Variant report

Variant	nsv884731
Chromosome Location	chr6:32307382-32329795
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:1287)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:32309236-32309268	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr6:32313528-32313764	GM12878	blood:	n/a	chr6:32313546-32313555
3	CEBPB	chr6:32321136-32321610	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr6:32317340-32317490	Caco-2	colon:	n/a	n/a
5	E2F4	chr6:32311658-32311738	MCF10A-Er-Src	breast:	n/a	n/a
6	EP300	chr6:32321139-32321500	Hela-S3	cervix:	n/a	n/a
7	FOS	chr6:32313504-32313882	MCF10A-Er-Src	breast:	n/a	chr6:32313731-32313742 chr6:32313530-32313539
8	FOS	chr6:32313531-32313873	MCF10A-Er-Src	breast:	n/a	chr6:32313731-32313742
9	FOS	chr6:32321115-32321505	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr6:32313508-32313881	MCF10A-Er-Src	breast:	n/a	chr6:32313731-32313742 chr6:32313530-32313539
11	FOS	chr6:32313505-32313875	HUVEC	blood vessel:	n/a	chr6:32313731-32313742 chr6:32313530-32313539
12	FOS	chr6:32314098-32314129	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr6:32317500-32317812	MCF10A-Er-Src	breast:	n/a	chr6:32317643-32317652
14	FOS	chr6:32317508-32317764	MCF10A-Er-Src	breast:	n/a	chr6:32317643-32317652
15	FOS	chr6:32321184-32321501	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr6:32321132-32321502	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr6:32317556-32317801	MCF10A-Er-Src	breast:	n/a	chr6:32317643-32317652
18	FOS	chr6:32321122-32321561	MCF10A-Er-Src	breast:	n/a	n/a
19	GATA2	chr6:32323035-32323624	HUVEC	blood vessel:	n/a	n/a
20	GATA2	chr6:32313457-32313814	HUVEC	blood vessel:	n/a	chr6:32313491-32313502
21	MAFK	chr6:32314185-32314297	HepG2	liver:	n/a	n/a
22	MAFK	chr6:32327890-32328075	HepG2	liver:	n/a	n/a
23	MYC	chr6:32310973-32311201	H1-hESC	embryonic stem cell:	n/a	n/a
24	MYC	chr6:32321278-32321564	MCF10A-Er-Src	breast:	n/a	n/a
25	NFYA	chr6:32317687-32317810	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr6:32317083-32317116	Gliobla	brain:	n/a	n/a
27	POLR2A	chr6:32324354-32324363	MCF-7	breast:	n/a	n/a
28	POLR2A	chr6:32324969-32325114	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr6:32324366-32324388	MCF-7	breast:	n/a	n/a
30	PRDM1	chr6:32323220-32323427	Hela-S3	cervix:	n/a	n/a
31	STAT3	chr6:32317512-32317778	MCF10A-Er-Src	breast:	n/a	n/a
32	STAT3	chr6:32321140-32321480	Hela-S3	cervix:	n/a	n/a
33	STAT3	chr6:32319840-32319996	MCF10A-Er-Src	breast:	n/a	n/a
34	STAT3	chr6:32321069-32321546	MCF10A-Er-Src	breast:	n/a	n/a
35	STAT3	chr6:32321347-32321420	MCF10A-Er-Src	breast:	n/a	n/a
36	STAT3	chr6:32321165-32321481	MCF10A-Er-Src	breast:	n/a	n/a
37	STAT3	chr6:32308261-32308444	MCF10A-Er-Src	breast:	n/a	n/a
38	STAT3	chr6:32321157-32321514	MCF10A-Er-Src	breast:	n/a	n/a

(count:1287 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32309323-32309373	AG04450	lung:	fetal
2	chr6:32315772-32315822	PrEC	prostate:	n/a
3	chr6:32324878-32324928	BE2_C	brain:	n/a
4	chr6:32324878-32324928	PFSK-1	brain:	n/a
5	chr6:32310527-32310577	GM06990	blood:	n/a
6	chr6:32320715-32320765	HRPEpiC	eye:	n/a
7	chr6:32309323-32309373	AG04450	lung:	fetal
8	chr6:32315772-32315822	PrEC	prostate:	n/a
9	chr6:32324878-32324928	BE2_C	brain:	n/a
10	chr6:32324878-32324928	PFSK-1	brain:	n/a
11	chr6:32310527-32310577	GM06990	blood:	n/a
12	chr6:32320715-32320765	HRPEpiC	eye:	n/a
13	chr6:32320708-32320758	NH-A	brain:	n/a
14	chr6:32308995-32309045	HL-60	blood:	n/a
15	chr6:32313583-32313633	HL-60	blood:	n/a
16	chr6:32311517-32311567	SAEC	small airway:	n/a
17	chr6:32320708-32320758	HNPCEpiC	eye:	n/a
18	chr6:32314717-32314767	SK-N-MC	brain:	n/a
19	chr6:32317528-32317578	GM12878	blood:	n/a
20	chr6:32312513-32312563	K562	blood:	n/a
21	chr6:32324878-32324928	GM12878	blood:	n/a
22	chr6:32324878-32324928	HRCEpiC	kidney:	n/a
23	chr6:32317528-32317578	AG10803	skin:	n/a
24	chr6:32309323-32309373	PrEC	prostate:	n/a
25	chr6:32312351-32312401	BJ	skin:	n/a
26	chr6:32309154-32309204	BE2_C	brain:	n/a
27	chr6:32308995-32309045	H1-hESC	embryonic stem cell:	embryo
28	chr6:32311517-32311567	A549	lung:	n/a
29	chr6:32314717-32314767	GM12891	blood:	n/a
30	chr6:32317143-32317193	PANC-1	pancreas:	n/a
31	chr6:32315253-32315303	BE2_C	brain:	n/a
32	chr6:32317429-32317479	GM12891	blood:	n/a
33	chr6:32317429-32317479	IMR90	lung:	fetal
34	chr6:32315253-32315303	K562	blood:	n/a
35	chr6:32326581-32326631	HepG2	liver:	n/a
36	chr6:32315772-32315822	K562	blood:	n/a
37	chr6:32320715-32320765	SK-N-SH	brain:	n/a
38	chr6:32324878-32324928	Hela-S3	cervix:	n/a
39	chr6:32329440-32329490	U87	brain:	n/a
40	chr6:32317028-32317078	AG04450	lung:	fetal
41	chr6:32320715-32320765	AoSMC	blood vessel:	n/a
42	chr6:32315772-32315822	GM12878	blood:	n/a
43	chr6:32317429-32317479	HCPEpiC	choroid plexus:	n/a
44	chr6:32312351-32312401	U87	brain:	n/a
45	chr6:32329440-32329490	A549	lung:	n/a
46	chr6:32313583-32313633	ProgFib	skin:	n/a
47	chr6:32310527-32310577	ProgFib	skin:	n/a
48	chr6:32320708-32320758	HIPEpiC	eye:	n/a
49	chr6:32317028-32317078	GM12892	blood:	n/a
50	chr6:32309154-32309204	MCF-7	breast:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:32312156..32313758-chr6:32316689..32318846,2	MCF-7	breast:
2	chr6:32312156..32313758-chr6:32316689..32318846,2	MCF-7	breast:
3	chr6:32066051..32069021-chr6:32305851..32308384,2	K562	blood:
4	chr6:32297324..32300713-chr6:32303639..32307978,4	K562	blood:
5	chr6:32310954..32313823-chr6:32318938..32321332,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-DRA-6	chr6:32317289-32317601	NONHSAT108900

No data

Variant related genes	Relation type
RNU6-603P	TF binding region
RNU6-603P	CpG island
ENSG00000223335	chromatin interactions

Extended variants
information (count: 599 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:599 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528554394	chr6:32310004-32310005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs540689198	chr6:32310007-32310008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561964906	chr6:32310009-32310010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529205962	chr6:32310066-32310067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191372139	chr6:32310097-32310098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs9268257	chr6:32310103-32310104	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs3129901	chr6:32310119-32310120	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs183816080	chr6:32310167-32310168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs3129902	chr6:32310194-32310195	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs3129903	chr6:32310211-32310212	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs188301070	chr6:32310290-32310291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs3129904	chr6:32310396-32310397	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs566972048	chr6:32310403-32310404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs117144699	chr6:32310404-32310405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs3132955	chr6:32310415-32310416	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs138908531	chr6:32310445-32310446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532340067	chr6:32310479-32310480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539646151	chr6:32310532-32310533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs117876908	chr6:32310538-32310539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572966083	chr6:32310613-32310614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs56016875	chr6:32310645-32310646	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs9268258	chr6:32310684-32310685	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs573738805	chr6:32310714-32310715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9268259	chr6:32310803-32310804	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs3117136	chr6:32310811-32310812	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs192786386	chr6:32310842-32310843	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs185268917	chr6:32310848-32310849	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs140179797	chr6:32310853-32310854	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs144049657	chr6:32310929-32310930	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs542844425	chr6:32310965-32310966	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs9268260	chr6:32310967-32310968	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs9268261	chr6:32310986-32310987	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs550572395	chr6:32311044-32311045	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs569207192	chr6:32311067-32311068	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539374406	chr6:32311089-32311090	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147358179	chr6:32311107-32311108	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs114094496	chr6:32311116-32311117	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs1555117	chr6:32311148-32311149	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs148394151	chr6:32311163-32311164	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs116680752	chr6:32311202-32311203	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs6902224	chr6:32311213-32311214	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs150952376	chr6:32311238-32311239	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs577940238	chr6:32311271-32311272	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532116317	chr6:32311272-32311273	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs376161396	chr6:32311297-32311298	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545377721	chr6:32311304-32311305	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs139595484	chr6:32311356-32311357	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs527917547	chr6:32311429-32311430	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs3132954	chr6:32311459-32311460	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs561793076	chr6:32311503-32311504	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Ovarian cancer	21781307	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:32310000-32311600	Enhancers	Primary B cells from peripheral blood	blood
2	chr6:32310600-32311000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:32310800-32311200	Bivalent Enhancer	GM12878-XiMat	blood
4	chr6:32311200-32311800	Enhancers	GM12878-XiMat	blood
5	chr6:32312200-32312600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:32312600-32315200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:32315000-32315600	Enhancers	Brain Cingulate Gyrus	brain
8	chr6:32315000-32315800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr6:32315200-32315600	Enhancers	Brain Hippocampus Middle	brain
10	chr6:32315200-32316000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:32315200-32316000	Enhancers	Brain Substantia Nigra	brain
12	chr6:32315400-32316000	Enhancers	Brain Angular Gyrus	brain
13	chr6:32317400-32317800	Enhancers	Hela-S3	cervix
14	chr6:32317800-32320800	Weak transcription	Hela-S3	cervix
15	chr6:32320800-32321800	Enhancers	Hela-S3	cervix
16	chr6:32320800-32322000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:32321800-32323000	Weak transcription	Hela-S3	cervix
18	chr6:32322000-32323200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:32322800-32323600	Enhancers	HUVEC	blood vessel
20	chr6:32323000-32323400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:32323000-32324200	Enhancers	Hela-S3	cervix
22	chr6:32323200-32324000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:32324200-32324600	Weak transcription	Hela-S3	cervix
24	chr6:32324600-32325600	Enhancers	Hela-S3	cervix
25	chr6:32325600-32332600	Weak transcription	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links