Variant report

Variant	esv1801819
Chromosome Location	chr12:9619681-9728768
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:487)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:9621679-9621874	HepG2	liver:	n/a	n/a
2	BATF	chr12:9623145-9623344	GM12878	blood:	n/a	n/a
3	BATF	chr12:9627069-9627370	GM12878	blood:	n/a	chr12:9627229-9627240
4	BATF	chr12:9627071-9627414	GM12878	blood:	n/a	chr12:9627229-9627240
5	BHLHE40	chr12:9621680-9621866	K562	blood:	n/a	n/a
6	BRCA1	chr12:9621725-9621746	GM12878	blood:	n/a	n/a
7	CEBPB	chr12:9621705-9621858	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr12:9626831-9627127	Hela-S3	cervix:	n/a	chr12:9626967-9626978
9	CEBPB	chr12:9728216-9728457	A549	lung:	n/a	n/a
10	CEBPB	chr12:9646117-9646284	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr12:9699973-9700136	IMR90	lung:	n/a	n/a
12	CEBPB	chr12:9626823-9627139	HepG2	liver:	n/a	chr12:9626967-9626978
13	CEBPB	chr12:9626847-9627088	A549	lung:	n/a	chr12:9626967-9626978
14	CEBPB	chr12:9621719-9621810	K562	blood:	n/a	n/a
15	CEBPB	chr12:9699995-9700109	A549	lung:	n/a	n/a
16	CEBPB	chr12:9626941-9627031	K562	blood:	n/a	chr12:9626967-9626978
17	CEBPB	chr12:9621651-9621793	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:9626864-9627128	K562	blood:	n/a	chr12:9626967-9626978
19	CEBPB	chr12:9621557-9621862	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:9635038-9635326	IMR90	lung:	n/a	chr12:9635144-9635153 chr12:9635144-9635153 chr12:9635144-9635153
21	CTCF	chr12:9621611-9621891	HepG2	liver:	n/a	n/a
22	CTCF	chr12:9620819-9620946	MCF-7	breast:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
23	CTCF	chr12:9621740-9621890	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr12:9621720-9621870	HCFaa	heart:	n/a	n/a
25	CTCF	chr12:9621740-9621890	K562	blood:	n/a	n/a
26	CTCF	chr12:9620840-9620990	HMF	breast:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
27	CTCF	chr12:9621567-9621972	HepG2	liver:	n/a	chr12:9621901-9621914
28	CTCF	chr12:9621474-9621980	A549	lung:	n/a	chr12:9621901-9621914
29	CTCF	chr12:9621720-9621870	HepG2	liver:	n/a	n/a
30	CTCF	chr12:9621676-9621905	Fibrobl	skin:	n/a	n/a
31	CTCF	chr12:9691717-9691734	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr12:9621700-9621850	BE2_C	brain:	n/a	n/a
33	CTCF	chr12:9621720-9621870	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr12:9621740-9621890	GM12864	blood:	n/a	n/a
35	CTCF	chr12:9620834-9620956	GM10248	blood:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
36	CTCF	chr12:9621680-9621830	AG09309	skin:	n/a	n/a
37	CTCF	chr12:9621720-9621870	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:9621700-9621850	GM12869	blood:	n/a	n/a
39	CTCF	chr12:9621760-9621910	HCT-116	colon:	n/a	n/a
40	CTCF	chr12:9665406-9665624	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr12:9620840-9620990	AG10803	skin:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
42	CTCF	chr12:9620795-9620990	GM12878	blood:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
43	CTCF	chr12:9621720-9621870	GM06990	blood:	n/a	n/a
44	CTCF	chr12:9665315-9665625	A549	lung:	n/a	n/a
45	CTCF	chr12:9726760-9726829	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr12:9620800-9620950	AG09319	gingival:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
47	CTCF	chr12:9620820-9620970	GM06990	blood:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
48	CTCF	chr12:9665390-9665555	ProgFib	skin:	n/a	n/a
49	CTCF	chr12:9621700-9621850	HAc	cerebellar:	n/a	n/a
50	CTCF	chr12:9621668-9621940	K562	blood:	n/a	chr12:9621901-9621914

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9720090-9720140	HRCEpiC	kidney:	n/a
2	chr12:9720554-9720604	NT2-D1	testis:	n/a
3	chr12:9723402-9723452	A549	lung:	n/a
4	chr12:9720554-9720604	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:9722091-9722141	HCM	heart:	n/a
6	chr12:9723402-9723452	GM19239	blood:	n/a
7	chr12:9720554-9720604	GM12891	blood:	n/a
8	chr12:9723402-9723452	SAEC	small airway:	n/a
9	chr12:9720090-9720140	ovcar-3	ovarian:	n/a
10	chr12:9720090-9720140	MCF10A-Er-Src	breast:	n/a
11	chr12:9723402-9723452	HEEpiC	esophagus:	n/a
12	chr12:9723402-9723452	HRE	kidney:	n/a
13	chr12:9722091-9722141	NH-A	brain:	n/a
14	chr12:9720554-9720604	AG04449	skin:	fetal
15	chr12:9720090-9720140	GM12878	blood:	n/a
16	chr12:9720554-9720604	GM06990	blood:	n/a
17	chr12:9720554-9720604	HRE	kidney:	n/a
18	chr12:9722091-9722141	HEEpiC	esophagus:	n/a
19	chr12:9722091-9722141	AoSMC	blood vessel:	n/a
20	chr12:9720090-9720140	A549	lung:	n/a
21	chr12:9722091-9722141	Caco-2	colon:	n/a
22	chr12:9720554-9720604	H1-hESC	embryonic stem cell:	embryo
23	chr12:9722091-9722141	MCF-7	breast:	n/a
24	chr12:9720090-9720140	SAEC	small airway:	n/a
25	chr12:9720090-9720140	SK-N-SH_RA	brain:	n/a
26	chr12:9723402-9723452	GM12891	blood:	n/a
27	chr12:9722091-9722141	A549	lung:	n/a
28	chr12:9723402-9723452	HRPEpiC	eye:	n/a
29	chr12:9720090-9720140	MCF-7	breast:	n/a
30	chr12:9720554-9720604	CMK	blood:	n/a
31	chr12:9723402-9723452	HCPEpiC	choroid plexus:	n/a
32	chr12:9722091-9722141	SAEC	small airway:	n/a
33	chr12:9723402-9723452	HPAEpiC	pulmonary alveolar:	n/a
34	chr12:9723402-9723452	AG04450	lung:	fetal
35	chr12:9720554-9720604	Jurkat	blood:	n/a
36	chr12:9722091-9722141	CMK	blood:	n/a
37	chr12:9723402-9723452	PANC-1	pancreas:	n/a
38	chr12:9720090-9720140	HEEpiC	esophagus:	n/a
39	chr12:9722091-9722141	GM12878	blood:	n/a
40	chr12:9722091-9722141	HIPEpiC	eye:	n/a
41	chr12:9720554-9720604	HRPEpiC	eye:	n/a
42	chr12:9720554-9720604	Caco-2	colon:	n/a
43	chr12:9722091-9722141	PrEC	prostate:	n/a
44	chr12:9722091-9722141	HUVEC	blood vessel:	n/a
45	chr12:9723402-9723452	AoSMC	blood vessel:	n/a
46	chr12:9720554-9720604	BE2_C	brain:	n/a
47	chr12:9720554-9720604	NHDF-neo	bronchial:	n/a
48	chr12:9720090-9720140	HMEC	breast:	n/a
49	chr12:9720554-9720604	HNPCEpiC	eye:	n/a
50	chr12:9720090-9720140	ECC-1	luminal epithelium:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9620489..9621323-chr12:31206721..31207493,2	MCF-7	breast:
2	chr12:9620209..9621328-chr12:31206996..31207808,4	MCF-7	breast:
3	chr12:9530894..9532008-chr12:9621312..9622244,4	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2D-9	chr12:9723357-9723488	NONHSAT026830
2	lnc-CLEC2D-9	chr12:9725984-9726130	NONHSAT026830
3	lnc-CLEC2D-9	chr12:9725599-9725666	NONHSAT026830
4	lnc-CLEC2D-9	chr12:9728714-9728863	NONHSAT026830
5	lnc-CLEC2D-9	chr12:9724057-9724169	NONHSAT026830
6	lnc-KLRB1-2	chr12:9690763-9691239	l_603_chr12:9690762-9691933_testes
7	lnc-CLEC2D-9	chr12:9728239-9728313	NONHSAT026830
8	lnc-CLEC2D-9	chr12:9727443-9727545	NONHSAT026830
9	lnc-KLRB1-2	chr12:9691704-9691933	l_603_chr12:9690762-9691933_testes

No data

Variant related genes	Relation type
ENSG00000266633	TF binding region
ENSG00000256975	TF binding region
ENSG00000214776	TF binding region
ENSG00000266633	CpG island
ENSG00000256975	CpG island
ENSG00000214776	CpG island

Extended variants
information (count: 2173 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2173 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369407169	chr12:9619696-9619697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs17804971	chr12:9619705-9619706	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs184628411	chr12:9619710-9619711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2536683	chr12:9619758-9619759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78348429	chr12:9619795-9619796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs398076410	chr12:9619796-9619797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545536059	chr12:9619821-9619822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2536681	chr12:9619843-9619844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575714438	chr12:9619949-9619950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113530230	chr12:9619981-9619982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2159779	chr12:9620106-9620107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
12	rs143504978	chr12:9620111-9620112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199705173	chr12:9620183-9620184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4015236	chr12:9620185-9620186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561669414	chr12:9620189-9620190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370322861	chr12:9620236-9620237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2109900	chr12:9620255-9620256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
18	rs200332999	chr12:9620420-9620421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547206658	chr12:9620521-9620522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2888915	chr12:9620544-9620545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs55690498	chr12:9620567-9620568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
22	rs377538666	chr12:9620614-9620615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529928959	chr12:9620630-9620631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2888917	chr12:9620638-9620639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs56124826	chr12:9620647-9620648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570162267	chr12:9620662-9620663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189949674	chr12:9620702-9620703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
28	rs55651903	chr12:9620720-9620721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs56137687	chr12:9620735-9620736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185226708	chr12:9620767-9620768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2374753	chr12:9620794-9620795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs55837995	chr12:9620876-9620877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs56085041	chr12:9620888-9620889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371185615	chr12:9620903-9620904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11614201	chr12:9620950-9620951	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs56222664	chr12:9620966-9620967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs3863335	chr12:9620975-9620976	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs55687140	chr12:9620977-9620978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567579058	chr12:9620994-9620995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139155704	chr12:9621028-9621029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs3928137	chr12:9621036-9621037	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs190876122	chr12:9621040-9621041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs553200528	chr12:9621047-9621048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140076647	chr12:9621099-9621100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143635416	chr12:9621110-9621111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11837514	chr12:9621130-9621131	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs146783378	chr12:9621187-9621188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565333088	chr12:9621194-9621195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113423943	chr12:9621224-9621225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575803474	chr12:9621254-9621255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:137 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9607200-9623000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:9608800-9642800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:9610200-9621000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:9611200-9621400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr12:9615200-9621600	Weak transcription	Fetal Muscle Leg	muscle
6	chr12:9615400-9622600	Weak transcription	Primary B cells from peripheral blood	blood
7	chr12:9617400-9621600	Weak transcription	Fetal Lung	lung
8	chr12:9617800-9622800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr12:9618200-9622600	Weak transcription	GM12878-XiMat	blood
10	chr12:9618800-9621000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:9619600-9621600	Enhancers	Fetal Heart	heart
12	chr12:9619600-9623600	Enhancers	Fetal Thymus	thymus
13	chr12:9620800-9621200	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr12:9620800-9623600	Enhancers	Primary T cells from cord blood	blood
15	chr12:9620800-9623600	Enhancers	Primary T cells fromperipheralblood	blood
16	chr12:9621000-9621200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr12:9621000-9621400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr12:9621000-9621600	Enhancers	HSMMtube	muscle
19	chr12:9621000-9621800	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr12:9621000-9621800	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr12:9621000-9621800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:9621000-9621800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr12:9621000-9622000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr12:9621000-9622000	Enhancers	HepG2	liver
25	chr12:9621000-9622200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr12:9621000-9623600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:9621200-9621400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr12:9621200-9621800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr12:9621200-9621800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr12:9621400-9621600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr12:9621400-9621800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr12:9621400-9621800	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr12:9621400-9622000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr12:9621400-9622000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:9621400-9622400	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr12:9621400-9623600	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr12:9621600-9621800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr12:9621600-9621800	Enhancers	Fetal Muscle Leg	muscle
39	chr12:9621600-9621800	Enhancers	Thymus	Thymus
40	chr12:9621600-9622000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr12:9621600-9622000	Enhancers	Liver	Liver
42	chr12:9621600-9622000	Enhancers	Fetal Lung	lung
43	chr12:9621600-9622000	Enhancers	Dnd41	blood
44	chr12:9621800-9622600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr12:9621800-9622800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr12:9621800-9623000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr12:9621800-9623000	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr12:9621800-9623000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr12:9621800-9623600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr12:9621800-9625800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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