Variant report

Variant	nsv559103
Chromosome Location	chr12:60383069-60483607
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:248)
CpG islands
(count:0)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:248 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:60471816-60472199	K562	blood:	n/a	n/a
2	BHLHE40	chr12:60471887-60471910	GM12878	blood:	n/a	n/a
3	CEBPB	chr12:60464408-60464802	MCF-7	breast:	n/a	n/a
4	CEBPB	chr12:60399603-60399803	A549	lung:	n/a	n/a
5	CEBPB	chr12:60394344-60394410	A549	lung:	n/a	n/a
6	CEBPB	chr12:60428211-60428406	HepG2	liver:	n/a	chr12:60428277-60428288
7	CEBPB	chr12:60428205-60428348	A549	lung:	n/a	chr12:60428277-60428288
8	CTCF	chr12:60431533-60431672	GM12878	blood:	n/a	n/a
9	CTCF	chr12:60415195-60415245	MCF-7	breast:	n/a	n/a
10	CTCF	chr12:60415080-60415230	MCF-7	breast:	n/a	n/a
11	CTCF	chr12:60393364-60393506	GM12878	blood:	n/a	n/a
12	CTCF	chr12:60415160-60415310	AG09309	skin:	n/a	n/a
13	CTCF	chr12:60452960-60453110	HCT-116	colon:	n/a	n/a
14	CTCF	chr12:60431540-60431690	HCT-116	colon:	n/a	n/a
15	CTCF	chr12:60452980-60453130	AG04450	lung:	n/a	n/a
16	CTCF	chr12:60415191-60415194	MCF-7	breast:	n/a	n/a
17	CTCF	chr12:60453060-60453210	AoAF	blood vessel:	n/a	n/a
18	CTCF	chr12:60394160-60394187	GM13976	blood:	n/a	n/a
19	CTCF	chr12:60394112-60394149	GM10248	blood:	n/a	n/a
20	CTCF	chr12:60453060-60453210	SAEC	small airway:	n/a	n/a
21	CTCF	chr12:60431569-60431633	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr12:60453040-60453190	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr12:60453100-60453250	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr12:60453040-60453190	NHEK	skin:	n/a	n/a
25	CTCF	chr12:60452940-60453090	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:60453000-60453150	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr12:60453000-60453150	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:60453040-60453190	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr12:60463523-60463609	Lung_OC	lung:	n/a	n/a
30	CTCF	chr12:60471701-60471732	GM13976	blood:	n/a	n/a
31	CTCF	chr12:60453060-60453210	HMF	breast:	n/a	n/a
32	CTCF	chr12:60477446-60477528	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:60453060-60453210	HCFaa	heart:	n/a	n/a
34	CTCF	chr12:60453060-60453210	HMEC	breast:	n/a	n/a
35	CTCF	chr12:60399040-60399190	GM06990	blood:	n/a	n/a
36	CTCF	chr12:60470260-60470410	A549	lung:	n/a	n/a
37	CTCF	chr12:60453060-60453210	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr12:60453040-60453190	AG04450	lung:	n/a	n/a
39	E2F4	chr12:60408741-60408749	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr12:60459063-60459331	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr12:60470080-60470120	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr12:60438565-60438706	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr12:60429046-60429069	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr12:60399741-60399899	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr12:60459734-60459892	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr12:60464284-60464649	MCF10A-Er-Src	breast:	n/a	n/a
47	EBF1	chr12:60465450-60465794	GM12878	blood:	n/a	n/a
48	ELF1	chr12:60435873-60436243	K562	blood:	n/a	chr12:60436015-60436028
49	EP300	chr12:60465597-60466133	MCF-7	breast:	n/a	n/a
50	ESR1	chr12:60437928-60438173	ECC-1	luminal epithelium:	n/a	n/a

No data

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:60481263..60483527-chr12:60485827..60488653,2	K562	blood:
2	chr12:60468174..60469728-chr12:60471025..60473459,2	MCF-7	breast:
3	chr12:60466814..60469463-chr12:60479017..60481348,2	MCF-7	breast:
4	chr12:60473802..60475803-chr12:60480234..60482937,2	MCF-7	breast:
5	chr12:60471895..60473733-chr12:60474074..60477071,2	MCF-7	breast:
6	chr12:60439937..60442180-chr12:60446699..60448272,2	MCF-7	breast:
7	chr12:60461970..60464211-chr12:60465232..60466795,2	MCF-7	breast:
8	chr12:60472741..60475079-chr12:60479250..60481071,2	K562	blood:
9	chr12:60463450..60465824-chr12:60478986..60481258,2	MCF-7	breast:
10	chr12:60465097..60467873-chr12:60470417..60472937,3	MCF-7	breast:
11	chr12:60466814..60469463-chr12:60479017..60481348,2	MCF-7	breast:
12	chr12:60463450..60465824-chr12:60478986..60481258,2	MCF-7	breast:
13	chr12:60473802..60475803-chr12:60480234..60482937,2	MCF-7	breast:
14	chr12:60465097..60467873-chr12:60470417..60472937,3	MCF-7	breast:
15	chr12:60419898..60420453-chr14:61344505..61345184,2	MCF-7	breast:
16	chr12:60468174..60469728-chr12:60471025..60473459,2	MCF-7	breast:
17	chr12:60424657..60427143-chr12:60427851..60429693,2	MCF-7	breast:
18	chr12:60442817..60444737-chr12:60445729..60447893,2	K562	blood:
19	chr12:60448484..60450647-chr12:60452739..60455616,2	K562	blood:
20	chr12:60466885..60469119-chr12:60493136..60496064,3	MCF-7	breast:
21	chr12:60442817..60444737-chr12:60445729..60447893,2	K562	blood:
22	chr12:60424657..60427143-chr12:60427851..60429693,2	MCF-7	breast:
23	chr12:60460447..60462196-chr12:60466989..60469396,2	K562	blood:
24	chr12:60460447..60462196-chr12:60466989..60469396,2	K562	blood:
25	chr12:60478315..60480971-chr12:60488037..60490719,3	MCF-7	breast:
26	chr12:60471895..60473733-chr12:60474074..60477071,2	MCF-7	breast:
27	chr12:60448484..60450647-chr12:60452739..60455616,2	K562	blood:
28	chr12:60454406..60456057-chr12:60465200..60468132,2	MCF-7	breast:
29	chr12:60459856..60461380-chr12:60466711..60469397,2	MCF-7	breast:
30	chr12:60461970..60464211-chr12:60465232..60466795,2	MCF-7	breast:
31	chr12:60459856..60461380-chr12:60466711..60469397,2	MCF-7	breast:
32	chr12:60454406..60456057-chr12:60465200..60468132,2	MCF-7	breast:
33	chr12:60439937..60442180-chr12:60446699..60448272,2	MCF-7	breast:
34	chr12:60437721..60438429-chr8:43096750..43097250,2	MCF-7	breast:
35	chr12:60472741..60475079-chr12:60479250..60481071,2	K562	blood:
36	chr1:107703503..107704327-chr12:60399253..60400075,2	MCF-7	breast:
37	chr12:60464696..60468583-chr12:60490353..60494821,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000257294	TF binding region
ENSG00000264437	TF binding region
ENSG00000257294	chromatin interactions

Extended variants
information (count: 3132 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3132 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9325169	chr12:60383069-60383070	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148105868	chr12:60383121-60383122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534952334	chr12:60383126-60383127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554995628	chr12:60383147-60383148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574789625	chr12:60383178-60383179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs386763486	chr12:60383191-60383192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543804630	chr12:60383214-60383215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563592831	chr12:60383221-60383222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142777816	chr12:60383231-60383232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545957479	chr12:60383265-60383266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559547331	chr12:60383268-60383269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375209351	chr12:60383277-60383278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74613393	chr12:60383317-60383318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76062717	chr12:60383330-60383331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577042066	chr12:60383339-60383340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529610776	chr12:60383355-60383356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146054922	chr12:60383389-60383390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569623912	chr12:60383400-60383401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538767511	chr12:60383424-60383425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559012458	chr12:60383425-60383426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552385058	chr12:60383431-60383432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565924971	chr12:60383469-60383470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538320755	chr12:60383485-60383486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534915387	chr12:60383495-60383496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371261145	chr12:60383565-60383566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75259522	chr12:60383569-60383570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139436915	chr12:60383584-60383585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537013623	chr12:60383594-60383595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530175584	chr12:60383595-60383596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557345478	chr12:60383644-60383645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11173267	chr12:60383709-60383710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11173268	chr12:60383712-60383713	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs545924487	chr12:60383717-60383718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142657794	chr12:60383775-60383776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572763649	chr12:60383809-60383810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573147883	chr12:60383850-60383851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111897531	chr12:60383889-60383890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542020708	chr12:60383899-60383900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7315509	chr12:60383927-60383928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150572473	chr12:60384122-60384123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531258637	chr12:60384166-60384167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139576065	chr12:60384258-60384259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149707563	chr12:60384294-60384295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563677464	chr12:60384295-60384296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145525623	chr12:60384300-60384301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552350231	chr12:60384307-60384308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565787216	chr12:60384318-60384319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528257824	chr12:60384343-60384344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548383508	chr12:60384380-60384381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568234520	chr12:60384392-60384393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60377400-60403800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:60382800-60383600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:60387000-60387400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:60391000-60392600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr12:60391200-60392600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:60391200-60392800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr12:60391400-60392800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr12:60391600-60392000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr12:60391800-60392600	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr12:60392600-60395200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:60395200-60395400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:60401200-60401600	Enhancers	Fetal Brain Female	brain
13	chr12:60404000-60405000	Enhancers	Fetal Intestine Small	intestine
14	chr12:60404000-60405200	Enhancers	Fetal Intestine Large	intestine
15	chr12:60404200-60404800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr12:60404400-60404800	Enhancers	Stomach Mucosa	stomach
17	chr12:60404800-60408000	Weak transcription	Stomach Mucosa	stomach
18	chr12:60405000-60407400	Weak transcription	Fetal Intestine Small	intestine
19	chr12:60405200-60408200	Weak transcription	Fetal Intestine Large	intestine
20	chr12:60407400-60408800	Enhancers	Fetal Intestine Small	intestine
21	chr12:60408000-60408800	Enhancers	Stomach Mucosa	stomach
22	chr12:60408200-60408800	Enhancers	Duodenum Mucosa	Duodenum
23	chr12:60408200-60409000	Enhancers	Fetal Intestine Large	intestine
24	chr12:60408800-60420600	Weak transcription	Fetal Intestine Small	intestine
25	chr12:60413200-60414200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:60414200-60418400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:60418400-60422000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:60419600-60427000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:60420600-60421600	Enhancers	Fetal Intestine Small	intestine
30	chr12:60426800-60428200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:60427000-60428200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:60427400-60427800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:60427400-60428200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr12:60428200-60429800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:60428800-60430800	Enhancers	HUVEC	blood vessel
36	chr12:60429400-60430200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr12:60429400-60430400	Enhancers	NHEK	skin
38	chr12:60429400-60430600	Enhancers	HMEC	breast
39	chr12:60429800-60430400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr12:60429800-60430600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:60429800-60430600	Enhancers	NHDF-Ad	bronchial
42	chr12:60436600-60437000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr12:60436800-60437000	Enhancers	HUVEC	blood vessel
44	chr12:60437000-60437400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:60437000-60438000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr12:60437000-60442400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:60437200-60437600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr12:60437400-60437800	Enhancers	HUVEC	blood vessel
49	chr12:60437400-60438000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:60453800-60454600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links