Variant report

Variant	nsv945965
Chromosome Location	chr1:57003085-57005467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:20)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:20 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:57005357-57005359	HepG2	liver:	n/a	n/a
2	CTCF	chr1:57005140-57005290	HPF	lung:	n/a	n/a
3	EP300	chr1:57005101-57005508	HepG2	liver:	n/a	chr1:57005262-57005272
4	EP300	chr1:57005071-57005470	HepG2	liver:	n/a	chr1:57005262-57005272
5	EP300	chr1:57003509-57003593	HepG2	liver:	n/a	n/a
6	FOXA1	chr1:57004950-57005487	HepG2	liver:	n/a	n/a
7	FOXA1	chr1:57005005-57005487	HepG2	liver:	n/a	n/a
8	FOXA1	chr1:57004991-57005552	HepG2	liver:	n/a	n/a
9	FOXA1	chr1:57004997-57005417	HepG2	liver:	n/a	n/a
10	FOXA2	chr1:57005046-57005426	A549	lung:	n/a	n/a
11	FOXA2	chr1:57004576-57005728	HepG2	liver:	n/a	n/a
12	FOXA2	chr1:57005057-57005448	HepG2	liver:	n/a	n/a
13	KAP1	chr1:57005115-57006318	HEK293	kidney:	n/a	chr1:57006131-57006139
14	MYBL2	chr1:57005098-57005489	HepG2	liver:	n/a	n/a
15	POLR2A	chr1:57003171-57004244	PFSK-1	brain:	n/a	n/a
16	POLR2A	chr1:57005117-57005670	PFSK-1	brain:	n/a	n/a
17	POLR2A	chr1:57003582-57003636	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr1:56998973-57004163	HepG2	liver:	n/a	n/a
19	STAT3	chr1:57004990-57005014	MCF10A-Er-Src	breast:	n/a	n/a
20	YY1	chr1:57005164-57005415	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:57004017-57004067	NT2-D1	testis:	n/a
2	chr1:57004017-57004067	AG04450	lung:	fetal
3	chr1:57004017-57004067	HAEpiC	amniotic membrane:	n/a
4	chr1:57004017-57004067	PFSK-1	brain:	n/a
5	chr1:57004017-57004067	GM06990	blood:	n/a
6	chr1:57004017-57004067	ovcar-3	ovarian:	n/a
7	chr1:57004017-57004067	HRPEpiC	eye:	n/a
8	chr1:57004017-57004067	NHDF-neo	bronchial:	n/a
9	chr1:57004017-57004067	HIPEpiC	eye:	n/a
10	chr1:57004017-57004067	MCF-7	breast:	n/a
11	chr1:57004017-57004067	NHBE	bronchial:	n/a
12	chr1:57004017-57004067	AoSMC	blood vessel:	n/a
13	chr1:57004017-57004067	U87	brain:	n/a
14	chr1:57004017-57004067	HCM	heart:	n/a
15	chr1:57004017-57004067	GM12892	blood:	n/a
16	chr1:57004017-57004067	GM12878	blood:	n/a
17	chr1:57004017-57004067	HUVEC	blood vessel:	n/a
18	chr1:57004017-57004067	Hepatocyte	liver:	n/a
19	chr1:57004017-57004067	HepG2	liver:	n/a
20	chr1:57004017-57004067	T-47D	breast:	n/a
21	chr1:57004017-57004067	RPTEC	kidney:	n/a
22	chr1:57004017-57004067	SK-N-SH_RA	brain:	n/a
23	chr1:57004017-57004067	HCPEpiC	choroid plexus:	n/a
24	chr1:57004017-57004067	PANC-1	pancreas:	n/a
25	chr1:57004017-57004067	HEEpiC	esophagus:	n/a
26	chr1:57004017-57004067	ECC-1	luminal epithelium:	n/a
27	chr1:57004017-57004067	Caco-2	colon:	n/a
28	chr1:57004017-57004067	ProgFib	skin:	n/a
29	chr1:57004017-57004067	HMEC	breast:	n/a
30	chr1:57004017-57004067	GM19239	blood:	n/a
31	chr1:57004017-57004067	AG09319	gingival:	n/a
32	chr1:57004017-57004067	AG04449	skin:	fetal
33	chr1:57004017-57004067	HCF	heart:	n/a
34	chr1:57004017-57004067	NH-A	brain:	n/a
35	chr1:57004017-57004067	AG10803	skin:	n/a
36	chr1:57004017-57004067	HRCEpiC	kidney:	n/a
37	chr1:57004017-57004067	K562	blood:	n/a
38	chr1:57004017-57004067	SAEC	small airway:	n/a
39	chr1:57004017-57004067	H1-hESC	embryonic stem cell:	embryo
40	chr1:57004017-57004067	HCT-116	colon:	n/a
41	chr1:57004017-57004067	HRE	kidney:	n/a
42	chr1:57004017-57004067	GM12891	blood:	n/a
43	chr1:57004017-57004067	PrEC	prostate:	n/a
44	chr1:57004017-57004067	Jurkat	blood:	n/a
45	chr1:57004017-57004067	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:57004017-57004067	LNCaP	prostate:	n/a
47	chr1:57004017-57004067	HNPCEpiC	eye:	n/a
48	chr1:57004017-57004067	MCF10A-Er-Src	breast:	n/a
49	chr1:57004017-57004067	IMR90	lung:	fetal
50	chr1:57004017-57004067	NB4	blood:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKAA2-9	chr1:57004124-57004583	NONHSAT003451

No data

Variant related genes	Relation type
RPL21P23	TF binding region
RPL21P23	CpG island

Extended variants
information (count: 93 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141007116	chr1:57003099-57003100	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs142472827	chr1:57003101-57003102	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs572740208	chr1:57003113-57003114	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs544787523	chr1:57003119-57003120	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs564863989	chr1:57003124-57003125	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs575167701	chr1:57003215-57003216	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs182984810	chr1:57003243-57003244	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs150822190	chr1:57003254-57003255	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs532249445	chr1:57003310-57003311	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs369781315	chr1:57003316-57003317	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs1418977	chr1:57003359-57003360	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs376467063	chr1:57003412-57003413	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs187841358	chr1:57003423-57003424	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs191503440	chr1:57003429-57003430	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs188233693	chr1:57003440-57003441	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs551984921	chr1:57003528-57003529	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs183234048	chr1:57003543-57003544	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs17114088	chr1:57003559-57003560	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs550550455	chr1:57003560-57003561	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs567195137	chr1:57003587-57003588	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs536232660	chr1:57003663-57003664	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs552683701	chr1:57003685-57003686	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs540425642	chr1:57003708-57003709	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs7519268	chr1:57003810-57003811	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs139258456	chr1:57003815-57003816	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs532488425	chr1:57003832-57003833	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs558295587	chr1:57003855-57003856	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs575183406	chr1:57003858-57003859	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs544132035	chr1:57003890-57003891	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs187537503	chr1:57003903-57003904	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs374935279	chr1:57003907-57003908	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs151327593	chr1:57003929-57003930	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs573992387	chr1:57003941-57003942	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs542993898	chr1:57003946-57003947	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs559916043	chr1:57003948-57003949	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs528571681	chr1:57003968-57003969	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs376357639	chr1:57004017-57004018	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs529965948	chr1:57004022-57004023	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs35726205	chr1:57004066-57004067	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs541447192	chr1:57004069-57004070	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs562902934	chr1:57004088-57004089	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs146583563	chr1:57004129-57004130	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs551028727	chr1:57004140-57004141	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs1777274	chr1:57004147-57004148	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs551898495	chr1:57004158-57004159	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs546160339	chr1:57004162-57004163	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs140969960	chr1:57004164-57004165	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs1759750	chr1:57004178-57004179	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558334283	chr1:57004209-57004210	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs192307907	chr1:57004249-57004250	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
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
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
Melanoma	17363583	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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56987000-57015000	Genic enhancers	NHDF-Ad	bronchial
2	chr1:56990000-57004000	Genic enhancers	Liver	Liver
3	chr1:56992800-57011200	Weak transcription	Stomach Mucosa	stomach
4	chr1:56993000-57004600	Weak transcription	Hela-S3	cervix
5	chr1:56993600-57007800	Weak transcription	Primary B cells from cord blood	blood
6	chr1:56993800-57004200	Weak transcription	NH-A	brain
7	chr1:56994000-57004000	Weak transcription	HUVEC	blood vessel
8	chr1:56994000-57012400	Weak transcription	Fetal Brain Male	brain
9	chr1:56994000-57012800	Weak transcription	Fetal Brain Female	brain
10	chr1:56994200-57004400	Strong transcription	Muscle Satellite Cultured Cells	--
11	chr1:56995000-57003400	Strong transcription	Fetal Muscle Trunk	muscle
12	chr1:56995000-57003600	Strong transcription	Osteobl	bone
13	chr1:56995200-57003800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:56995600-57004600	Weak transcription	Colon Smooth Muscle	Colon
15	chr1:56995800-57004000	Genic enhancers	HepG2	liver
16	chr1:56996600-57004000	Strong transcription	HSMM	muscle
17	chr1:56996600-57005200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:56997000-57003400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr1:56997200-57004600	Genic enhancers	Placenta	Placenta
20	chr1:56997600-57004400	Genic enhancers	Fetal Muscle Leg	muscle
21	chr1:56997800-57003600	Genic enhancers	Skeletal Muscle Female	skeletal muscle
22	chr1:56998600-57003800	Strong transcription	Fetal Stomach	stomach
23	chr1:56999400-57012800	Weak transcription	HSMMtube	muscle
24	chr1:57000000-57003800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr1:57000000-57004200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr1:57000200-57005000	Weak transcription	Rectal Smooth Muscle	rectum
27	chr1:57000200-57008200	Weak transcription	Fetal Kidney	kidney
28	chr1:57000400-57004000	Strong transcription	NHLF	lung
29	chr1:57000400-57011000	Weak transcription	Gastric	stomach
30	chr1:57000400-57013000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:57000600-57003800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr1:57000600-57005400	Weak transcription	Colonic Mucosa	Colon
33	chr1:57000800-57004000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr1:57001000-57004000	Genic enhancers	Fetal Intestine Large	intestine
35	chr1:57001000-57004200	Enhancers	Pancreas	Pancrea
36	chr1:57001200-57018800	Weak transcription	A549	lung
37	chr1:57001400-57004600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:57001800-57003400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr1:57001800-57003400	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr1:57001800-57003600	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr1:57001800-57018600	Weak transcription	Small Intestine	intestine
42	chr1:57001800-57021800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr1:57002000-57003200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr1:57002000-57004000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr1:57002000-57004000	Enhancers	Fetal Thymus	thymus
46	chr1:57002200-57004400	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr1:57002200-57004400	Enhancers	Psoas Muscle	Psoas
48	chr1:57002400-57003400	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr1:57002400-57003600	Weak transcription	Brain Angular Gyrus	brain
50	chr1:57002400-57004600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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