Variant report

Variant	nsv833197
Chromosome Location	chr16:31957340-32088251
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	BATF	chr16:32050371-32050791	GM12878	blood:	n/a	n/a
2	BATF	chr16:32059227-32059446	GM12878	blood:	n/a	n/a
3	BATF	chr16:32059238-32059578	GM12878	blood:	n/a	n/a
4	BATF	chr16:32001426-32001621	GM12878	blood:	n/a	n/a
5	BATF	chr16:31967621-31968011	GM12878	blood:	n/a	n/a
6	BATF	chr16:32007628-32007992	GM12878	blood:	n/a	n/a
7	BCL11A	chr16:32001120-32001954	GM12878	blood:	n/a	n/a
8	BCL11A	chr16:31967573-31967758	GM12878	blood:	n/a	n/a
9	BCL11A	chr16:32059954-32060170	GM12878	blood:	n/a	n/a
10	BCL11A	chr16:32001344-32001697	GM12878	blood:	n/a	n/a
11	BHLHE40	chr16:31985679-31985857	HepG2	liver:	n/a	chr16:31985733-31985749
12	CBX3	chr16:31967501-31967949	K562	blood:	n/a	n/a
13	CBX3	chr16:32050646-32050949	K562	blood:	n/a	n/a
14	CBX3	chr16:31967467-31967998	K562	blood:	n/a	n/a
15	CBX3	chr16:32007689-32008189	K562	blood:	n/a	n/a
16	CBX3	chr16:32050399-32050591	K562	blood:	n/a	n/a
17	CEBPB	chr16:32073025-32073229	HepG2	liver:	n/a	chr16:32073200-32073211
18	CEBPB	chr16:31992231-31992592	K562	blood:	n/a	chr16:31992407-31992418
19	CEBPB	chr16:31992189-31992618	K562	blood:	n/a	chr16:31992407-31992418
20	CEBPB	chr16:31992336-31992524	K562	blood:	n/a	chr16:31992407-31992418
21	CEBPB	chr16:31992228-31992528	HepG2	liver:	n/a	chr16:31992407-31992418
22	CHD2	chr16:32051321-32051488	HepG2	liver:	n/a	n/a
23	CTCF	chr16:31967664-31967950	K562	blood:	n/a	n/a
24	CTCF	chr16:32051361-32051543	MCF-7	breast:	n/a	chr16:32051440-32051456 chr16:32051444-32051454
25	CTCF	chr16:32007655-32007981	Gliobla	brain:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
26	CTCF	chr16:31967680-31967830	AG04449	skin:	n/a	n/a
27	CTCF	chr16:32050079-32051239	A549	lung:	n/a	chr16:32050439-32050448
28	CTCF	chr16:32007727-32007925	HepG2	liver:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
29	CTCF	chr16:31967591-31967934	GM20000	blood:	n/a	n/a
30	CTCF	chr16:31967620-31967770	GM12874	blood:	n/a	n/a
31	CTCF	chr16:31985617-31985910	Medullo	brain:	n/a	chr16:31985751-31985764 chr16:31985749-31985765 chr16:31985748-31985766 chr16:31985753-31985763
32	CTCF	chr16:32007692-32007970	Medullo	brain:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
33	CTCF	chr16:31985663-31985835	MCF-7	breast:	n/a	chr16:31985751-31985764 chr16:31985749-31985765 chr16:31985748-31985766 chr16:31985753-31985763
34	CTCF	chr16:32050298-32050615	MCF-7	breast:	n/a	chr16:32050439-32050448
35	CTCF	chr16:31967620-31967770	HEK293	kidney:	n/a	n/a
36	CTCF	chr16:32050241-32050867	K562	blood:	n/a	chr16:32050439-32050448
37	CTCF	chr16:31967660-31967810	HVMF	connective:	n/a	n/a
38	CTCF	chr16:31985588-31985901	HepG2	liver:	n/a	chr16:31985751-31985764 chr16:31985749-31985765 chr16:31985748-31985766 chr16:31985753-31985763
39	CTCF	chr16:32049969-32051693	K562	blood:	n/a	chr16:32051440-32051456 chr16:32050439-32050448 chr16:32051444-32051454
40	CTCF	chr16:32051320-32051470	SK-N-SH_RA	brain:	n/a	chr16:32051440-32051456 chr16:32051444-32051454
41	CTCF	chr16:32007705-32007944	MCF-7	breast:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
42	CTCF	chr16:32050560-32050710	GM12866	blood:	n/a	n/a
43	CTCF	chr16:32000915-32001033	GM10266	blood:	n/a	n/a
44	CTCF	chr16:32077680-32077830	Caco-2	colon:	n/a	chr16:32077744-32077754 chr16:32077740-32077756
45	CTCF	chr16:32000986-32001089	Lung_OC	lung:	n/a	n/a
46	CTCF	chr16:32050453-32050675	MCF-7	breast:	n/a	n/a
47	CTCF	chr16:31967593-31967818	T-47D	breast:	n/a	n/a
48	CTCF	chr16:31967620-31967770	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr16:31967640-31967790	GM12867	blood:	n/a	n/a
50	CTCF	chr16:32007770-32007974	MCF-7	breast:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:31997067-31997117	SK-N-MC	brain:	n/a
2	chr16:31997067-31997117	PFSK-1	brain:	n/a
3	chr16:32037687-32037737	HNPCEpiC	eye:	n/a
4	chr16:32037687-32037737	NHBE	bronchial:	n/a
5	chr16:31995423-31995473	SK-N-SH_RA	brain:	n/a
6	chr16:32037687-32037737	SKMC	muscle:	n/a
7	chr16:31995423-31995473	AG09319	gingival:	n/a
8	chr16:32049224-32049274	HRCEpiC	kidney:	n/a
9	chr16:32049224-32049274	GM12878	blood:	n/a
10	chr16:31990956-31991006	RPTEC	kidney:	n/a
11	chr16:31995423-31995473	AG04449	skin:	fetal
12	chr16:32049224-32049274	NT2-D1	testis:	n/a
13	chr16:31990956-31991006	GM12878	blood:	n/a
14	chr16:31997067-31997117	HUVEC	blood vessel:	n/a
15	chr16:31993479-31993529	HEEpiC	esophagus:	n/a
16	chr16:31993479-31993529	HCT-116	colon:	n/a
17	chr16:31995423-31995473	NH-A	brain:	n/a
18	chr16:31997067-31997117	PANC-1	pancreas:	n/a
19	chr16:31990956-31991006	NHDF-neo	bronchial:	n/a
20	chr16:31995423-31995473	AG09309	skin:	n/a
21	chr16:31995423-31995473	SK-N-SH	brain:	n/a
22	chr16:31990956-31991006	NH-A	brain:	n/a
23	chr16:32049224-32049274	HUVEC	blood vessel:	n/a
24	chr16:31995423-31995473	HEEpiC	esophagus:	n/a
25	chr16:32037687-32037737	AG10803	skin:	n/a
26	chr16:31990956-31991006	HL-60	blood:	n/a
27	chr16:32037687-32037737	SK-N-MC	brain:	n/a
28	chr16:31990956-31991006	CMK	blood:	n/a
29	chr16:32049224-32049274	HL-60	blood:	n/a
30	chr16:32049224-32049274	H1-hESC	embryonic stem cell:	embryo
31	chr16:31993231-31993281	GM12892	blood:	n/a
32	chr16:31993479-31993529	ovcar-3	ovarian:	n/a
33	chr16:31993231-31993281	GM19239	blood:	n/a
34	chr16:31993231-31993281	HCF	heart:	n/a
35	chr16:32049224-32049274	HepG2	liver:	n/a
36	chr16:32049224-32049274	AG04450	lung:	fetal
37	chr16:31997067-31997117	HEEpiC	esophagus:	n/a
38	chr16:31997067-31997117	AoSMC	blood vessel:	n/a
39	chr16:31997067-31997117	HCM	heart:	n/a
40	chr16:31995423-31995473	GM12878	blood:	n/a
41	chr16:31993479-31993529	AoSMC	blood vessel:	n/a
42	chr16:32037687-32037737	HRPEpiC	eye:	n/a
43	chr16:32037687-32037737	HepG2	liver:	n/a
44	chr16:31993231-31993281	HRE	kidney:	n/a
45	chr16:31993231-31993281	AG09309	skin:	n/a
46	chr16:31990956-31991006	AG10803	skin:	n/a
47	chr16:31997067-31997117	SK-N-SH	brain:	n/a
48	chr16:32049224-32049274	BJ	skin:	n/a
49	chr16:31997067-31997117	HMEC	breast:	n/a
50	chr16:32049224-32049274	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:106598214..106598843-chr16:32050606..32051126,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF267-3	chr16:31963481-31963794	NONHSAT141978
2	lnc-ZNF267-4	chr16:31975124-31975400	NONHSAT141983
3	lnc-ZNF267-4	chr16:31973257-31973743	NONHSAT141979
4	lnc-ZNF267-4	chr16:31972893-31972899	NONHSAT141979

Variant related genes	Relation type
ENSG00000261289	TF binding region
ENSG00000223931	TF binding region
ENSG00000260628	TF binding region
ENSG00000197476	TF binding region
IGHV1OR16-1	TF binding region
IGHV3OR16-9	TF binding region
ENSG00000260218	TF binding region
IGHV1OR16-3	TF binding region
ENSG00000261289	CpG island
ENSG00000223931	CpG island
ENSG00000260628	CpG island
ENSG00000197476	CpG island
IGHV1OR16-1	CpG island
IGHV3OR16-9	CpG island
ENSG00000260218	CpG island
IGHV1OR16-3	CpG island

Extended variants
information (count: 455 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551666934	chr16:31957363-31957364	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs9941272	chr16:31957368-31957369	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs369901859	chr16:31957374-31957375	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs530579862	chr16:31957399-31957400	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs549153533	chr16:31957424-31957425	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs567397033	chr16:31957444-31957445	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs534393560	chr16:31957466-31957467	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs140203166	chr16:31957512-31957513	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs150026057	chr16:31957533-31957534	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs538271657	chr16:31957550-31957551	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs557321671	chr16:31957574-31957575	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs575900216	chr16:31957615-31957616	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs542990010	chr16:31957618-31957619	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs555140050	chr16:31957688-31957689	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs573383875	chr16:31957697-31957698	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs115652703	chr16:31957736-31957737	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs553388994	chr16:31957764-31957765	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs150501991	chr16:31957813-31957814	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs565393797	chr16:31957868-31957869	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs532521544	chr16:31957960-31957961	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs373127546	chr16:31957965-31957966	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs544626439	chr16:31957993-31957994	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs77653565	chr16:31958018-31958019	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs145337082	chr16:31958021-31958022	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs149203502	chr16:31958061-31958062	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs549037245	chr16:31958062-31958063	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs567440527	chr16:31958084-31958085	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs376023296	chr16:31958135-31958136	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs34607688	chr16:31958137-31958138	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs74017550	chr16:31958152-31958153	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs145149706	chr16:31958186-31958187	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs1395526	chr16:31958211-31958212	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs565660295	chr16:31958216-31958217	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs538203969	chr16:31958235-31958236	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs539550616	chr16:31958335-31958336	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs568804454	chr16:31958355-31958356	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs78739538	chr16:31958382-31958383	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs142148616	chr16:31958389-31958390	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs35438798	chr16:31958391-31958392	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs571078509	chr16:31958399-31958400	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs146888134	chr16:31958426-31958427	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs115078246	chr16:31958437-31958438	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs140473210	chr16:31958451-31958452	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs201363460	chr16:31958485-31958486	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs559053730	chr16:31958496-31958497	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs531273259	chr16:31958497-31958498	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs577407610	chr16:31958546-31958547	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs145649173	chr16:31958573-31958574	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs562880679	chr16:31958584-31958585	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs574777131	chr16:31958644-31958645	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Sezary syndrome	18413736	CNVD
Wilms tumour	21544195	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31957000-31958800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr16:31962600-31963000	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr16:31962600-31963400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr16:31962800-31963400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr16:31962800-31963600	Enhancers	Primary T cells fromperipheralblood	blood
6	chr16:31962800-31963600	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr16:31963200-31963400	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr16:31963200-31964000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr16:31963600-31964200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr16:31964200-31964400	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr16:31964200-31964400	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr16:31971800-31972200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr16:32002400-32002800	Enhancers	HepG2	liver
14	chr16:32051200-32051600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr16:32051400-32051600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr16:32051400-32051600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr16:32077600-32078000	Enhancers	Dnd41	blood

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