Variant report

Variant	esv3332298
Chromosome Location	chr12:9500121-9519487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:439)
CpG islands
(count:245)
Chromatin interactive
region (count:8)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr12:9500046-9500362	K562	blood:	n/a	n/a
3	ATF1	chr12:9517037-9517719	K562	blood:	n/a	n/a
4	ATF2	chr12:9514231-9515229	GM12878	blood:	n/a	n/a
5	ATF2	chr12:9516298-9518464	GM12878	blood:	n/a	n/a
6	ATF2	chr12:9514144-9518351	GM12878	blood:	n/a	n/a
7	ATF2	chr12:9515316-9516084	GM12878	blood:	n/a	n/a
8	BACH1	chr12:9507019-9507395	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr12:9516711-9516911	K562	blood:	n/a	n/a
10	BATF	chr12:9515676-9516129	GM12878	blood:	n/a	chr12:9515939-9515950
11	BATF	chr12:9516818-9517792	GM12878	blood:	n/a	n/a
12	BATF	chr12:9516696-9517884	GM12878	blood:	n/a	n/a
13	BATF	chr12:9514492-9515074	GM12878	blood:	n/a	n/a
14	BATF	chr12:9506976-9507254	GM12878	blood:	n/a	n/a
15	BATF	chr12:9507017-9507310	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:9506964-9507320	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:9516896-9517726	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:9507015-9507175	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:9516825-9517859	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:9514518-9515013	GM12878	blood:	n/a	chr12:9514548-9514557
21	BCL11A	chr12:9514587-9514903	GM12878	blood:	n/a	n/a
22	BCL3	chr12:9514179-9515157	GM12878	blood:	n/a	chr12:9514548-9514557
23	BCL3	chr12:9516773-9518016	GM12878	blood:	n/a	n/a
24	BCL3	chr12:9514536-9515106	GM12878	blood:	n/a	chr12:9514548-9514557
25	BCL3	chr12:9516906-9517768	GM12878	blood:	n/a	n/a
26	BCLAF1	chr12:9514439-9515090	GM12878	blood:	n/a	chr12:9514548-9514557
27	BCLAF1	chr12:9516321-9518443	GM12878	blood:	n/a	n/a
28	BCLAF1	chr12:9516391-9518359	GM12878	blood:	n/a	n/a
29	BCLAF1	chr12:9514268-9515127	GM12878	blood:	n/a	chr12:9514548-9514557
30	BHLHE40	chr12:9516856-9517910	GM12878	blood:	n/a	n/a
31	BHLHE40	chr12:9507035-9507312	HepG2	liver:	n/a	n/a
32	BHLHE40	chr12:9515984-9516100	GM12878	blood:	n/a	n/a
33	BHLHE40	chr12:9507008-9507323	HepG2	liver:	n/a	n/a
34	BHLHE40	chr12:9514468-9515061	GM12878	blood:	n/a	n/a
35	BRCA1	chr12:9516868-9517658	GM12878	blood:	n/a	n/a
36	CBX3	chr12:9506684-9507036	K562	blood:	n/a	n/a
37	CBX3	chr12:9506667-9507079	K562	blood:	n/a	n/a
38	CCNT2	chr12:9516802-9517040	K562	blood:	n/a	n/a
39	CEBPB	chr12:9499834-9500361	HCT-116	colon:	n/a	n/a
40	CEBPB	chr12:9516410-9518549	GM12878	blood:	n/a	chr12:9518109-9518122 chr12:9518111-9518122
41	CEBPB	chr12:9514223-9515124	GM12878	blood:	n/a	n/a
42	CEBPB	chr12:9516935-9517320	GM12878	blood:	n/a	n/a
43	CEBPB	chr12:9503781-9504020	HepG2	liver:	n/a	n/a
44	CEBPB	chr12:9500023-9500302	IMR90	lung:	n/a	n/a
45	CEBPB	chr12:9499940-9500276	Hela-S3	cervix:	n/a	n/a
46	CHD1	chr12:9516965-9517934	GM12878	blood:	n/a	n/a
47	CHD1	chr12:9514867-9515131	GM12878	blood:	n/a	n/a
48	CHD2	chr12:9505536-9505671	HepG2	liver:	n/a	n/a
49	CHD2	chr12:9516713-9518340	GM12878	blood:	n/a	n/a
50	CHD2	chr12:9515653-9516070	GM12878	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9517562-9517612	T-47D	breast:	n/a
2	chr12:9517562-9517612	T-47D	breast:	n/a
3	chr12:9501845-9501895	NHBE	bronchial:	n/a
4	chr12:9501783-9501833	SK-N-SH_RA	brain:	n/a
5	chr12:9517562-9517612	HAEpiC	amniotic membrane:	n/a
6	chr12:9501783-9501833	SKMC	muscle:	n/a
7	chr12:9501783-9501833	GM06990	blood:	n/a
8	chr12:9501783-9501833	K562	blood:	n/a
9	chr12:9501845-9501895	T-47D	breast:	n/a
10	chr12:9501915-9501965	HEEpiC	esophagus:	n/a
11	chr12:9501915-9501965	Hela-S3	cervix:	n/a
12	chr12:9517562-9517612	A549	lung:	n/a
13	chr12:9517562-9517612	NHDF-neo	bronchial:	n/a
14	chr12:9517562-9517612	NT2-D1	testis:	n/a
15	chr12:9501783-9501833	HAEpiC	amniotic membrane:	n/a
16	chr12:9501845-9501895	HNPCEpiC	eye:	n/a
17	chr12:9501783-9501833	HNPCEpiC	eye:	n/a
18	chr12:9501783-9501833	HRCEpiC	kidney:	n/a
19	chr12:9501915-9501965	T-47D	breast:	n/a
20	chr12:9501783-9501833	HRE	kidney:	n/a
21	chr12:9501783-9501833	Caco-2	colon:	n/a
22	chr12:9501845-9501895	GM06990	blood:	n/a
23	chr12:9501845-9501895	HL-60	blood:	n/a
24	chr12:9501915-9501965	HIPEpiC	eye:	n/a
25	chr12:9501783-9501833	HUVEC	blood vessel:	n/a
26	chr12:9501915-9501965	HRCEpiC	kidney:	n/a
27	chr12:9501845-9501895	Caco-2	colon:	n/a
28	chr12:9501783-9501833	GM19239	blood:	n/a
29	chr12:9501845-9501895	Hela-S3	cervix:	n/a
30	chr12:9517562-9517612	GM19239	blood:	n/a
31	chr12:9501783-9501833	HCF	heart:	n/a
32	chr12:9501783-9501833	MCF-7	breast:	n/a
33	chr12:9501915-9501965	HCF	heart:	n/a
34	chr12:9501783-9501833	HRPEpiC	eye:	n/a
35	chr12:9517562-9517612	HRE	kidney:	n/a
36	chr12:9517562-9517612	HCT-116	colon:	n/a
37	chr12:9517562-9517612	GM12891	blood:	n/a
38	chr12:9501845-9501895	SK-N-SH	brain:	n/a
39	chr12:9501845-9501895	ECC-1	luminal epithelium:	n/a
40	chr12:9517562-9517612	SK-N-SH	brain:	n/a
41	chr12:9517562-9517612	HCM	heart:	n/a
42	chr12:9501915-9501965	Jurkat	blood:	n/a
43	chr12:9517562-9517612	HCF	heart:	n/a
44	chr12:9501915-9501965	NHBE	bronchial:	n/a
45	chr12:9501845-9501895	ovcar-3	ovarian:	n/a
46	chr12:9501783-9501833	NB4	blood:	n/a
47	chr12:9517562-9517612	NH-A	brain:	n/a
48	chr12:9501845-9501895	PANC-1	pancreas:	n/a
49	chr12:9501783-9501833	NH-A	brain:	n/a
50	chr12:9517562-9517612	PFSK-1	brain:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9499156..9500827-chr12:9501599..9503470,2	MCF-7	breast:
2	chr12:9514472..9517285-chr12:9517571..9520331,3	K562	blood:
3	chr12:9516871..9518767-chr12:9528942..9530878,2	MCF-7	breast:
4	chr12:9493453..9495524-chr12:9502233..9505001,2	K562	blood:
5	chr12:9499156..9500827-chr12:9501599..9503470,2	MCF-7	breast:
6	chr12:9512017..9514493-chr12:9517939..9520276,2	MCF-7	breast:
7	chr12:9492332..9494947-chr12:9501072..9502931,2	MCF-7	breast:
8	chr12:9514676..9517481-chr12:9908794..9910668,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2D-6	chr12:9500555-9500599	XLOC_009650
2	lnc-PZP-10	chr12:9502714-9503413	NONHSAT026583
3	lnc-CLEC2D-5	chr12:9504271-9504480	XLOC_009651
4	lnc-CLEC2D-5	chr12:9504271-9504944	NONHSAT026731
5	lnc-CLEC2D-5	chr12:9502564-9502713	NONHSAT026731
6	lnc-CLEC2D-6	chr12:9500409-9501023	NONHSAT026706
7	lnc-PZP-4	chr12:9516719-9517139	XLOC_010009
8	lnc-PZP-10	chr12:9500060-9500507	NONHSAT026583
9	lnc-CLEC2D-5	chr12:9502422-9502713	XLOC_009651
10	lnc-CLEC2D-4	chr12:9518908-9519370	XLOC_009652

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: 558 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:558 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200591574	chr12:9500161-9500162	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs370105486	chr12:9500255-9500256	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs76230046	chr12:9500283-9500284	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs190446689	chr12:9500315-9500316	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs145372492	chr12:9500323-9500324	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs147664009	chr12:9500350-9500351	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs115874390	chr12:9500427-9500428	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs79948976	chr12:9500484-9500485	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs561902395	chr12:9500485-9500486	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs183073560	chr12:9500486-9500487	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs1991192	chr12:9500499-9500500	Strong transcription Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs547937818	chr12:9500770-9500771	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs187050429	chr12:9500914-9500915	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs78326657	chr12:9500942-9500943	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs75336702	chr12:9500976-9500977	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs114675908	chr12:9501092-9501093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376324247	chr12:9501093-9501094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116549621	chr12:9501095-9501096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112887373	chr12:9501108-9501109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368253015	chr12:9501177-9501178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559852521	chr12:9501180-9501181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569904511	chr12:9501305-9501306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138895091	chr12:9501332-9501333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536192160	chr12:9501369-9501370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71265060	chr12:9501401-9501402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372536202	chr12:9501507-9501508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs386760176	chr12:9501518-9501519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs60839170	chr12:9501519-9501520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116003189	chr12:9501589-9501590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs58195943	chr12:9501601-9501602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141614032	chr12:9501606-9501607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs58135855	chr12:9501609-9501610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs59060075	chr12:9501610-9501611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs61251860	chr12:9501617-9501618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7971165	chr12:9501631-9501632	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs56654357	chr12:9501639-9501640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs60784396	chr12:9501659-9501660	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs58326473	chr12:9501679-9501680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs59403662	chr12:9501689-9501690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61421192	chr12:9501690-9501691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12298872	chr12:9501697-9501698	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs368866336	chr12:9501708-9501709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs59378313	chr12:9501713-9501714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12371486	chr12:9501725-9501726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149711023	chr12:9501757-9501758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10843491	chr12:9501770-9501771	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs11050392	chr12:9501776-9501777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373011097	chr12:9501779-9501780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11050393	chr12:9501784-9501785	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs147398621	chr12:9501792-9501793	Weak transcription Strong transcription	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:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9490200-9504400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:9492800-9500200	Enhancers	Primary T cells from cord blood	blood
3	chr12:9493200-9502400	Weak transcription	Fetal Muscle Trunk	muscle
4	chr12:9493400-9500400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr12:9494000-9502600	Weak transcription	HSMM	muscle
6	chr12:9496200-9500800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr12:9498000-9500800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:9498200-9502600	Weak transcription	Dnd41	blood
9	chr12:9498400-9502600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr12:9498400-9502600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:9498400-9502800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:9498600-9500800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr12:9498600-9500800	Enhancers	NHEK	skin
14	chr12:9498600-9505000	Strong transcription	Fetal Lung	lung
15	chr12:9498800-9500800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:9498800-9501000	Enhancers	HMEC	breast
17	chr12:9499000-9500600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr12:9499000-9502600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr12:9499000-9502600	Weak transcription	Fetal Thymus	thymus
20	chr12:9499000-9506000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr12:9499400-9500200	Enhancers	Right Atrium	heart
22	chr12:9499400-9500400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr12:9499400-9500400	Enhancers	Osteobl	bone
24	chr12:9499600-9503000	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr12:9500000-9500200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr12:9500000-9500400	Enhancers	GM12878-XiMat	blood
27	chr12:9500000-9500400	Enhancers	HepG2	liver
28	chr12:9500000-9500800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:9500200-9501600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr12:9500200-9503400	Weak transcription	Primary T cells from cord blood	blood
31	chr12:9500400-9502200	Weak transcription	HepG2	liver
32	chr12:9500400-9502400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr12:9500400-9502600	Weak transcription	Osteobl	bone
34	chr12:9500400-9502800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr12:9500600-9501000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr12:9500800-9501800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr12:9500800-9502200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr12:9500800-9502600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr12:9500800-9502800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr12:9500800-9502800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr12:9501000-9502200	Weak transcription	HMEC	breast
42	chr12:9501000-9502400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr12:9501600-9502000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr12:9501800-9504600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr12:9502000-9502400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:9502200-9502800	Enhancers	Fetal Heart	heart
47	chr12:9502200-9502800	Enhancers	HepG2	liver
48	chr12:9502200-9503600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:9502200-9504000	Enhancers	HMEC	breast
50	chr12:9502400-9503000	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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