Variant report

Variant	esv3584654
Chromosome Location	chr12:11433876-11523026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:254)
CpG islands
(count:488)
Chromatin interactive
region (count:2)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:11501400-11501725	K562	blood:	n/a	n/a
2	BCL3	chr12:11501361-11501642	GM12878	blood:	n/a	n/a
3	BCL3	chr12:11501365-11501771	GM12878	blood:	n/a	n/a
4	CEBPB	chr12:11514261-11514433	Hela-S3	cervix:	n/a	chr12:11514316-11514325
5	CEBPB	chr12:11458075-11458297	HepG2	liver:	n/a	chr12:11458153-11458164
6	CEBPB	chr12:11478711-11479007	HepG2	liver:	n/a	chr12:11478828-11478841 chr12:11478830-11478839 chr12:11478828-11478839 chr12:11478829-11478840
7	CEBPB	chr12:11457994-11458258	A549	lung:	n/a	chr12:11458153-11458164
8	CREB1	chr12:11501341-11501827	HepG2	liver:	n/a	n/a
9	CREB1	chr12:11501439-11501709	A549	lung:	n/a	n/a
10	CREB1	chr12:11501156-11501972	K562	blood:	n/a	n/a
11	CREB1	chr12:11501322-11501785	K562	blood:	n/a	n/a
12	CREB1	chr12:11501275-11501755	HepG2	liver:	n/a	n/a
13	CTCF	chr12:11505990-11506144	K562	blood:	n/a	n/a
14	CTCF	chr12:11500840-11500990	AG04450	lung:	n/a	n/a
15	CTCF	chr12:11501300-11501450	SAEC	small airway:	n/a	n/a
16	CTCF	chr12:11500891-11501001	LNCaP	prostate:	n/a	n/a
17	CTCF	chr12:11500907-11500926	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:11500800-11500950	GM12874	blood:	n/a	n/a
19	CTCF	chr12:11506052-11506137	MCF-7	breast:	n/a	n/a
20	CTCF	chr12:11500900-11501050	RPTEC	kidney:	n/a	n/a
21	CTCF	chr12:11500800-11500950	GM12873	blood:	n/a	n/a
22	CTCF	chr12:11500858-11500979	MCF-7	breast:	n/a	n/a
23	CTCF	chr12:11505592-11505641	GM20000	blood:	n/a	n/a
24	CTCF	chr12:11500920-11501070	GM12872	blood:	n/a	n/a
25	CTCF	chr12:11500780-11500930	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:11500840-11500990	HPF	lung:	n/a	n/a
27	CTCF	chr12:11500766-11501020	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:11501680-11501830	GM12866	blood:	n/a	n/a
29	CTCF	chr12:11500860-11501010	GM12873	blood:	n/a	n/a
30	CTCF	chr12:11500780-11500930	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr12:11500780-11500930	Caco-2	colon:	n/a	n/a
32	CTCF	chr12:11500689-11501045	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr12:11500860-11501010	HCFaa	heart:	n/a	n/a
34	CTCF	chr12:11501587-11501601	A549	lung:	n/a	n/a
35	CTCF	chr12:11500860-11501010	GM12872	blood:	n/a	n/a
36	CTCF	chr12:11505978-11506004	Lung_OC	lung:	n/a	n/a
37	CTCF	chr12:11500880-11501030	HVMF	connective:	n/a	n/a
38	CTCF	chr12:11500860-11501010	HEK293	kidney:	n/a	n/a
39	CTCF	chr12:11500800-11500950	GM12871	blood:	n/a	n/a
40	CTCF	chr12:11500793-11501045	HepG2	liver:	n/a	n/a
41	CTCF	chr12:11492997-11493057	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr12:11500840-11500990	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr12:11506136-11506201	GM20000	blood:	n/a	n/a
44	CTCF	chr12:11500840-11500990	GM12878	blood:	n/a	n/a
45	CTCF	chr12:11501600-11501750	HEK293	kidney:	n/a	n/a
46	CTCF	chr12:11500840-11500990	HL-60	blood:	n/a	n/a
47	CTCF	chr12:11500840-11500990	NHEK	skin:	n/a	n/a
48	CTCF	chr12:11500873-11500995	K562	blood:	n/a	n/a
49	CTCF	chr12:11500920-11501070	AG04450	lung:	n/a	n/a
50	CTCF	chr12:11500820-11500970	GM12801	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11509583-11509633	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:11460710-11460760	HCPEpiC	choroid plexus:	n/a
3	chr12:11463937-11463987	SKMC	muscle:	n/a
4	chr12:11509583-11509633	Jurkat	blood:	n/a
5	chr12:11463937-11463987	BJ	skin:	n/a
6	chr12:11464607-11464657	PFSK-1	brain:	n/a
7	chr12:11508049-11508099	CMK	blood:	n/a
8	chr12:11463379-11463429	IMR90	lung:	fetal
9	chr12:11464607-11464657	HCT-116	colon:	n/a
10	chr12:11508049-11508099	MCF10A-Er-Src	breast:	n/a
11	chr12:11508049-11508099	AG09319	gingival:	n/a
12	chr12:11461798-11461848	GM12891	blood:	n/a
13	chr12:11463379-11463429	HCF	heart:	n/a
14	chr12:11508049-11508099	HRPEpiC	eye:	n/a
15	chr12:11460710-11460760	GM06990	blood:	n/a
16	chr12:11463844-11463894	PrEC	prostate:	n/a
17	chr12:11461798-11461848	GM19239	blood:	n/a
18	chr12:11461798-11461848	HCT-116	colon:	n/a
19	chr12:11463379-11463429	Hepatocyte	liver:	n/a
20	chr12:11464607-11464657	SK-N-SH	brain:	n/a
21	chr12:11460710-11460760	SKMC	muscle:	n/a
22	chr12:11461798-11461848	HepG2	liver:	n/a
23	chr12:11463379-11463429	HEEpiC	esophagus:	n/a
24	chr12:11464607-11464657	BJ	skin:	n/a
25	chr12:11464607-11464657	A549	lung:	n/a
26	chr12:11463379-11463429	Caco-2	colon:	n/a
27	chr12:11508049-11508099	U87	brain:	n/a
28	chr12:11464607-11464657	GM12878	blood:	n/a
29	chr12:11461798-11461848	PANC-1	pancreas:	n/a
30	chr12:11508049-11508099	GM12878	blood:	n/a
31	chr12:11463937-11463987	Jurkat	blood:	n/a
32	chr12:11509583-11509633	HRCEpiC	kidney:	n/a
33	chr12:11508049-11508099	HAEpiC	amniotic membrane:	n/a
34	chr12:11508049-11508099	PrEC	prostate:	n/a
35	chr12:11461798-11461848	AG09309	skin:	n/a
36	chr12:11508049-11508099	Jurkat	blood:	n/a
37	chr12:11509583-11509633	Hepatocyte	liver:	n/a
38	chr12:11463937-11463987	HNPCEpiC	eye:	n/a
39	chr12:11463937-11463987	GM12892	blood:	n/a
40	chr12:11464607-11464657	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:11464607-11464657	AG09319	gingival:	n/a
42	chr12:11464607-11464657	HepG2	liver:	n/a
43	chr12:11464607-11464657	LNCaP	prostate:	n/a
44	chr12:11508049-11508099	ECC-1	luminal epithelium:	n/a
45	chr12:11463379-11463429	HRCEpiC	kidney:	n/a
46	chr12:11464607-11464657	GM19239	blood:	n/a
47	chr12:11464607-11464657	U87	brain:	n/a
48	chr12:11460710-11460760	Hela-S3	cervix:	n/a
49	chr12:11460710-11460760	PANC-1	pancreas:	n/a
50	chr12:11461798-11461848	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11494392..11497234-chr12:11500928..11503308,2	K562	blood:
2	chr12:11494392..11497234-chr12:11500928..11503308,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRB4-1	chr12:11461584-11461816	NONHSAT026935
2	lnc-PRB4-1	chr12:11462305-11462339	NONHSAT026935
3	lnc-PRB4-1	chr12:11463270-11463369	NONHSAT026935
4	lnc-PRB4-1	chr12:11461162-11461375	NONHSAT026935

No data

Variant related genes	Relation type
PRB4	TF binding region
PRB1	TF binding region
PRB4	CpG island
PRB1	CpG island

Extended variants
information (count: 3017 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:3017 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370942027	chr12:11433889-11433890	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs145586433	chr12:11433907-11433908	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs148892444	chr12:11433926-11433927	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs553268745	chr12:11433937-11433938	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs546208612	chr12:11433984-11433985	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs573320193	chr12:11433985-11433986	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs535592321	chr12:11434011-11434012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555800278	chr12:11434038-11434039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575551324	chr12:11434049-11434050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562828415	chr12:11434054-11434055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538762042	chr12:11434056-11434057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143604665	chr12:11434106-11434107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147555187	chr12:11434112-11434113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540464079	chr12:11434113-11434114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560077249	chr12:11434118-11434119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529051364	chr12:11434136-11434137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141977740	chr12:11434172-11434173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199870610	chr12:11434216-11434217	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs111382824	chr12:11434225-11434226	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs562557797	chr12:11434242-11434243	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs113095186	chr12:11434250-11434251	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs3984946	chr12:11434258-11434259	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs560706104	chr12:11434261-11434262	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs570836241	chr12:11434300-11434301	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs368821117	chr12:11434354-11434355	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs138711610	chr12:11434384-11434385	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs183193134	chr12:11434418-11434419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566971576	chr12:11434444-11434445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535996301	chr12:11434475-11434476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555586870	chr12:11434500-11434501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141230985	chr12:11434522-11434523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371190062	chr12:11434580-11434581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538291385	chr12:11434597-11434598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187522781	chr12:11434598-11434599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377390097	chr12:11434650-11434651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs578027195	chr12:11434700-11434701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150444389	chr12:11434707-11434708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567680050	chr12:11434789-11434790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560367255	chr12:11434791-11434792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370386525	chr12:11434825-11434826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116797235	chr12:11434834-11434835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367958323	chr12:11434863-11434864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542767026	chr12:11434893-11434894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562486270	chr12:11434896-11434897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546459842	chr12:11434919-11434920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531283873	chr12:11434927-11434928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138272366	chr12:11434941-11434942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564555075	chr12:11434943-11434944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527265215	chr12:11434998-11434999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566785575	chr12:11435008-11435009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	17237825	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	22522925	CNVD
Mental retardation	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	20531469	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11407400-11440200	Weak transcription	Primary T cells from cord blood	blood
2	chr12:11433400-11434000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:11433400-11434200	Strong transcription	Adipose Nuclei	Adipose
4	chr12:11433800-11434000	ZNF genes & repeats	Liver	Liver
5	chr12:11434200-11434400	ZNF genes & repeats	Adipose Nuclei	Adipose
6	chr12:11449800-11450600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
7	chr12:11450200-11450600	Enhancers	Stomach Mucosa	stomach
8	chr12:11450200-11450800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
9	chr12:11450200-11450800	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr12:11450200-11450800	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr12:11450200-11450800	Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr12:11450400-11450800	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr12:11450400-11450800	Active TSS	Rectal Mucosa Donor 31	rectum
14	chr12:11460200-11460800	Enhancers	HUVEC	blood vessel
15	chr12:11461200-11462200	Enhancers	Spleen	Spleen
16	chr12:11467000-11467200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:11473600-11475800	Enhancers	Fetal Heart	heart
18	chr12:11474600-11475000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:11475400-11478200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr12:11478200-11479200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr12:11478800-11479400	Enhancers	HMEC	breast
22	chr12:11479000-11479200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr12:11479200-11480200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr12:11479200-11493000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr12:11486800-11487000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr12:11493000-11493200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr12:11493000-11493400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:11493000-11494200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:11494200-11496400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:11496600-11496800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:11496800-11499400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:11497200-11497800	Enhancers	HepG2	liver
33	chr12:11497800-11498600	Enhancers	Fetal Intestine Small	intestine
34	chr12:11498200-11498600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr12:11504000-11505000	Enhancers	HUVEC	blood vessel
36	chr12:11505000-11510400	Weak transcription	HUVEC	blood vessel
37	chr12:11506600-11507000	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr12:11510000-11511000	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr12:11510000-11511200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr12:11510400-11511000	Enhancers	HUVEC	blood vessel
41	chr12:11511000-11512400	Weak transcription	HUVEC	blood vessel
42	chr12:11511200-11519600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr12:11512400-11514000	Enhancers	HUVEC	blood vessel
44	chr12:11513000-11513800	Enhancers	HMEC	breast
45	chr12:11513000-11514000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr12:11513000-11514000	Enhancers	NHEK	skin
47	chr12:11513400-11513600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr12:11513600-11514200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr12:11513600-11521200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:11516600-11517000	Enhancers	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links