Variant report

Variant	nsv1486
Chromosome Location	chr15:35494248-35536549
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	ARID3A	chr15:35502061-35502453	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:35510461-35510693	HepG2	liver:	n/a	n/a
3	BHLHE40	chr15:35498695-35498725	HepG2	liver:	n/a	n/a
4	BHLHE40	chr15:35502067-35502394	HepG2	liver:	n/a	n/a
5	CBX3	chr15:35498477-35498877	K562	blood:	n/a	n/a
6	CEBPB	chr15:35498159-35498446	K562	blood:	n/a	chr15:35498302-35498315
7	CEBPB	chr15:35502092-35502398	HepG2	liver:	n/a	chr15:35502324-35502335
8	CEBPB	chr15:35502044-35502495	HepG2	liver:	n/a	chr15:35502324-35502335
9	CEBPB	chr15:35507105-35507432	IMR90	lung:	n/a	chr15:35507273-35507285 chr15:35507261-35507272
10	CEBPB	chr15:35502026-35502519	HepG2	liver:	n/a	chr15:35502324-35502335
11	CEBPB	chr15:35502178-35502397	HepG2	liver:	n/a	chr15:35502324-35502335
12	CTCF	chr15:35498600-35498750	HepG2	liver:	n/a	chr15:35498658-35498676
13	CTCF	chr15:35498640-35498790	GM12866	blood:	n/a	chr15:35498658-35498676
14	CTCF	chr15:35512800-35512950	HMF	breast:	n/a	n/a
15	CTCF	chr15:35498580-35498730	GM12866	blood:	n/a	chr15:35498658-35498676
16	CTCF	chr15:35498560-35498710	HepG2	liver:	n/a	chr15:35498658-35498676
17	CTCF	chr15:35498555-35498774	GM13977	blood:	n/a	chr15:35498658-35498676
18	CTCF	chr15:35498620-35498770	GM12865	blood:	n/a	chr15:35498658-35498676
19	CTCF	chr15:35498560-35498710	SK-N-SH_RA	brain:	n/a	chr15:35498658-35498676
20	CTCF	chr15:35498600-35498750	HCPEpiC	choroid plexus:	n/a	chr15:35498658-35498676
21	CTCF	chr15:35498676-35498707	GM13976	blood:	n/a	n/a
22	CTCF	chr15:35498663-35498731	A549	lung:	n/a	n/a
23	CTCF	chr15:35498600-35498750	SAEC	small airway:	n/a	chr15:35498658-35498676
24	CTCF	chr15:35498600-35498750	AG04450	lung:	n/a	chr15:35498658-35498676
25	CTCF	chr15:35498571-35498756	HepG2	liver:	n/a	chr15:35498658-35498676
26	CTCF	chr15:35498600-35498750	GM12873	blood:	n/a	chr15:35498658-35498676
27	CTCF	chr15:35498580-35498730	HA-sp	spinal cord:	n/a	chr15:35498658-35498676
28	CTCF	chr15:35498600-35498750	GM12871	blood:	n/a	chr15:35498658-35498676
29	CTCF	chr15:35498620-35498770	Caco-2	colon:	n/a	chr15:35498658-35498676
30	CTCF	chr15:35498600-35498750	WERI-Rb-1	eye:	n/a	chr15:35498658-35498676
31	CTCF	chr15:35498580-35498730	HCPEpiC	choroid plexus:	n/a	chr15:35498658-35498676
32	CTCF	chr15:35498544-35498802	GM12878	blood:	n/a	chr15:35498658-35498676
33	CTCF	chr15:35498620-35498770	NHLF	lung:	n/a	chr15:35498658-35498676
34	CTCF	chr15:35498560-35498710	HFF	foreskin:	n/a	chr15:35498658-35498676
35	CTCF	chr15:35498657-35498683	MCF-7	breast:	n/a	chr15:35498658-35498676
36	CTCF	chr15:35498540-35498690	GM12865	blood:	n/a	chr15:35498658-35498676
37	CTCF	chr15:35498600-35498750	HUVEC	blood vessel:	n/a	chr15:35498658-35498676
38	CTCF	chr15:35498620-35498770	HRE	kidney:	n/a	chr15:35498658-35498676
39	CTCF	chr15:35498688-35498787	Lung_OC	lung:	n/a	n/a
40	CTCF	chr15:35498520-35498670	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr15:35498594-35498753	GM20000	blood:	n/a	chr15:35498658-35498676
42	CTCF	chr15:35498580-35498730	WERI-Rb-1	eye:	n/a	chr15:35498658-35498676
43	CTCF	chr15:35498620-35498770	GM12874	blood:	n/a	chr15:35498658-35498676
44	CTCF	chr15:35498600-35498750	HVMF	connective:	n/a	chr15:35498658-35498676
45	CTCF	chr15:35498484-35498829	K562	blood:	n/a	chr15:35498658-35498676
46	CTCF	chr15:35498600-35498750	HPF	lung:	n/a	chr15:35498658-35498676
47	CTCF	chr15:35498620-35498770	WI-38	lung:	n/a	chr15:35498658-35498676
48	CTCF	chr15:35498622-35498707	Kidney_OC	kidney:	n/a	chr15:35498658-35498676
49	CTCF	chr15:35498600-35498750	HMF	breast:	n/a	chr15:35498658-35498676
50	CTCF	chr15:35498560-35498710	AG04449	skin:	n/a	chr15:35498658-35498676

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:35529521-35529571	A549	lung:	n/a
2	chr15:35529521-35529571	A549	lung:	n/a
3	chr15:35529612-35529662	HCT-116	colon:	n/a
4	chr15:35529473-35529523	NH-A	brain:	n/a
5	chr15:35529473-35529523	BE2_C	brain:	n/a
6	chr15:35529560-35529610	ECC-1	luminal epithelium:	n/a
7	chr15:35529473-35529523	ovcar-3	ovarian:	n/a
8	chr15:35529560-35529610	HIPEpiC	eye:	n/a
9	chr15:35529473-35529523	A549	lung:	n/a
10	chr15:35529612-35529662	ProgFib	skin:	n/a
11	chr15:35529169-35529219	CMK	blood:	n/a
12	chr15:35529560-35529610	ovcar-3	ovarian:	n/a
13	chr15:35529560-35529610	HRPEpiC	eye:	n/a
14	chr15:35529169-35529219	ProgFib	skin:	n/a
15	chr15:35529473-35529523	GM12878	blood:	n/a
16	chr15:35529521-35529571	IMR90	lung:	fetal
17	chr15:35529169-35529219	GM19239	blood:	n/a
18	chr15:35529473-35529523	HEEpiC	esophagus:	n/a
19	chr15:35529612-35529662	T-47D	breast:	n/a
20	chr15:35529169-35529219	HAEpiC	amniotic membrane:	n/a
21	chr15:35529612-35529662	PANC-1	pancreas:	n/a
22	chr15:35529169-35529219	SAEC	small airway:	n/a
23	chr15:35529473-35529523	HCPEpiC	choroid plexus:	n/a
24	chr15:35529612-35529662	AG04449	skin:	fetal
25	chr15:35529473-35529523	AG09309	skin:	n/a
26	chr15:35529473-35529523	ProgFib	skin:	n/a
27	chr15:35529612-35529662	NHBE	bronchial:	n/a
28	chr15:35529473-35529523	HRPEpiC	eye:	n/a
29	chr15:35529169-35529219	SK-N-SH_RA	brain:	n/a
30	chr15:35529612-35529662	GM06990	blood:	n/a
31	chr15:35529521-35529571	HUVEC	blood vessel:	n/a
32	chr15:35529521-35529571	K562	blood:	n/a
33	chr15:35529521-35529571	HMEC	breast:	n/a
34	chr15:35529169-35529219	GM12891	blood:	n/a
35	chr15:35529169-35529219	HUVEC	blood vessel:	n/a
36	chr15:35529521-35529571	HAEpiC	amniotic membrane:	n/a
37	chr15:35529169-35529219	MCF10A-Er-Src	breast:	n/a
38	chr15:35529169-35529219	H1-hESC	embryonic stem cell:	embryo
39	chr15:35529473-35529523	SK-N-MC	brain:	n/a
40	chr15:35529560-35529610	GM19239	blood:	n/a
41	chr15:35529473-35529523	MCF-7	breast:	n/a
42	chr15:35529169-35529219	AG09319	gingival:	n/a
43	chr15:35529560-35529610	NB4	blood:	n/a
44	chr15:35529521-35529571	HNPCEpiC	eye:	n/a
45	chr15:35529560-35529610	AG09319	gingival:	n/a
46	chr15:35529473-35529523	BJ	skin:	n/a
47	chr15:35529169-35529219	NHDF-neo	bronchial:	n/a
48	chr15:35529473-35529523	SAEC	small airway:	n/a
49	chr15:35529169-35529219	HCF	heart:	n/a
50	chr15:35529612-35529662	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:35492720..35494706-chr15:35497193..35498842,2	K562	blood:
2	chr15:35494938..35497759-chr15:35498704..35501139,2	K562	blood:
3	chr15:35497735..35499624-chr15:35509642..35511524,2	K562	blood:
4	chr15:35494938..35497759-chr15:35498704..35501139,2	K562	blood:
5	chr15:35370781..35371294-chr15:35498222..35498748,2	K562	blood:
6	chr15:35497735..35499624-chr15:35509642..35511524,2	K562	blood:
7	chr15:35515840..35517484-chr15:35522294..35524054,2	K562	blood:
8	chr15:35515840..35517484-chr15:35522294..35524054,2	K562	blood:
9	chr15:35509284..35511880-chr15:35539205..35541715,2	K562	blood:
10	chr15:35492720..35494706-chr15:35497193..35498842,2	K562	blood:
11	chr15:35464572..35466280-chr15:35519004..35521985,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATPBD4-3	chr15:35512076-35512541	NONHSAT041623
2	lnc-AC114546.1-11	chr15:35529527-35530264	NR_003144
3	lnc-ATPBD4-3	chr15:35504992-35505452	NONHSAT041623

Variant related genes	Relation type
ANP32AP1	TF binding region
ANP32AP1	CpG island

Extended variants
information (count: 1284 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574635366	chr15:35494252-35494253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542142079	chr15:35494339-35494340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553664797	chr15:35494371-35494372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572180283	chr15:35494381-35494382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546038177	chr15:35494391-35494392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147699570	chr15:35494420-35494421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142845309	chr15:35494432-35494433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531439565	chr15:35494458-35494459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4924646	chr15:35494537-35494538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561755030	chr15:35494628-35494629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368370924	chr15:35494717-35494718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147407964	chr15:35494754-35494755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557228082	chr15:35494801-35494802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548039952	chr15:35494802-35494803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575572381	chr15:35494840-35494841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373855793	chr15:35494862-35494863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79968399	chr15:35494866-35494867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4924647	chr15:35494907-35494908	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs551561623	chr15:35494964-35494965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569811897	chr15:35494987-35494988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537190000	chr15:35495033-35495034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72707067	chr15:35495058-35495059	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs8038846	chr15:35495074-35495075	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs534732257	chr15:35495103-35495104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183513297	chr15:35495104-35495105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72707068	chr15:35495113-35495114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545976712	chr15:35495174-35495175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187815285	chr15:35495221-35495222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576187264	chr15:35495227-35495228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149911013	chr15:35495289-35495290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs193146065	chr15:35495373-35495374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371076882	chr15:35495384-35495385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148331079	chr15:35495389-35495390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371170149	chr15:35495424-35495425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561649116	chr15:35495457-35495458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375488112	chr15:35495477-35495478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143939683	chr15:35495484-35495485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573544797	chr15:35495572-35495573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs58808674	chr15:35495601-35495602	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs148057897	chr15:35495671-35495672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78271350	chr15:35495707-35495708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533492143	chr15:35495717-35495718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185638759	chr15:35495739-35495740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79810676	chr15:35495851-35495852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530837843	chr15:35495882-35495883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549429916	chr15:35495954-35495955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567672669	chr15:35495979-35495980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534978712	chr15:35496003-35496004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143153164	chr15:35496024-35496025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565979947	chr15:35496034-35496035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:35484200-35502000	Weak transcription	Left Ventricle	heart
2	chr15:35489000-35504600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr15:35500400-35500800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr15:35500400-35500800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr15:35500400-35500800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr15:35500400-35501000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr15:35500600-35501800	Enhancers	Liver	Liver
8	chr15:35501600-35502800	Enhancers	HepG2	liver
9	chr15:35501800-35502200	Flanking Active TSS	Liver	Liver
10	chr15:35501800-35504200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr15:35501800-35506000	Enhancers	Fetal Brain Male	brain
12	chr15:35502000-35502200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr15:35502000-35502400	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr15:35502000-35502400	Enhancers	Left Ventricle	heart
15	chr15:35502000-35504800	Enhancers	Fetal Heart	heart
16	chr15:35502200-35502800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr15:35502200-35503600	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr15:35502200-35504400	Enhancers	Liver	Liver
19	chr15:35502800-35503800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr15:35503400-35503800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr15:35504000-35504200	Enhancers	Esophagus	oesophagus
22	chr15:35504200-35504800	Enhancers	Fetal Brain Female	brain
23	chr15:35504400-35510400	Weak transcription	Liver	Liver
24	chr15:35504600-35505600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr15:35505200-35505400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr15:35505200-35505600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr15:35506000-35510400	Weak transcription	Fetal Brain Male	brain
28	chr15:35510000-35511000	Enhancers	HepG2	liver
29	chr15:35510200-35511000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr15:35510400-35510600	Enhancers	Fetal Brain Male	brain
31	chr15:35510400-35510800	Enhancers	Liver	Liver
32	chr15:35510600-35510800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr15:35510600-35511400	Weak transcription	Fetal Brain Male	brain
34	chr15:35511000-35511200	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr15:35511400-35511600	Enhancers	Fetal Brain Male	brain
36	chr15:35511600-35512000	Enhancers	Rectal Smooth Muscle	rectum
37	chr15:35511800-35512000	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr15:35511800-35513600	Enhancers	Fetal Stomach	stomach
39	chr15:35513400-35513600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr15:35513400-35513800	Enhancers	Ovary	ovary
41	chr15:35521400-35523400	Weak transcription	Pancreas	Pancrea
42	chr15:35522200-35522600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr15:35522200-35523800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr15:35523000-35523400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
45	chr15:35523000-35524400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr15:35523800-35525200	Weak transcription	Adipose Nuclei	Adipose
47	chr15:35524400-35526400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr15:35524800-35525400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr15:35525400-35525600	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
50	chr15:35526400-35526600	Enhancers	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links