Variant report

Variant	nsv981781
Chromosome Location	chr7:127322449-127326404
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	ATF2	chr7:127324105-127324646	GM12878	blood:	n/a	n/a
2	BATF	chr7:127324206-127324538	GM12878	blood:	n/a	n/a
3	BCL3	chr7:127324155-127324588	GM12878	blood:	n/a	chr7:127324250-127324257 chr7:127324557-127324566
4	CTCF	chr7:127325760-127325910	HRE	kidney:	n/a	n/a
5	CTCF	chr7:127325866-127325919	GM12892	blood:	n/a	n/a
6	CTCF	chr7:127325800-127325950	GM12873	blood:	n/a	n/a
7	CTCF	chr7:127325820-127325970	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr7:127325820-127325970	GM12873	blood:	n/a	n/a
9	CTCF	chr7:127325800-127325950	GM12866	blood:	n/a	n/a
10	CTCF	chr7:127325780-127325930	GM12865	blood:	n/a	n/a
11	CTCF	chr7:127325720-127325870	GM12872	blood:	n/a	n/a
12	CTCF	chr7:127325806-127325927	Spleen_OC	spleen:	n/a	n/a
13	CTCF	chr7:127325850-127325936	GM19238	blood:	n/a	n/a
14	CTCF	chr7:127325800-127325950	GM12864	blood:	n/a	n/a
15	CTCF	chr7:127325760-127325910	GM12873	blood:	n/a	n/a
16	CTCF	chr7:127325792-127325886	GM13976	blood:	n/a	n/a
17	CTCF	chr7:127325720-127325870	GM12870	blood:	n/a	n/a
18	CTCF	chr7:127325760-127325910	GM12865	blood:	n/a	n/a
19	CTCF	chr7:127325760-127325910	GM12874	blood:	n/a	n/a
20	CTCF	chr7:127325760-127325910	GM12872	blood:	n/a	n/a
21	CTCF	chr7:127325820-127325970	GM12869	blood:	n/a	n/a
22	CTCF	chr7:127325580-127325830	HL-60	blood:	n/a	n/a
23	CTCF	chr7:127325823-127325894	GM13977	blood:	n/a	n/a
24	CTCF	chr7:127325800-127325950	GM12801	blood:	n/a	n/a
25	CTCF	chr7:127325760-127325910	GM12864	blood:	n/a	n/a
26	CTCF	chr7:127325654-127326036	GM12878	blood:	n/a	n/a
27	CTCF	chr7:127325760-127325910	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr7:127325720-127325870	GM12874	blood:	n/a	n/a
29	CTCF	chr7:127325740-127325890	GM12878	blood:	n/a	n/a
30	CTCF	chr7:127325720-127325870	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:127325840-127325990	GM12868	blood:	n/a	n/a
32	CTCF	chr7:127325800-127325950	GM12870	blood:	n/a	n/a
33	CTCF	chr7:127325800-127325950	GM06990	blood:	n/a	n/a
34	CTCF	chr7:127325800-127325950	GM12875	blood:	n/a	n/a
35	CTCF	chr7:127325803-127325954	GM12878	blood:	n/a	n/a
36	CTCF	chr7:127325800-127325950	GM12865	blood:	n/a	n/a
37	CTCF	chr7:127325786-127325883	GM10248	blood:	n/a	n/a
38	CTCF	chr7:127325820-127325970	HMEC	breast:	n/a	n/a
39	CUX1	chr7:127324198-127324614	GM12878	blood:	n/a	n/a
40	EBF1	chr7:127325692-127326066	GM12878	blood:	n/a	n/a
41	EBF1	chr7:127322114-127322456	GM12878	blood:	n/a	n/a
42	EBF1	chr7:127323929-127324709	GM12878	blood:	n/a	chr7:127324333-127324342 chr7:127324331-127324344 chr7:127324083-127324096 chr7:127324085-127324094 chr7:127324085-127324094 chr7:127324084-127324094 chr7:127324331-127324342 chr7:127324332-127324342
43	EBF1	chr7:127325693-127326095	GM12878	blood:	n/a	n/a
44	EBF1	chr7:127325664-127326095	GM12878	blood:	n/a	n/a
45	EBF1	chr7:127324065-127324571	GM12878	blood:	n/a	chr7:127324333-127324342 chr7:127324331-127324344 chr7:127324083-127324096 chr7:127324085-127324094 chr7:127324085-127324094 chr7:127324084-127324094 chr7:127324331-127324342 chr7:127324332-127324342
46	EBF1	chr7:127324050-127324536	GM12878	blood:	n/a	chr7:127324333-127324342 chr7:127324331-127324344 chr7:127324083-127324096 chr7:127324085-127324094 chr7:127324085-127324094 chr7:127324084-127324094 chr7:127324331-127324342 chr7:127324332-127324342
47	EP300	chr7:127322267-127322633	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr7:127324220-127324537	GM12878	blood:	n/a	n/a
49	GTF2F1	chr7:127324594-127324767	H1-hESC	embryonic stem cell:	n/a	n/a
50	IRF3	chr7:127324713-127324715	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:127322349..127324124-chr7:127326869..127328716,2	MCF-7	breast:
2	chr7:127322078..127323617-chr7:127325626..127327156,2	K562	blood:
3	chr7:127324074..127325812-chr7:127338072..127340357,2	K562	blood:
4	chr7:127321239..127323993-chr7:127348040..127350478,2	K562	blood:

Variant related genes	Relation type
SND1	TF binding region
ENSG00000197157	chromatin interactions

Extended variants
information (count: 136 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:136 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181195510	chr7:127322453-127322454	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs537900875	chr7:127322469-127322470	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs555838179	chr7:127322488-127322489	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs577858615	chr7:127322529-127322530	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs186213604	chr7:127322536-127322537	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561220847	chr7:127322597-127322598	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs712707	chr7:127322614-127322615	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs574402938	chr7:127322652-127322653	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs712708	chr7:127322685-127322686	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs559889142	chr7:127322713-127322714	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs35815054	chr7:127322716-127322717	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs189267536	chr7:127322722-127322723	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs528638388	chr7:127322863-127322864	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs972088	chr7:127322989-127322990	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs79707236	chr7:127322992-127322993	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs537636786	chr7:127323054-127323055	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs972089	chr7:127323067-127323068	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs112118036	chr7:127323083-127323084	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs116505734	chr7:127323085-127323086	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs10244461	chr7:127323096-127323097	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs35816796	chr7:127323107-127323108	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs972090	chr7:127323121-127323122	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs73723031	chr7:127323126-127323127	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs548704690	chr7:127323133-127323134	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs115438455	chr7:127323202-127323203	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs537434573	chr7:127323249-127323250	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs549501621	chr7:127323313-127323314	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs570986374	chr7:127323328-127323329	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs538868322	chr7:127323359-127323360	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs535875741	chr7:127323373-127323374	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs553914017	chr7:127323420-127323421	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs566249019	chr7:127323480-127323481	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373398029	chr7:127323517-127323518	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs376599186	chr7:127323518-127323519	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs57444252	chr7:127323523-127323524	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs552513364	chr7:127323565-127323566	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs576421746	chr7:127323643-127323644	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs180688680	chr7:127323663-127323664	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs559118210	chr7:127323700-127323701	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs528907639	chr7:127323751-127323752	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs577380395	chr7:127323798-127323799	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs145200824	chr7:127323852-127323853	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs186308938	chr7:127323856-127323857	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs550370225	chr7:127323860-127323861	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs149129874	chr7:127323956-127323957	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs6979634	chr7:127323965-127323966	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs190864462	chr7:127323999-127324000	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs183054622	chr7:127324002-127324003	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs373258989	chr7:127324014-127324015	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs571024984	chr7:127324025-127324026	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Glioblastoma multiforme	21510904	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
Myxofibrosarcoma	20639860	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127293200-127326600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr7:127294800-127327400	Weak transcription	Fetal Kidney	kidney
3	chr7:127295400-127326400	Weak transcription	Thymus	Thymus
4	chr7:127296200-127326600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr7:127299000-127334400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr7:127304600-127326600	Weak transcription	Fetal Stomach	stomach
7	chr7:127305200-127326600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:127306600-127323600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr7:127307000-127324200	Weak transcription	Fetal Heart	heart
10	chr7:127307000-127324200	Weak transcription	Stomach Mucosa	stomach
11	chr7:127307000-127330200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr7:127307200-127323200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr7:127307800-127324400	Weak transcription	Small Intestine	intestine
14	chr7:127308000-127323600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:127308200-127326600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr7:127308400-127326600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr7:127308800-127323600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr7:127308800-127323600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr7:127308800-127333600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr7:127309400-127333600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr7:127309600-127339600	Weak transcription	Brain Germinal Matrix	brain
22	chr7:127310600-127326400	Weak transcription	Fetal Muscle Leg	muscle
23	chr7:127311200-127326600	Weak transcription	Hela-S3	cervix
24	chr7:127312000-127323200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr7:127314200-127323600	Weak transcription	Gastric	stomach
26	chr7:127314400-127323200	Weak transcription	Left Ventricle	heart
27	chr7:127314400-127323400	Weak transcription	Pancreas	Pancrea
28	chr7:127314400-127326000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr7:127314400-127326600	Weak transcription	Spleen	Spleen
30	chr7:127314400-127327600	Weak transcription	Brain Anterior Caudate	brain
31	chr7:127314400-127330400	Weak transcription	Esophagus	oesophagus
32	chr7:127316400-127323800	Weak transcription	Ovary	ovary
33	chr7:127316400-127326600	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr7:127317000-127326600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:127318200-127325800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:127318200-127333800	Weak transcription	Brain Angular Gyrus	brain
37	chr7:127318600-127326200	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr7:127318800-127323600	Weak transcription	Adipose Nuclei	Adipose
39	chr7:127318800-127323800	Weak transcription	Brain Hippocampus Middle	brain
40	chr7:127319000-127323600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:127319200-127323200	Weak transcription	Psoas Muscle	Psoas
42	chr7:127319200-127323600	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr7:127319200-127323600	Weak transcription	Fetal Lung	lung
44	chr7:127319200-127324000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:127319200-127326200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr7:127319200-127326200	Weak transcription	Rectal Smooth Muscle	rectum
47	chr7:127319200-127326400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr7:127319200-127326600	Weak transcription	Lung	lung
49	chr7:127319200-127326600	Weak transcription	HSMM	muscle
50	chr7:127319200-127330400	Weak transcription	Aorta	Aorta

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