11165951,2	MCF-7	breast:
8	chr12:11253040..11255708-chr12:11259363..11262255,2	K562	blood:
9	chr12:11271454..11274346-chr12:11279643..11282306,2	MCF-7	breast:
10	chr12:11253040..11255708-chr12:11259363..11262255,2	K562	blood:
11	chr12:11210669..11211248-chr5:109800405..109801099,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRH1-1	chr12:11199619-11199640	NONHSAT026908
2	lnc-PRH1-1	chr12:11273435-11273779	NONHSAT026920
3	lnc-TAS2R43-1	chr12:11229915-11230841	NONHSAT140056
4	lnc-PRH1-1	chr12:11199619-11199787	NR_037918
5	lnc-PRH1-1	chr12:11199619-11199787	NONHSAT026907
6	lnc-PRH1-1	chr12:11199619-11199736	NONHSAT026915
7	lnc-PRH1-1	chr12:11187381-11187484	NR_037918
8	lnc-PRH1-1	chr12:11199619-11199787	NONHSAT026912
9	lnc-PRH1-1	chr12:11199612-11199787	NONHSAT026916
10	lnc-TAS2R43-1	chr12:11229368-11231770	NONHSAT026918
11	lnc-PRH1-1	chr12:11187381-11187484	NONHSAT026912
12	lnc-PRH1-1	chr12:11199619-11199713	NONHSAT026914
13	lnc-TAS2R46-1	chr12:11200931-11201855	NONHSAT026917
14	lnc-PRH1-1	chr12:11273609-11273779	NONHSAT026916

No data

Variant related genes	Relation type
TAS2R46	TF binding region
TAS2R19	TF binding region
TAS2R31	TF binding region
ENSG00000256400	TF binding region
ENSG00000268301	TF binding region
PRR4	TF binding region
TAS2R63P	TF binding region
TAS2R43	TF binding region
TAS2R64P	TF binding region
TAS2R46	CpG island
TAS2R19	CpG island
TAS2R31	CpG island
ENSG00000256400	CpG island
ENSG00000268301	CpG island
PRR4	CpG island
TAS2R63P	CpG island
TAS2R43	CpG island
TAS2R64P	CpG island
ENSG00000256712	chromatin interactions
ENSG00000256537	chromatin interactions
ENSG00000111215	chromatin interactions
ENSG00000212127	chromatin interactions

Extended variants
information (count: 6544 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:6544 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4763611	chr12:11165117-11165118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144428914	chr12:11165131-11165132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548200082	chr12:11165146-11165147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575241960	chr12:11165150-11165151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189885131	chr12:11165202-11165203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1376249	chr12:11165233-11165234	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs4763612	chr12:11165300-11165301	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs545986428	chr12:11165301-11165302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559845006	chr12:11165375-11165376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1376250	chr12:11165394-11165395	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs542236623	chr12:11165427-11165428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561907128	chr12:11165435-11165436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539667290	chr12:11165436-11165437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182104635	chr12:11165438-11165439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4763613	chr12:11165446-11165447	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs563940513	chr12:11165470-11165471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186592201	chr12:11165478-11165479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7306087	chr12:11165540-11165541	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs546465128	chr12:11165587-11165588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4553441	chr12:11165643-11165644	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs145399674	chr12:11165771-11165772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1868760	chr12:11165826-11165827	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs192258352	chr12:11165855-11165856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs367969912	chr12:11165867-11165868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1868761	chr12:11165933-11165934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs7974464	chr12:11165976-11165977	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs1868762	chr12:11165984-11165985	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs149222911	chr12:11166002-11166003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553268865	chr12:11166007-11166008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573309549	chr12:11166169-11166170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541922303	chr12:11166181-11166182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555350074	chr12:11166184-11166185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200319064	chr12:11166198-11166199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534827291	chr12:11166236-11166237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117620570	chr12:11166389-11166390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564077879	chr12:11166419-11166420	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533038974	chr12:11166431-11166432	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1349390	chr12:11166463-11166464	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs183551224	chr12:11166471-11166472	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs58796988	chr12:11166491-11166492	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11054164	chr12:11166536-11166537	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs529001470	chr12:11166538-11166539	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1901189	chr12:11166574-11166575	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs1901190	chr12:11166578-11166579	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs201419568	chr12:11166581-11166582	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531382410	chr12:11166589-11166590	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79136508	chr12:11166591-11166592	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566487892	chr12:11166706-11166707	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201624325	chr12:11166716-11166717	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11054165	chr12:11166735-11166736	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Acute myeloid leukemia	17237825	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11114400-11180200	Weak transcription	Primary B cells from peripheral blood	blood
2	chr12:11122000-11170200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr12:11122200-11168000	Weak transcription	HUVEC	blood vessel
4	chr12:11129200-11167600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr12:11134800-11166800	Weak transcription	NHDF-Ad	bronchial
6	chr12:11136400-11180200	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr12:11136600-11180200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr12:11136600-11196400	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr12:11137400-11203000	Weak transcription	Hela-S3	cervix
10	chr12:11143400-11167600	Weak transcription	Fetal Intestine Small	intestine
11	chr12:11143400-11178800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr12:11145400-11177600	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr12:11146200-11167400	Weak transcription	Fetal Intestine Large	intestine
14	chr12:11147000-11165200	Weak transcription	Esophagus	oesophagus
15	chr12:11147000-11166400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr12:11147000-11168400	Weak transcription	Liver	Liver
17	chr12:11147000-11178600	Weak transcription	Fetal Stomach	stomach
18	chr12:11147000-11185400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr12:11147200-11168600	Weak transcription	Spleen	Spleen
20	chr12:11147200-11169200	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr12:11147200-11171200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr12:11147200-11176200	Weak transcription	Aorta	Aorta
23	chr12:11147200-11180400	Weak transcription	Pancreas	Pancrea
24	chr12:11148400-11178200	Weak transcription	Dnd41	blood
25	chr12:11149000-11168600	Weak transcription	Left Ventricle	heart
26	chr12:11154000-11169000	Weak transcription	Primary T cells from cord blood	blood
27	chr12:11154200-11167400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr12:11154200-11168000	Weak transcription	Fetal Muscle Leg	muscle
29	chr12:11154200-11174200	Weak transcription	Primary B cells from cord blood	blood
30	chr12:11154200-11178000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr12:11154200-11178200	Weak transcription	A549	lung
32	chr12:11154200-11178800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr12:11154400-11168000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr12:11159400-11168600	Weak transcription	Gastric	stomach
35	chr12:11159400-11182000	Weak transcription	NHEK	skin
36	chr12:11159600-11178200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr12:11160800-11165800	Weak transcription	NH-A	brain
38	chr12:11161400-11178200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:11161400-11179200	Weak transcription	Fetal Kidney	kidney
40	chr12:11162400-11172800	Weak transcription	Fetal Brain Female	brain
41	chr12:11162600-11167800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:11163400-11177600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr12:11163400-11178000	Weak transcription	GM12878-XiMat	blood
44	chr12:11163600-11178800	Weak transcription	Ovary	ovary
45	chr12:11163800-11178000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr12:11164000-11165200	Weak transcription	Brain Substantia Nigra	brain
47	chr12:11164400-11178600	Weak transcription	Fetal Thymus	thymus
48	chr12:11164600-11168200	Weak transcription	Stomach Mucosa	stomach
49	chr12:11164800-11171800	Weak transcription	Lung	lung
50	chr12:11165000-11170000	Weak transcription	Fetal Muscle Trunk	muscle

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