Variant report

Variant	esv2760260
Chromosome Location	chr12:9504060-9519172
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:398)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:398 , 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	ATF1	chr12:9515879-9516104	K562	blood:	n/a	n/a
2	ATF1	chr12:9517037-9517719	K562	blood:	n/a	n/a
3	ATF2	chr12:9514231-9515229	GM12878	blood:	n/a	n/a
4	ATF2	chr12:9515316-9516084	GM12878	blood:	n/a	n/a
5	ATF2	chr12:9514144-9518351	GM12878	blood:	n/a	n/a
6	ATF2	chr12:9516298-9518464	GM12878	blood:	n/a	n/a
7	BACH1	chr12:9507019-9507395	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:9516711-9516911	K562	blood:	n/a	n/a
9	BATF	chr12:9516818-9517792	GM12878	blood:	n/a	n/a
10	BATF	chr12:9516696-9517884	GM12878	blood:	n/a	n/a
11	BATF	chr12:9514492-9515074	GM12878	blood:	n/a	n/a
12	BATF	chr12:9515676-9516129	GM12878	blood:	n/a	chr12:9515939-9515950
13	BATF	chr12:9506976-9507254	GM12878	blood:	n/a	n/a
14	BATF	chr12:9507017-9507310	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:9507015-9507175	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:9516825-9517859	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:9506964-9507320	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:9514587-9514903	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:9516896-9517726	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:9514518-9515013	GM12878	blood:	n/a	chr12:9514548-9514557
21	BCL3	chr12:9516773-9518016	GM12878	blood:	n/a	n/a
22	BCL3	chr12:9514536-9515106	GM12878	blood:	n/a	chr12:9514548-9514557
23	BCL3	chr12:9516906-9517768	GM12878	blood:	n/a	n/a
24	BCL3	chr12:9514179-9515157	GM12878	blood:	n/a	chr12:9514548-9514557
25	BCLAF1	chr12:9514439-9515090	GM12878	blood:	n/a	chr12:9514548-9514557
26	BCLAF1	chr12:9516391-9518359	GM12878	blood:	n/a	n/a
27	BCLAF1	chr12:9516321-9518443	GM12878	blood:	n/a	n/a
28	BCLAF1	chr12:9514268-9515127	GM12878	blood:	n/a	chr12:9514548-9514557
29	BHLHE40	chr12:9516856-9517910	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:9507008-9507323	HepG2	liver:	n/a	n/a
31	BHLHE40	chr12:9515984-9516100	GM12878	blood:	n/a	n/a
32	BHLHE40	chr12:9507035-9507312	HepG2	liver:	n/a	n/a
33	BHLHE40	chr12:9514468-9515061	GM12878	blood:	n/a	n/a
34	BRCA1	chr12:9516868-9517658	GM12878	blood:	n/a	n/a
35	CBX3	chr12:9506684-9507036	K562	blood:	n/a	n/a
36	CBX3	chr12:9506667-9507079	K562	blood:	n/a	n/a
37	CCNT2	chr12:9516802-9517040	K562	blood:	n/a	n/a
38	CEBPB	chr12:9516935-9517320	GM12878	blood:	n/a	n/a
39	CEBPB	chr12:9516410-9518549	GM12878	blood:	n/a	chr12:9518109-9518122 chr12:9518111-9518122
40	CEBPB	chr12:9514223-9515124	GM12878	blood:	n/a	n/a
41	CHD1	chr12:9514867-9515131	GM12878	blood:	n/a	n/a
42	CHD1	chr12:9516965-9517934	GM12878	blood:	n/a	n/a
43	CHD2	chr12:9515653-9516070	GM12878	blood:	n/a	n/a
44	CHD2	chr12:9505536-9505671	HepG2	liver:	n/a	n/a
45	CHD2	chr12:9514272-9515006	GM12878	blood:	n/a	n/a
46	CHD2	chr12:9516713-9518340	GM12878	blood:	n/a	n/a
47	CREB1	chr12:9514610-9515109	GM12878	blood:	n/a	n/a
48	CREB1	chr12:9516804-9517992	GM12878	blood:	n/a	n/a
49	CTCF	chr12:9506040-9506190	GM12869	blood:	n/a	n/a
50	CTCF	chr12:9506959-9507031	GM10266	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9517562-9517612	HCM	heart:	n/a
2	chr12:9517562-9517612	A549	lung:	n/a
3	chr12:9517562-9517612	HCT-116	colon:	n/a
4	chr12:9517562-9517612	HCPEpiC	choroid plexus:	n/a
5	chr12:9517562-9517612	HepG2	liver:	n/a
6	chr12:9517562-9517612	GM12892	blood:	n/a
7	chr12:9517562-9517612	H1-hESC	embryonic stem cell:	embryo
8	chr12:9517562-9517612	BJ	skin:	n/a
9	chr12:9517562-9517612	AG09309	skin:	n/a
10	chr12:9517562-9517612	GM12878	blood:	n/a
11	chr12:9517562-9517612	Hela-S3	cervix:	n/a
12	chr12:9517562-9517612	ProgFib	skin:	n/a
13	chr12:9517562-9517612	AoSMC	blood vessel:	n/a
14	chr12:9517562-9517612	HEEpiC	esophagus:	n/a
15	chr12:9517562-9517612	SK-N-SH_RA	brain:	n/a
16	chr12:9517562-9517612	PrEC	prostate:	n/a
17	chr12:9517562-9517612	NT2-D1	testis:	n/a
18	chr12:9517562-9517612	NH-A	brain:	n/a
19	chr12:9517562-9517612	GM12891	blood:	n/a
20	chr12:9517562-9517612	HMEC	breast:	n/a
21	chr12:9517562-9517612	AG09319	gingival:	n/a
22	chr12:9517562-9517612	HL-60	blood:	n/a
23	chr12:9517562-9517612	AG10803	skin:	n/a
24	chr12:9517562-9517612	HRCEpiC	kidney:	n/a
25	chr12:9517562-9517612	Jurkat	blood:	n/a
26	chr12:9517562-9517612	SK-N-MC	brain:	n/a
27	chr12:9517562-9517612	CMK	blood:	n/a
28	chr12:9517562-9517612	HCF	heart:	n/a
29	chr12:9517562-9517612	GM19239	blood:	n/a
30	chr12:9517562-9517612	Hepatocyte	liver:	n/a
31	chr12:9517562-9517612	MCF10A-Er-Src	breast:	n/a
32	chr12:9517562-9517612	BE2_C	brain:	n/a
33	chr12:9517562-9517612	ECC-1	luminal epithelium:	n/a
34	chr12:9517562-9517612	U87	brain:	n/a
35	chr12:9517562-9517612	RPTEC	kidney:	n/a
36	chr12:9517562-9517612	HAEpiC	amniotic membrane:	n/a
37	chr12:9517562-9517612	NHBE	bronchial:	n/a
38	chr12:9517562-9517612	AG04449	skin:	fetal
39	chr12:9517562-9517612	HNPCEpiC	eye:	n/a
40	chr12:9517562-9517612	PANC-1	pancreas:	n/a
41	chr12:9517562-9517612	HEK293	kidney:	embryo
42	chr12:9517562-9517612	NHDF-neo	bronchial:	n/a
43	chr12:9517562-9517612	LNCaP	prostate:	n/a
44	chr12:9517562-9517612	SKMC	muscle:	n/a
45	chr12:9517562-9517612	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:9517562-9517612	SK-N-SH	brain:	n/a
47	chr12:9517562-9517612	SAEC	small airway:	n/a
48	chr12:9517562-9517612	HUVEC	blood vessel:	n/a
49	chr12:9517562-9517612	K562	blood:	n/a
50	chr12:9517562-9517612	GM06990	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9516871..9518767-chr12:9528942..9530878,2	MCF-7	breast:
2	chr12:9512017..9514493-chr12:9517939..9520276,2	MCF-7	breast:
3	chr12:9493453..9495524-chr12:9502233..9505001,2	K562	blood:
4	chr12:9514676..9517481-chr12:9908794..9910668,2	K562	blood:
5	chr12:9514472..9517285-chr12:9517571..9520331,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2D-4	chr12:9518908-9519370	XLOC_009652
2	lnc-CLEC2D-5	chr12:9504271-9504480	XLOC_009651
3	lnc-PZP-4	chr12:9516719-9517139	XLOC_010009
4	lnc-CLEC2D-5	chr12:9504271-9504944	NONHSAT026731

No data

Variant related genes	Relation type
ENSG00000260423	TF binding region
ENSG00000260423	CpG island
ENSG00000260423	chromatin interactions
ANXA8L1	miRNA target sites

Extended variants
information (count: 412 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145363404	chr12:9504082-9504083	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75052022	chr12:9504105-9504106	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140764328	chr12:9504201-9504202	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79345945	chr12:9504290-9504291	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs12372791	chr12:9504294-9504295	Weak transcription Enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs78557867	chr12:9504319-9504320	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs73240745	chr12:9504345-9504346	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs556909381	chr12:9504429-9504430	Weak transcription Enhancers Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
9	rs375911037	chr12:9504449-9504450	Weak transcription Enhancers Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
10	rs186035523	chr12:9504465-9504466	Weak transcription Enhancers Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
11	rs28735913	chr12:9504496-9504497	Weak transcription Enhancers Strong transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs149336908	chr12:9504524-9504525	Weak transcription Enhancers Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
13	rs528450136	chr12:9504557-9504558	Weak transcription Enhancers Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
14	rs75930824	chr12:9504575-9504576	Weak transcription Enhancers Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
15	rs112345810	chr12:9504641-9504642	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs373035201	chr12:9504700-9504701	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs76151236	chr12:9504740-9504741	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs111940520	chr12:9504771-9504772	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs138126591	chr12:9504825-9504826	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs113778106	chr12:9504830-9504831	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs546777713	chr12:9504866-9504867	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs368412509	chr12:9504913-9504914	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs376108437	chr12:9504945-9504946	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77657421	chr12:9504969-9504970	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs6144607	chr12:9504970-9504971	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144434316	chr12:9505012-9505013	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12309329	chr12:9505013-9505014	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
28	rs549090794	chr12:9505063-9505064	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111719819	chr12:9505077-9505078	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7302974	chr12:9505139-9505140	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs557709329	chr12:9505152-9505153	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368783781	chr12:9505231-9505232	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs7304119	chr12:9505305-9505306	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs7134386	chr12:9505317-9505318	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs77898800	chr12:9505327-9505328	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143595714	chr12:9505328-9505329	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556882383	chr12:9505349-9505350	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7134498	chr12:9505364-9505365	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs542744025	chr12:9505442-9505443	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201660940	chr12:9505520-9505521	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs180899505	chr12:9505525-9505526	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75008738	chr12:9505584-9505585	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549679299	chr12:9505597-9505598	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs117266654	chr12:9505598-9505599	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377088187	chr12:9505631-9505632	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73240746	chr12:9505649-9505650	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545016472	chr12:9505736-9505737	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs35408348	chr12:9505763-9505764	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147278324	chr12:9505916-9505917	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368226426	chr12:9505981-9505982	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9490200-9504400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:9498600-9505000	Strong transcription	Fetal Lung	lung
3	chr12:9499000-9506000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr12:9501800-9504600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr12:9502600-9504200	Enhancers	Primary hematopoietic stem cells	blood
6	chr12:9502600-9504400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:9502600-9504400	Enhancers	Dnd41	blood
8	chr12:9502800-9507200	Weak transcription	Fetal Heart	heart
9	chr12:9503200-9506000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr12:9503400-9504200	Enhancers	Primary T cells from cord blood	blood
11	chr12:9503400-9506000	Enhancers	HepG2	liver
12	chr12:9503800-9504200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:9503800-9504800	Weak transcription	Fetal Thymus	thymus
14	chr12:9503800-9505800	Weak transcription	Thymus	Thymus
15	chr12:9504000-9504600	Weak transcription	HMEC	breast
16	chr12:9504000-9505200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr12:9504200-9504400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr12:9504200-9505000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr12:9504400-9506800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:9505000-9506600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
21	chr12:9505000-9508000	ZNF genes & repeats	Fetal Lung	lung
22	chr12:9505200-9507000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr12:9505800-9506400	ZNF genes & repeats	Thymus	Thymus
24	chr12:9506000-9506200	ZNF genes & repeats	Stomach Smooth Muscle	stomach
25	chr12:9506000-9506400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
26	chr12:9506000-9506600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:9506000-9506800	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
28	chr12:9506000-9507000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
29	chr12:9506000-9507200	ZNF genes & repeats	HepG2	liver
30	chr12:9506200-9506800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr12:9506800-9516000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:9507000-9516800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr12:9507000-9517200	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr12:9507200-9507400	Active TSS	Fetal Heart	heart
35	chr12:9507200-9514200	Weak transcription	HepG2	liver
36	chr12:9508000-9512400	Weak transcription	Fetal Lung	lung
37	chr12:9512400-9516200	Strong transcription	Fetal Lung	lung
38	chr12:9513400-9514200	Enhancers	GM12878-XiMat	blood
39	chr12:9514200-9514600	Flanking Active TSS	GM12878-XiMat	blood
40	chr12:9514200-9515000	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr12:9514200-9515000	Enhancers	HepG2	liver
42	chr12:9514400-9514800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
43	chr12:9514400-9515000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr12:9514400-9515200	Enhancers	Primary B cells from peripheral blood	blood
45	chr12:9514400-9515600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr12:9514600-9515600	Enhancers	GM12878-XiMat	blood
47	chr12:9514800-9515000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr12:9514800-9515000	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr12:9514800-9517200	Enhancers	Primary T cells fromperipheralblood	blood
50	chr12:9515000-9515400	Weak transcription	HepG2	liver

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