Variant report

Variant	nsv972418
Chromosome Location	chr9:94865248-94870773
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:32)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:32 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr9:94866561-94866595	GM20000	blood:	n/a	n/a
2	CTCF	chr9:94869293-94869344	Lung_OC	lung:	n/a	n/a
3	EP300	chr9:94867153-94867413	GM12878	blood:	n/a	n/a
4	GABPA	chr9:94865387-94865608	Hela-S3	cervix:	n/a	n/a
5	JUND	chr9:94867157-94867339	HepG2	liver:	n/a	n/a
6	MXI1	chr9:94870130-94870146	GM12878	blood:	n/a	n/a
7	PAX5	chr9:94866842-94867466	GM12878	blood:	n/a	n/a
8	POLR2A	chr9:94865632-94865703	GM12878	blood:	n/a	n/a
9	POLR2A	chr9:94869898-94869966	A549	lung:	n/a	n/a
10	POLR2A	chr9:94865722-94866312	GM12878	blood:	n/a	n/a
11	POLR2A	chr9:94866084-94866822	GM12892	blood:	n/a	n/a
12	POLR2A	chr9:94866863-94867414	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr9:94865357-94866739	GM12891	blood:	n/a	n/a
14	POLR2A	chr9:94866860-94867401	GM12878	blood:	n/a	n/a
15	POLR2A	chr9:94866086-94866421	GM12878	blood:	n/a	n/a
16	POLR2A	chr9:94867859-94868371	GM12878	blood:	n/a	n/a
17	POLR2A	chr9:94866172-94866846	GM12891	blood:	n/a	n/a
18	POLR2A	chr9:94869391-94869425	HepG2	liver:	n/a	n/a
19	POLR2A	chr9:94865220-94867614	GM12892	blood:	n/a	n/a
20	POLR2A	chr9:94865384-94866817	GM12891	blood:	n/a	n/a
21	POLR2A	chr9:94865000-94866680	GM12892	blood:	n/a	n/a
22	POLR2A	chr9:94865380-94866053	GM12891	blood:	n/a	n/a
23	POLR2A	chr9:94865298-94865749	GM12878	blood:	n/a	n/a
24	POLR2A	chr9:94868745-94868904	K562	blood:	n/a	n/a
25	POLR2A	chr9:94865126-94867729	GM12878	blood:	n/a	n/a
26	POU2F2	chr9:94865623-94866281	GM12878	blood:	n/a	n/a
27	POU2F2	chr9:94866849-94867362	GM12878	blood:	n/a	n/a
28	SPI1	chr9:94866942-94867153	K562	blood:	n/a	n/a
29	TAF1	chr9:94865265-94865484	Hela-S3	cervix:	n/a	n/a
30	TCF12	chr9:94866961-94867318	GM12878	blood:	n/a	n/a
31	USF1	chr9:94867229-94867372	HepG2	liver:	n/a	n/a
32	ZBTB33	chr9:94865413-94865626	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:94868003-94868053	HIPEpiC	eye:	n/a
2	chr9:94868003-94868053	MCF-7	breast:	n/a
3	chr9:94868003-94868053	NT2-D1	testis:	n/a
4	chr9:94868003-94868053	A549	lung:	n/a
5	chr9:94868003-94868053	AG04449	skin:	fetal
6	chr9:94868003-94868053	ovcar-3	ovarian:	n/a
7	chr9:94868003-94868053	PrEC	prostate:	n/a
8	chr9:94868003-94868053	BJ	skin:	n/a
9	chr9:94868003-94868053	SK-N-MC	brain:	n/a
10	chr9:94868003-94868053	CMK	blood:	n/a
11	chr9:94868003-94868053	LNCaP	prostate:	n/a
12	chr9:94868003-94868053	PANC-1	pancreas:	n/a
13	chr9:94868003-94868053	HRE	kidney:	n/a
14	chr9:94868003-94868053	T-47D	breast:	n/a
15	chr9:94868003-94868053	SKMC	muscle:	n/a
16	chr9:94868003-94868053	Jurkat	blood:	n/a
17	chr9:94868003-94868053	HEK293	kidney:	embryo
18	chr9:94868003-94868053	HepG2	liver:	n/a
19	chr9:94868003-94868053	Hepatocyte	liver:	n/a
20	chr9:94868003-94868053	IMR90	lung:	fetal
21	chr9:94868003-94868053	Hela-S3	cervix:	n/a
22	chr9:94868003-94868053	MCF10A-Er-Src	breast:	n/a
23	chr9:94868003-94868053	PFSK-1	brain:	n/a
24	chr9:94868003-94868053	H1-hESC	embryonic stem cell:	embryo
25	chr9:94868003-94868053	HUVEC	blood vessel:	n/a
26	chr9:94868003-94868053	AG04450	lung:	fetal
27	chr9:94868003-94868053	SAEC	small airway:	n/a
28	chr9:94868003-94868053	SK-N-SH	brain:	n/a
29	chr9:94868003-94868053	GM12891	blood:	n/a
30	chr9:94868003-94868053	NHBE	bronchial:	n/a
31	chr9:94868003-94868053	U87	brain:	n/a
32	chr9:94868003-94868053	HAEpiC	amniotic membrane:	n/a
33	chr9:94868003-94868053	GM12878	blood:	n/a
34	chr9:94868003-94868053	NB4	blood:	n/a
35	chr9:94868003-94868053	ECC-1	luminal epithelium:	n/a
36	chr9:94868003-94868053	HRCEpiC	kidney:	n/a
37	chr9:94868003-94868053	SK-N-SH_RA	brain:	n/a
38	chr9:94868003-94868053	AG09319	gingival:	n/a
39	chr9:94868003-94868053	AoSMC	blood vessel:	n/a
40	chr9:94868003-94868053	HRPEpiC	eye:	n/a
41	chr9:94868003-94868053	Caco-2	colon:	n/a
42	chr9:94868003-94868053	AG10803	skin:	n/a
43	chr9:94868003-94868053	RPTEC	kidney:	n/a
44	chr9:94868003-94868053	HPAEpiC	pulmonary alveolar:	n/a
45	chr9:94868003-94868053	K562	blood:	n/a
46	chr9:94868003-94868053	HCT-116	colon:	n/a
47	chr9:94868003-94868053	AG09309	skin:	n/a
48	chr9:94868003-94868053	HCF	heart:	n/a
49	chr9:94868003-94868053	HEEpiC	esophagus:	n/a
50	chr9:94868003-94868053	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:94867851..94872295-chr9:94876110..94878962,5	MCF-7	breast:
2	chr9:94860200..94862194-chr9:94864408..94866012,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000228069	TF binding region
ENSG00000238288	TF binding region
ENSG00000232179	TF binding region
MTND4P15	TF binding region
ENSG00000240791	TF binding region
ENSG00000228069	CpG island
ENSG00000238288	CpG island
ENSG00000232179	CpG island
MTND4P15	CpG island
ENSG00000240791	CpG island
ENSG00000090054	chromatin interactions

Extended variants
information (count: 248 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:248 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564798985	chr9:94865256-94865257	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs186327385	chr9:94865264-94865265	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs141807564	chr9:94865265-94865266	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs192449242	chr9:94865310-94865311	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs529644723	chr9:94865319-94865320	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs548041592	chr9:94865387-94865388	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs569631464	chr9:94865390-94865391	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs530592353	chr9:94865393-94865394	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs373938649	chr9:94865439-94865440	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs570592067	chr9:94865471-94865472	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs535111059	chr9:94865472-94865473	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs143822872	chr9:94865516-94865517	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs183338107	chr9:94865538-94865539	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs3957485	chr9:94865588-94865589	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs200845011	chr9:94865606-94865607	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3996336	chr9:94865621-94865622	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535857028	chr9:94865628-94865629	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9697261	chr9:94865656-94865657	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs575914246	chr9:94865657-94865658	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373658660	chr9:94865691-94865692	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558314759	chr9:94865717-94865718	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573398069	chr9:94865788-94865789	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188845946	chr9:94865799-94865800	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540723983	chr9:94865811-94865812	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs559031971	chr9:94865825-94865826	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs9696251	chr9:94865873-94865874	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs541447489	chr9:94865876-94865877	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs563166133	chr9:94865878-94865879	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs191141911	chr9:94865892-94865893	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs60827996	chr9:94865899-94865900	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs141864158	chr9:94865911-94865912	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs552230724	chr9:94865927-94865928	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs570624618	chr9:94865935-94865936	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs113261064	chr9:94865952-94865953	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs528301031	chr9:94865968-94865969	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs541118113	chr9:94865985-94865986	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs117470035	chr9:94865986-94865987	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs370866816	chr9:94866006-94866007	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs200597238	chr9:94866027-94866028	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs568581930	chr9:94866039-94866040	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs7037848	chr9:94866040-94866041	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs7021040	chr9:94866051-94866052	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs569190977	chr9:94866090-94866091	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs368667785	chr9:94866147-94866148	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs541111664	chr9:94866152-94866153	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs551720125	chr9:94866154-94866155	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs58224960	chr9:94866162-94866163	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs573346388	chr9:94866187-94866188	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs534139756	chr9:94866191-94866192	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs552622568	chr9:94866194-94866195	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94817800-94877000	Weak transcription	Fetal Heart	heart
2	chr9:94830800-94873800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr9:94840200-94865400	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr9:94840600-94872000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr9:94842800-94866000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr9:94842800-94867600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr9:94842800-94876600	Weak transcription	Colonic Mucosa	Colon
8	chr9:94843000-94866000	Weak transcription	Lung	lung
9	chr9:94851400-94865400	Weak transcription	Thymus	Thymus
10	chr9:94851400-94876600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr9:94851600-94865600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr9:94851800-94866000	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr9:94851800-94867600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr9:94853200-94865400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr9:94857000-94875400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr9:94857200-94866200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr9:94857400-94865600	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr9:94857800-94866200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr9:94858200-94867600	Weak transcription	Brain Angular Gyrus	brain
20	chr9:94858200-94869000	Weak transcription	Primary B cells from peripheral blood	blood
21	chr9:94858200-94873600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr9:94858400-94865600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr9:94858400-94866000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:94858400-94872200	Weak transcription	K562	blood
25	chr9:94858600-94865400	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr9:94858600-94869400	Weak transcription	Primary hematopoietic stem cells	blood
27	chr9:94858800-94873400	Weak transcription	GM12878-XiMat	blood
28	chr9:94859000-94870000	Weak transcription	HepG2	liver
29	chr9:94859200-94867600	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr9:94859600-94872800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr9:94860400-94872000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr9:94860800-94865400	Weak transcription	Fetal Muscle Trunk	muscle
33	chr9:94860800-94865600	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr9:94860800-94865600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr9:94860800-94865600	Weak transcription	Aorta	Aorta
36	chr9:94860800-94865600	Weak transcription	Duodenum Mucosa	Duodenum
37	chr9:94860800-94865600	Weak transcription	Fetal Stomach	stomach
38	chr9:94860800-94865600	Weak transcription	Left Ventricle	heart
39	chr9:94860800-94865600	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr9:94860800-94865600	Weak transcription	Rectal Smooth Muscle	rectum
41	chr9:94860800-94865600	Weak transcription	Right Ventricle	heart
42	chr9:94860800-94866000	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr9:94860800-94872600	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr9:94860800-94873600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr9:94860800-94876000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr9:94860800-94876000	Weak transcription	Brain Substantia Nigra	brain
47	chr9:94860800-94877000	Weak transcription	Brain Cingulate Gyrus	brain
48	chr9:94860800-94877200	Weak transcription	Stomach Mucosa	stomach
49	chr9:94861000-94865600	Weak transcription	Fetal Muscle Leg	muscle
50	chr9:94861000-94865600	Weak transcription	Rectal Mucosa Donor 29	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links