Variant report

Variant	esv6546
Chromosome Location	chr12:11172416-11228413
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:300)
CpG islands
(count:672)
Chromatin interactive
region (count:1)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:300 , 50 per page) page: 1 2 3 4 5 6

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	chr12:11176072-11176303	HepG2	liver:	n/a	n/a
3	BATF	chr12:11186631-11186911	GM12878	blood:	n/a	n/a
4	BATF	chr12:11225254-11225547	GM12878	blood:	n/a	n/a
5	BATF	chr12:11228218-11228560	GM12878	blood:	n/a	n/a
6	BATF	chr12:11216721-11217010	GM12878	blood:	n/a	n/a
7	BATF	chr12:11186566-11186883	GM12878	blood:	n/a	n/a
8	BCL11A	chr12:11228248-11228517	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:11186584-11186913	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:11228293-11228667	GM12878	blood:	n/a	n/a
11	CEBPB	chr12:11223987-11224332	HepG2	liver:	n/a	n/a
12	CEBPB	chr12:11222658-11222813	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:11226186-11226481	HepG2	liver:	n/a	n/a
14	CTCF	chr12:11178806-11179001	K562	blood:	n/a	n/a
15	CTCF	chr12:11178800-11178950	NHEK	skin:	n/a	n/a
16	CTCF	chr12:11178880-11179030	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr12:11178860-11179010	GM12871	blood:	n/a	n/a
18	CTCF	chr12:11178863-11178966	NHEK	skin:	n/a	n/a
19	CTCF	chr12:11178700-11178990	HPF	lung:	n/a	n/a
20	CTCF	chr12:11178800-11178950	SAEC	small airway:	n/a	n/a
21	CTCF	chr12:11178780-11178930	RPTEC	kidney:	n/a	n/a
22	CTCF	chr12:11178880-11179030	A549	lung:	n/a	n/a
23	CTCF	chr12:11209880-11210030	GM12872	blood:	n/a	n/a
24	CTCF	chr12:11178872-11178912	GM12891	blood:	n/a	n/a
25	CTCF	chr12:11178820-11178970	NB4	blood:	n/a	n/a
26	CTCF	chr12:11178820-11178970	MCF-7	breast:	n/a	n/a
27	CTCF	chr12:11176040-11176190	BE2_C	brain:	n/a	n/a
28	CTCF	chr12:11178791-11179030	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:11178880-11179030	HEK293	kidney:	n/a	n/a
30	CTCF	chr12:11178770-11179057	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:11178840-11178990	GM12872	blood:	n/a	n/a
32	CTCF	chr12:11178746-11178994	HepG2	liver:	n/a	n/a
33	CTCF	chr12:11178782-11179023	MCF-7	breast:	n/a	n/a
34	CTCF	chr12:11206452-11206523	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr12:11207523-11207552	GM10248	blood:	n/a	n/a
36	CTCF	chr12:11178760-11178910	GM12869	blood:	n/a	n/a
37	CTCF	chr12:11178880-11179030	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr12:11178820-11178970	GM12866	blood:	n/a	n/a
39	CTCF	chr12:11178820-11178970	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr12:11178800-11178950	HMF	breast:	n/a	n/a
41	CTCF	chr12:11178840-11178990	GM12865	blood:	n/a	n/a
42	CTCF	chr12:11178840-11178990	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr12:11178869-11178995	LNCaP	prostate:	n/a	n/a
44	CTCF	chr12:11183077-11183136	GM10248	blood:	n/a	n/a
45	CTCF	chr12:11178779-11179099	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr12:11178920-11179070	GM12868	blood:	n/a	n/a
47	CTCF	chr12:11178807-11179031	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr12:11178840-11178990	Caco-2	colon:	n/a	n/a
49	CTCF	chr12:11178720-11178870	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr12:11178840-11178990	HEK293	kidney:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11215083-11215133	ECC-1	luminal epithelium:	n/a
2	chr12:11215083-11215133	ECC-1	luminal epithelium:	n/a
3	chr12:11184149-11184199	AoSMC	blood vessel:	n/a
4	chr12:11215083-11215133	PFSK-1	brain:	n/a
5	chr12:11184037-11184087	HRCEpiC	kidney:	n/a
6	chr12:11184037-11184087	HCT-116	colon:	n/a
7	chr12:11184347-11184397	U87	brain:	n/a
8	chr12:11184415-11184465	SKMC	muscle:	n/a
9	chr12:11184005-11184055	AG09319	gingival:	n/a
10	chr12:11176574-11176624	HMEC	breast:	n/a
11	chr12:11184149-11184199	HCT-116	colon:	n/a
12	chr12:11174898-11174948	SKMC	muscle:	n/a
13	chr12:11174898-11174948	HRE	kidney:	n/a
14	chr12:11174898-11174948	PrEC	prostate:	n/a
15	chr12:11184415-11184465	NHBE	bronchial:	n/a
16	chr12:11185058-11185108	ECC-1	luminal epithelium:	n/a
17	chr12:11184415-11184465	ProgFib	skin:	n/a
18	chr12:11185058-11185108	Jurkat	blood:	n/a
19	chr12:11174898-11174948	BJ	skin:	n/a
20	chr12:11184415-11184465	NH-A	brain:	n/a
21	chr12:11184347-11184397	HEEpiC	esophagus:	n/a
22	chr12:11184149-11184199	SKMC	muscle:	n/a
23	chr12:11176574-11176624	AG09309	skin:	n/a
24	chr12:11184347-11184397	MCF10A-Er-Src	breast:	n/a
25	chr12:11176574-11176624	PrEC	prostate:	n/a
26	chr12:11174898-11174948	SK-N-SH	brain:	n/a
27	chr12:11184149-11184199	HL-60	blood:	n/a
28	chr12:11174898-11174948	HNPCEpiC	eye:	n/a
29	chr12:11176386-11176436	Hela-S3	cervix:	n/a
30	chr12:11216351-11216401	NH-A	brain:	n/a
31	chr12:11184347-11184397	SK-N-MC	brain:	n/a
32	chr12:11176386-11176436	AG09319	gingival:	n/a
33	chr12:11176386-11176436	HRCEpiC	kidney:	n/a
34	chr12:11174898-11174948	HIPEpiC	eye:	n/a
35	chr12:11215083-11215133	GM12892	blood:	n/a
36	chr12:11184415-11184465	AoSMC	blood vessel:	n/a
37	chr12:11174898-11174948	GM19239	blood:	n/a
38	chr12:11184347-11184397	SAEC	small airway:	n/a
39	chr12:11184415-11184465	AG10803	skin:	n/a
40	chr12:11216351-11216401	HCM	heart:	n/a
41	chr12:11184037-11184087	HMEC	breast:	n/a
42	chr12:11174898-11174948	IMR90	lung:	fetal
43	chr12:11184037-11184087	PANC-1	pancreas:	n/a
44	chr12:11184005-11184055	NHDF-neo	bronchial:	n/a
45	chr12:11184415-11184465	SK-N-SH	brain:	n/a
46	chr12:11176386-11176436	HepG2	liver:	n/a
47	chr12:11185058-11185108	Hela-S3	cervix:	n/a
48	chr12:11176574-11176624	GM12878	blood:	n/a
49	chr12:11184415-11184465	IMR90	lung:	fetal
50	chr12:11184415-11184465	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11210669..11211248-chr5:109800405..109801099,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
TAS2R46	TF binding region
TAS2R19	TF binding region
TAS2R31	TF binding region
ENSG00000268301	TF binding region
PRR4	TF binding region
TAS2R63P	TF binding region
TAS2R46	CpG island
TAS2R19	CpG island
TAS2R31	CpG island
ENSG00000268301	CpG island
PRR4	CpG island
TAS2R63P	CpG island

Extended variants
information (count: 3307 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3307 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs66539429	chr12:11172437-11172438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1868768	chr12:11172439-11172440	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs72475476	chr12:11172444-11172445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs66479728	chr12:11172479-11172480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562433266	chr12:11172480-11172481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531241174	chr12:11172489-11172490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550946939	chr12:11172494-11172495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs3863330	chr12:11172502-11172503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79838297	chr12:11172506-11172507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs76925949	chr12:11172508-11172509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs72475477	chr12:11172544-11172545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547148309	chr12:11172591-11172592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566646110	chr12:11172622-11172623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535522711	chr12:11172624-11172625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73047151	chr12:11172629-11172630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs75766932	chr12:11172632-11172633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187011506	chr12:11172651-11172652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79946923	chr12:11172668-11172669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs114717411	chr12:11172673-11172674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201339529	chr12:11172674-11172675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200134770	chr12:11172677-11172678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144306455	chr12:11172700-11172701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs367754399	chr12:11172709-11172710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371859002	chr12:11172710-11172711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375853110	chr12:11172712-11172713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368925723	chr12:11172736-11172737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557805703	chr12:11172737-11172738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs201311898	chr12:11172764-11172765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201927465	chr12:11172772-11172773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375583271	chr12:11172779-11172780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199923030	chr12:11172783-11172784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200859219	chr12:11172786-11172787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79907914	chr12:11172796-11172797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375707470	chr12:11172836-11172837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375209290	chr12:11172839-11172840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs386760336	chr12:11172841-11172842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs67622503	chr12:11172842-11172843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368668561	chr12:11172843-11172844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139303523	chr12:11172872-11172873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78993399	chr12:11172877-11172878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76052458	chr12:11172899-11172900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112134780	chr12:11172906-11172907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560364015	chr12:11172907-11172908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200241499	chr12:11172910-11172911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373186212	chr12:11172926-11172927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376925609	chr12:11172936-11172937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371359008	chr12:11172947-11172948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374072303	chr12:11172950-11172951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573798460	chr12:11172951-11172952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377660685	chr12:11172960-11172961	Weak transcription	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:823 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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	chr12:11154200-11174200	Weak transcription	Primary B cells from cord blood	blood
14	chr12:11154200-11178000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:11154200-11178200	Weak transcription	A549	lung
16	chr12:11154200-11178800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr12:11159400-11182000	Weak transcription	NHEK	skin
18	chr12:11159600-11178200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr12:11161400-11178200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:11161400-11179200	Weak transcription	Fetal Kidney	kidney
21	chr12:11162400-11172800	Weak transcription	Fetal Brain Female	brain
22	chr12:11163400-11177600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr12:11163400-11178000	Weak transcription	GM12878-XiMat	blood
24	chr12:11163600-11178800	Weak transcription	Ovary	ovary
25	chr12:11163800-11178000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr12:11164400-11178600	Weak transcription	Fetal Thymus	thymus
27	chr12:11165000-11180800	Weak transcription	HSMM	muscle
28	chr12:11165400-11180200	Weak transcription	Esophagus	oesophagus
29	chr12:11165600-11174200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr12:11166000-11192000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr12:11166200-11210000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr12:11166600-11199600	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr12:11167000-11178200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr12:11167400-11201800	Weak transcription	Stomach Smooth Muscle	stomach
35	chr12:11167600-11178000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr12:11167600-11180000	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr12:11167800-11178600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr12:11168000-11177600	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr12:11168800-11201000	Weak transcription	Colon Smooth Muscle	Colon
40	chr12:11168800-11205800	Weak transcription	Osteobl	bone
41	chr12:11169000-11177000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:11169000-11178200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr12:11169000-11180200	Weak transcription	Adipose Nuclei	Adipose
44	chr12:11169200-11174200	Weak transcription	Right Atrium	heart
45	chr12:11169200-11178000	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr12:11169200-11178200	Weak transcription	Liver	Liver
47	chr12:11169400-11174200	Weak transcription	Primary T cells from cord blood	blood
48	chr12:11169400-11176200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr12:11169400-11178000	Weak transcription	Fetal Muscle Leg	muscle
50	chr12:11169400-11180200	Weak transcription	Gastric	stomach

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