Variant report

Variant	nsv898767
Chromosome Location	chr12:10553930-10622047
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:636)
CpG islands
(count:611)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10562084-10562332	K562	blood:	n/a	n/a
2	ARID3A	chr12:10592356-10592503	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:10563882-10564383	HepG2	liver:	n/a	n/a
4	ATF1	chr12:10562095-10562363	K562	blood:	n/a	n/a
5	BATF	chr12:10583308-10583579	GM12878	blood:	n/a	chr12:10583461-10583472
6	BATF	chr12:10598779-10599011	GM12878	blood:	n/a	chr12:10598893-10598904
7	BCL11A	chr12:10583293-10583483	GM12878	blood:	n/a	n/a
8	BCL11A	chr12:10598783-10598965	GM12878	blood:	n/a	n/a
9	BCL3	chr12:10592167-10592607	A549	lung:	n/a	n/a
10	BHLHE40	chr12:10562058-10562261	K562	blood:	n/a	n/a
11	BHLHE40	chr12:10559427-10559772	K562	blood:	n/a	n/a
12	BHLHE40	chr12:10559410-10559764	GM12878	blood:	n/a	n/a
13	BRCA1	chr12:10574950-10575149	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr12:10562044-10562186	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr12:10608263-10608767	HCT-116	colon:	n/a	n/a
16	CEBPB	chr12:10592194-10592559	A549	lung:	n/a	n/a
17	CEBPB	chr12:10574940-10575149	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:10573229-10573321	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:10605885-10606198	A549	lung:	n/a	chr12:10606038-10606049
20	CEBPB	chr12:10585773-10585908	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:10563736-10564412	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:10557191-10557468	K562	blood:	n/a	n/a
23	CEBPB	chr12:10605864-10606214	HepG2	liver:	n/a	chr12:10606038-10606049
24	CEBPB	chr12:10605854-10606222	Hela-S3	cervix:	n/a	chr12:10606038-10606049
25	CEBPB	chr12:10563800-10564310	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr12:10590205-10590581	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr12:10590386-10590401	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:10592348-10592508	HepG2	liver:	n/a	n/a
29	CEBPB	chr12:10563725-10564405	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr12:10574947-10575139	K562	blood:	n/a	n/a
31	CEBPB	chr12:10600201-10600212	A549	lung:	n/a	n/a
32	CEBPB	chr12:10588520-10588745	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:10605878-10606169	IMR90	lung:	n/a	chr12:10606038-10606049
34	CEBPB	chr12:10574805-10575159	K562	blood:	n/a	n/a
35	CEBPB	chr12:10590272-10590510	K562	blood:	n/a	n/a
36	CEBPB	chr12:10592190-10592807	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:10577271-10577431	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr12:10574938-10575152	A549	lung:	n/a	n/a
39	CEBPB	chr12:10574839-10575068	K562	blood:	n/a	n/a
40	CEBPB	chr12:10574775-10575160	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr12:10562055-10562317	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr12:10562076-10562277	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr12:10590372-10590413	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr12:10574937-10575144	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr12:10563840-10563990	SAEC	small airway:	n/a	n/a
46	CTCF	chr12:10569981-10570054	GM13976	blood:	n/a	n/a
47	CTCF	chr12:10593047-10593172	Fibrobl	skin:	n/a	n/a
48	CTCF	chr12:10577713-10577786	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr12:10563840-10563990	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr12:10563860-10564010	GM12866	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10570179-10570229	HUVEC	blood vessel:	n/a
2	chr12:10570179-10570229	HUVEC	blood vessel:	n/a
3	chr12:10570179-10570229	H1-hESC	embryonic stem cell:	embryo
4	chr12:10583355-10583405	HL-60	blood:	n/a
5	chr12:10586130-10586180	BJ	skin:	n/a
6	chr12:10599740-10599790	U87	brain:	n/a
7	chr12:10605936-10605986	AG09309	skin:	n/a
8	chr12:10605936-10605986	GM19239	blood:	n/a
9	chr12:10588483-10588533	K562	blood:	n/a
10	chr12:10608067-10608117	K562	blood:	n/a
11	chr12:10607364-10607414	Caco-2	colon:	n/a
12	chr12:10599740-10599790	SK-N-SH_RA	brain:	n/a
13	chr12:10560602-10560652	NHDF-neo	bronchial:	n/a
14	chr12:10588483-10588533	HCM	heart:	n/a
15	chr12:10607364-10607414	HEEpiC	esophagus:	n/a
16	chr12:10607364-10607414	SK-N-SH	brain:	n/a
17	chr12:10608067-10608117	HIPEpiC	eye:	n/a
18	chr12:10605936-10605986	MCF10A-Er-Src	breast:	n/a
19	chr12:10570179-10570229	NT2-D1	testis:	n/a
20	chr12:10570179-10570229	PANC-1	pancreas:	n/a
21	chr12:10607364-10607414	GM19239	blood:	n/a
22	chr12:10560602-10560652	MCF10A-Er-Src	breast:	n/a
23	chr12:10586130-10586180	PrEC	prostate:	n/a
24	chr12:10608067-10608117	HMEC	breast:	n/a
25	chr12:10599740-10599790	HRE	kidney:	n/a
26	chr12:10560602-10560652	AG04450	lung:	fetal
27	chr12:10608067-10608117	HL-60	blood:	n/a
28	chr12:10583355-10583405	HepG2	liver:	n/a
29	chr12:10608067-10608117	HCPEpiC	choroid plexus:	n/a
30	chr12:10607364-10607414	BE2_C	brain:	n/a
31	chr12:10608067-10608117	HRPEpiC	eye:	n/a
32	chr12:10583355-10583405	NT2-D1	testis:	n/a
33	chr12:10586130-10586180	SK-N-SH_RA	brain:	n/a
34	chr12:10570179-10570229	NHDF-neo	bronchial:	n/a
35	chr12:10608067-10608117	RPTEC	kidney:	n/a
36	chr12:10607364-10607414	Hepatocyte	liver:	n/a
37	chr12:10599740-10599790	PrEC	prostate:	n/a
38	chr12:10605936-10605986	PANC-1	pancreas:	n/a
39	chr12:10608067-10608117	AG04449	skin:	fetal
40	chr12:10586130-10586180	H1-hESC	embryonic stem cell:	embryo
41	chr12:10607538-10607588	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:10570179-10570229	K562	blood:	n/a
43	chr12:10607538-10607588	HCPEpiC	choroid plexus:	n/a
44	chr12:10608067-10608117	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:10599740-10599790	CMK	blood:	n/a
46	chr12:10560602-10560652	LNCaP	prostate:	n/a
47	chr12:10560602-10560652	CMK	blood:	n/a
48	chr12:10607364-10607414	ovcar-3	ovarian:	n/a
49	chr12:10607364-10607414	Hela-S3	cervix:	n/a
50	chr12:10560602-10560652	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
2	chr12:10561211..10561774-chr17:76182659..76183234,2	Hela-S3	cervix:
3	chr1:28974955..28975586-chr12:10563608..10564342,2	Hela-S3	cervix:
4	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
5	chr12:10554334..10554872-chr16:81477760..81478703,2	Hela-S3	cervix:
6	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
7	chr12:10559960..10560793-chrX:131351678..131352452,2	Hela-S3	cervix:
8	chr12:10563346..10565218-chr12:11316267..11318781,2	K562	blood:
9	chr12:10604438..10606172-chr12:10606795..10608691,2	K562	blood:
10	chr12:10604438..10606172-chr12:10606795..10608691,2	K562	blood:
11	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2S3L.1-6	chr12:10601202-10602083	l_610_chr12:10597245-10602083_whiteBloodCell
2	lnc-EIF2S3L.1-6	chr12:10597246-10597382	l_610_chr12:10597245-10602083_whiteBloodCell

No data

Variant related genes	Relation type
KLRC2	TF binding region
KLRC3	TF binding region
KLRC4	TF binding region
KLRC1	TF binding region
KLRC4-KLRK1	TF binding region
ENSG00000255641	TF binding region
KLRC2	CpG island
KLRC3	CpG island
KLRC4	CpG island
KLRC1	CpG island
KLRC4-KLRK1	CpG island
ENSG00000255641	CpG island
ENSG00000245648	chromatin interactions
ENSG00000134545	chromatin interactions
ENSG00000123728	chromatin interactions
ENSG00000255641	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000205810	chromatin interactions
ENSG00000205809	chromatin interactions
ENSG00000167900	chromatin interactions

Extended variants
information (count: 2845 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2845 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2617165	chr12:10553930-10553931	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs75199620	chr12:10553965-10553966	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs74648437	chr12:10553983-10553984	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs75366872	chr12:10554030-10554031	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs561452755	chr12:10554063-10554064	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs7955196	chr12:10554074-10554075	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs544741051	chr12:10554077-10554078	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs77756011	chr12:10554091-10554092	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs543601927	chr12:10554093-10554094	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs551648835	chr12:10554101-10554102	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs376721808	chr12:10554186-10554187	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs565128811	chr12:10554265-10554266	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs572009406	chr12:10554292-10554293	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs540828845	chr12:10554402-10554403	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs560432062	chr12:10554447-10554448	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs529660271	chr12:10554487-10554488	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs57563883	chr12:10554511-10554512	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs35612288	chr12:10554534-10554535	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs532674856	chr12:10554557-10554558	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs562904064	chr12:10554585-10554586	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs531715334	chr12:10554619-10554620	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs74914637	chr12:10554620-10554621	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs12816829	chr12:10554632-10554633	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs12821887	chr12:10554679-10554680	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs547574019	chr12:10554703-10554704	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs59368977	chr12:10554714-10554715	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs567124400	chr12:10554739-10554740	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs35968979	chr12:10554784-10554785	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs145658066	chr12:10554820-10554821	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs59903818	chr12:10554840-10554841	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs75997663	chr12:10554867-10554868	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs558224280	chr12:10554869-10554870	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs572107852	chr12:10554881-10554882	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs568556659	chr12:10554912-10554913	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs540766010	chr12:10554954-10554955	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs560777692	chr12:10554963-10554964	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs574268221	chr12:10554973-10554974	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs2734561	chr12:10554985-10554986	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs73256293	chr12:10555027-10555028	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs532011021	chr12:10555049-10555050	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545394909	chr12:10555105-10555106	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2617166	chr12:10555179-10555180	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140392750	chr12:10555197-10555198	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527835327	chr12:10555225-10555226	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs547568665	chr12:10555242-10555243	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs546271611	chr12:10555257-10555258	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs146487711	chr12:10555311-10555312	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs566268193	chr12:10555317-10555318	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs79034876	chr12:10555350-10555351	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs140967823	chr12:10555366-10555367	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10547800-10559400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:10548600-10557400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr12:10548600-10564000	Weak transcription	Brain Angular Gyrus	brain
4	chr12:10549200-10559400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr12:10550600-10555200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr12:10550600-10559000	Weak transcription	Primary T cells from cord blood	blood
7	chr12:10550600-10562000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr12:10550800-10564000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:10552000-10556600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr12:10552200-10554000	Enhancers	Hela-S3	cervix
11	chr12:10553600-10554400	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr12:10553800-10554000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
13	chr12:10553800-10554800	Active TSS	Primary T killer memory cells from peripheral blood	blood
14	chr12:10554000-10554800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr12:10554000-10557600	Weak transcription	Hela-S3	cervix
16	chr12:10554400-10557400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr12:10554800-10555000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
18	chr12:10554800-10557200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr12:10555000-10555200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr12:10555200-10555400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
21	chr12:10555400-10556800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr12:10556600-10557400	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
23	chr12:10556800-10557000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
24	chr12:10557000-10557200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
25	chr12:10557200-10557800	Transcr. at gene 5' and 3'	Primary T killer naive cells fromperipheralblood	blood
26	chr12:10557200-10560000	Active TSS	Primary T killer memory cells from peripheral blood	blood
27	chr12:10557400-10557800	Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr12:10557400-10558200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr12:10557400-10558200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr12:10557600-10558400	Strong transcription	Hela-S3	cervix
31	chr12:10557800-10559000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr12:10557800-10559400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
33	chr12:10558000-10558200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr12:10558000-10558600	Enhancers	NHEK	skin
35	chr12:10558200-10559000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr12:10558200-10562200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr12:10558200-10562200	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
38	chr12:10558400-10559400	Weak transcription	Hela-S3	cervix
39	chr12:10558600-10559000	Weak transcription	NHEK	skin
40	chr12:10558800-10559600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr12:10558800-10560000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr12:10558800-10562400	Active TSS	Primary T cells fromperipheralblood	blood
43	chr12:10559000-10559200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
44	chr12:10559000-10559200	Enhancers	Adipose Nuclei	Adipose
45	chr12:10559000-10559400	Active TSS	Primary T cells from cord blood	blood
46	chr12:10559000-10559600	Enhancers	Primary hematopoietic stem cells	blood
47	chr12:10559000-10559800	Enhancers	Primary B cells from cord blood	blood
48	chr12:10559000-10559800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr12:10559000-10559800	Enhancers	NHEK	skin
50	chr12:10559000-10560000	Enhancers	Primary monocytes fromperipheralblood	blood

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