Variant report

Variant	nsv871733
Chromosome Location	chr1:103459537-103509323
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:103502292-103502351	K562	blood:	n/a	n/a
2	CEBPB	chr1:103468048-103468248	HepG2	liver:	n/a	chr1:103468160-103468173 chr1:103468074-103468085 chr1:103468076-103468085
3	CEBPB	chr1:103463557-103463788	A549	lung:	n/a	chr1:103463691-103463704 chr1:103463691-103463702 chr1:103463691-103463702 chr1:103463712-103463725 chr1:103463691-103463704
4	CEBPB	chr1:103462260-103462460	HepG2	liver:	n/a	chr1:103462355-103462366 chr1:103462357-103462368
5	CEBPB	chr1:103489916-103490117	HepG2	liver:	n/a	chr1:103489991-103490002 chr1:103489991-103490000
6	CTCF	chr1:103467700-103467850	BJ	skin:	n/a	chr1:103467740-103467748
7	CTCF	chr1:103467620-103467770	BE2_C	brain:	n/a	chr1:103467740-103467748
8	CTCF	chr1:103489061-103489081	Fibrobl	skin:	n/a	n/a
9	ELK1	chr1:103474216-103474272	GM12878	blood:	n/a	n/a
10	EP300	chr1:103495066-103495343	SK-N-SH_RA	brain:	n/a	n/a
11	EP300	chr1:103482033-103482177	K562	blood:	n/a	chr1:103482034-103482043
12	EP300	chr1:103497514-103497813	SK-N-SH_RA	brain:	n/a	chr1:103497580-103497588 chr1:103497645-103497652
13	FAM48A	chr1:103481060-103481095	GM12878	blood:	n/a	n/a
14	GATA3	chr1:103483910-103484121	SH-SY5Y	brain:	n/a	chr1:103483910-103483926 chr1:103484011-103484019 chr1:103484008-103484021 chr1:103483984-103483991 chr1:103483911-103483921 chr1:103484010-103484019 chr1:103483957-103483973 chr1:103483959-103483971 chr1:103484012-103484019
15	GATA3	chr1:103495167-103495348	SH-SY5Y	brain:	n/a	n/a
16	GATA3	chr1:103469326-103469402	SH-SY5Y	brain:	n/a	chr1:103469390-103469400
17	GATA3	chr1:103460939-103461128	SH-SY5Y	brain:	n/a	chr1:103461085-103461101
18	GATA3	chr1:103500817-103500879	SH-SY5Y	brain:	n/a	n/a
19	JUND	chr1:103467623-103468040	H1-hESC	embryonic stem cell:	n/a	chr1:103467779-103467791 chr1:103467781-103467790 chr1:103467782-103467789 chr1:103467780-103467790 chr1:103467781-103467789
20	JUND	chr1:103498509-103498704	H1-hESC	embryonic stem cell:	n/a	n/a
21	MAFF	chr1:103500871-103501071	HepG2	liver:	n/a	chr1:103500984-103501002
22	MAFF	chr1:103500931-103500933	K562	blood:	n/a	n/a
23	MAFK	chr1:103500893-103501127	IMR90	lung:	n/a	chr1:103500986-103500997 chr1:103500986-103500997 chr1:103500987-103500998 chr1:103500986-103501001 chr1:103500985-103500999 chr1:103500986-103501002
24	MAFK	chr1:103488526-103488726	IMR90	lung:	n/a	n/a
25	MAFK	chr1:103500873-103501086	HepG2	liver:	n/a	chr1:103500986-103500997 chr1:103500986-103500997 chr1:103500987-103500998 chr1:103500986-103501001 chr1:103500985-103500999 chr1:103500986-103501002
26	MAFK	chr1:103488469-103488807	HepG2	liver:	n/a	chr1:103488748-103488768
27	MAFK	chr1:103500869-103501153	HepG2	liver:	n/a	chr1:103500986-103500997 chr1:103500986-103500997 chr1:103500987-103500998 chr1:103500986-103501001 chr1:103500985-103500999 chr1:103500986-103501002
28	MAX	chr1:103498532-103498732	NB4	blood:	n/a	n/a
29	MAZ	chr1:103477655-103477827	HepG2	liver:	n/a	n/a
30	MXI1	chr1:103464776-103464780	GM12878	blood:	n/a	n/a
31	MXI1	chr1:103476805-103476816	K562	blood:	n/a	n/a
32	MXI1	chr1:103461574-103461774	GM12878	blood:	n/a	n/a
33	MXI1	chr1:103467282-103467392	GM12878	blood:	n/a	n/a
34	NFYA	chr1:103491625-103491853	GM12878	blood:	n/a	n/a
35	POLR2A	chr1:103489703-103489763	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr1:103498773-103498930	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr1:103467208-103467320	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr1:103468500-103468715	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr1:103497360-103497385	MCF10A-Er-Src	breast:	n/a	n/a
40	RAD21	chr1:103467626-103467874	H1-hESC	embryonic stem cell:	n/a	chr1:103467737-103467751
41	STAT3	chr1:103504306-103504321	MCF10A-Er-Src	breast:	n/a	n/a
42	STAT3	chr1:103462687-103462967	MCF10A-Er-Src	breast:	n/a	n/a
43	STAT3	chr1:103483766-103483976	MCF10A-Er-Src	breast:	n/a	n/a
44	STAT3	chr1:103491597-103491691	MCF10A-Er-Src	breast:	n/a	n/a
45	TCF7L2	chr1:103491184-103491804	PANC-1	pancreas:	n/a	chr1:103491573-103491582

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:103471408..103474127-chr1:103476869..103478860,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1B-5	chr1:103467481-103467525	NONHSAT004880
2	lnc-AMY1B-5	chr1:103468303-103468347	NONHSAT004880
3	lnc-AMY1B-5	chr1:103466993-103467187	NONHSAT004880
4	lnc-AMY1B-5	chr1:103470000-103470037	NONHSAT004880
5	lnc-AMY1B-5	chr1:103467984-103468037	NONHSAT004880

Variant related genes	Relation type
COL11A1	TF binding region
ENSG00000060718	chromatin interactions
FOXO1	miRNA target sites
NHLRC3	miRNA target sites
TMPO	miRNA target sites
MBD4	miRNA target sites

Extended variants
information (count: 2112 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2112 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11809524	chr1:103459537-103459538	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
2	rs78308033	chr1:103459539-103459540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541016617	chr1:103459545-103459546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10782915	chr1:103459558-103459559	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs549076753	chr1:103459566-103459567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541659709	chr1:103459567-103459568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533023246	chr1:103459595-103459596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78089634	chr1:103459604-103459605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563867734	chr1:103459609-103459610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs76617635	chr1:103459622-103459623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188440095	chr1:103459687-103459688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567614966	chr1:103459708-103459709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534733653	chr1:103459750-103459751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138322762	chr1:103459782-103459783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571674501	chr1:103459817-103459818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142814221	chr1:103459827-103459828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560287740	chr1:103459848-103459849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557680351	chr1:103459866-103459867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200963201	chr1:103459878-103459879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs71483860	chr1:103459879-103459880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs61815932	chr1:103459880-103459881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370255696	chr1:103459881-103459882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555740759	chr1:103459884-103459885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573965109	chr1:103459900-103459901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78218587	chr1:103459920-103459921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72683293	chr1:103459944-103459945	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs372298244	chr1:103459947-103459948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191724641	chr1:103459959-103459960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146046288	chr1:103459982-103459983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs3102058	chr1:103460014-103460015	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs78504529	chr1:103460043-103460044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549154846	chr1:103460105-103460106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561276506	chr1:103460111-103460112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528733548	chr1:103460133-103460134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184012978	chr1:103460135-103460136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71664952	chr1:103460182-103460183	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs538762258	chr1:103460227-103460228	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551103665	chr1:103460248-103460249	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569244813	chr1:103460256-103460257	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537275217	chr1:103460258-103460259	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs531747421	chr1:103460328-103460329	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567585568	chr1:103460372-103460373	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534877680	chr1:103460373-103460374	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552702838	chr1:103460452-103460453	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577518869	chr1:103460478-103460479	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550171417	chr1:103460576-103460577	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544674362	chr1:103460627-103460628	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545306501	chr1:103460646-103460647	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs557057854	chr1:103460652-103460653	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142004246	chr1:103460678-103460679	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103369600-103498600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:103386200-103482000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:103400200-103462000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:103415800-103485200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:103423000-103468200	Weak transcription	HSMMtube	muscle
6	chr1:103423800-103476000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:103425000-103478000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr1:103446800-103497800	Weak transcription	HSMM	muscle
9	chr1:103449200-103545200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:103450800-103470200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:103453200-103467400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr1:103453400-103490000	Weak transcription	NH-A	brain
13	chr1:103454000-103468400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:103457200-103459800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr1:103457200-103462800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr1:103458600-103460800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:103459000-103460200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:103459200-103461800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:103459400-103460600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr1:103459800-103460800	Strong transcription	Cortex derived primary cultured neurospheres	brain
21	chr1:103460200-103461800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:103460200-103516400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr1:103460800-103465600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:103460800-103466600	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr1:103461800-103466800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:103462800-103463800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr1:103463800-103466600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:103466600-103467000	Strong transcription	Cortex derived primary cultured neurospheres	brain
29	chr1:103466600-103471200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:103466800-103469400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:103467000-103469400	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr1:103467400-103468400	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr1:103468400-103471400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:103468400-103478600	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr1:103469400-103469800	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr1:103469400-103471400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:103469800-103486600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr1:103470200-103471400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr1:103471200-103475000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:103471400-103471800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:103471400-103476600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:103471400-103486600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:103471800-103474400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr1:103474400-103476800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:103474800-103483600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:103475000-103476200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr1:103475800-103516600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:103476200-103486800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:103476600-103477600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:103476800-103477000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links