Variant report

Variant	esv1805234
Chromosome Location	chr12:10571907-10596286
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:375)
CpG islands
(count:184)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10592356-10592503	HepG2	liver:	n/a	n/a
2	BATF	chr12:10583308-10583579	GM12878	blood:	n/a	chr12:10583461-10583472
3	BCL11A	chr12:10583293-10583483	GM12878	blood:	n/a	n/a
4	BCL3	chr12:10592167-10592607	A549	lung:	n/a	n/a
5	BRCA1	chr12:10574950-10575149	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr12:10590272-10590510	K562	blood:	n/a	n/a
7	CEBPB	chr12:10574938-10575152	A549	lung:	n/a	n/a
8	CEBPB	chr12:10590386-10590401	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:10574947-10575139	K562	blood:	n/a	n/a
10	CEBPB	chr12:10585773-10585908	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr12:10574839-10575068	K562	blood:	n/a	n/a
12	CEBPB	chr12:10592194-10592559	A549	lung:	n/a	n/a
13	CEBPB	chr12:10574775-10575160	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr12:10592348-10592508	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:10574805-10575159	K562	blood:	n/a	n/a
16	CEBPB	chr12:10577271-10577431	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:10588520-10588745	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:10592190-10592807	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:10573229-10573321	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:10574940-10575149	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:10590205-10590581	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr12:10574937-10575144	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr12:10590372-10590413	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr12:10577678-10577792	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr12:10577654-10577777	A549	lung:	n/a	n/a
26	CTCF	chr12:10577713-10577786	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr12:10593084-10593189	Gliobla	brain:	n/a	n/a
28	CTCF	chr12:10577736-10577759	LNCaP	prostate:	n/a	n/a
29	CTCF	chr12:10591453-10591491	A549	lung:	n/a	n/a
30	CTCF	chr12:10593932-10594014	A549	lung:	n/a	n/a
31	CTCF	chr12:10577638-10577785	Fibrobl	skin:	n/a	n/a
32	CTCF	chr12:10593138-10593151	NHEK	skin:	n/a	n/a
33	CTCF	chr12:10593047-10593172	Fibrobl	skin:	n/a	n/a
34	CTCF	chr12:10592724-10592809	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr12:10577683-10577798	HepG2	liver:	n/a	n/a
36	CTCF	chr12:10593080-10593174	MCF-7	breast:	n/a	n/a
37	CTCF	chr12:10577725-10577792	GM19240	blood:	n/a	n/a
38	CTCF	chr12:10577689-10577783	GM19238	blood:	n/a	n/a
39	CTCF	chr12:10582110-10582224	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:10572135-10572203	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr12:10582121-10582214	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:10593082-10593151	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:10593058-10593183	A549	lung:	n/a	n/a
44	CTCF	chr12:10593072-10593203	GM19239	blood:	n/a	n/a
45	CTCF	chr12:10577729-10577796	LNCaP	prostate:	n/a	n/a
46	CTCF	chr12:10593095-10593127	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:10593076-10593192	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr12:10582123-10582221	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:10577339-10577398	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr12:10577670-10577781	GM19239	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10583355-10583405	MCF-7	breast:	n/a
2	chr12:10583355-10583405	MCF-7	breast:	n/a
3	chr12:10586130-10586180	LNCaP	prostate:	n/a
4	chr12:10586130-10586180	A549	lung:	n/a
5	chr12:10586130-10586180	SAEC	small airway:	n/a
6	chr12:10588483-10588533	HRE	kidney:	n/a
7	chr12:10586130-10586180	HL-60	blood:	n/a
8	chr12:10583355-10583405	HAEpiC	amniotic membrane:	n/a
9	chr12:10588483-10588533	NT2-D1	testis:	n/a
10	chr12:10588483-10588533	SAEC	small airway:	n/a
11	chr12:10586130-10586180	AoSMC	blood vessel:	n/a
12	chr12:10588483-10588533	HEEpiC	esophagus:	n/a
13	chr12:10586130-10586180	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:10588483-10588533	ECC-1	luminal epithelium:	n/a
15	chr12:10583355-10583405	HUVEC	blood vessel:	n/a
16	chr12:10583355-10583405	U87	brain:	n/a
17	chr12:10583355-10583405	Jurkat	blood:	n/a
18	chr12:10586130-10586180	ovcar-3	ovarian:	n/a
19	chr12:10586130-10586180	HCT-116	colon:	n/a
20	chr12:10588483-10588533	HCT-116	colon:	n/a
21	chr12:10583355-10583405	HEK293	kidney:	embryo
22	chr12:10588483-10588533	SK-N-SH_RA	brain:	n/a
23	chr12:10586130-10586180	SK-N-SH	brain:	n/a
24	chr12:10583355-10583405	PrEC	prostate:	n/a
25	chr12:10586130-10586180	Jurkat	blood:	n/a
26	chr12:10583355-10583405	HepG2	liver:	n/a
27	chr12:10586130-10586180	HAEpiC	amniotic membrane:	n/a
28	chr12:10586130-10586180	HEEpiC	esophagus:	n/a
29	chr12:10583355-10583405	HRE	kidney:	n/a
30	chr12:10588483-10588533	IMR90	lung:	fetal
31	chr12:10583355-10583405	HCPEpiC	choroid plexus:	n/a
32	chr12:10583355-10583405	PFSK-1	brain:	n/a
33	chr12:10583355-10583405	T-47D	breast:	n/a
34	chr12:10586130-10586180	NB4	blood:	n/a
35	chr12:10586130-10586180	AG10803	skin:	n/a
36	chr12:10583355-10583405	SAEC	small airway:	n/a
37	chr12:10586130-10586180	U87	brain:	n/a
38	chr12:10586130-10586180	PFSK-1	brain:	n/a
39	chr12:10588483-10588533	HCM	heart:	n/a
40	chr12:10583355-10583405	NT2-D1	testis:	n/a
41	chr12:10588483-10588533	PFSK-1	brain:	n/a
42	chr12:10586130-10586180	SK-N-SH_RA	brain:	n/a
43	chr12:10583355-10583405	NB4	blood:	n/a
44	chr12:10583355-10583405	Hela-S3	cervix:	n/a
45	chr12:10583355-10583405	GM06990	blood:	n/a
46	chr12:10586130-10586180	MCF10A-Er-Src	breast:	n/a
47	chr12:10583355-10583405	HRPEpiC	eye:	n/a
48	chr12:10583355-10583405	SK-N-SH_RA	brain:	n/a
49	chr12:10583355-10583405	AG09319	gingival:	n/a
50	chr12:10586130-10586180	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
2	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:

No data

Variant related genes	Relation type
KLRC3	TF binding region
ENSG00000255641	TF binding region
KLRC2	TF binding region
KLRC3	CpG island
ENSG00000255641	CpG island
KLRC2	CpG island
ENSG00000205810	chromatin interactions
ENSG00000255641	chromatin interactions
ENSG00000205809	chromatin interactions

Extended variants
information (count: 999 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:999 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553163047	chr12:10571923-10571924	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs201650760	chr12:10571927-10571928	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370455334	chr12:10571928-10571929	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566795987	chr12:10571952-10571953	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372389161	chr12:10571956-10571957	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555367100	chr12:10572003-10572004	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74060400	chr12:10572095-10572096	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs543779648	chr12:10572098-10572099	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557437135	chr12:10572190-10572191	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs577281298	chr12:10572221-10572222	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs546028953	chr12:10572250-10572251	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs556172558	chr12:10572433-10572434	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs201234318	chr12:10572443-10572444	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs528811637	chr12:10572466-10572467	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs200300248	chr12:10572497-10572498	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs562370907	chr12:10572506-10572507	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs368697230	chr12:10572535-10572536	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs143188402	chr12:10572544-10572545	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs530948587	chr12:10572580-10572581	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs550946066	chr12:10572606-10572607	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs570967280	chr12:10572621-10572622	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs2682492	chr12:10572687-10572688	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs192024260	chr12:10572732-10572733	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs546817910	chr12:10572749-10572750	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs566525691	chr12:10572750-10572751	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs184093784	chr12:10572769-10572770	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs72475442	chr12:10572777-10572778	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs188533289	chr12:10572782-10572783	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs537460324	chr12:10572804-10572805	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs570118795	chr12:10572822-10572823	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs2253365	chr12:10572839-10572840	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs577364168	chr12:10572876-10572877	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs191444104	chr12:10572903-10572904	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs184286957	chr12:10572921-10572922	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs374017336	chr12:10572937-10572938	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs190402940	chr12:10572939-10572940	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs367596202	chr12:10572948-10572949	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs182280345	chr12:10572951-10572952	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs201837367	chr12:10572957-10572958	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs142093820	chr12:10572974-10572975	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs376033608	chr12:10572975-10572976	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs2741881	chr12:10572982-10572983	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs186837131	chr12:10572986-10572987	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs533491021	chr12:10572999-10573000	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs555408556	chr12:10573005-10573006	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs546761115	chr12:10573027-10573028	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs560598198	chr12:10573044-10573045	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs139064875	chr12:10573048-10573049	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs368635736	chr12:10573054-10573055	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs2682491	chr12:10573094-10573095	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance

Variant related diseases (count:86)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10562200-10572800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr12:10570600-10572600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr12:10571400-10572600	Weak transcription	Hela-S3	cervix
4	chr12:10571600-10573800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
5	chr12:10572600-10573000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
6	chr12:10572600-10573200	Active TSS	Hela-S3	cervix
7	chr12:10572600-10573600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:10572800-10573000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr12:10572800-10573600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr12:10572800-10573600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr12:10572800-10573600	Enhancers	Muscle Satellite Cultured Cells	--
12	chr12:10572800-10573600	Enhancers	A549	lung
13	chr12:10572800-10573600	Enhancers	Osteobl	bone
14	chr12:10572800-10573800	Enhancers	HUVEC	blood vessel
15	chr12:10573200-10573600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr12:10573200-10573600	Enhancers	Hela-S3	cervix
17	chr12:10573600-10575200	Weak transcription	Hela-S3	cervix
18	chr12:10573600-10578200	Weak transcription	A549	lung
19	chr12:10573800-10585600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:10575200-10575800	Enhancers	Hela-S3	cervix
21	chr12:10575800-10584400	Weak transcription	Hela-S3	cervix
22	chr12:10578000-10578800	Active TSS	Brain Hippocampus Middle	brain
23	chr12:10578000-10579000	Active TSS	Brain Anterior Caudate	brain
24	chr12:10578000-10579000	Active TSS	Brain Cingulate Gyrus	brain
25	chr12:10578000-10579000	Active TSS	Brain Inferior Temporal Lobe	brain
26	chr12:10578000-10579000	Active TSS	Brain Substantia Nigra	brain
27	chr12:10578200-10578400	Enhancers	A549	lung
28	chr12:10578200-10578800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr12:10578200-10579000	Active TSS	Brain Angular Gyrus	brain
30	chr12:10582600-10584200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr12:10584200-10588000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr12:10584400-10584600	Strong transcription	Hela-S3	cervix
33	chr12:10584600-10585400	Weak transcription	Hela-S3	cervix
34	chr12:10585400-10585600	Genic enhancers	Hela-S3	cervix
35	chr12:10585600-10585800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:10585600-10586200	Transcr. at gene 5' and 3'	Hela-S3	cervix
37	chr12:10585800-10589000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
38	chr12:10586200-10587000	Active TSS	Hela-S3	cervix
39	chr12:10587000-10588000	Weak transcription	Hela-S3	cervix
40	chr12:10588000-10588400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr12:10588000-10588600	Active TSS	Fetal Thymus	thymus
42	chr12:10588000-10588800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr12:10588000-10588800	Active TSS	Brain Anterior Caudate	brain
44	chr12:10588000-10588800	Active TSS	Hela-S3	cervix
45	chr12:10588200-10588800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr12:10588200-10588800	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr12:10588200-10589000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr12:10588200-10589000	Enhancers	A549	lung
49	chr12:10588200-10589000	Enhancers	HUVEC	blood vessel
50	chr12:10588400-10588800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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