Variant report

Variant	nsv683
Chromosome Location	chr12:40951473-40996258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:179)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:179 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:40955261-40955752	GM12878	blood:	n/a	n/a
2	ATF2	chr12:40953538-40954231	GM12878	blood:	n/a	n/a
3	ATF2	chr12:40953520-40954269	GM12878	blood:	n/a	n/a
4	ATF2	chr12:40954996-40955723	GM12878	blood:	n/a	n/a
5	BCL3	chr12:40953531-40954178	GM12878	blood:	n/a	n/a
6	BCL3	chr12:40953675-40954068	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:40955455-40955598	GM12878	blood:	n/a	n/a
8	CEBPB	chr12:40977595-40977950	IMR90	lung:	n/a	chr12:40977774-40977785
9	CEBPB	chr12:40969826-40970115	HepG2	liver:	n/a	chr12:40970015-40970026 chr12:40969981-40969992
10	CEBPB	chr12:40977615-40977929	K562	blood:	n/a	chr12:40977774-40977785
11	CEBPB	chr12:40977598-40977943	A549	lung:	n/a	chr12:40977774-40977785
12	CEBPB	chr12:40954576-40954630	K562	blood:	n/a	n/a
13	CEBPB	chr12:40969858-40970163	A549	lung:	n/a	chr12:40970015-40970026 chr12:40969981-40969992
14	CEBPB	chr12:40971941-40972115	HepG2	liver:	n/a	chr12:40971944-40971956
15	CEBPB	chr12:40969835-40970109	IMR90	lung:	n/a	chr12:40970015-40970026 chr12:40969981-40969992
16	CEBPB	chr12:40977556-40977925	HepG2	liver:	n/a	chr12:40977774-40977785
17	CHD1	chr12:40955462-40955553	GM12878	blood:	n/a	n/a
18	CHD2	chr12:40955581-40955594	GM12878	blood:	n/a	n/a
19	CTCF	chr12:40959140-40959290	HMEC	breast:	n/a	chr12:40959238-40959247 chr12:40959235-40959245
20	CTCF	chr12:40959060-40959210	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr12:40986780-40986818	Lung_OC	lung:	n/a	n/a
22	CTCF	chr12:40959140-40959290	GM06990	blood:	n/a	chr12:40959238-40959247 chr12:40959235-40959245
23	CTCF	chr12:40959180-40959330	HCT-116	colon:	n/a	chr12:40959238-40959247 chr12:40959235-40959245
24	CTCF	chr12:40959380-40959530	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr12:40959220-40959370	GM12873	blood:	n/a	chr12:40959238-40959247 chr12:40959235-40959245
26	CTCF	chr12:40959140-40959290	Caco-2	colon:	n/a	chr12:40959238-40959247 chr12:40959235-40959245
27	CTCF	chr12:40959260-40959410	RPTEC	kidney:	n/a	n/a
28	CTCF	chr12:40977678-40977736	GM12878	blood:	n/a	n/a
29	CTCF	chr12:40952780-40952930	GM12871	blood:	n/a	n/a
30	CTCF	chr12:40952700-40952850	GM12873	blood:	n/a	n/a
31	CTCF	chr12:40977523-40977822	GM12878	blood:	n/a	n/a
32	CTCF	chr12:40952780-40952930	GM12873	blood:	n/a	n/a
33	CTCF	chr12:40959280-40959430	BE2_C	brain:	n/a	n/a
34	CTCF	chr12:40959200-40959350	A549	lung:	n/a	chr12:40959238-40959247 chr12:40959235-40959245
35	CTCF	chr12:40952840-40952990	GM12878	blood:	n/a	n/a
36	CTCF	chr12:40952720-40952870	GM12874	blood:	n/a	n/a
37	CTCF	chr12:40959100-40959250	BE2_C	brain:	n/a	chr12:40959238-40959247 chr12:40959235-40959245
38	CTCF	chr12:40959120-40959270	MCF-7	breast:	n/a	chr12:40959238-40959247 chr12:40959235-40959245
39	CTCF	chr12:40977600-40977750	HMEC	breast:	n/a	n/a
40	CTCF	chr12:40959260-40959410	GM12872	blood:	n/a	n/a
41	CTCF	chr12:40959340-40959490	GM06990	blood:	n/a	n/a
42	CTCF	chr12:40959160-40959310	HMEC	breast:	n/a	chr12:40959238-40959247 chr12:40959235-40959245
43	CUX1	chr12:40971952-40971969	K562	blood:	n/a	n/a
44	CUX1	chr12:40953638-40954081	GM12878	blood:	n/a	n/a
45	CUX1	chr12:40954844-40955067	GM12878	blood:	n/a	n/a
46	E2F4	chr12:40966028-40966056	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr12:40982223-40982245	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr12:40984493-40984502	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr12:40990119-40990244	MCF10A-Er-Src	breast:	n/a	n/a
50	EBF1	chr12:40952505-40953128	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40959011-40959061	HRCEpiC	kidney:	n/a
2	chr12:40959011-40959061	CMK	blood:	n/a
3	chr12:40959011-40959061	GM12891	blood:	n/a
4	chr12:40959011-40959061	HRPEpiC	eye:	n/a
5	chr12:40959011-40959061	SKMC	muscle:	n/a
6	chr12:40959011-40959061	Caco-2	colon:	n/a
7	chr12:40959011-40959061	GM19239	blood:	n/a
8	chr12:40959011-40959061	K562	blood:	n/a
9	chr12:40959011-40959061	IMR90	lung:	fetal
10	chr12:40959011-40959061	BJ	skin:	n/a
11	chr12:40959011-40959061	HCPEpiC	choroid plexus:	n/a
12	chr12:40959011-40959061	HAEpiC	amniotic membrane:	n/a
13	chr12:40959011-40959061	NHBE	bronchial:	n/a
14	chr12:40959011-40959061	HPAEpiC	pulmonary alveolar:	n/a
15	chr12:40959011-40959061	GM12892	blood:	n/a
16	chr12:40959011-40959061	ovcar-3	ovarian:	n/a
17	chr12:40959011-40959061	HCF	heart:	n/a
18	chr12:40959011-40959061	HNPCEpiC	eye:	n/a
19	chr12:40959011-40959061	PFSK-1	brain:	n/a
20	chr12:40959011-40959061	RPTEC	kidney:	n/a
21	chr12:40959011-40959061	NT2-D1	testis:	n/a
22	chr12:40959011-40959061	SAEC	small airway:	n/a
23	chr12:40959011-40959061	HIPEpiC	eye:	n/a
24	chr12:40959011-40959061	MCF10A-Er-Src	breast:	n/a
25	chr12:40959011-40959061	HL-60	blood:	n/a
26	chr12:40959011-40959061	NH-A	brain:	n/a
27	chr12:40959011-40959061	Hela-S3	cervix:	n/a
28	chr12:40959011-40959061	HRE	kidney:	n/a
29	chr12:40959011-40959061	NHDF-neo	bronchial:	n/a
30	chr12:40959011-40959061	AG09309	skin:	n/a
31	chr12:40959011-40959061	HCT-116	colon:	n/a
32	chr12:40959011-40959061	U87	brain:	n/a
33	chr12:40959011-40959061	PrEC	prostate:	n/a
34	chr12:40959011-40959061	MCF-7	breast:	n/a
35	chr12:40959011-40959061	HepG2	liver:	n/a
36	chr12:40959011-40959061	GM06990	blood:	n/a
37	chr12:40959011-40959061	ECC-1	luminal epithelium:	n/a
38	chr12:40959011-40959061	T-47D	breast:	n/a
39	chr12:40959011-40959061	ProgFib	skin:	n/a
40	chr12:40959011-40959061	Jurkat	blood:	n/a
41	chr12:40959011-40959061	AG09319	gingival:	n/a
42	chr12:40959011-40959061	LNCaP	prostate:	n/a
43	chr12:40959011-40959061	HEK293	kidney:	embryo
44	chr12:40959011-40959061	SK-N-SH_RA	brain:	n/a
45	chr12:40959011-40959061	PANC-1	pancreas:	n/a
46	chr12:40959011-40959061	SK-N-MC	brain:	n/a
47	chr12:40959011-40959061	H1-hESC	embryonic stem cell:	embryo
48	chr12:40959011-40959061	SK-N-SH	brain:	n/a
49	chr12:40959011-40959061	GM12878	blood:	n/a
50	chr12:40959011-40959061	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:40974030..40975876-chr12:40978694..40980782,2	K562	blood:
2	chr12:40718883..40719693-chr12:40958776..40959283,2	MCF-7	breast:
3	chr12:40974030..40975876-chr12:40978694..40980782,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MUC19-1	chr12:40959315-40959346	NONHSAT027728
2	lnc-MUC19-1	chr12:40959435-40959597	NONHSAT027728
3	lnc-MUC19-1	chr12:40959928-40959965	NONHSAT027728
4	lnc-MUC19-1	chr12:40957333-40957362	NONHSAT027728
5	lnc-MUC19-1	chr12:40955364-40955411	NONHSAT027728
6	lnc-MUC19-1	chr12:40955141-40955194	NONHSAT027728
7	lnc-MUC19-1	chr12:40954338-40954391	NONHSAT027728
8	lnc-MUC19-1	chr12:40961400-40961514	NONHSAT027728
9	lnc-MUC19-1	chr12:40953037-40953090	NONHSAT027728
10	lnc-MUC19-1	chr12:40951895-40951936	NONHSAT027728
11	lnc-MUC19-1	chr12:40954806-40954856	NONHSAT027728
12	lnc-MUC19-1	chr12:40962809-40962844	NONHSAT027728
13	lnc-MUC19-1	chr12:40963498-40963606	NONHSAT027728
14	lnc-MUC19-1	chr12:40964265-40964562	NONHSAT027728

No data

Variant related genes	Relation type
RNU6-713P	TF binding region
MUC19	TF binding region
RNU6-713P	CpG island
MUC19	CpG island

Extended variants
information (count: 1037 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566949235	chr12:40951535-40951536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534743532	chr12:40951546-40951547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367684999	chr12:40951570-40951571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs3751167	chr12:40951596-40951597	Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs3751168	chr12:40951605-40951606	Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs368894329	chr12:40951642-40951643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs3829294	chr12:40951756-40951757	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs575651228	chr12:40951761-40951762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542554778	chr12:40951764-40951765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561168301	chr12:40951775-40951776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528260594	chr12:40951776-40951777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540739094	chr12:40951778-40951779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144615166	chr12:40951810-40951811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532372993	chr12:40951841-40951842	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs3751169	chr12:40951845-40951846	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs3751170	chr12:40951866-40951867	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs3751171	chr12:40951890-40951891	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs548577558	chr12:40951896-40951897	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs567088239	chr12:40951902-40951903	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs534098475	chr12:40951913-40951914	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs3751172	chr12:40951950-40951951	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs3751173	chr12:40951961-40951962	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs538727990	chr12:40952024-40952025	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs188083126	chr12:40952041-40952042	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs530005515	chr12:40952042-40952043	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs575293342	chr12:40952050-40952051	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs548868337	chr12:40952096-40952097	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs3751174	chr12:40952143-40952144	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs111274801	chr12:40952201-40952202	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs60098016	chr12:40952216-40952217	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs375006338	chr12:40952233-40952234	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs192076460	chr12:40952320-40952321	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs565046750	chr12:40952370-40952371	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs576961862	chr12:40952405-40952406	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs544295026	chr12:40952407-40952408	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs562570543	chr12:40952439-40952440	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs143524149	chr12:40952560-40952561	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs148032303	chr12:40952640-40952641	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs560594892	chr12:40952644-40952645	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs17128457	chr12:40952648-40952649	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs183158087	chr12:40952664-40952665	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs571054980	chr12:40952847-40952848	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs187847685	chr12:40952854-40952855	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs141740719	chr12:40952856-40952857	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs147206981	chr12:40952869-40952870	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs11613339	chr12:40952895-40952896	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs1352938	chr12:40952934-40952935	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs573012106	chr12:40952935-40952936	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs56322620	chr12:40952943-40952944	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs558375557	chr12:40952964-40952965	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40947400-40967800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:40949600-40951800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr12:40951800-40952200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:40952600-40954800	Enhancers	GM12878-XiMat	blood
5	chr12:40954800-40955800	Flanking Active TSS	GM12878-XiMat	blood
6	chr12:40955800-40956000	Enhancers	GM12878-XiMat	blood
7	chr12:40956000-40963600	Weak transcription	GM12878-XiMat	blood
8	chr12:40960200-40961200	Enhancers	A549	lung
9	chr12:40961400-40962200	Weak transcription	A549	lung
10	chr12:40962400-40962600	Weak transcription	A549	lung
11	chr12:40962800-40964400	Enhancers	A549	lung
12	chr12:40962800-40964600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr12:40963200-40964400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr12:40963200-40964400	Enhancers	NHDF-Ad	bronchial
15	chr12:40963200-40964800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:40963600-40963800	Enhancers	GM12878-XiMat	blood
17	chr12:40974200-40974400	ZNF genes & repeats	Pancreas	Pancrea
18	chr12:40977200-40977400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:40977400-40978000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr12:40978000-40979600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr12:40979600-40981200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr12:40980200-40980600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr12:40981200-40981800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:40982200-40984800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:40983600-40984200	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr12:40984000-40984800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr12:40985400-40985600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr12:40985600-40986000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr12:40985600-40986400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr12:40986000-40986400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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