Variant report

Variant	esv3489126
Chromosome Location	chr12:11175760-11202498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:186)
CpG islands
(count:488)
Chromatin interactive
region (count:0)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:186 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:11176072-11176303	HepG2	liver:	n/a	n/a
2	BATF	chr12:11186566-11186883	GM12878	blood:	n/a	n/a
3	BATF	chr12:11186631-11186911	GM12878	blood:	n/a	n/a
4	BCL11A	chr12:11186584-11186913	GM12878	blood:	n/a	n/a
5	CTCF	chr12:11178800-11178950	GM12868	blood:	n/a	n/a
6	CTCF	chr12:11178820-11178970	HCT-116	colon:	n/a	n/a
7	CTCF	chr12:11178840-11178990	AG09319	gingival:	n/a	n/a
8	CTCF	chr12:11178779-11179099	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr12:11178840-11178990	GM12865	blood:	n/a	n/a
10	CTCF	chr12:11176040-11176190	BE2_C	brain:	n/a	n/a
11	CTCF	chr12:11178820-11178970	HFF-Myc	foreskin:	n/a	n/a
12	CTCF	chr12:11178820-11178970	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr12:11178780-11178930	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr12:11178800-11178950	HMF	breast:	n/a	n/a
15	CTCF	chr12:11178800-11178950	HFF	foreskin:	n/a	n/a
16	CTCF	chr12:11178746-11178994	HepG2	liver:	n/a	n/a
17	CTCF	chr12:11178840-11178990	BE2_C	brain:	n/a	n/a
18	CTCF	chr12:11178760-11178910	GM12869	blood:	n/a	n/a
19	CTCF	chr12:11178792-11179039	MCF-7	breast:	n/a	n/a
20	CTCF	chr12:11178792-11179011	MCF-7	breast:	n/a	n/a
21	CTCF	chr12:11178820-11179007	K562	blood:	n/a	n/a
22	CTCF	chr12:11178780-11178930	GM12878	blood:	n/a	n/a
23	CTCF	chr12:11178840-11178990	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr12:11187719-11187757	GM13976	blood:	n/a	n/a
25	CTCF	chr12:11178700-11178850	GM12870	blood:	n/a	n/a
26	CTCF	chr12:11178860-11179010	GM12872	blood:	n/a	n/a
27	CTCF	chr12:11178800-11178950	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr12:11183077-11183136	GM10248	blood:	n/a	n/a
29	CTCF	chr12:11178820-11178970	AG09309	skin:	n/a	n/a
30	CTCF	chr12:11178840-11178990	HMF	breast:	n/a	n/a
31	CTCF	chr12:11178840-11178990	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr12:11178820-11178970	HepG2	liver:	n/a	n/a
33	CTCF	chr12:11178902-11178949	HepG2	liver:	n/a	n/a
34	CTCF	chr12:11178860-11179010	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr12:11178869-11178995	LNCaP	prostate:	n/a	n/a
36	CTCF	chr12:11178800-11178950	SAEC	small airway:	n/a	n/a
37	CTCF	chr12:11176080-11176230	HepG2	liver:	n/a	n/a
38	CTCF	chr12:11178700-11178850	HCM	heart:	n/a	n/a
39	CTCF	chr12:11178819-11178997	A549	lung:	n/a	n/a
40	CTCF	chr12:11178782-11179023	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:11178860-11179010	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr12:11178720-11178870	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr12:11178800-11178950	HVMF	connective:	n/a	n/a
44	CTCF	chr12:11178900-11179050	BJ	skin:	n/a	n/a
45	CTCF	chr12:11178840-11178990	HepG2	liver:	n/a	n/a
46	CTCF	chr12:11178880-11179030	GM12864	blood:	n/a	n/a
47	CTCF	chr12:11178840-11178990	GM12872	blood:	n/a	n/a
48	CTCF	chr12:11178800-11178950	GM12874	blood:	n/a	n/a
49	CTCF	chr12:11178920-11179070	GM12868	blood:	n/a	n/a
50	CTCF	chr12:11178806-11179001	K562	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11184037-11184087	GM06990	blood:	n/a
2	chr12:11184005-11184055	GM12878	blood:	n/a
3	chr12:11184037-11184087	HAEpiC	amniotic membrane:	n/a
4	chr12:11184415-11184465	HRCEpiC	kidney:	n/a
5	chr12:11185058-11185108	AG09319	gingival:	n/a
6	chr12:11184005-11184055	SK-N-MC	brain:	n/a
7	chr12:11184005-11184055	HRPEpiC	eye:	n/a
8	chr12:11176574-11176624	PANC-1	pancreas:	n/a
9	chr12:11185058-11185108	H1-hESC	embryonic stem cell:	embryo
10	chr12:11184005-11184055	HPAEpiC	pulmonary alveolar:	n/a
11	chr12:11184005-11184055	BE2_C	brain:	n/a
12	chr12:11176574-11176624	HRCEpiC	kidney:	n/a
13	chr12:11185058-11185108	BJ	skin:	n/a
14	chr12:11184037-11184087	GM12892	blood:	n/a
15	chr12:11176386-11176436	T-47D	breast:	n/a
16	chr12:11185058-11185108	HRE	kidney:	n/a
17	chr12:11176574-11176624	BE2_C	brain:	n/a
18	chr12:11185058-11185108	NH-A	brain:	n/a
19	chr12:11184149-11184199	Jurkat	blood:	n/a
20	chr12:11184149-11184199	HRE	kidney:	n/a
21	chr12:11184347-11184397	HNPCEpiC	eye:	n/a
22	chr12:11185058-11185108	GM19239	blood:	n/a
23	chr12:11176386-11176436	NT2-D1	testis:	n/a
24	chr12:11184005-11184055	Jurkat	blood:	n/a
25	chr12:11184149-11184199	BJ	skin:	n/a
26	chr12:11184037-11184087	PFSK-1	brain:	n/a
27	chr12:11184005-11184055	PANC-1	pancreas:	n/a
28	chr12:11176386-11176436	HepG2	liver:	n/a
29	chr12:11184037-11184087	ovcar-3	ovarian:	n/a
30	chr12:11184037-11184087	AG09319	gingival:	n/a
31	chr12:11184347-11184397	ProgFib	skin:	n/a
32	chr12:11184037-11184087	BJ	skin:	n/a
33	chr12:11176386-11176436	CMK	blood:	n/a
34	chr12:11184149-11184199	NH-A	brain:	n/a
35	chr12:11184149-11184199	HCF	heart:	n/a
36	chr12:11184347-11184397	GM19239	blood:	n/a
37	chr12:11184005-11184055	U87	brain:	n/a
38	chr12:11184149-11184199	GM12878	blood:	n/a
39	chr12:11184347-11184397	HAEpiC	amniotic membrane:	n/a
40	chr12:11176386-11176436	Hepatocyte	liver:	n/a
41	chr12:11184005-11184055	AG10803	skin:	n/a
42	chr12:11185058-11185108	SAEC	small airway:	n/a
43	chr12:11184005-11184055	AoSMC	blood vessel:	n/a
44	chr12:11184149-11184199	Caco-2	colon:	n/a
45	chr12:11176386-11176436	BE2_C	brain:	n/a
46	chr12:11184347-11184397	GM06990	blood:	n/a
47	chr12:11184037-11184087	SAEC	small airway:	n/a
48	chr12:11184149-11184199	T-47D	breast:	n/a
49	chr12:11184149-11184199	GM12892	blood:	n/a
50	chr12:11185058-11185108	Jurkat	blood:	n/a

No data

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRH1-1	chr12:11199612-11199787	NONHSAT026916
2	lnc-PRH1-1	chr12:11199619-11199713	NONHSAT026914
3	lnc-TAS2R46-1	chr12:11200931-11201855	NONHSAT026917
4	lnc-PRH1-1	chr12:11199619-11199787	NR_037918
5	lnc-PRH1-1	chr12:11187381-11187484	NR_037918
6	lnc-PRH1-1	chr12:11199619-11199640	NONHSAT026908
7	lnc-PRH1-1	chr12:11187381-11187484	NONHSAT026912
8	lnc-PRH1-1	chr12:11199619-11199736	NONHSAT026915
9	lnc-PRH1-1	chr12:11199619-11199787	NONHSAT026912
10	lnc-PRH1-1	chr12:11199619-11199787	NONHSAT026907

No data

Variant related genes	Relation type
TAS2R19	TF binding region
TAS2R31	TF binding region
ENSG00000268301	TF binding region
PRR4	TF binding region
TAS2R63P	TF binding region
TAS2R19	CpG island
TAS2R31	CpG island
ENSG00000268301	CpG island
PRR4	CpG island
TAS2R63P	CpG island

Extended variants
information (count: 1428 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1428 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576651965	chr12:11175763-11175764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148679471	chr12:11175803-11175804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553106055	chr12:11175836-11175837	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs192338593	chr12:11175859-11175860	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs573446052	chr12:11175920-11175921	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs367768566	chr12:11175922-11175923	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs115693778	chr12:11175953-11175954	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs117814982	chr12:11175954-11175955	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs184501210	chr12:11175997-11175998	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs561362411	chr12:11176015-11176016	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs188816613	chr12:11176020-11176021	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs72475482	chr12:11176082-11176083	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs181342679	chr12:11176095-11176096	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs377019686	chr12:11176108-11176109	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs201972961	chr12:11176166-11176167	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs371989861	chr12:11176175-11176176	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs76538183	chr12:11176202-11176203	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs77244775	chr12:11176211-11176212	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs563627433	chr12:11176240-11176241	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs532276920	chr12:11176251-11176252	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs552366700	chr12:11176278-11176279	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs74663851	chr12:11176290-11176291	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs565498233	chr12:11176300-11176301	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs113511950	chr12:11176341-11176342	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs113914286	chr12:11176345-11176346	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs78505428	chr12:11176372-11176373	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs147579631	chr12:11176384-11176385	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs79525198	chr12:11176386-11176387	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs142086361	chr12:11176401-11176402	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs199730642	chr12:11176417-11176418	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs184605537	chr12:11176452-11176453	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537086593	chr12:11176470-11176471	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs118025805	chr12:11176506-11176507	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570350745	chr12:11176516-11176517	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538922322	chr12:11176662-11176663	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559108439	chr12:11176673-11176674	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572722156	chr12:11176681-11176682	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372131683	chr12:11176682-11176683	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201548128	chr12:11176711-11176712	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs199768156	chr12:11176712-11176713	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200707869	chr12:11176726-11176727	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201681281	chr12:11176739-11176740	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541626603	chr12:11176743-11176744	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12371085	chr12:11176761-11176762	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs574963439	chr12:11176795-11176796	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs67001148	chr12:11176802-11176803	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11054172	chr12:11176820-11176821	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs201614484	chr12:11176823-11176824	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372582209	chr12:11176829-11176830	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563501637	chr12:11176836-11176837	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:559 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11114400-11180200	Weak transcription	Primary B cells from peripheral blood	blood
2	chr12:11136400-11180200	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr12:11136600-11180200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr12:11136600-11196400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr12:11137400-11203000	Weak transcription	Hela-S3	cervix
6	chr12:11143400-11178800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr12:11145400-11177600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr12:11147000-11178600	Weak transcription	Fetal Stomach	stomach
9	chr12:11147000-11185400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:11147200-11176200	Weak transcription	Aorta	Aorta
11	chr12:11147200-11180400	Weak transcription	Pancreas	Pancrea
12	chr12:11148400-11178200	Weak transcription	Dnd41	blood
13	chr12:11154200-11178000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr12:11154200-11178200	Weak transcription	A549	lung
15	chr12:11154200-11178800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr12:11159400-11182000	Weak transcription	NHEK	skin
17	chr12:11159600-11178200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr12:11161400-11178200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr12:11161400-11179200	Weak transcription	Fetal Kidney	kidney
20	chr12:11163400-11177600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr12:11163400-11178000	Weak transcription	GM12878-XiMat	blood
22	chr12:11163600-11178800	Weak transcription	Ovary	ovary
23	chr12:11163800-11178000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr12:11164400-11178600	Weak transcription	Fetal Thymus	thymus
25	chr12:11165000-11180800	Weak transcription	HSMM	muscle
26	chr12:11165400-11180200	Weak transcription	Esophagus	oesophagus
27	chr12:11166000-11192000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr12:11166200-11210000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr12:11166600-11199600	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr12:11167000-11178200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr12:11167400-11201800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr12:11167600-11178000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr12:11167600-11180000	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr12:11167800-11178600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:11168000-11177600	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr12:11168800-11201000	Weak transcription	Colon Smooth Muscle	Colon
37	chr12:11168800-11205800	Weak transcription	Osteobl	bone
38	chr12:11169000-11177000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:11169000-11178200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr12:11169000-11180200	Weak transcription	Adipose Nuclei	Adipose
41	chr12:11169200-11178000	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr12:11169200-11178200	Weak transcription	Liver	Liver
43	chr12:11169400-11176200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr12:11169400-11178000	Weak transcription	Fetal Muscle Leg	muscle
45	chr12:11169400-11180200	Weak transcription	Gastric	stomach
46	chr12:11169400-11180800	Weak transcription	Right Ventricle	heart
47	chr12:11169400-11182000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr12:11169400-11182400	Weak transcription	Spleen	Spleen
49	chr12:11169400-11201600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr12:11169400-11219400	Weak transcription	HUVEC	blood vessel

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links