Variant report

Variant	esv3436788
Chromosome Location	chr12:9499151-9519686
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:452)
CpG islands
(count:244)
Chromatin interactive
region (count:8)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:452 , 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	ATF1	chr12:9517037-9517719	K562	blood:	n/a	n/a
2	ATF1	chr12:9515879-9516104	K562	blood:	n/a	n/a
3	ATF1	chr12:9500046-9500362	K562	blood:	n/a	n/a
4	ATF1	chr12:9499390-9499755	K562	blood:	n/a	n/a
5	ATF2	chr12:9516298-9518464	GM12878	blood:	n/a	n/a
6	ATF2	chr12:9515316-9516084	GM12878	blood:	n/a	n/a
7	ATF2	chr12:9514144-9518351	GM12878	blood:	n/a	n/a
8	ATF2	chr12:9514231-9515229	GM12878	blood:	n/a	n/a
9	BACH1	chr12:9516711-9516911	K562	blood:	n/a	n/a
10	BACH1	chr12:9507019-9507395	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr12:9515676-9516129	GM12878	blood:	n/a	chr12:9515939-9515950
12	BATF	chr12:9514492-9515074	GM12878	blood:	n/a	n/a
13	BATF	chr12:9506976-9507254	GM12878	blood:	n/a	n/a
14	BATF	chr12:9516696-9517884	GM12878	blood:	n/a	n/a
15	BATF	chr12:9507017-9507310	GM12878	blood:	n/a	n/a
16	BATF	chr12:9516818-9517792	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:9507015-9507175	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:9506964-9507320	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:9516896-9517726	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:9516825-9517859	GM12878	blood:	n/a	n/a
21	BCL11A	chr12:9514518-9515013	GM12878	blood:	n/a	chr12:9514548-9514557
22	BCL11A	chr12:9514587-9514903	GM12878	blood:	n/a	n/a
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	chr12:9514179-9515157	GM12878	blood:	n/a	chr12:9514548-9514557
26	BCL3	chr12:9516906-9517768	GM12878	blood:	n/a	n/a
27	BCLAF1	chr12:9516391-9518359	GM12878	blood:	n/a	n/a
28	BCLAF1	chr12:9516321-9518443	GM12878	blood:	n/a	n/a
29	BCLAF1	chr12:9514268-9515127	GM12878	blood:	n/a	chr12:9514548-9514557
30	BCLAF1	chr12:9514439-9515090	GM12878	blood:	n/a	chr12:9514548-9514557
31	BHLHE40	chr12:9507035-9507312	HepG2	liver:	n/a	n/a
32	BHLHE40	chr12:9499426-9499609	K562	blood:	n/a	n/a
33	BHLHE40	chr12:9515984-9516100	GM12878	blood:	n/a	n/a
34	BHLHE40	chr12:9507008-9507323	HepG2	liver:	n/a	n/a
35	BHLHE40	chr12:9514468-9515061	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:9516856-9517910	GM12878	blood:	n/a	n/a
37	BRCA1	chr12:9516868-9517658	GM12878	blood:	n/a	n/a
38	CBX3	chr12:9506684-9507036	K562	blood:	n/a	n/a
39	CBX3	chr12:9506667-9507079	K562	blood:	n/a	n/a
40	CCNT2	chr12:9516802-9517040	K562	blood:	n/a	n/a
41	CEBPB	chr12:9516935-9517320	GM12878	blood:	n/a	n/a
42	CEBPB	chr12:9514223-9515124	GM12878	blood:	n/a	n/a
43	CEBPB	chr12:9500023-9500302	IMR90	lung:	n/a	n/a
44	CEBPB	chr12:9499834-9500361	HCT-116	colon:	n/a	n/a
45	CEBPB	chr12:9499940-9500276	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr12:9503781-9504020	HepG2	liver:	n/a	n/a
47	CEBPB	chr12:9516410-9518549	GM12878	blood:	n/a	chr12:9518109-9518122 chr12:9518111-9518122
48	CHD1	chr12:9514867-9515131	GM12878	blood:	n/a	n/a
49	CHD1	chr12:9516965-9517934	GM12878	blood:	n/a	n/a
50	CHD2	chr12:9514272-9515006	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9501783-9501833	NHBE	bronchial:	n/a
2	chr12:9501783-9501833	NHDF-neo	bronchial:	n/a
3	chr12:9501845-9501895	NH-A	brain:	n/a
4	chr12:9517562-9517612	HEEpiC	esophagus:	n/a
5	chr12:9501783-9501833	GM06990	blood:	n/a
6	chr12:9501845-9501895	RPTEC	kidney:	n/a
7	chr12:9517562-9517612	SK-N-MC	brain:	n/a
8	chr12:9517562-9517612	GM06990	blood:	n/a
9	chr12:9501783-9501833	HPAEpiC	pulmonary alveolar:	n/a
10	chr12:9501915-9501965	GM19239	blood:	n/a
11	chr12:9501915-9501965	HCF	heart:	n/a
12	chr12:9517562-9517612	HCM	heart:	n/a
13	chr12:9517562-9517612	AG09309	skin:	n/a
14	chr12:9501783-9501833	HNPCEpiC	eye:	n/a
15	chr12:9501845-9501895	IMR90	lung:	fetal
16	chr12:9517562-9517612	NB4	blood:	n/a
17	chr12:9517562-9517612	NT2-D1	testis:	n/a
18	chr12:9501783-9501833	ProgFib	skin:	n/a
19	chr12:9501915-9501965	K562	blood:	n/a
20	chr12:9501783-9501833	SKMC	muscle:	n/a
21	chr12:9501783-9501833	MCF10A-Er-Src	breast:	n/a
22	chr12:9501845-9501895	HCPEpiC	choroid plexus:	n/a
23	chr12:9501845-9501895	HRCEpiC	kidney:	n/a
24	chr12:9501845-9501895	BE2_C	brain:	n/a
25	chr12:9501915-9501965	HIPEpiC	eye:	n/a
26	chr12:9517562-9517612	HRPEpiC	eye:	n/a
27	chr12:9501915-9501965	PFSK-1	brain:	n/a
28	chr12:9501783-9501833	SK-N-SH	brain:	n/a
29	chr12:9501915-9501965	SKMC	muscle:	n/a
30	chr12:9501845-9501895	Hela-S3	cervix:	n/a
31	chr12:9501783-9501833	AG04449	skin:	fetal
32	chr12:9517562-9517612	NHDF-neo	bronchial:	n/a
33	chr12:9501845-9501895	Hepatocyte	liver:	n/a
34	chr12:9501845-9501895	MCF-7	breast:	n/a
35	chr12:9517562-9517612	MCF-7	breast:	n/a
36	chr12:9517562-9517612	HCPEpiC	choroid plexus:	n/a
37	chr12:9501783-9501833	HepG2	liver:	n/a
38	chr12:9501845-9501895	SK-N-SH	brain:	n/a
39	chr12:9501915-9501965	CMK	blood:	n/a
40	chr12:9501915-9501965	HRCEpiC	kidney:	n/a
41	chr12:9517562-9517612	SAEC	small airway:	n/a
42	chr12:9501845-9501895	HAEpiC	amniotic membrane:	n/a
43	chr12:9501845-9501895	HEK293	kidney:	embryo
44	chr12:9501915-9501965	PrEC	prostate:	n/a
45	chr12:9501783-9501833	HL-60	blood:	n/a
46	chr12:9517562-9517612	BE2_C	brain:	n/a
47	chr12:9501915-9501965	HepG2	liver:	n/a
48	chr12:9501915-9501965	A549	lung:	n/a
49	chr12:9501845-9501895	HUVEC	blood vessel:	n/a
50	chr12:9517562-9517612	K562	blood:	n/a

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

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

(count:13 , 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	chr12:9502422-9502713	XLOC_009651
3	lnc-PZP-4	chr12:9516719-9517139	XLOC_010009
4	lnc-CLEC2D-5	chr12:9502564-9502713	NONHSAT026731
5	lnc-CLEC2D-6	chr12:9499309-9499722	XLOC_009650
6	lnc-CLEC2D-5	chr12:9504271-9504944	NONHSAT026731
7	lnc-CLEC2D-6	chr12:9500555-9500599	XLOC_009650
8	lnc-CLEC2D-6	chr12:9500409-9501023	NONHSAT026706
9	lnc-CLEC2D-5	chr12:9504271-9504480	XLOC_009651
10	lnc-PZP-10	chr12:9502714-9503413	NONHSAT026583
11	lnc-CLEC2D-6	chr12:9499308-9499722	NONHSAT026706
12	lnc-PZP-10	chr12:9500060-9500507	NONHSAT026583
13	lnc-PZP-10	chr12:9499320-9499524	NONHSAT026583

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: 594 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:594 , 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	rs553385920	chr12:9499154-9499155	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs201450758	chr12:9499175-9499176	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35207429	chr12:9499176-9499177	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200896241	chr12:9499177-9499178	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs397777191	chr12:9499178-9499179	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373499595	chr12:9499226-9499227	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114340189	chr12:9499266-9499267	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570891776	chr12:9499351-9499352	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs539820177	chr12:9499355-9499356	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs181192545	chr12:9499390-9499391	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs3954124	chr12:9499513-9499514	Weak transcription Enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs576688974	chr12:9499570-9499571	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs185302551	chr12:9499585-9499586	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs188601373	chr12:9499634-9499635	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs535734440	chr12:9499672-9499673	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs180737946	chr12:9499773-9499774	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555931481	chr12:9499791-9499792	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200003682	chr12:9499797-9499798	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186064470	chr12:9499802-9499803	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192211456	chr12:9499823-9499824	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4882990	chr12:9499841-9499842	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs184049081	chr12:9499877-9499878	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56994845	chr12:9499881-9499882	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs117632161	chr12:9499952-9499953	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116880083	chr12:9500038-9500039	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186947517	chr12:9500046-9500047	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141565955	chr12:9500051-9500052	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77499855	chr12:9500070-9500071	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs200591574	chr12:9500161-9500162	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs370105486	chr12:9500255-9500256	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs76230046	chr12:9500283-9500284	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs190446689	chr12:9500315-9500316	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs145372492	chr12:9500323-9500324	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs147664009	chr12:9500350-9500351	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs115874390	chr12:9500427-9500428	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs79948976	chr12:9500484-9500485	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs561902395	chr12:9500485-9500486	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs183073560	chr12:9500486-9500487	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs1991192	chr12:9500499-9500500	Strong transcription Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs547937818	chr12:9500770-9500771	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs187050429	chr12:9500914-9500915	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs78326657	chr12:9500942-9500943	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs75336702	chr12:9500976-9500977	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs114675908	chr12:9501092-9501093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376324247	chr12:9501093-9501094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116549621	chr12:9501095-9501096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112887373	chr12:9501108-9501109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368253015	chr12:9501177-9501178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559852521	chr12:9501180-9501181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569904511	chr12:9501305-9501306	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:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9490200-9504400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:9490800-9500000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:9492800-9500200	Enhancers	Primary T cells from cord blood	blood
4	chr12:9493200-9502400	Weak transcription	Fetal Muscle Trunk	muscle
5	chr12:9493400-9500400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr12:9494000-9499400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr12:9494000-9499400	Weak transcription	Osteobl	bone
8	chr12:9494000-9502600	Weak transcription	HSMM	muscle
9	chr12:9496200-9500800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr12:9497000-9499400	Weak transcription	Fetal Muscle Leg	muscle
11	chr12:9497000-9499600	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr12:9497000-9500000	Weak transcription	HepG2	liver
13	chr12:9498000-9499600	Enhancers	Primary T cells fromperipheralblood	blood
14	chr12:9498000-9500800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr12:9498200-9500000	Weak transcription	GM12878-XiMat	blood
16	chr12:9498200-9502600	Weak transcription	Dnd41	blood
17	chr12:9498400-9499400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr12:9498400-9502600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr12:9498400-9502600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:9498400-9502800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr12:9498600-9500800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr12:9498600-9500800	Enhancers	NHEK	skin
23	chr12:9498600-9505000	Strong transcription	Fetal Lung	lung
24	chr12:9498800-9500800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr12:9498800-9501000	Enhancers	HMEC	breast
26	chr12:9499000-9500600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr12:9499000-9502600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr12:9499000-9502600	Weak transcription	Fetal Thymus	thymus
29	chr12:9499000-9506000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr12:9499200-9500000	Enhancers	K562	blood
31	chr12:9499400-9499800	Enhancers	Fetal Muscle Leg	muscle
32	chr12:9499400-9500000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:9499400-9500200	Enhancers	Right Atrium	heart
34	chr12:9499400-9500400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr12:9499400-9500400	Enhancers	Osteobl	bone
36	chr12:9499600-9499800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr12:9499600-9503000	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr12:9500000-9500200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr12:9500000-9500400	Enhancers	GM12878-XiMat	blood
40	chr12:9500000-9500400	Enhancers	HepG2	liver
41	chr12:9500000-9500800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr12:9500200-9501600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:9500200-9503400	Weak transcription	Primary T cells from cord blood	blood
44	chr12:9500400-9502200	Weak transcription	HepG2	liver
45	chr12:9500400-9502400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr12:9500400-9502600	Weak transcription	Osteobl	bone
47	chr12:9500400-9502800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr12:9500600-9501000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr12:9500800-9501800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr12:9500800-9502200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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