Variant report

Variant	nsv1004586
Chromosome Location	chr4:16341873-16375164
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:489)
Chromatin interactive
region (count:12)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr4:16362360-16362692	K562	blood:	n/a	n/a
2	CTCF	chr4:16374276-16374380	LNCaP	prostate:	n/a	n/a
3	E2F4	chr4:16366375-16366575	MCF10A-Er-Src	breast:	n/a	n/a
4	E2F4	chr4:16360641-16360852	MCF10A-Er-Src	breast:	n/a	n/a
5	E2F4	chr4:16363661-16363799	MCF10A-Er-Src	breast:	n/a	n/a
6	E2F6	chr4:16362597-16362767	K562	blood:	n/a	n/a
7	ELF1	chr4:16362212-16362798	MCF-7	breast:	n/a	n/a
8	ELF1	chr4:16362289-16362761	MCF-7	breast:	n/a	n/a
9	HA-E2F1	chr4:16362306-16363059	MCF-7	breast:	n/a	n/a
10	IRF1	chr4:16357311-16357460	K562	blood:	n/a	n/a
11	MAFF	chr4:16348525-16348762	HepG2	liver:	n/a	n/a
12	MAFK	chr4:16348552-16348793	HepG2	liver:	n/a	n/a
13	MAFK	chr4:16346479-16346552	HepG2	liver:	n/a	n/a
14	MAFK	chr4:16348561-16348761	HepG2	liver:	n/a	n/a
15	MAFK	chr4:16367690-16367765	HepG2	liver:	n/a	n/a
16	MAX	chr4:16354947-16355115	NB4	blood:	n/a	chr4:16354987-16354997
17	MAX	chr4:16362167-16362522	K562	blood:	n/a	n/a
18	MAX	chr4:16362445-16362769	MCF-7	breast:	n/a	n/a
19	MYC	chr4:16362408-16362824	MCF-7	breast:	n/a	n/a
20	MYC	chr4:16362427-16362723	MCF-7	breast:	n/a	n/a
21	MYC	chr4:16345444-16345447	MCF10A-Er-Src	breast:	n/a	n/a
22	MYC	chr4:16362417-16362669	MCF-7	breast:	n/a	n/a
23	MYC	chr4:16362429-16362626	H1-hESC	embryonic stem cell:	n/a	n/a
24	PML	chr4:16362453-16362761	MCF-7	breast:	n/a	n/a
25	POLR2A	chr4:16368672-16368763	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr4:16362107-16362125	MCF-7	breast:	n/a	n/a
27	POLR2A	chr4:16362271-16362913	MCF-7	breast:	n/a	n/a
28	POLR2A	chr4:16359970-16360061	K562	blood:	n/a	n/a
29	POLR2A	chr4:16362130-16363282	MCF-7	breast:	n/a	n/a
30	POLR2A	chr4:16362252-16362898	MCF-7	breast:	n/a	n/a
31	POLR2A	chr4:16362267-16362328	K562	blood:	n/a	n/a
32	POLR2A	chr4:16362508-16362535	ProgFib	skin:	n/a	n/a
33	POLR2A	chr4:16366829-16367151	H1-neurons	neurons:	n/a	n/a
34	POLR2A	chr4:16365781-16365862	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr4:16353183-16353327	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr4:16362334-16362650	K562	blood:	n/a	n/a
37	POLR2A	chr4:16344102-16344244	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr4:16362561-16362776	ProgFib	skin:	n/a	n/a
39	POLR2A	chr4:16354902-16355014	ProgFib	skin:	n/a	n/a
40	REST	chr4:16366769-16367224	H1-neurons	neurons:	n/a	n/a
41	SPI1	chr4:16351942-16352161	HL-60	blood:	n/a	chr4:16352067-16352076 chr4:16352065-16352078 chr4:16352066-16352079 chr4:16352068-16352075
42	SPI1	chr4:16351981-16352131	K562	blood:	n/a	chr4:16352067-16352076 chr4:16352065-16352078 chr4:16352066-16352079 chr4:16352068-16352075
43	SPI1	chr4:16351828-16352357	HL-60	blood:	n/a	chr4:16352067-16352076 chr4:16352065-16352078 chr4:16352066-16352079 chr4:16352068-16352075
44	SPI1	chr4:16350375-16350792	HL-60	blood:	n/a	n/a
45	STAT3	chr4:16347199-16347317	MCF10A-Er-Src	breast:	n/a	n/a
46	STAT3	chr4:16358956-16359156	MCF10A-Er-Src	breast:	n/a	n/a
47	STAT3	chr4:16346598-16346719	MCF10A-Er-Src	breast:	n/a	n/a
48	TAF1	chr4:16362443-16362735	MCF-7	breast:	n/a	n/a
49	USF1	chr4:16349162-16349540	H1-hESC	embryonic stem cell:	n/a	n/a
50	YY1	chr4:16362352-16362611	K562	blood:	n/a	chr4:16362484-16362496

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:16362664-16362714	GM19239	blood:	n/a
2	chr4:16362664-16362714	GM19239	blood:	n/a
3	chr4:16363266-16363316	GM12878	blood:	n/a
4	chr4:16363266-16363316	A549	lung:	n/a
5	chr4:16362664-16362714	NH-A	brain:	n/a
6	chr4:16366593-16366643	SK-N-MC	brain:	n/a
7	chr4:16362422-16362472	HNPCEpiC	eye:	n/a
8	chr4:16362340-16362390	RPTEC	kidney:	n/a
9	chr4:16362666-16362716	HEK293	kidney:	embryo
10	chr4:16362340-16362390	GM12878	blood:	n/a
11	chr4:16362340-16362390	NH-A	brain:	n/a
12	chr4:16366593-16366643	AG09319	gingival:	n/a
13	chr4:16366593-16366643	ovcar-3	ovarian:	n/a
14	chr4:16363266-16363316	HCF	heart:	n/a
15	chr4:16362340-16362390	A549	lung:	n/a
16	chr4:16366593-16366643	Caco-2	colon:	n/a
17	chr4:16359846-16359896	T-47D	breast:	n/a
18	chr4:16362664-16362714	ProgFib	skin:	n/a
19	chr4:16362584-16362634	HRPEpiC	eye:	n/a
20	chr4:16362340-16362390	NB4	blood:	n/a
21	chr4:16362666-16362716	ovcar-3	ovarian:	n/a
22	chr4:16366593-16366643	AG04450	lung:	fetal
23	chr4:16362584-16362634	GM12878	blood:	n/a
24	chr4:16359846-16359896	SK-N-SH	brain:	n/a
25	chr4:16362666-16362716	BE2_C	brain:	n/a
26	chr4:16362666-16362716	Hepatocyte	liver:	n/a
27	chr4:16363266-16363316	PFSK-1	brain:	n/a
28	chr4:16362422-16362472	HIPEpiC	eye:	n/a
29	chr4:16366593-16366643	H1-hESC	embryonic stem cell:	embryo
30	chr4:16366593-16366643	T-47D	breast:	n/a
31	chr4:16362584-16362634	AG09319	gingival:	n/a
32	chr4:16362584-16362634	ProgFib	skin:	n/a
33	chr4:16362340-16362390	HRCEpiC	kidney:	n/a
34	chr4:16362664-16362714	NT2-D1	testis:	n/a
35	chr4:16362664-16362714	HEK293	kidney:	embryo
36	chr4:16362584-16362634	U87	brain:	n/a
37	chr4:16362664-16362714	SAEC	small airway:	n/a
38	chr4:16362340-16362390	HUVEC	blood vessel:	n/a
39	chr4:16362422-16362472	H1-hESC	embryonic stem cell:	embryo
40	chr4:16362666-16362716	BJ	skin:	n/a
41	chr4:16362666-16362716	SAEC	small airway:	n/a
42	chr4:16362584-16362634	HepG2	liver:	n/a
43	chr4:16362664-16362714	IMR90	lung:	fetal
44	chr4:16362666-16362716	CMK	blood:	n/a
45	chr4:16366593-16366643	HEEpiC	esophagus:	n/a
46	chr4:16363266-16363316	AG04450	lung:	fetal
47	chr4:16362340-16362390	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:16363266-16363316	HEEpiC	esophagus:	n/a
49	chr4:16362664-16362714	SK-N-SH_RA	brain:	n/a
50	chr4:16362422-16362472	NH-A	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:16360973..16364086-chr4:16365820..16368451,4	MCF-7	breast:
2	chr4:16355756..16359124-chr4:16361383..16363978,4	MCF-7	breast:
3	chr19:56161626..56162436-chr4:16357679..16358532,2	MCF-7	breast:
4	chr4:16320021..16320816-chr4:16349710..16350236,2	MCF-7	breast:
5	chr4:16363037..16365847-chr4:16366056..16368462,2	K562	blood:
6	chr4:16355873..16357763-chr4:16357802..16360791,2	MCF-7	breast:
7	chr4:16364655..16366735-chr4:16377619..16379236,2	K562	blood:
8	chr4:16360699..16362829-chr4:16383139..16385452,2	MCF-7	breast:
9	chr4:16331798..16335655-chr4:16340723..16344531,3	K562	blood:
10	chr4:16258640..16260295-chr4:16352186..16354704,2	K562	blood:
11	chr4:16355873..16357763-chr4:16357802..16360791,2	MCF-7	breast:
12	chr4:16361224..16363467-chr4:16364801..16367359,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAPT1-3	chr4:16362507-16362611	NONHSAT095687
2	lnc-CD38-2	chr4:16357242-16357365	NONHSAT095684
3	lnc-CD38-2	chr4:16357243-16357365	XLOC_003469

No data

Variant related genes	Relation type
ZEB2P1	TF binding region
ZEB2P1	CpG island
ENSG00000249506	chromatin interactions

Extended variants
information (count: 732 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187636393	chr4:16341883-16341884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561026004	chr4:16341932-16341933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530248957	chr4:16341947-16341948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141765178	chr4:16341985-16341986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563549002	chr4:16342014-16342015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192369989	chr4:16342019-16342020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6825333	chr4:16342027-16342028	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs73239739	chr4:16342049-16342050	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs76391943	chr4:16342078-16342079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78100048	chr4:16342079-16342080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6825514	chr4:16342102-16342103	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs185007183	chr4:16342103-16342104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6849196	chr4:16342123-16342124	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs146204899	chr4:16342207-16342208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188942524	chr4:16342263-16342264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139230856	chr4:16342383-16342384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570240362	chr4:16342411-16342412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538930522	chr4:16342425-16342426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192100626	chr4:16342452-16342453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572435490	chr4:16342473-16342474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79837768	chr4:16342480-16342481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs9291643	chr4:16342501-16342502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185285634	chr4:16342517-16342518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189833806	chr4:16342574-16342575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142335677	chr4:16342636-16342637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574013501	chr4:16342669-16342670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371192745	chr4:16342682-16342683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116993694	chr4:16342729-16342730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546090612	chr4:16342730-16342731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559662656	chr4:16342732-16342733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528428261	chr4:16342790-16342791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548197418	chr4:16342792-16342793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181435078	chr4:16342842-16342843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530482326	chr4:16342864-16342865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550666496	chr4:16342878-16342879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150520510	chr4:16342913-16342914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539202577	chr4:16342925-16342926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185897965	chr4:16342967-16342968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566025193	chr4:16342987-16342988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189257395	chr4:16343005-16343006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554498940	chr4:16343011-16343012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181769725	chr4:16343049-16343050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543514951	chr4:16343054-16343055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186190828	chr4:16343112-16343113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375648268	chr4:16343122-16343123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576133077	chr4:16343147-16343148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545158851	chr4:16343165-16343166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565154846	chr4:16343213-16343214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546003557	chr4:16343284-16343285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115888505	chr4:16343314-16343315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:16338600-16353200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:16349800-16350000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:16350000-16352800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:16350200-16350600	Enhancers	Spleen	Spleen
5	chr4:16351400-16351600	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:16351400-16354000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr4:16351600-16351800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:16351600-16351800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr4:16351600-16351800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:16351600-16352200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr4:16351600-16352200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr4:16351800-16352800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr4:16351800-16353000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr4:16352000-16353000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr4:16352200-16352600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr4:16352200-16353000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr4:16352200-16353200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr4:16352200-16353800	Enhancers	Brain Germinal Matrix	brain
19	chr4:16352600-16355000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr4:16352800-16353800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:16352800-16353800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr4:16352800-16353800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:16352800-16353800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr4:16352800-16353800	Enhancers	Fetal Brain Female	brain
25	chr4:16353000-16353600	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr4:16353000-16353800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr4:16353000-16353800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:16353000-16353800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:16353000-16353800	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr4:16353000-16353800	Enhancers	Brain Cingulate Gyrus	brain
31	chr4:16353200-16353400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr4:16353200-16353800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr4:16353200-16353800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:16353200-16353800	Enhancers	Brain Substantia Nigra	brain
35	chr4:16353400-16353800	Enhancers	Brain Hippocampus Middle	brain
36	chr4:16353800-16354600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:16353800-16355000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:16354800-16355000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:16355000-16355200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:16357200-16358400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr4:16359200-16359600	Enhancers	Fetal Stomach	stomach
42	chr4:16362200-16362600	Active TSS	K562	blood
43	chr4:16362400-16363000	Active TSS	Placenta	Placenta
44	chr4:16362400-16363200	ZNF genes & repeats	Pancreas	Pancrea
45	chr4:16362600-16362800	Flanking Active TSS	K562	blood
46	chr4:16366600-16367200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr4:16366600-16367200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr4:16366800-16367200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr4:16367000-16367200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:16367000-16368200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links