Variant report

Variant	nsv606
Chromosome Location	chr12:10552632-10612899
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:626)
CpG islands
(count:610)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:626 , 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	chr12:10592356-10592503	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:10563882-10564383	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:10562084-10562332	K562	blood:	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	chr12:10559410-10559764	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:10559427-10559772	K562	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	chr12:10592190-10592807	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:10574940-10575149	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:10577271-10577431	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:10590205-10590581	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:10573229-10573321	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:10574775-10575160	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:10600201-10600212	A549	lung:	n/a	n/a
23	CEBPB	chr12:10585773-10585908	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr12:10557191-10557468	K562	blood:	n/a	n/a
25	CEBPB	chr12:10574805-10575159	K562	blood:	n/a	n/a
26	CEBPB	chr12:10592348-10592508	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:10605854-10606222	Hela-S3	cervix:	n/a	chr12:10606038-10606049
28	CEBPB	chr12:10590386-10590401	HepG2	liver:	n/a	n/a
29	CEBPB	chr12:10590272-10590510	K562	blood:	n/a	n/a
30	CEBPB	chr12:10563800-10564310	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr12:10605864-10606214	HepG2	liver:	n/a	chr12:10606038-10606049
32	CEBPB	chr12:10588520-10588745	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:10563736-10564412	HepG2	liver:	n/a	n/a
34	CEBPB	chr12:10563725-10564405	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr12:10605885-10606198	A549	lung:	n/a	chr12:10606038-10606049
36	CEBPB	chr12:10574938-10575152	A549	lung:	n/a	n/a
37	CEBPB	chr12:10574947-10575139	K562	blood:	n/a	n/a
38	CEBPB	chr12:10592194-10592559	A549	lung:	n/a	n/a
39	CEBPB	chr12:10605878-10606169	IMR90	lung:	n/a	chr12:10606038-10606049
40	CEBPB	chr12:10562055-10562317	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr12:10574839-10575068	K562	blood:	n/a	n/a
42	CHD2	chr12:10574937-10575144	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr12:10562076-10562277	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr12:10590372-10590413	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr12:10582110-10582224	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:10563860-10564010	GM12872	blood:	n/a	n/a
47	CTCF	chr12:10563880-10564030	RPTEC	kidney:	n/a	n/a
48	CTCF	chr12:10563860-10564010	SAEC	small airway:	n/a	n/a
49	CTCF	chr12:10577702-10577734	LNCaP	prostate:	n/a	n/a
50	CTCF	chr12:10563840-10563990	GM12869	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10607538-10607588	NT2-D1	testis:	n/a
2	chr12:10608067-10608117	NT2-D1	testis:	n/a
3	chr12:10599740-10599790	CMK	blood:	n/a
4	chr12:10560602-10560652	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:10560602-10560652	NB4	blood:	n/a
6	chr12:10570179-10570229	H1-hESC	embryonic stem cell:	embryo
7	chr12:10583355-10583405	GM12892	blood:	n/a
8	chr12:10583355-10583405	HCM	heart:	n/a
9	chr12:10560602-10560652	T-47D	breast:	n/a
10	chr12:10570179-10570229	AoSMC	blood vessel:	n/a
11	chr12:10570179-10570229	NHDF-neo	bronchial:	n/a
12	chr12:10560602-10560652	SK-N-SH	brain:	n/a
13	chr12:10607364-10607414	ProgFib	skin:	n/a
14	chr12:10588483-10588533	LNCaP	prostate:	n/a
15	chr12:10607538-10607588	H1-hESC	embryonic stem cell:	embryo
16	chr12:10588483-10588533	GM19239	blood:	n/a
17	chr12:10583355-10583405	LNCaP	prostate:	n/a
18	chr12:10586130-10586180	Jurkat	blood:	n/a
19	chr12:10599740-10599790	HMEC	breast:	n/a
20	chr12:10583355-10583405	HCPEpiC	choroid plexus:	n/a
21	chr12:10607364-10607414	K562	blood:	n/a
22	chr12:10560602-10560652	ECC-1	luminal epithelium:	n/a
23	chr12:10586130-10586180	PrEC	prostate:	n/a
24	chr12:10588483-10588533	HAEpiC	amniotic membrane:	n/a
25	chr12:10560602-10560652	PANC-1	pancreas:	n/a
26	chr12:10607538-10607588	HL-60	blood:	n/a
27	chr12:10605936-10605986	U87	brain:	n/a
28	chr12:10599740-10599790	T-47D	breast:	n/a
29	chr12:10570179-10570229	K562	blood:	n/a
30	chr12:10583355-10583405	IMR90	lung:	fetal
31	chr12:10607364-10607414	PANC-1	pancreas:	n/a
32	chr12:10608067-10608117	ProgFib	skin:	n/a
33	chr12:10560602-10560652	Hepatocyte	liver:	n/a
34	chr12:10608067-10608117	AG04449	skin:	fetal
35	chr12:10608067-10608117	T-47D	breast:	n/a
36	chr12:10608067-10608117	GM12878	blood:	n/a
37	chr12:10607538-10607588	HMEC	breast:	n/a
38	chr12:10586130-10586180	LNCaP	prostate:	n/a
39	chr12:10586130-10586180	HEK293	kidney:	embryo
40	chr12:10607364-10607414	HEEpiC	esophagus:	n/a
41	chr12:10608067-10608117	HAEpiC	amniotic membrane:	n/a
42	chr12:10583355-10583405	AoSMC	blood vessel:	n/a
43	chr12:10607538-10607588	Jurkat	blood:	n/a
44	chr12:10607364-10607414	HIPEpiC	eye:	n/a
45	chr12:10607364-10607414	T-47D	breast:	n/a
46	chr12:10607538-10607588	PFSK-1	brain:	n/a
47	chr12:10560602-10560652	HL-60	blood:	n/a
48	chr12:10588483-10588533	HL-60	blood:	n/a
49	chr12:10608067-10608117	Jurkat	blood:	n/a
50	chr12:10570179-10570229	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:10604438..10606172-chr12:10606795..10608691,2	K562	blood:
2	chr12:10563346..10565218-chr12:11316267..11318781,2	K562	blood:
3	chr1:28974955..28975586-chr12:10563608..10564342,2	Hela-S3	cervix:
4	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
5	chr12:10561211..10561774-chr17:76182659..76183234,2	Hela-S3	cervix:
6	chr12:10554334..10554872-chr16:81477760..81478703,2	Hela-S3	cervix:
7	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
8	chr12:10559960..10560793-chrX:131351678..131352452,2	Hela-S3	cervix:
9	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
10	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:
11	chr12:10604438..10606172-chr12:10606795..10608691,2	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
ENSG00000255641	chromatin interactions
ENSG00000205809	chromatin interactions
ENSG00000245648	chromatin interactions
ENSG00000123728	chromatin interactions
ENSG00000167900	chromatin interactions
ENSG00000205810	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000134545	chromatin interactions

Extended variants
information (count: 2564 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2564 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536360013	chr12:10552633-10552634	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576831541	chr12:10552682-10552683	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559932011	chr12:10552686-10552687	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34350399	chr12:10552693-10552694	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150921047	chr12:10552702-10552703	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528867423	chr12:10552753-10552754	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12827347	chr12:10552762-10552763	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs562265456	chr12:10552765-10552766	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531272014	chr12:10552814-10552815	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550773814	chr12:10552872-10552873	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145140097	chr12:10552879-10552880	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533503518	chr12:10552896-10552897	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192280560	chr12:10552898-10552899	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs12825500	chr12:10552899-10552900	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs150948362	chr12:10552953-10552954	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534781811	chr12:10552958-10552959	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139474211	chr12:10552964-10552965	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569380991	chr12:10552969-10552970	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538295322	chr12:10552977-10552978	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12830618	chr12:10553030-10553031	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs577757473	chr12:10553037-10553038	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs540192160	chr12:10553108-10553109	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs11836503	chr12:10553174-10553175	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs573827699	chr12:10553183-10553184	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs538878538	chr12:10553188-10553189	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs182847322	chr12:10553217-10553218	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372923753	chr12:10553224-10553225	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs728010	chr12:10553267-10553268	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs34460670	chr12:10553287-10553288	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs3056209	chr12:10553354-10553355	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369933156	chr12:10553355-10553356	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs397689176	chr12:10553357-10553358	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs202026830	chr12:10553358-10553359	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187044036	chr12:10553401-10553402	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544704309	chr12:10553474-10553475	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377250436	chr12:10553484-10553485	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564567018	chr12:10553515-10553516	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533557562	chr12:10553546-10553547	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs728011	chr12:10553618-10553619	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs567166121	chr12:10553648-10553649	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs529568769	chr12:10553715-10553716	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs549400297	chr12:10553721-10553722	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs149660129	chr12:10553743-10553744	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs371222287	chr12:10553762-10553763	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs538381353	chr12:10553840-10553841	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs551836046	chr12:10553844-10553845	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs35896263	chr12:10553855-10553856	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs571381763	chr12:10553857-10553858	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs35392979	chr12:10553864-10553865	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs7980470	chr12:10553888-10553889	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:250 , 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	chr12:10549000-10553000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr12:10549200-10559400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:10550600-10555200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr12:10550600-10559000	Weak transcription	Primary T cells from cord blood	blood
8	chr12:10550600-10562000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr12:10550800-10564000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:10551800-10553000	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr12:10552000-10553000	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr12:10552000-10556600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:10552200-10554000	Enhancers	Hela-S3	cervix
14	chr12:10552400-10553000	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr12:10553000-10553200	Enhancers	Primary hematopoietic stem cells	blood
16	chr12:10553000-10553200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
17	chr12:10553000-10553600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr12:10553000-10553600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr12:10553200-10553800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr12:10553600-10553800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
21	chr12:10553600-10554400	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr12:10553800-10554000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
23	chr12:10553800-10554800	Active TSS	Primary T killer memory cells from peripheral blood	blood
24	chr12:10554000-10554800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr12:10554000-10557600	Weak transcription	Hela-S3	cervix
26	chr12:10554400-10557400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr12:10554800-10555000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
28	chr12:10554800-10557200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr12:10555000-10555200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr12:10555200-10555400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
31	chr12:10555400-10556800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr12:10556600-10557400	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
33	chr12:10556800-10557000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
34	chr12:10557000-10557200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
35	chr12:10557200-10557800	Transcr. at gene 5' and 3'	Primary T killer naive cells fromperipheralblood	blood
36	chr12:10557200-10560000	Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr12:10557400-10557800	Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr12:10557400-10558200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr12:10557400-10558200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr12:10557600-10558400	Strong transcription	Hela-S3	cervix
41	chr12:10557800-10559000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr12:10557800-10559400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
43	chr12:10558000-10558200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr12:10558000-10558600	Enhancers	NHEK	skin
45	chr12:10558200-10559000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr12:10558200-10562200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr12:10558200-10562200	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
48	chr12:10558400-10559400	Weak transcription	Hela-S3	cervix
49	chr12:10558600-10559000	Weak transcription	NHEK	skin
50	chr12:10558800-10559600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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