Variant report

Variant	nsv557469
Chromosome Location	chr12:10573580-10598784
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:360)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:360 , 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	BATF	chr12:10598779-10599011	GM12878	blood:	n/a	chr12:10598893-10598904
4	BCL11A	chr12:10583293-10583483	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:10598783-10598965	GM12878	blood:	n/a	n/a
6	BCL3	chr12:10592167-10592607	A549	lung:	n/a	n/a
7	BRCA1	chr12:10574950-10575149	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr12:10574775-10575160	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:10585773-10585908	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:10588520-10588745	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr12:10590205-10590581	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:10574839-10575068	K562	blood:	n/a	n/a
13	CEBPB	chr12:10574938-10575152	A549	lung:	n/a	n/a
14	CEBPB	chr12:10577271-10577431	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr12:10590386-10590401	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:10574805-10575159	K562	blood:	n/a	n/a
17	CEBPB	chr12:10590272-10590510	K562	blood:	n/a	n/a
18	CEBPB	chr12:10574940-10575149	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:10592190-10592807	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:10592348-10592508	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:10574947-10575139	K562	blood:	n/a	n/a
22	CEBPB	chr12:10592194-10592559	A549	lung:	n/a	n/a
23	CHD2	chr12:10574937-10575144	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr12:10590372-10590413	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr12:10577681-10577775	NHEK	skin:	n/a	n/a
26	CTCF	chr12:10593084-10593189	Gliobla	brain:	n/a	n/a
27	CTCF	chr12:10577654-10577777	A549	lung:	n/a	n/a
28	CTCF	chr12:10582123-10582221	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:10593080-10593174	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:10593072-10593203	GM19239	blood:	n/a	n/a
31	CTCF	chr12:10577339-10577398	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr12:10577664-10577750	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:10597587-10597650	Fibrobl	skin:	n/a	n/a
34	CTCF	chr12:10577702-10577734	LNCaP	prostate:	n/a	n/a
35	CTCF	chr12:10583540-10583606	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr12:10577689-10577783	GM19238	blood:	n/a	n/a
37	CTCF	chr12:10593058-10593183	A549	lung:	n/a	n/a
38	CTCF	chr12:10592724-10592809	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr12:10593047-10593172	Fibrobl	skin:	n/a	n/a
40	CTCF	chr12:10577713-10577786	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr12:10577725-10577792	GM19240	blood:	n/a	n/a
42	CTCF	chr12:10593095-10593127	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:10582117-10582206	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:10577638-10577785	Fibrobl	skin:	n/a	n/a
45	CTCF	chr12:10593932-10594014	A549	lung:	n/a	n/a
46	CTCF	chr12:10593138-10593151	NHEK	skin:	n/a	n/a
47	CTCF	chr12:10577678-10577792	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr12:10574917-10574984	GM19239	blood:	n/a	n/a
49	CTCF	chr12:10593076-10593192	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr12:10577670-10577781	GM19239	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10583355-10583405	NHDF-neo	bronchial:	n/a
2	chr12:10586130-10586180	NB4	blood:	n/a
3	chr12:10588483-10588533	GM12891	blood:	n/a
4	chr12:10588483-10588533	HCT-116	colon:	n/a
5	chr12:10586130-10586180	HIPEpiC	eye:	n/a
6	chr12:10586130-10586180	HRCEpiC	kidney:	n/a
7	chr12:10583355-10583405	NHBE	bronchial:	n/a
8	chr12:10586130-10586180	ovcar-3	ovarian:	n/a
9	chr12:10583355-10583405	GM12891	blood:	n/a
10	chr12:10583355-10583405	HMEC	breast:	n/a
11	chr12:10583355-10583405	AG04450	lung:	fetal
12	chr12:10583355-10583405	Hepatocyte	liver:	n/a
13	chr12:10583355-10583405	LNCaP	prostate:	n/a
14	chr12:10586130-10586180	BE2_C	brain:	n/a
15	chr12:10586130-10586180	NH-A	brain:	n/a
16	chr12:10583355-10583405	SKMC	muscle:	n/a
17	chr12:10586130-10586180	PrEC	prostate:	n/a
18	chr12:10583355-10583405	AG04449	skin:	fetal
19	chr12:10588483-10588533	A549	lung:	n/a
20	chr12:10586130-10586180	AG09319	gingival:	n/a
21	chr12:10588483-10588533	AG10803	skin:	n/a
22	chr12:10588483-10588533	AoSMC	blood vessel:	n/a
23	chr12:10588483-10588533	AG09319	gingival:	n/a
24	chr12:10588483-10588533	AG04450	lung:	fetal
25	chr12:10583355-10583405	PFSK-1	brain:	n/a
26	chr12:10586130-10586180	HUVEC	blood vessel:	n/a
27	chr12:10586130-10586180	ECC-1	luminal epithelium:	n/a
28	chr12:10588483-10588533	IMR90	lung:	fetal
29	chr12:10586130-10586180	HCM	heart:	n/a
30	chr12:10588483-10588533	HCF	heart:	n/a
31	chr12:10588483-10588533	H1-hESC	embryonic stem cell:	embryo
32	chr12:10586130-10586180	Hepatocyte	liver:	n/a
33	chr12:10588483-10588533	NB4	blood:	n/a
34	chr12:10586130-10586180	GM12892	blood:	n/a
35	chr12:10588483-10588533	Caco-2	colon:	n/a
36	chr12:10588483-10588533	K562	blood:	n/a
37	chr12:10586130-10586180	GM19239	blood:	n/a
38	chr12:10583355-10583405	HCF	heart:	n/a
39	chr12:10583355-10583405	BE2_C	brain:	n/a
40	chr12:10586130-10586180	HRE	kidney:	n/a
41	chr12:10583355-10583405	ovcar-3	ovarian:	n/a
42	chr12:10588483-10588533	HMEC	breast:	n/a
43	chr12:10586130-10586180	LNCaP	prostate:	n/a
44	chr12:10583355-10583405	MCF10A-Er-Src	breast:	n/a
45	chr12:10588483-10588533	NH-A	brain:	n/a
46	chr12:10588483-10588533	SK-N-MC	brain:	n/a
47	chr12:10588483-10588533	SK-N-SH	brain:	n/a
48	chr12:10586130-10586180	HL-60	blood:	n/a
49	chr12:10588483-10588533	HEEpiC	esophagus:	n/a
50	chr12:10583355-10583405	GM12878	blood:	n/a

(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:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2S3L.1-6	chr12:10597246-10597382	l_610_chr12:10597245-10602083_whiteBloodCell

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
ENSG00000255641	chromatin interactions
ENSG00000205809	chromatin interactions
ENSG00000205810	chromatin interactions

Extended variants
information (count: 1048 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1048 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17548969	chr12:10573580-10573581	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs578080293	chr12:10573607-10573608	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs34733928	chr12:10573619-10573620	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs560393441	chr12:10573626-10573627	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs529600735	chr12:10573646-10573647	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs34171381	chr12:10573656-10573657	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs529382549	chr12:10573684-10573685	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs35125944	chr12:10573695-10573696	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs34986157	chr12:10573701-10573702	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs531535123	chr12:10573716-10573717	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs551279069	chr12:10573766-10573767	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs571181924	chr12:10573768-10573769	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs533555021	chr12:10573777-10573778	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547328849	chr12:10573778-10573779	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs567289282	chr12:10573780-10573781	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs201129621	chr12:10573794-10573795	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs17513944	chr12:10573796-10573797	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs200564723	chr12:10573797-10573798	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs61919130	chr12:10573802-10573803	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs536343452	chr12:10573886-10573887	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs28651942	chr12:10573895-10573896	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs556022411	chr12:10573933-10573934	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575888794	chr12:10573957-10573958	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs4763199	chr12:10573963-10573964	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs17513937	chr12:10574001-10574002	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs61919131	chr12:10574022-10574023	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs558508464	chr12:10574115-10574116	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs578240215	chr12:10574161-10574162	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs55988715	chr12:10574165-10574166	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560538432	chr12:10574245-10574246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574078415	chr12:10574266-10574267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61919132	chr12:10574336-10574337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543092011	chr12:10574438-10574439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562609015	chr12:10574525-10574526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61919133	chr12:10574533-10574534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544756091	chr12:10574540-10574541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564843643	chr12:10574563-10574564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375578495	chr12:10574580-10574581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547124863	chr12:10574642-10574643	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs567229277	chr12:10574656-10574657	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs61919134	chr12:10574684-10574685	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs3759267	chr12:10574759-10574760	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs529783273	chr12:10574899-10574900	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs549916493	chr12:10574942-10574943	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs373714669	chr12:10574963-10574964	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs569737478	chr12:10574983-10574984	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs538452756	chr12:10574988-10574989	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs558376329	chr12:10574989-10574990	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs571895491	chr12:10575111-10575112	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs112715177	chr12:10575128-10575129	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

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:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10571600-10573800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
2	chr12:10572600-10573600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:10572800-10573600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr12:10572800-10573600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr12:10572800-10573600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr12:10572800-10573600	Enhancers	A549	lung
7	chr12:10572800-10573600	Enhancers	Osteobl	bone
8	chr12:10572800-10573800	Enhancers	HUVEC	blood vessel
9	chr12:10573200-10573600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr12:10573200-10573600	Enhancers	Hela-S3	cervix
11	chr12:10573600-10575200	Weak transcription	Hela-S3	cervix
12	chr12:10573600-10578200	Weak transcription	A549	lung
13	chr12:10573800-10585600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr12:10575200-10575800	Enhancers	Hela-S3	cervix
15	chr12:10575800-10584400	Weak transcription	Hela-S3	cervix
16	chr12:10578000-10578800	Active TSS	Brain Hippocampus Middle	brain
17	chr12:10578000-10579000	Active TSS	Brain Anterior Caudate	brain
18	chr12:10578000-10579000	Active TSS	Brain Cingulate Gyrus	brain
19	chr12:10578000-10579000	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr12:10578000-10579000	Active TSS	Brain Substantia Nigra	brain
21	chr12:10578200-10578400	Enhancers	A549	lung
22	chr12:10578200-10578800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
23	chr12:10578200-10579000	Active TSS	Brain Angular Gyrus	brain
24	chr12:10582600-10584200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr12:10584200-10588000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr12:10584400-10584600	Strong transcription	Hela-S3	cervix
27	chr12:10584600-10585400	Weak transcription	Hela-S3	cervix
28	chr12:10585400-10585600	Genic enhancers	Hela-S3	cervix
29	chr12:10585600-10585800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
30	chr12:10585600-10586200	Transcr. at gene 5' and 3'	Hela-S3	cervix
31	chr12:10585800-10589000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
32	chr12:10586200-10587000	Active TSS	Hela-S3	cervix
33	chr12:10587000-10588000	Weak transcription	Hela-S3	cervix
34	chr12:10588000-10588400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr12:10588000-10588600	Active TSS	Fetal Thymus	thymus
36	chr12:10588000-10588800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr12:10588000-10588800	Active TSS	Brain Anterior Caudate	brain
38	chr12:10588000-10588800	Active TSS	Hela-S3	cervix
39	chr12:10588200-10588800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr12:10588200-10588800	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr12:10588200-10589000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr12:10588200-10589000	Enhancers	A549	lung
43	chr12:10588200-10589000	Enhancers	HUVEC	blood vessel
44	chr12:10588400-10588800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:10588800-10589400	Enhancers	Hela-S3	cervix
46	chr12:10588800-10592600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr12:10589000-10590600	Weak transcription	A549	lung
48	chr12:10589000-10591200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr12:10589400-10593800	Weak transcription	Hela-S3	cervix
50	chr12:10590600-10591200	Enhancers	A549	lung

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