Variant report

Variant	esv3405329
Chromosome Location	chr12:7656734-7712687
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:150)
CpG islands
(count:122)
Chromatin interactive
region (count:0)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:150 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:7665324-7665556	HepG2	liver:	n/a	n/a
2	ATF1	chr12:7708380-7708732	K562	blood:	n/a	n/a
3	BACH1	chr12:7665246-7665532	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr12:7667208-7667453	HepG2	liver:	n/a	chr12:7667346-7667357
5	CEBPB	chr12:7665279-7665520	A549	lung:	n/a	n/a
6	CEBPB	chr12:7665239-7665592	HepG2	liver:	n/a	n/a
7	CEBPB	chr12:7695458-7695696	IMR90	lung:	n/a	n/a
8	CEBPB	chr12:7672170-7672423	HepG2	liver:	n/a	chr12:7672273-7672284
9	CEBPB	chr12:7665221-7665590	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:7708182-7708891	HCT-116	colon:	n/a	chr12:7708755-7708772
11	CEBPB	chr12:7672141-7672341	IMR90	lung:	n/a	chr12:7672273-7672284
12	CEBPB	chr12:7665221-7665533	IMR90	lung:	n/a	n/a
13	CEBPB	chr12:7672163-7672360	A549	lung:	n/a	chr12:7672273-7672284
14	CEBPB	chr12:7667228-7667466	A549	lung:	n/a	chr12:7667346-7667357
15	CTCF	chr12:7688386-7688420	GM20000	blood:	n/a	n/a
16	CTCF	chr12:7673011-7673049	Lung_OC	lung:	n/a	n/a
17	CTCF	chr12:7665320-7665470	AG04449	skin:	n/a	n/a
18	CTCF	chr12:7665300-7665450	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr12:7669900-7670050	GM12866	blood:	n/a	n/a
20	CTCF	chr12:7670909-7670933	Lung_OC	lung:	n/a	n/a
21	CTCF	chr12:7671378-7671402	GM10248	blood:	n/a	n/a
22	CTCF	chr12:7699652-7699695	GM20000	blood:	n/a	n/a
23	E2F4	chr12:7676576-7676792	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr12:7665258-7665616	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr12:7708441-7708622	MCF10A-Er-Src	breast:	n/a	n/a
26	EP300	chr12:7665236-7665382	HepG2	liver:	n/a	n/a
27	FAM48A	chr12:7669384-7669534	GM12878	blood:	n/a	n/a
28	FOS	chr12:7708404-7708686	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr12:7663986-7664150	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr12:7708319-7708782	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr12:7665211-7665611	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr12:7665199-7665767	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr12:7708319-7708748	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr12:7708346-7708701	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr12:7665210-7665713	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr12:7665203-7665720	MCF10A-Er-Src	breast:	n/a	n/a
37	FOSL1	chr12:7665062-7665685	HCT-116	colon:	n/a	n/a
38	FOSL2	chr12:7665236-7665617	HepG2	liver:	n/a	chr12:7665387-7665398
39	FOSL2	chr12:7665208-7665495	SK-N-SH	brain:	n/a	chr12:7665387-7665398
40	FOSL2	chr12:7665208-7665603	A549	lung:	n/a	chr12:7665387-7665398
41	FOSL2	chr12:7665200-7665584	HepG2	liver:	n/a	chr12:7665387-7665398
42	FOSL2	chr12:7665261-7665476	A549	lung:	n/a	chr12:7665387-7665398
43	FOXA1	chr12:7662431-7662659	HepG2	liver:	n/a	n/a
44	FOXA1	chr12:7696446-7696782	HepG2	liver:	n/a	n/a
45	FOXA1	chr12:7662326-7662653	HepG2	liver:	n/a	n/a
46	FOXA1	chr12:7662422-7662764	HepG2	liver:	n/a	n/a
47	FOXA1	chr12:7662417-7662689	HepG2	liver:	n/a	n/a
48	FOXA2	chr12:7662208-7662752	A549	lung:	n/a	n/a
49	FOXA2	chr12:7662465-7662627	HepG2	liver:	n/a	n/a
50	GABPA	chr12:7656308-7656751	HL-60	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:7657479-7657529	HCT-116	colon:	n/a
2	chr12:7657396-7657446	SK-N-MC	brain:	n/a
3	chr12:7657479-7657529	HPAEpiC	pulmonary alveolar:	n/a
4	chr12:7657479-7657529	NB4	blood:	n/a
5	chr12:7657396-7657446	H1-hESC	embryonic stem cell:	embryo
6	chr12:7657479-7657529	SKMC	muscle:	n/a
7	chr12:7657396-7657446	PANC-1	pancreas:	n/a
8	chr12:7657479-7657529	AG04449	skin:	fetal
9	chr12:7657479-7657529	CMK	blood:	n/a
10	chr12:7657396-7657446	A549	lung:	n/a
11	chr12:7657479-7657529	HepG2	liver:	n/a
12	chr12:7657479-7657529	HCF	heart:	n/a
13	chr12:7657396-7657446	CMK	blood:	n/a
14	chr12:7657396-7657446	ProgFib	skin:	n/a
15	chr12:7657396-7657446	PFSK-1	brain:	n/a
16	chr12:7657479-7657529	HRPEpiC	eye:	n/a
17	chr12:7657479-7657529	Jurkat	blood:	n/a
18	chr12:7657396-7657446	MCF10A-Er-Src	breast:	n/a
19	chr12:7657479-7657529	MCF10A-Er-Src	breast:	n/a
20	chr12:7657396-7657446	MCF-7	breast:	n/a
21	chr12:7657479-7657529	Caco-2	colon:	n/a
22	chr12:7657479-7657529	SAEC	small airway:	n/a
23	chr12:7657479-7657529	BE2_C	brain:	n/a
24	chr12:7657396-7657446	RPTEC	kidney:	n/a
25	chr12:7657396-7657446	HL-60	blood:	n/a
26	chr12:7657479-7657529	GM12892	blood:	n/a
27	chr12:7657479-7657529	Hepatocyte	liver:	n/a
28	chr12:7657396-7657446	HMEC	breast:	n/a
29	chr12:7657479-7657529	HIPEpiC	eye:	n/a
30	chr12:7657396-7657446	SK-N-SH_RA	brain:	n/a
31	chr12:7657396-7657446	HAEpiC	amniotic membrane:	n/a
32	chr12:7657396-7657446	SK-N-SH	brain:	n/a
33	chr12:7657479-7657529	LNCaP	prostate:	n/a
34	chr12:7657479-7657529	GM12878	blood:	n/a
35	chr12:7657396-7657446	U87	brain:	n/a
36	chr12:7657396-7657446	BJ	skin:	n/a
37	chr12:7657396-7657446	ovcar-3	ovarian:	n/a
38	chr12:7657479-7657529	MCF-7	breast:	n/a
39	chr12:7657396-7657446	HRCEpiC	kidney:	n/a
40	chr12:7657396-7657446	NHDF-neo	bronchial:	n/a
41	chr12:7657396-7657446	AoSMC	blood vessel:	n/a
42	chr12:7657479-7657529	HMEC	breast:	n/a
43	chr12:7657396-7657446	LNCaP	prostate:	n/a
44	chr12:7657396-7657446	K562	blood:	n/a
45	chr12:7657396-7657446	HCT-116	colon:	n/a
46	chr12:7657479-7657529	K562	blood:	n/a
47	chr12:7657396-7657446	Hepatocyte	liver:	n/a
48	chr12:7657396-7657446	T-47D	breast:	n/a
49	chr12:7657479-7657529	NT2-D1	testis:	n/a
50	chr12:7657396-7657446	ECC-1	luminal epithelium:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPPA3-3	chr12:7707947-7708115	NONHSAT026260
2	lnc-ACSM4-4	chr12:7668781-7668856	NONHSAT026258
3	lnc-ACSM4-4	chr12:7667942-7668184	NONHSAT026258
4	lnc-DPPA3-2	chr12:7703127-7703471	NONHSAT026261
5	lnc-DPPA3-3	chr12:7702815-7702958	NONHSAT026260
6	lnc-ACSM4-5	chr12:7670415-7670900	NONHSAT026259
7	lnc-DPPA3-2	chr12:7708132-7708164	NONHSAT026261
8	lnc-ACSM4-5	chr12:7669251-7670028	NONHSAT026259

No data

Variant related genes	Relation type
CD163	TF binding region
CD163	CpG island

Extended variants
information (count: 561 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:561 , 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	rs189256013	chr12:7656759-7656760	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs181915361	chr12:7656769-7656770	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs11054195	chr12:7656849-7656850	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs79166970	chr12:7656858-7656859	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs139178848	chr12:7656860-7656861	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs10772428	chr12:7656902-7656903	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs75608120	chr12:7656997-7656998	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs554000332	chr12:7657074-7657075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs28364798	chr12:7657121-7657122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185750464	chr12:7657141-7657142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373078894	chr12:7657213-7657214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188949472	chr12:7657220-7657221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544833173	chr12:7657271-7657272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546508718	chr12:7657283-7657284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11054197	chr12:7657322-7657323	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs74056494	chr12:7657396-7657397	Enhancers Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs79302630	chr12:7657399-7657400	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs181125459	chr12:7657403-7657404	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs10845306	chr12:7657427-7657428	Enhancers Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs572146632	chr12:7657430-7657431	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs374131366	chr12:7657431-7657432	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs376174761	chr12:7657479-7657480	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs141702097	chr12:7657518-7657519	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs7301572	chr12:7657543-7657544	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs186538286	chr12:7657592-7657593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191296998	chr12:7657667-7657668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112952776	chr12:7657707-7657708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182774688	chr12:7657709-7657710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374466463	chr12:7657710-7657711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185379464	chr12:7657713-7657714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190930904	chr12:7657726-7657727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183388725	chr12:7657757-7657758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530304312	chr12:7657999-7658000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187391472	chr12:7658002-7658003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193108437	chr12:7658082-7658083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183620602	chr12:7658088-7658089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539211383	chr12:7658136-7658137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150507900	chr12:7658222-7658223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188165623	chr12:7658225-7658226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9669287	chr12:7658277-7658278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9669288	chr12:7658289-7658290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9667992	chr12:7658295-7658296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556636892	chr12:7658372-7658373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12828625	chr12:7658388-7658389	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs183499270	chr12:7658477-7658478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139633441	chr12:7658482-7658483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188234807	chr12:7658485-7658486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11054199	chr12:7658577-7658578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs367873467	chr12:7658581-7658582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9668124	chr12:7658645-7658646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21364760	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	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Medullary thyroid carcinoma	18765511	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:7650600-7657000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
2	chr12:7655600-7657400	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr12:7656200-7657200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:7656200-7658000	Weak transcription	Liver	Liver
5	chr12:7656400-7657600	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr12:7657000-7657400	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr12:7657400-7663400	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr12:7657600-7662600	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr12:7659200-7662000	Weak transcription	Liver	Liver
10	chr12:7662000-7662600	Enhancers	Liver	Liver
11	chr12:7662600-7663000	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
12	chr12:7662600-7663600	Weak transcription	Liver	Liver
13	chr12:7663000-7663600	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr12:7663400-7666200	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr12:7663400-7666400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:7663600-7664000	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr12:7663600-7665600	Enhancers	Liver	Liver
18	chr12:7664000-7665000	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr12:7664600-7665400	Enhancers	HepG2	liver
20	chr12:7664800-7665800	Enhancers	NHDF-Ad	bronchial
21	chr12:7664800-7666000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:7665000-7665600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr12:7665000-7665600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr12:7665000-7665800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr12:7665000-7666200	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr12:7665200-7665600	Enhancers	Placenta	Placenta
27	chr12:7679600-7680600	ZNF genes & repeats	Liver	Liver
28	chr12:7680200-7680400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr12:7690000-7691200	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr12:7690000-7691400	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr12:7691200-7694000	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr12:7691400-7694000	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr12:7693400-7694200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr12:7694000-7694200	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr12:7694000-7697400	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr12:7694200-7694400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr12:7694200-7694800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr12:7694200-7695200	Enhancers	Fetal Muscle Leg	muscle
39	chr12:7694200-7696600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr12:7694200-7696800	Enhancers	Placenta	Placenta
41	chr12:7694400-7695000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr12:7694400-7695200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:7694600-7695000	Enhancers	Primary B cells from cord blood	blood
44	chr12:7694600-7696600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:7694800-7695000	Active TSS	Osteobl	bone
46	chr12:7694800-7695200	Enhancers	NHDF-Ad	bronchial
47	chr12:7694800-7695600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr12:7694800-7695800	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr12:7694800-7696600	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr12:7695000-7695200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links