Variant report

Variant	esv3431632
Chromosome Location	chr2:181987257-181989255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:56)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:56 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:181988331-181989010	GM12878	blood:	n/a	n/a
2	ATF2	chr2:181988390-181988888	GM12878	blood:	n/a	n/a
3	BATF	chr2:181988398-181988791	GM12878	blood:	n/a	n/a
4	BATF	chr2:181988440-181988955	GM12878	blood:	n/a	chr2:181988871-181988881 chr2:181988867-181988877
5	BCL11A	chr2:181988467-181988832	GM12878	blood:	n/a	n/a
6	BCLAF1	chr2:181988271-181988945	GM12878	blood:	n/a	chr2:181988869-181988878
7	BHLHE40	chr2:181988446-181988761	GM12878	blood:	n/a	n/a
8	CEBPB	chr2:181988319-181989251	GM12878	blood:	n/a	n/a
9	CHD2	chr2:181988491-181988834	GM12878	blood:	n/a	n/a
10	CUX1	chr2:181988354-181988790	GM12878	blood:	n/a	n/a
11	EBF1	chr2:181988434-181989055	GM12878	blood:	n/a	n/a
12	EP300	chr2:181988417-181988859	GM12878	blood:	n/a	chr2:181988715-181988725 chr2:181988721-181988735
13	EP300	chr2:181988452-181988805	GM12878	blood:	n/a	chr2:181988715-181988725 chr2:181988721-181988735
14	EP300	chr2:181988428-181988875	GM12878	blood:	n/a	chr2:181988715-181988725 chr2:181988721-181988735
15	FOS	chr2:181988662-181989073	HUVEC	blood vessel:	n/a	chr2:181988868-181988879 chr2:181988870-181988878
16	FOXM1	chr2:181988343-181988989	GM12878	blood:	n/a	n/a
17	FOXM1	chr2:181988325-181988980	GM12878	blood:	n/a	n/a
18	GATA2	chr2:181988406-181989508	HUVEC	blood vessel:	n/a	chr2:181988531-181988538 chr2:181988718-181988729 chr2:181988958-181988972
19	IKZF1	chr2:181988448-181989050	GM12878	blood:	n/a	n/a
20	IRF4	chr2:181988395-181988861	GM12878	blood:	n/a	n/a
21	MAFF	chr2:181989235-181989490	HepG2	liver:	n/a	chr2:181989337-181989355
22	MAFK	chr2:181989236-181989465	HepG2	liver:	n/a	n/a
23	MAFK	chr2:181989208-181989489	IMR90	lung:	n/a	n/a
24	MAZ	chr2:181988473-181988864	GM12878	blood:	n/a	n/a
25	MEF2A	chr2:181988341-181988802	GM12878	blood:	n/a	n/a
26	MTA3	chr2:181988330-181988983	GM12878	blood:	n/a	n/a
27	MTA3	chr2:181988398-181988919	GM12878	blood:	n/a	n/a
28	MXI1	chr2:181988414-181988812	GM12878	blood:	n/a	n/a
29	NFATC1	chr2:181988400-181989063	GM12878	blood:	n/a	n/a
30	NFATC1	chr2:181988389-181988885	GM12878	blood:	n/a	n/a
31	NFIC	chr2:181988240-181989826	GM12878	blood:	n/a	n/a
32	NFIC	chr2:181988293-181989052	GM12878	blood:	n/a	n/a
33	PAX5	chr2:181988378-181988894	GM12878	blood:	n/a	n/a
34	PAX5	chr2:181988465-181988722	GM12878	blood:	n/a	n/a
35	PML	chr2:181988276-181989022	GM12878	blood:	n/a	n/a
36	PML	chr2:181988486-181988840	GM12878	blood:	n/a	n/a
37	POLR2A	chr2:181988419-181988932	GM12892	blood:	n/a	n/a
38	POLR2A	chr2:181988728-181988835	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr2:181988430-181988848	GM12891	blood:	n/a	n/a
40	POLR2A	chr2:181988522-181988747	GM12878	blood:	n/a	n/a
41	POLR2A	chr2:181988507-181988809	GM12891	blood:	n/a	n/a
42	POLR2A	chr2:181988530-181989063	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr2:181988510-181988818	GM12891	blood:	n/a	n/a
44	RELA	chr2:181988449-181988913	GM12891	blood:	n/a	n/a
45	RUNX3	chr2:181988378-181988952	GM12878	blood:	n/a	n/a
46	RUNX3	chr2:181988321-181988978	GM12878	blood:	n/a	n/a
47	SMC3	chr2:181988375-181988887	GM12878	blood:	n/a	n/a
48	SP1	chr2:181988420-181988846	GM12878	blood:	n/a	n/a
49	SPI1	chr2:181988315-181988941	HL-60	blood:	n/a	n/a
50	SPI1	chr2:181988422-181988649	GM12891	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:181987552-181987602	ECC-1	luminal epithelium:	n/a
2	chr2:181987552-181987602	HIPEpiC	eye:	n/a
3	chr2:181987552-181987602	H1-hESC	embryonic stem cell:	embryo
4	chr2:181987552-181987602	BE2_C	brain:	n/a
5	chr2:181987552-181987602	HRCEpiC	kidney:	n/a
6	chr2:181987552-181987602	HMEC	breast:	n/a
7	chr2:181987552-181987602	GM12892	blood:	n/a
8	chr2:181987552-181987602	HepG2	liver:	n/a
9	chr2:181987552-181987602	BJ	skin:	n/a
10	chr2:181987552-181987602	AG09309	skin:	n/a
11	chr2:181987552-181987602	HRE	kidney:	n/a
12	chr2:181987552-181987602	GM12878	blood:	n/a
13	chr2:181987552-181987602	HCM	heart:	n/a
14	chr2:181987552-181987602	HRPEpiC	eye:	n/a
15	chr2:181987552-181987602	PANC-1	pancreas:	n/a
16	chr2:181987552-181987602	GM19239	blood:	n/a
17	chr2:181987552-181987602	CMK	blood:	n/a
18	chr2:181987552-181987602	A549	lung:	n/a
19	chr2:181987552-181987602	HCF	heart:	n/a
20	chr2:181987552-181987602	SK-N-MC	brain:	n/a
21	chr2:181987552-181987602	ovcar-3	ovarian:	n/a
22	chr2:181987552-181987602	RPTEC	kidney:	n/a
23	chr2:181987552-181987602	K562	blood:	n/a
24	chr2:181987552-181987602	AoSMC	blood vessel:	n/a
25	chr2:181987552-181987602	PrEC	prostate:	n/a
26	chr2:181987552-181987602	HUVEC	blood vessel:	n/a
27	chr2:181987552-181987602	HEK293	kidney:	embryo
28	chr2:181987552-181987602	AG09319	gingival:	n/a
29	chr2:181987552-181987602	AG04449	skin:	fetal
30	chr2:181987552-181987602	SK-N-SH_RA	brain:	n/a
31	chr2:181987552-181987602	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:181987552-181987602	NB4	blood:	n/a
33	chr2:181987552-181987602	NT2-D1	testis:	n/a
34	chr2:181987552-181987602	Hepatocyte	liver:	n/a
35	chr2:181987552-181987602	GM06990	blood:	n/a
36	chr2:181987552-181987602	IMR90	lung:	fetal
37	chr2:181987552-181987602	GM12891	blood:	n/a
38	chr2:181987552-181987602	MCF-7	breast:	n/a
39	chr2:181987552-181987602	AG04450	lung:	fetal
40	chr2:181987552-181987602	HCPEpiC	choroid plexus:	n/a
41	chr2:181987552-181987602	Hela-S3	cervix:	n/a
42	chr2:181987552-181987602	SAEC	small airway:	n/a
43	chr2:181987552-181987602	NHBE	bronchial:	n/a
44	chr2:181987552-181987602	HCT-116	colon:	n/a
45	chr2:181987552-181987602	MCF10A-Er-Src	breast:	n/a
46	chr2:181987552-181987602	NH-A	brain:	n/a
47	chr2:181987552-181987602	ProgFib	skin:	n/a
48	chr2:181987552-181987602	LNCaP	prostate:	n/a
49	chr2:181987552-181987602	NHDF-neo	bronchial:	n/a
50	chr2:181987552-181987602	AG10803	skin:	n/a

No data

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2E3-1	chr2:181988562-181988707	XLOC_001776
2	lnc-CERKL-2	chr2:181988623-181988706	NONHSAT075862
3	lnc-UBE2E3-1	chr2:181988659-181988707	XLOC_001776
4	lnc-UBE2E3-1	chr2:181988623-181988707	XLOC_001776
5	lnc-UBE2E3-1	chr2:181988669-181988707	XLOC_001776
6	lnc-UBE2E3-1	chr2:181988564-181988707	ENSG00000234663
7	lnc-UBE2E3-1	chr2:181988564-181988707	XLOC_001776

No data

Variant related genes	Relation type
ENSG00000234663	TF binding region
ENSG00000234663	CpG island
TBPL1	miRNA target sites
NAP1L2	miRNA target sites

Extended variants
information (count: 76 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:76 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76843483	chr2:181987282-181987283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142309026	chr2:181987367-181987368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544816406	chr2:181987382-181987383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564981925	chr2:181987387-181987388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530677474	chr2:181987407-181987408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550811326	chr2:181987493-181987494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567551942	chr2:181987500-181987501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572137174	chr2:181987501-181987502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541137256	chr2:181987515-181987516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs13020845	chr2:181987553-181987554	Weak transcription Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs549357938	chr2:181987604-181987605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs10206586	chr2:181987614-181987615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs62178852	chr2:181987711-181987712	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs557786108	chr2:181987757-181987758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571432783	chr2:181987758-181987759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190763071	chr2:181987759-181987760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557164599	chr2:181987817-181987818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs59052759	chr2:181987969-181987970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs397760533	chr2:181987971-181987972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183763324	chr2:181987980-181987981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188293936	chr2:181988015-181988016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192984704	chr2:181988019-181988020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182966388	chr2:181988021-181988022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34412259	chr2:181988037-181988038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186980365	chr2:181988050-181988051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs13416165	chr2:181988067-181988068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183623373	chr2:181988069-181988070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189514464	chr2:181988073-181988074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs193041867	chr2:181988074-181988075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368767622	chr2:181988094-181988095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10207097	chr2:181988098-181988099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs13428145	chr2:181988121-181988122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181562552	chr2:181988198-181988199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186335374	chr2:181988202-181988203	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs552922489	chr2:181988239-181988240	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs62178853	chr2:181988256-181988257	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs551658003	chr2:181988300-181988301	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs572708388	chr2:181988349-181988350	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs544991689	chr2:181988350-181988351	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs564946063	chr2:181988351-181988352	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs530657518	chr2:181988356-181988357	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs188360125	chr2:181988363-181988364	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs138982499	chr2:181988414-181988415	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs79619894	chr2:181988476-181988477	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs180905859	chr2:181988490-181988491	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs140449252	chr2:181988493-181988494	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs116224953	chr2:181988533-181988534	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs377587614	chr2:181988593-181988594	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs150426240	chr2:181988625-181988626	Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs571388596	chr2:181988660-181988661	Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181981400-181988600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:181983600-181988400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:181984800-181988200	Enhancers	Primary T cells from cord blood	blood
4	chr2:181985000-181988400	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr2:181985000-181988800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr2:181985000-181990200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:181985200-181987800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr2:181985200-181988000	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr2:181985600-181988400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:181985800-181988400	Weak transcription	HMEC	breast
11	chr2:181985800-181988400	Weak transcription	NH-A	brain
12	chr2:181986000-181988200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr2:181986200-181988400	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr2:181986400-181988600	Weak transcription	HSMM	muscle
15	chr2:181986600-181989000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr2:181986800-181987600	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr2:181986800-181988400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr2:181987000-181988600	Weak transcription	HSMMtube	muscle
19	chr2:181987000-181988800	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr2:181987200-181988000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr2:181987400-181988400	Enhancers	Dnd41	blood
22	chr2:181987400-181989000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr2:181987600-181988400	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr2:181987800-181988400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr2:181988000-181988200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr2:181988000-181988400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr2:181988200-181988400	Flanking Active TSS	Primary T cells from cord blood	blood
28	chr2:181988200-181988400	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr2:181988200-181988400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:181988200-181988600	Enhancers	Primary B cells from cord blood	blood
31	chr2:181988200-181988600	Enhancers	Muscle Satellite Cultured Cells	--
32	chr2:181988400-181988600	Active TSS	Primary T helper naive cells from peripheral blood	blood
33	chr2:181988400-181988600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
34	chr2:181988400-181988600	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr2:181988400-181988800	Active TSS	Primary T cells from cord blood	blood
36	chr2:181988400-181988800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
37	chr2:181988400-181988800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr2:181988400-181989000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr2:181988400-181989000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:181988400-181989000	Enhancers	Primary B cells from peripheral blood	blood
41	chr2:181988400-181989000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr2:181988400-181989000	Enhancers	HMEC	breast
43	chr2:181988400-181989200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr2:181988400-181989200	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr2:181988400-181989400	Active TSS	Primary T cells fromperipheralblood	blood
46	chr2:181988400-181989400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chr2:181988400-181989400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr2:181988400-181989600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr2:181988400-181989600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr2:181988400-181989600	Enhancers	Primary hematopoietic stem cells short term culture	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links