Variant report

Variant	nsv536762
Chromosome Location	chr3:146671616-146900202
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:524)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr3:146685849-146686581	HCT-116	colon:	n/a	n/a
2	CBX3	chr3:146752227-146752413	K562	blood:	n/a	n/a
3	CBX3	chr3:146752123-146752575	HCT-116	colon:	n/a	n/a
4	CBX3	chr3:146685751-146686637	HCT-116	colon:	n/a	n/a
5	CBX3	chr3:146752237-146752423	K562	blood:	n/a	n/a
6	CEBPB	chr3:146723680-146723890	HepG2	liver:	n/a	chr3:146723818-146723829
7	CEBPB	chr3:146848265-146848581	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr3:146768098-146768323	A549	lung:	n/a	chr3:146768228-146768239
9	CEBPB	chr3:146694613-146694842	HepG2	liver:	n/a	chr3:146694708-146694719 chr3:146694708-146694721
10	CEBPB	chr3:146805457-146805698	HepG2	liver:	n/a	chr3:146805474-146805487 chr3:146805476-146805487
11	CEBPB	chr3:146715450-146715793	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:146723668-146723949	IMR90	lung:	n/a	chr3:146723818-146723829
13	CEBPB	chr3:146768067-146768370	IMR90	lung:	n/a	chr3:146768228-146768239
14	CEBPB	chr3:146685602-146686183	IMR90	lung:	n/a	n/a
15	CEBPB	chr3:146768077-146768388	HepG2	liver:	n/a	chr3:146768228-146768239
16	CEBPB	chr3:146780117-146780277	A549	lung:	n/a	n/a
17	CEBPB	chr3:146686339-146686461	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr3:146687179-146687451	IMR90	lung:	n/a	n/a
19	CEBPB	chr3:146685570-146686464	HCT-116	colon:	n/a	n/a
20	CEBPB	chr3:146685262-146686134	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:146835463-146835774	MCF-7	breast:	n/a	n/a
22	CEBPB	chr3:146805441-146805642	K562	blood:	n/a	chr3:146805474-146805487 chr3:146805476-146805487
23	CEBPB	chr3:146687962-146688145	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:146685521-146686346	HCT-116	colon:	n/a	n/a
25	CTCF	chr3:146838120-146838270	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr3:146837820-146838218	IMR90	lung:	n/a	chr3:146838011-146838032
27	CTCF	chr3:146847310-146847394	GM13977	blood:	n/a	n/a
28	CTCF	chr3:146837798-146838236	HepG2	liver:	n/a	chr3:146838011-146838032
29	CTCF	chr3:146837940-146838090	AG09309	skin:	n/a	chr3:146838011-146838032
30	CTCF	chr3:146837940-146838090	AG10803	skin:	n/a	chr3:146838011-146838032
31	CTCF	chr3:146838012-146838044	GM13977	blood:	n/a	n/a
32	CTCF	chr3:146837900-146838050	HepG2	liver:	n/a	chr3:146838011-146838032
33	CTCF	chr3:146878840-146878990	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:146837949-146838106	MCF-7	breast:	n/a	chr3:146838011-146838032
35	CTCF	chr3:146887476-146887481	GM13977	blood:	n/a	n/a
36	CTCF	chr3:146744623-146744858	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr3:146744660-146744810	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr3:146837928-146838111	LNCaP	prostate:	n/a	chr3:146838011-146838032
39	CTCF	chr3:146837960-146838110	HPAF	blood vessel:	n/a	chr3:146838011-146838032
40	CTCF	chr3:146718231-146718297	GM13976	blood:	n/a	n/a
41	CTCF	chr3:146838240-146838390	BJ	skin:	n/a	n/a
42	CTCF	chr3:146847317-146847387	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr3:146679757-146679825	Lung_OC	lung:	n/a	n/a
44	CTCF	chr3:146847348-146847365	GM19240	blood:	n/a	n/a
45	CTCF	chr3:146852245-146852287	GM13976	blood:	n/a	n/a
46	CTCF	chr3:146838100-146838250	HAc	cerebellar:	n/a	n/a
47	CTCF	chr3:146837964-146838059	SK-N-SH_RA	brain:	n/a	chr3:146838011-146838032
48	CTCF	chr3:146837940-146838090	AG04449	skin:	n/a	chr3:146838011-146838032
49	CTCF	chr3:146881239-146881303	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr3:146879723-146879802	GM20000	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:146756728-146756778	AG09319	gingival:	n/a
2	chr3:146756728-146756778	LNCaP	prostate:	n/a
3	chr3:146756728-146756778	T-47D	breast:	n/a
4	chr3:146756728-146756778	NHDF-neo	bronchial:	n/a
5	chr3:146756728-146756778	ECC-1	luminal epithelium:	n/a
6	chr3:146756728-146756778	SK-N-SH	brain:	n/a
7	chr3:146756728-146756778	RPTEC	kidney:	n/a
8	chr3:146756728-146756778	PrEC	prostate:	n/a
9	chr3:146756728-146756778	HL-60	blood:	n/a
10	chr3:146756728-146756778	SKMC	muscle:	n/a
11	chr3:146756728-146756778	BJ	skin:	n/a
12	chr3:146756728-146756778	Jurkat	blood:	n/a
13	chr3:146756728-146756778	Hela-S3	cervix:	n/a
14	chr3:146756728-146756778	ProgFib	skin:	n/a
15	chr3:146756728-146756778	PFSK-1	brain:	n/a
16	chr3:146756728-146756778	AoSMC	blood vessel:	n/a
17	chr3:146756728-146756778	AG04450	lung:	fetal
18	chr3:146756728-146756778	H1-hESC	embryonic stem cell:	embryo
19	chr3:146756728-146756778	U87	brain:	n/a
20	chr3:146756728-146756778	AG04449	skin:	fetal
21	chr3:146756728-146756778	HRPEpiC	eye:	n/a
22	chr3:146756728-146756778	Hepatocyte	liver:	n/a
23	chr3:146756728-146756778	NH-A	brain:	n/a
24	chr3:146756728-146756778	HCM	heart:	n/a
25	chr3:146756728-146756778	PANC-1	pancreas:	n/a
26	chr3:146756728-146756778	CMK	blood:	n/a
27	chr3:146756728-146756778	NHBE	bronchial:	n/a
28	chr3:146756728-146756778	HepG2	liver:	n/a
29	chr3:146756728-146756778	HIPEpiC	eye:	n/a
30	chr3:146756728-146756778	HCT-116	colon:	n/a
31	chr3:146756728-146756778	AG09309	skin:	n/a
32	chr3:146756728-146756778	MCF-7	breast:	n/a
33	chr3:146756728-146756778	K562	blood:	n/a
34	chr3:146756728-146756778	GM12878	blood:	n/a
35	chr3:146756728-146756778	HMEC	breast:	n/a
36	chr3:146756728-146756778	AG10803	skin:	n/a
37	chr3:146756728-146756778	NT2-D1	testis:	n/a
38	chr3:146756728-146756778	HRCEpiC	kidney:	n/a
39	chr3:146756728-146756778	HRE	kidney:	n/a
40	chr3:146756728-146756778	ovcar-3	ovarian:	n/a
41	chr3:146756728-146756778	A549	lung:	n/a
42	chr3:146756728-146756778	HCPEpiC	choroid plexus:	n/a
43	chr3:146756728-146756778	HEEpiC	esophagus:	n/a
44	chr3:146756728-146756778	IMR90	lung:	fetal
45	chr3:146756728-146756778	HPAEpiC	pulmonary alveolar:	n/a
46	chr3:146756728-146756778	NB4	blood:	n/a
47	chr3:146756728-146756778	GM12891	blood:	n/a
48	chr3:146756728-146756778	HCF	heart:	n/a
49	chr3:146756728-146756778	Caco-2	colon:	n/a
50	chr3:146756728-146756778	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:146724156..146724656-chr7:158811116..158812074,2	MCF-7	breast:
2	chr3:146698311..146701060-chr3:146701293..146703528,2	MCF-7	breast:
3	chr3:146714192..146714735-chr3:146728166..146728967,2	MCF-7	breast:
4	chr3:146715446..146717460-chr3:146722255..146724620,2	K562	blood:
5	chr3:146837603..146838491-chr3:146909373..146910222,2	MCF-7	breast:
6	chr3:146698311..146701060-chr3:146701293..146703528,2	MCF-7	breast:
7	chr3:146715446..146717460-chr3:146722255..146724620,2	K562	blood:
8	chr3:146862726..146863568-chr7:549720..550401,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZIC4-5	chr3:146760793-146761118	NONHSAT092573
2	lnc-ZIC4-5	chr3:146761390-146761517	NONHSAT092573
3	lnc-ZIC4-3	chr3:146874252-146874348	ENSG00000243620.1

No data

Variant related genes	Relation type
RNU6-505P	TF binding region
ENSG00000251800	TF binding region
RNU6-505P	CpG island
ENSG00000251800	CpG island
ENSG00000207156	chromatin interactions

Extended variants
information (count: 3133 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3133 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540984935	chr3:146671643-146671644	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs543165023	chr3:146671655-146671656	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs558106570	chr3:146671678-146671679	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs555172340	chr3:146671715-146671716	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs543472838	chr3:146671717-146671718	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs563482981	chr3:146671761-146671762	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs529443865	chr3:146671762-146671763	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs543239898	chr3:146671763-146671764	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs191053218	chr3:146671782-146671783	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs528754407	chr3:146671789-146671790	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs551789523	chr3:146671814-146671815	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570385232	chr3:146671846-146671847	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182130577	chr3:146671864-146671865	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573447676	chr3:146671908-146671909	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376858289	chr3:146671915-146671916	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371572163	chr3:146671943-146671944	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77695484	chr3:146671986-146671987	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540714881	chr3:146671989-146671990	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186765181	chr3:146671990-146671991	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555507423	chr3:146672016-146672017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs199985017	chr3:146672035-146672036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148202110	chr3:146672048-146672049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192598571	chr3:146672059-146672060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374183205	chr3:146672080-146672081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199863551	chr3:146672127-146672128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371345102	chr3:146672131-146672132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79205883	chr3:146672132-146672133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201018228	chr3:146672164-146672165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs58730662	chr3:146672166-146672167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150810030	chr3:146672190-146672191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372917440	chr3:146672201-146672202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112170772	chr3:146672282-146672283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188708518	chr3:146672306-146672307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192842842	chr3:146672330-146672331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139141281	chr3:146672358-146672359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542775705	chr3:146672386-146672387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559850975	chr3:146672422-146672423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142574059	chr3:146672446-146672447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184893934	chr3:146672447-146672448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146078642	chr3:146672454-146672455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563567502	chr3:146672463-146672464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189407906	chr3:146672466-146672467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549839039	chr3:146672469-146672470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555921250	chr3:146672502-146672503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141562352	chr3:146672518-146672519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563290464	chr3:146672630-146672631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76212396	chr3:146672714-146672715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548810395	chr3:146672716-146672717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13094317	chr3:146672734-146672735	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs534555674	chr3:146672739-146672740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autism	21956041	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146671200-146671800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:146671200-146671800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:146671200-146671800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:146671200-146671800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:146671200-146671800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr3:146671200-146671800	Enhancers	Fetal Brain Male	brain
7	chr3:146671200-146671800	Enhancers	NHDF-Ad	bronchial
8	chr3:146671200-146672000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr3:146671200-146672000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr3:146671200-146672000	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr3:146671200-146672200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr3:146671400-146672000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:146671400-146672000	Enhancers	Fetal Lung	lung
14	chr3:146671400-146672200	Enhancers	Osteobl	bone
15	chr3:146671600-146671800	Flanking Active TSS	NH-A	brain
16	chr3:146671800-146672000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr3:146671800-146672000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:146671800-146672200	Enhancers	NH-A	brain
19	chr3:146671800-146674400	Weak transcription	Fetal Brain Male	brain
20	chr3:146671800-146684800	Weak transcription	NHDF-Ad	bronchial
21	chr3:146672000-146672200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:146672000-146675800	Weak transcription	Fetal Lung	lung
23	chr3:146674400-146674800	Enhancers	Fetal Brain Male	brain
24	chr3:146675800-146676000	Enhancers	Fetal Lung	lung
25	chr3:146684000-146684200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr3:146684000-146685600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr3:146684400-146685400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr3:146684400-146687200	Enhancers	Hela-S3	cervix
29	chr3:146684600-146685800	Enhancers	Osteobl	bone
30	chr3:146684600-146687600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr3:146684800-146685400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr3:146684800-146685800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr3:146684800-146685800	Enhancers	NHDF-Ad	bronchial
34	chr3:146684800-146686000	Enhancers	NHLF	lung
35	chr3:146684800-146686200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr3:146684800-146686200	Enhancers	HSMMtube	muscle
37	chr3:146684800-146686600	Enhancers	HSMM	muscle
38	chr3:146685000-146685800	Enhancers	NH-A	brain
39	chr3:146685000-146687800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr3:146685000-146688200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr3:146685400-146685600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr3:146685400-146685800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr3:146685400-146686000	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr3:146685600-146686000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:146685600-146686000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr3:146685600-146686200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr3:146685600-146686600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr3:146685600-146686600	Enhancers	HMEC	breast
49	chr3:146685600-146686800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr3:146685600-146686800	Enhancers	HUVEC	blood vessel

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