Variant report

Variant	esv13569
Chromosome Location	chr10:43325598-43331203
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:43327236-43327383	K562	blood:	n/a	n/a
2	FOXA1	chr10:43328734-43329005	HepG2	liver:	n/a	n/a
3	MYC	chr10:43330815-43330841	K562	blood:	n/a	n/a
4	POLR2A	chr10:43327904-43328237	K562	blood:	n/a	n/a
5	POLR2A	chr10:43328780-43329247	GM12891	blood:	n/a	n/a
6	POLR2A	chr10:43325974-43326042	K562	blood:	n/a	n/a
7	POLR2A	chr10:43327475-43327486	K562	blood:	n/a	n/a
8	POLR2A	chr10:43327726-43327798	K562	blood:	n/a	n/a
9	POLR2A	chr10:43328824-43329188	GM12878	blood:	n/a	n/a
10	POLR2A	chr10:43328894-43329029	Gliobla	brain:	n/a	n/a
11	POLR2A	chr10:43327624-43327656	ProgFib	skin:	n/a	n/a
12	POLR2A	chr10:43327797-43328297	GM12891	blood:	n/a	n/a
13	POLR2A	chr10:43329116-43329139	HepG2	liver:	n/a	n/a
14	POLR2A	chr10:43328786-43329220	GM12891	blood:	n/a	n/a
15	POLR2A	chr10:43327828-43328248	GM12891	blood:	n/a	n/a
16	POLR2A	chr10:43329056-43329200	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr10:43328782-43329438	K562	blood:	n/a	n/a
18	POLR2A	chr10:43327327-43328303	GM12892	blood:	n/a	n/a
19	POLR2A	chr10:43327855-43328430	K562	blood:	n/a	n/a
20	POLR2A	chr10:43327877-43328245	K562	blood:	n/a	n/a
21	POLR2A	chr10:43327704-43327706	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr10:43328789-43329192	K562	blood:	n/a	n/a
23	POLR2A	chr10:43328785-43328873	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr10:43329039-43329175	MCF-7	breast:	n/a	n/a
25	POLR2A	chr10:43328883-43329024	MCF-7	breast:	n/a	n/a
26	POLR2A	chr10:43326051-43326143	K562	blood:	n/a	n/a
27	POLR2A	chr10:43329030-43329038	MCF-7	breast:	n/a	n/a
28	POLR2A	chr10:43328912-43328965	GM12878	blood:	n/a	n/a
29	POLR2A	chr10:43326148-43326278	K562	blood:	n/a	n/a
30	POLR2A	chr10:43327867-43328337	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr10:43327338-43327480	K562	blood:	n/a	n/a
32	POLR2A	chr10:43328110-43328219	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr10:43328334-43328364	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr10:43327438-43327626	K562	blood:	n/a	n/a
35	POLR2A	chr10:43325401-43325601	K562	blood:	n/a	n/a
36	POLR2A	chr10:43327713-43327714	K562	blood:	n/a	n/a
37	POLR2A	chr10:43327421-43327617	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr10:43327538-43327567	K562	blood:	n/a	n/a
39	POLR2A	chr10:43327627-43327822	K562	blood:	n/a	n/a
40	POLR2A	chr10:43327883-43328307	GM12891	blood:	n/a	n/a
41	POLR2A	chr10:43327973-43328227	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr10:43327628-43328156	K562	blood:	n/a	n/a
43	SPI1	chr10:43325845-43326039	K562	blood:	n/a	chr10:43325987-43325994 chr10:43325934-43325947 chr10:43325935-43325944 chr10:43325933-43325946 chr10:43325934-43325947
44	SPI1	chr10:43325788-43326078	HL-60	blood:	n/a	chr10:43325987-43325994 chr10:43325934-43325947 chr10:43326031-43326044 chr10:43325935-43325944 chr10:43325933-43325946 chr10:43325934-43325947

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43329092-43329142	AG09309	skin:	n/a
2	chr10:43329092-43329142	GM12891	blood:	n/a
3	chr10:43329092-43329142	HepG2	liver:	n/a
4	chr10:43329092-43329142	PrEC	prostate:	n/a
5	chr10:43329092-43329142	GM12892	blood:	n/a
6	chr10:43329092-43329142	AG10803	skin:	n/a
7	chr10:43329092-43329142	BJ	skin:	n/a
8	chr10:43329092-43329142	ECC-1	luminal epithelium:	n/a
9	chr10:43329092-43329142	ovcar-3	ovarian:	n/a
10	chr10:43329092-43329142	GM12878	blood:	n/a
11	chr10:43329092-43329142	SK-N-SH	brain:	n/a
12	chr10:43329092-43329142	NB4	blood:	n/a
13	chr10:43329092-43329142	HEEpiC	esophagus:	n/a
14	chr10:43329092-43329142	HUVEC	blood vessel:	n/a
15	chr10:43329092-43329142	SK-N-SH_RA	brain:	n/a
16	chr10:43329092-43329142	HRE	kidney:	n/a
17	chr10:43329092-43329142	MCF-7	breast:	n/a
18	chr10:43329092-43329142	HAEpiC	amniotic membrane:	n/a
19	chr10:43329092-43329142	AG04450	lung:	fetal
20	chr10:43329092-43329142	Hepatocyte	liver:	n/a
21	chr10:43329092-43329142	HRCEpiC	kidney:	n/a
22	chr10:43329092-43329142	NHBE	bronchial:	n/a
23	chr10:43329092-43329142	A549	lung:	n/a
24	chr10:43329092-43329142	HPAEpiC	pulmonary alveolar:	n/a
25	chr10:43329092-43329142	NH-A	brain:	n/a
26	chr10:43329092-43329142	SKMC	muscle:	n/a
27	chr10:43329092-43329142	AG09319	gingival:	n/a
28	chr10:43329092-43329142	HL-60	blood:	n/a
29	chr10:43329092-43329142	HCT-116	colon:	n/a
30	chr10:43329092-43329142	NHDF-neo	bronchial:	n/a
31	chr10:43329092-43329142	K562	blood:	n/a
32	chr10:43329092-43329142	ProgFib	skin:	n/a
33	chr10:43329092-43329142	Jurkat	blood:	n/a
34	chr10:43329092-43329142	HRPEpiC	eye:	n/a
35	chr10:43329092-43329142	RPTEC	kidney:	n/a
36	chr10:43329092-43329142	HEK293	kidney:	embryo
37	chr10:43329092-43329142	BE2_C	brain:	n/a
38	chr10:43329092-43329142	PFSK-1	brain:	n/a
39	chr10:43329092-43329142	MCF10A-Er-Src	breast:	n/a
40	chr10:43329092-43329142	T-47D	breast:	n/a
41	chr10:43329092-43329142	AoSMC	blood vessel:	n/a
42	chr10:43329092-43329142	HCM	heart:	n/a
43	chr10:43329092-43329142	HCPEpiC	choroid plexus:	n/a
44	chr10:43329092-43329142	HNPCEpiC	eye:	n/a
45	chr10:43329092-43329142	HIPEpiC	eye:	n/a
46	chr10:43329092-43329142	GM06990	blood:	n/a
47	chr10:43329092-43329142	HMEC	breast:	n/a
48	chr10:43329092-43329142	H1-hESC	embryonic stem cell:	embryo
49	chr10:43329092-43329142	IMR90	lung:	fetal
50	chr10:43329092-43329142	LNCaP	prostate:	n/a

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	BMS1	hsa-miR-30a-5p	chr10:43327447-43327468

Variant related genes	Relation type
RNU6-885P	TF binding region
RNU6-885P	CpG island

Extended variants
information (count: 252 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10900276	chr10:43325606-43325607	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542443357	chr10:43325653-43325654	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs368570049	chr10:43325658-43325659	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs41295810	chr10:43325664-43325665	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs201739639	chr10:43325682-43325683	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372559744	chr10:43325695-43325696	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369831218	chr10:43325700-43325701	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374194864	chr10:43325769-43325770	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377616718	chr10:43325777-43325778	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552907353	chr10:43325792-43325793	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144403555	chr10:43325798-43325799	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370668862	chr10:43325825-43325826	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200894282	chr10:43325832-43325833	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs201022846	chr10:43325839-43325840	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550664789	chr10:43325840-43325841	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377058786	chr10:43325843-43325844	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568964255	chr10:43325844-43325845	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141528123	chr10:43325847-43325848	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201871271	chr10:43325851-43325852	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199956903	chr10:43325869-43325870	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201582130	chr10:43325881-43325882	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374201960	chr10:43325895-43325896	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368682397	chr10:43325896-43325897	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372101358	chr10:43325897-43325898	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369244218	chr10:43325901-43325902	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113245167	chr10:43325906-43325907	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567754844	chr10:43325924-43325925	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530174757	chr10:43325927-43325928	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562625754	chr10:43325942-43325943	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142499238	chr10:43325945-43325946	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs180899227	chr10:43325957-43325958	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186188200	chr10:43325973-43325974	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556223757	chr10:43325981-43325982	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574917732	chr10:43325988-43325989	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542053017	chr10:43326076-43326077	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570201162	chr10:43326092-43326093	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140410360	chr10:43326172-43326173	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538975912	chr10:43326218-43326219	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144257025	chr10:43326227-43326228	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147835947	chr10:43326256-43326257	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369848139	chr10:43326274-43326275	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191583834	chr10:43326296-43326297	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541781231	chr10:43326297-43326298	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181709983	chr10:43326348-43326349	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186197369	chr10:43326351-43326352	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150743357	chr10:43326358-43326359	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139118520	chr10:43326364-43326365	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375762235	chr10:43326371-43326372	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111882453	chr10:43326376-43326377	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547986001	chr10:43326393-43326394	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43279800-43328200	Strong transcription	Primary T helper cells fromperipheralblood	blood
2	chr10:43293200-43332400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr10:43301800-43325800	Weak transcription	NHLF	lung
4	chr10:43303600-43325800	Weak transcription	Colon Smooth Muscle	Colon
5	chr10:43303600-43332200	Weak transcription	NHDF-Ad	bronchial
6	chr10:43308200-43328200	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr10:43309800-43330000	Weak transcription	Small Intestine	intestine
8	chr10:43310400-43327400	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr10:43311200-43329000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr10:43311400-43329000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr10:43311600-43328200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr10:43312000-43328400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr10:43313400-43325600	Weak transcription	Hela-S3	cervix
14	chr10:43313400-43325800	Weak transcription	Fetal Brain Male	brain
15	chr10:43314400-43325600	Weak transcription	Brain Anterior Caudate	brain
16	chr10:43314400-43325800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr10:43314400-43332200	Weak transcription	Right Atrium	heart
18	chr10:43314600-43325800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr10:43314600-43329800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr10:43317800-43328200	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr10:43317800-43328200	Strong transcription	Fetal Intestine Large	intestine
22	chr10:43317800-43328200	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr10:43317800-43328200	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr10:43318200-43327200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr10:43318800-43325800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr10:43318800-43327000	Weak transcription	HSMM	muscle
27	chr10:43319200-43326400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr10:43320000-43325600	Weak transcription	HSMMtube	muscle
29	chr10:43320000-43329000	Weak transcription	Fetal Heart	heart
30	chr10:43320000-43332600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr10:43320400-43326800	Strong transcription	Fetal Intestine Small	intestine
32	chr10:43320400-43328400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr10:43320800-43325800	Weak transcription	Fetal Kidney	kidney
34	chr10:43321000-43325600	Weak transcription	Primary hematopoietic stem cells	blood
35	chr10:43321400-43325600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr10:43321400-43325800	Weak transcription	Fetal Lung	lung
37	chr10:43321400-43332800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr10:43321600-43325600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr10:43321600-43328200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr10:43321600-43332200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr10:43321800-43328200	Strong transcription	Fetal Stomach	stomach
42	chr10:43322200-43325800	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr10:43322200-43328200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr10:43322400-43325800	Weak transcription	Brain Cingulate Gyrus	brain
45	chr10:43323000-43325600	Weak transcription	Esophagus	oesophagus
46	chr10:43323000-43325600	Weak transcription	Right Ventricle	heart
47	chr10:43323000-43325800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr10:43323000-43332400	Weak transcription	Psoas Muscle	Psoas
49	chr10:43323200-43325800	Weak transcription	Left Ventricle	heart
50	chr10:43323200-43325800	Weak transcription	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links