Variant report

Variant	nsv972254
Chromosome Location	chr8:124818093-124822653
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	CEBPB	chr8:124818902-124819212	HepG2	liver:	n/a	n/a
2	FOXA1	chr8:124818817-124819285	HepG2	liver:	n/a	n/a
3	FOXA2	chr8:124818901-124819208	HepG2	liver:	n/a	n/a
4	HNF4A	chr8:124818815-124819102	HepG2	liver:	n/a	chr8:124819017-124819030 chr8:124819017-124819029 chr8:124819015-124819030 chr8:124819017-124819030 chr8:124819016-124819029 chr8:124819015-124819030 chr8:124819017-124819030 chr8:124819016-124819030 chr8:124819017-124819029 chr8:124819014-124819032 chr8:124819016-124819030 chr8:124819015-124819030 chr8:124819015-124819030
5	HNF4G	chr8:124818912-124819117	HepG2	liver:	n/a	chr8:124819017-124819030 chr8:124819017-124819029 chr8:124819015-124819030 chr8:124819017-124819030 chr8:124819016-124819029 chr8:124819015-124819030 chr8:124819017-124819030 chr8:124819016-124819030 chr8:124819017-124819029 chr8:124819014-124819032 chr8:124819016-124819030 chr8:124819016-124819031 chr8:124819015-124819030
6	IRF1	chr8:124821621-124821758	K562	blood:	n/a	n/a
7	MAFF	chr8:124821300-124821860	K562	blood:	n/a	chr8:124821660-124821678
8	MAFF	chr8:124821154-124821865	HepG2	liver:	n/a	chr8:124821660-124821678
9	MAFK	chr8:124821489-124821857	H1-hESC	embryonic stem cell:	n/a	chr8:124821662-124821677 chr8:124821661-124821675 chr8:124821663-124821683
10	MAFK	chr8:124821350-124822009	GM12878	blood:	n/a	chr8:124821662-124821677 chr8:124821661-124821675 chr8:124821663-124821683
11	MAFK	chr8:124821457-124821857	Hela-S3	cervix:	n/a	chr8:124821662-124821677 chr8:124821661-124821675 chr8:124821663-124821683
12	MAFK	chr8:124821183-124821859	HepG2	liver:	n/a	chr8:124821662-124821677 chr8:124821303-124821314 chr8:124821304-124821315 chr8:124821661-124821675 chr8:124821663-124821683 chr8:124821304-124821315
13	MAFK	chr8:124821165-124821877	IMR90	lung:	n/a	chr8:124821662-124821677 chr8:124821303-124821314 chr8:124821304-124821315 chr8:124821661-124821675 chr8:124821663-124821683 chr8:124821304-124821315
14	MAFK	chr8:124821121-124821871	HepG2	liver:	n/a	chr8:124821662-124821677 chr8:124821303-124821314 chr8:124821304-124821315 chr8:124821661-124821675 chr8:124821663-124821683 chr8:124821304-124821315
15	MAFK	chr8:124821315-124821868	K562	blood:	n/a	chr8:124821662-124821677 chr8:124821661-124821675 chr8:124821663-124821683
16	POLR2A	chr8:124818373-124818391	HUVEC	blood vessel:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:124816253..124817960-chr8:124822217..124824038,2	K562	blood:
2	chr8:124774301..124776211-chr8:124822631..124825115,2	MCF-7	breast:
3	chr8:124818284..124820707-chr8:125487320..125489749,2	K562	blood:
4	chr8:124817123..124819367-chr8:124820502..124822341,2	K562	blood:
5	chr8:124812507..124814669-chr8:124816701..124818733,2	K562	blood:
6	chr8:124814412..124816720-chr8:124818333..124820559,2	MCF-7	breast:

Variant related genes	Relation type
FAM91A1	TF binding region
ENSG00000176853	chromatin interactions

Extended variants
information (count: 175 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:175 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187308635	chr8:124818100-124818101	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs558903764	chr8:124818111-124818112	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2272683	chr8:124818182-124818183	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs541437239	chr8:124818222-124818223	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs572027493	chr8:124818233-124818234	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs116439597	chr8:124818269-124818270	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372298206	chr8:124818270-124818271	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs115823649	chr8:124818296-124818297	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs551150661	chr8:124818302-124818303	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs368395786	chr8:124818303-124818304	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs372339138	chr8:124818307-124818308	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs375006283	chr8:124818323-124818324	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs369174862	chr8:124818372-124818373	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs372640947	chr8:124818386-124818387	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs545357572	chr8:124818387-124818388	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs570996822	chr8:124818407-124818408	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2272684	chr8:124818447-124818448	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs193192740	chr8:124818449-124818450	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs200021331	chr8:124818454-124818455	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs373449561	chr8:124818499-124818500	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs377443489	chr8:124818503-124818504	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs59400236	chr8:124818556-124818557	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs146258986	chr8:124818631-124818632	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555802036	chr8:124818661-124818662	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs542443499	chr8:124818688-124818689	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs376795557	chr8:124818691-124818692	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375184844	chr8:124818750-124818751	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575887385	chr8:124818754-124818755	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs377450588	chr8:124818781-124818782	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs543311610	chr8:124818782-124818783	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184743691	chr8:124818784-124818785	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs560500407	chr8:124818825-124818826	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs561961156	chr8:124818912-124818913	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs539644497	chr8:124819084-124819085	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs552614129	chr8:124819119-124819120	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs111568076	chr8:124819142-124819143	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs529063160	chr8:124819146-124819147	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs72715045	chr8:124819171-124819172	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs541376055	chr8:124819179-124819180	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs561391973	chr8:124819212-124819213	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559560938	chr8:124819229-124819230	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs189851767	chr8:124819256-124819257	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs373785327	chr8:124819266-124819267	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs544611207	chr8:124819267-124819268	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs142526574	chr8:124819295-124819296	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533336538	chr8:124819314-124819315	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs533378932	chr8:124819322-124819323	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs556297525	chr8:124819409-124819410	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547226131	chr8:124819431-124819432	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146339695	chr8:124819434-124819435	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:146)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124785800-124829000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr8:124786000-124825200	Strong transcription	Fetal Thymus	thymus
3	chr8:124786200-124825200	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr8:124786400-124827200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr8:124787000-124822800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr8:124787000-124827000	Strong transcription	Primary T helper cells fromperipheralblood	blood
7	chr8:124787600-124818800	Strong transcription	Liver	Liver
8	chr8:124789200-124824600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr8:124789400-124821600	Weak transcription	Stomach Mucosa	stomach
10	chr8:124789400-124825200	Strong transcription	Rectal Mucosa Donor 31	rectum
11	chr8:124789800-124827400	Strong transcription	Primary T helper cells PMA-I stimulated	--
12	chr8:124790000-124827800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:124790200-124828600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:124790800-124825200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr8:124791000-124828600	Strong transcription	Primary B cells from cord blood	blood
16	chr8:124791000-124828600	Strong transcription	Primary B cells from peripheral blood	blood
17	chr8:124791200-124828600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr8:124791200-124828600	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr8:124791200-124829000	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr8:124791200-124829200	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr8:124794200-124825000	Strong transcription	Primary hematopoietic stem cells	blood
22	chr8:124797800-124826000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:124798400-124826400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr8:124799400-124821400	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr8:124799600-124822600	Weak transcription	Small Intestine	intestine
26	chr8:124800200-124822600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr8:124806800-124828400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:124808200-124825000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr8:124808400-124819400	Weak transcription	Spleen	Spleen
30	chr8:124808400-124820000	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr8:124808400-124831600	Weak transcription	Esophagus	oesophagus
32	chr8:124808600-124819200	Weak transcription	Fetal Heart	heart
33	chr8:124808600-124822800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr8:124809000-124819400	Weak transcription	Right Ventricle	heart
35	chr8:124809200-124819600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:124809800-124819200	Weak transcription	Aorta	Aorta
37	chr8:124809800-124833600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:124810200-124829600	Weak transcription	Pancreas	Pancrea
39	chr8:124810600-124818400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr8:124810600-124819400	Weak transcription	Fetal Stomach	stomach
41	chr8:124810600-124831600	Weak transcription	Gastric	stomach
42	chr8:124811200-124818800	Weak transcription	Thymus	Thymus
43	chr8:124811600-124818400	Weak transcription	Lung	lung
44	chr8:124811600-124830400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr8:124812600-124821000	Weak transcription	Brain Cingulate Gyrus	brain
46	chr8:124812800-124829800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr8:124813000-124830600	Weak transcription	Colonic Mucosa	Colon
48	chr8:124813200-124818400	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr8:124813200-124829000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr8:124813400-124818600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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