Variant report

Variant	esv3379494
Chromosome Location	chr6:166918862-166923360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:32)
CpG islands
(count:491)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
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	ATF1	chr6:166920915-166921134	K562	blood:	n/a	n/a
2	BCL3	chr6:166920921-166921755	GM12878	blood:	n/a	n/a
3	BCL3	chr6:166920966-166921730	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:166921400-166921720	K562	blood:	n/a	n/a
5	BRCA1	chr6:166921291-166921301	GM12878	blood:	n/a	n/a
6	CTCF	chr6:166921511-166921583	GM19239	blood:	n/a	n/a
7	CTCF	chr6:166920520-166920670	HepG2	liver:	n/a	n/a
8	CTCF	chr6:166921025-166921035	GM19239	blood:	n/a	n/a
9	CTCF	chr6:166920452-166920633	K562	blood:	n/a	n/a
10	CTCF	chr6:166920523-166920637	K562	blood:	n/a	n/a
11	CTCF	chr6:166921062-166921362	GM19239	blood:	n/a	n/a
12	CTCF	chr6:166920970-166920987	GM19239	blood:	n/a	n/a
13	CTCF	chr6:166920430-166920711	K562	blood:	n/a	n/a
14	MAX	chr6:166921149-166921322	NB4	blood:	n/a	n/a
15	MAX	chr6:166921371-166921703	K562	blood:	n/a	chr6:166921589-166921600
16	MYC	chr6:166921365-166921621	MCF-7	breast:	n/a	chr6:166921589-166921600
17	MYC	chr6:166921150-166921275	HUVEC	blood vessel:	n/a	n/a
18	NFATC1	chr6:166921056-166921751	GM12878	blood:	n/a	n/a
19	NFATC1	chr6:166921017-166921785	GM12878	blood:	n/a	n/a
20	PBX3	chr6:166921003-166921679	GM12878	blood:	n/a	n/a
21	POLR2A	chr6:166921495-166921507	MCF-7	breast:	n/a	n/a
22	POLR2A	chr6:166920908-166921043	HepG2	liver:	n/a	n/a
23	POLR2A	chr6:166921371-166921443	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr6:166921212-166921371	HepG2	liver:	n/a	n/a
25	POU2F2	chr6:166920945-166921705	GM12891	blood:	n/a	n/a
26	RAD21	chr6:166920453-166920621	H1-hESC	embryonic stem cell:	n/a	n/a
27	RAD21	chr6:166920420-166920682	H1-hESC	embryonic stem cell:	n/a	n/a
28	SIN3A	chr6:166921673-166921935	H1-hESC	embryonic stem cell:	n/a	chr6:166921845-166921859 chr6:166921925-166921934
29	STAT5A	chr6:166921130-166921737	GM12878	blood:	n/a	n/a
30	SUZ12	chr6:166920842-166921608	H1-hESC	embryonic stem cell:	n/a	n/a
31	TCF3	chr6:166921210-166921606	GM12878	blood:	n/a	n/a
32	TCF3	chr6:166921237-166921708	GM12878	blood:	n/a	n/a

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166921890-166921940	SAEC	small airway:	n/a
2	chr6:166921760-166921810	SAEC	small airway:	n/a
3	chr6:166921807-166921857	AG09319	gingival:	n/a
4	chr6:166921890-166921940	SAEC	small airway:	n/a
5	chr6:166921760-166921810	SAEC	small airway:	n/a
6	chr6:166921807-166921857	AG09319	gingival:	n/a
7	chr6:166921760-166921810	PFSK-1	brain:	n/a
8	chr6:166921760-166921810	HepG2	liver:	n/a
9	chr6:166919577-166919627	PANC-1	pancreas:	n/a
10	chr6:166921807-166921857	Hepatocyte	liver:	n/a
11	chr6:166919277-166919327	AG04450	lung:	fetal
12	chr6:166922861-166922911	AG04450	lung:	fetal
13	chr6:166921890-166921940	ovcar-3	ovarian:	n/a
14	chr6:166921807-166921857	NT2-D1	testis:	n/a
15	chr6:166922861-166922911	Hela-S3	cervix:	n/a
16	chr6:166919189-166919239	HUVEC	blood vessel:	n/a
17	chr6:166922861-166922911	MCF-7	breast:	n/a
18	chr6:166922861-166922911	SK-N-SH	brain:	n/a
19	chr6:166921890-166921940	GM12878	blood:	n/a
20	chr6:166919277-166919327	BE2_C	brain:	n/a
21	chr6:166919277-166919327	Caco-2	colon:	n/a
22	chr6:166919189-166919239	BJ	skin:	n/a
23	chr6:166922861-166922911	HEEpiC	esophagus:	n/a
24	chr6:166921760-166921810	NHDF-neo	bronchial:	n/a
25	chr6:166919577-166919627	GM12878	blood:	n/a
26	chr6:166919189-166919239	HIPEpiC	eye:	n/a
27	chr6:166919277-166919327	ovcar-3	ovarian:	n/a
28	chr6:166919277-166919327	GM19239	blood:	n/a
29	chr6:166919577-166919627	AG04450	lung:	fetal
30	chr6:166921890-166921940	HCT-116	colon:	n/a
31	chr6:166921760-166921810	HEK293	kidney:	embryo
32	chr6:166921890-166921940	T-47D	breast:	n/a
33	chr6:166921890-166921940	H1-hESC	embryonic stem cell:	embryo
34	chr6:166922861-166922911	Hepatocyte	liver:	n/a
35	chr6:166921890-166921940	K562	blood:	n/a
36	chr6:166921890-166921940	SK-N-SH	brain:	n/a
37	chr6:166919277-166919327	NH-A	brain:	n/a
38	chr6:166919277-166919327	GM12878	blood:	n/a
39	chr6:166919577-166919627	AG10803	skin:	n/a
40	chr6:166919577-166919627	SAEC	small airway:	n/a
41	chr6:166922931-166922981	AG04450	lung:	fetal
42	chr6:166919577-166919627	CMK	blood:	n/a
43	chr6:166919577-166919627	NH-A	brain:	n/a
44	chr6:166921890-166921940	PrEC	prostate:	n/a
45	chr6:166921807-166921857	HNPCEpiC	eye:	n/a
46	chr6:166921807-166921857	NHBE	bronchial:	n/a
47	chr6:166919577-166919627	AG04449	skin:	fetal
48	chr6:166921807-166921857	AG04449	skin:	fetal
49	chr6:166921807-166921857	K562	blood:	n/a
50	chr6:166921807-166921857	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:166914781..166916706-chr6:166917616..166920240,2	K562	blood:
2	chr6:166917042..166919348-chr6:166921352..166923866,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1913	chr6:166922852-166922873	MIMAT0007888

No data

Variant related genes	Relation type
MIR1913	TF binding region
MIR1913	CpG island
ENSG00000071242	chromatin interactions
ENSG00000222958	chromatin interactions
SRSF4	Mature miRNA region

Extended variants
information (count: 229 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:229 , 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	rs76744913	chr6:166918877-166918878	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs574260033	chr6:166918919-166918920	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs559111020	chr6:166918990-166918991	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs115390509	chr6:166918992-166918993	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs548134908	chr6:166919036-166919037	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs563621446	chr6:166919081-166919082	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs530390899	chr6:166919082-166919083	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs186751953	chr6:166919112-166919113	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145214104	chr6:166919114-166919115	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs534706659	chr6:166919116-166919117	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs546759994	chr6:166919129-166919130	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs568629937	chr6:166919139-166919140	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs11751521	chr6:166919145-166919146	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs557346068	chr6:166919154-166919155	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs116063702	chr6:166919186-166919187	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs539781885	chr6:166919190-166919191	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs557710534	chr6:166919198-166919199	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs572940748	chr6:166919242-166919243	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540287681	chr6:166919246-166919247	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs561847783	chr6:166919248-166919249	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs574261407	chr6:166919257-166919258	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs189539119	chr6:166919266-166919267	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs563371274	chr6:166919267-166919268	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs180943725	chr6:166919284-166919285	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs552234440	chr6:166919287-166919288	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs564062441	chr6:166919294-166919295	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs138490480	chr6:166919298-166919299	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs559770653	chr6:166919311-166919312	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185775386	chr6:166919344-166919345	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs568182625	chr6:166919350-166919351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192392338	chr6:166919377-166919378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141079492	chr6:166919390-166919391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569380412	chr6:166919397-166919398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540124425	chr6:166919465-166919466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558037901	chr6:166919470-166919471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150247410	chr6:166919520-166919521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117081496	chr6:166919542-166919543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138862388	chr6:166919543-166919544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563925845	chr6:166919550-166919551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538977460	chr6:166919557-166919558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373350464	chr6:166919560-166919561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574062696	chr6:166919561-166919562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544406126	chr6:166919578-166919579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557115056	chr6:166919619-166919620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527619688	chr6:166919630-166919631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546080535	chr6:166919633-166919634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564375959	chr6:166919637-166919638	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376588231	chr6:166919691-166919692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528063954	chr6:166919715-166919716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528134157	chr6:166919730-166919731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	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	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166862400-166920600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:166890600-166925200	Weak transcription	Colon Smooth Muscle	Colon
3	chr6:166893000-166923200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:166893600-166921400	Weak transcription	Fetal Brain Male	brain
5	chr6:166894800-166928400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:166897600-166922400	Weak transcription	HSMMtube	muscle
7	chr6:166899400-166929400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:166901000-166954800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:166901400-166922000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:166902200-166954400	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr6:166902400-166922600	Weak transcription	Thymus	Thymus
12	chr6:166902400-166923600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr6:166902600-166952800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr6:166903000-166919200	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr6:166903000-166925400	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr6:166903800-166922000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr6:166904000-166923800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr6:166905000-166925200	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr6:166905000-166928200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:166905000-166928400	Weak transcription	HSMM	muscle
21	chr6:166906200-166921000	Weak transcription	Fetal Kidney	kidney
22	chr6:166906600-166923200	Strong transcription	Gastric	stomach
23	chr6:166906600-166923800	Strong transcription	Fetal Stomach	stomach
24	chr6:166906600-166925000	Strong transcription	Adipose Nuclei	Adipose
25	chr6:166906600-166925200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr6:166906800-166919800	Strong transcription	Brain Germinal Matrix	brain
27	chr6:166907000-166923200	Strong transcription	Fetal Brain Female	brain
28	chr6:166907800-166923000	Strong transcription	Lung	lung
29	chr6:166909200-166921600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr6:166909200-166921800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:166909400-166928400	Strong transcription	Muscle Satellite Cultured Cells	--
32	chr6:166909600-166943800	Weak transcription	Colonic Mucosa	Colon
33	chr6:166910400-166923200	Strong transcription	Cortex derived primary cultured neurospheres	brain
34	chr6:166910600-166920600	Weak transcription	Fetal Lung	lung
35	chr6:166910600-166923400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr6:166910800-166923800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr6:166911000-166919000	Strong transcription	Pancreas	Pancrea
38	chr6:166911000-166922200	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr6:166911000-166923200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr6:166911200-166928200	Weak transcription	NH-A	brain
41	chr6:166911400-166924400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr6:166911800-166923800	Strong transcription	Stomach Smooth Muscle	stomach
43	chr6:166912200-166919400	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr6:166912200-166927600	Weak transcription	HMEC	breast
45	chr6:166912200-166931200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr6:166913000-166929000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr6:166913000-166952000	Weak transcription	Primary T cells from cord blood	blood
48	chr6:166914400-166921000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr6:166915000-166920600	Weak transcription	Fetal Intestine Large	intestine
50	chr6:166915800-166921000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links