Variant report

Variant	esv2762980
Chromosome Location	chr12:51527963-51561056
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:82)
CpG islands
(count:0)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:82 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:51554827-51555101	K562	blood:	n/a	n/a
2	BRCA1	chr12:51547596-51547679	Hela-S3	cervix:	n/a	n/a
3	CBX3	chr12:51554769-51555115	K562	blood:	n/a	n/a
4	CEBPB	chr12:51532671-51532970	Hela-S3	cervix:	n/a	chr12:51532800-51532811
5	CEBPB	chr12:51532631-51532977	HepG2	liver:	n/a	chr12:51532800-51532811
6	CEBPB	chr12:51540965-51541114	HepG2	liver:	n/a	chr12:51541076-51541087
7	CEBPB	chr12:51532651-51532978	K562	blood:	n/a	chr12:51532800-51532811
8	CEBPB	chr12:51532641-51532975	IMR90	lung:	n/a	chr12:51532800-51532811
9	CEBPB	chr12:51554899-51555231	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:51532640-51532954	A549	lung:	n/a	chr12:51532800-51532811
11	CEBPB	chr12:51532663-51532966	ECC-1	luminal epithelium:	n/a	chr12:51532800-51532811
12	CEBPB	chr12:51532659-51532968	H1-hESC	embryonic stem cell:	n/a	chr12:51532800-51532811
13	CTCF	chr12:51556155-51556178	GM10266	blood:	n/a	n/a
14	CTCF	chr12:51533420-51533570	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr12:51544076-51544180	GM10248	blood:	n/a	n/a
16	CTCF	chr12:51553980-51554130	GM12865	blood:	n/a	n/a
17	CTCF	chr12:51533440-51533590	HEK293	kidney:	n/a	n/a
18	EBF1	chr12:51554944-51555085	GM12878	blood:	n/a	chr12:51555041-51555052
19	EBF1	chr12:51554908-51555141	GM12878	blood:	n/a	chr12:51555041-51555052
20	EP300	chr12:51554816-51555056	K562	blood:	n/a	n/a
21	EP300	chr12:51559148-51559320	K562	blood:	n/a	n/a
22	EP300	chr12:51554772-51555232	HepG2	liver:	n/a	n/a
23	FOS	chr12:51532762-51532858	MCF10A-Er-Src	breast:	n/a	n/a
24	FOXA1	chr12:51554805-51555245	HepG2	liver:	n/a	n/a
25	FOXA1	chr12:51554884-51555262	HepG2	liver:	n/a	n/a
26	FOXA1	chr12:51554904-51555263	HepG2	liver:	n/a	n/a
27	FOXA1	chr12:51554756-51555232	HepG2	liver:	n/a	n/a
28	FOXA2	chr12:51554798-51555219	HepG2	liver:	n/a	n/a
29	GATA2	chr12:51540456-51540771	SH-SY5Y	brain:	n/a	n/a
30	GATA3	chr12:51540506-51540734	T-47D	breast:	n/a	chr12:51540621-51540629
31	GATA3	chr12:51536888-51537010	SH-SY5Y	brain:	n/a	n/a
32	GATA3	chr12:51540448-51540797	SH-SY5Y	brain:	n/a	chr12:51540621-51540629
33	GATA3	chr12:51530952-51531070	SH-SY5Y	brain:	n/a	n/a
34	HDAC2	chr12:51554889-51555234	HepG2	liver:	n/a	n/a
35	JUN	chr12:51532735-51532881	HepG2	liver:	n/a	chr12:51532797-51532810
36	JUND	chr12:51554861-51555065	K562	blood:	n/a	n/a
37	JUND	chr12:51532757-51532957	HepG2	liver:	n/a	n/a
38	MAFF	chr12:51550194-51550511	HepG2	liver:	n/a	chr12:51550336-51550354
39	MAFF	chr12:51550171-51550512	K562	blood:	n/a	chr12:51550336-51550354
40	MAFF	chr12:51533258-51533607	HepG2	liver:	n/a	chr12:51533418-51533436
41	MAFF	chr12:51554811-51555099	K562	blood:	n/a	n/a
42	MAFK	chr12:51550171-51550523	HepG2	liver:	n/a	chr12:51550338-51550353
43	MAFK	chr12:51533298-51533590	IMR90	lung:	n/a	chr12:51533420-51533435
44	MAFK	chr12:51550176-51550523	IMR90	lung:	n/a	chr12:51550338-51550353
45	MAFK	chr12:51550217-51550474	K562	blood:	n/a	chr12:51550338-51550353
46	MAFK	chr12:51533256-51533593	HepG2	liver:	n/a	chr12:51533420-51533435
47	MAFK	chr12:51533284-51533576	HepG2	liver:	n/a	chr12:51533420-51533435
48	MAFK	chr12:51533383-51533481	K562	blood:	n/a	chr12:51533420-51533435
49	MAFK	chr12:51554819-51555043	K562	blood:	n/a	n/a
50	MAFK	chr12:51550179-51550515	HepG2	liver:	n/a	chr12:51550338-51550353

No data

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:51557800..51560550-chr12:51563372..51565178,2	K562	blood:
2	chr12:51544206..51546525-chr12:51548031..51551174,3	MCF-7	breast:
3	chr12:51534963..51537834-chr12:51539860..51541619,2	K562	blood:
4	chr12:51557800..51560128-chr12:51563372..51565944,2	K562	blood:
5	chr12:51554796..51557300-chr12:51565911..51568570,2	K562	blood:
6	chr12:51453861..51455456-chr12:51525275..51527997,2	K562	blood:
7	chr12:51557818..51560220-chr12:51566523..51568651,2	K562	blood:
8	chr12:51554796..51556370-chr12:51565911..51567778,2	K562	blood:
9	chr12:51530226..51532781-chr12:51632391..51634176,2	K562	blood:
10	chr12:51545382..51548232-chr12:51608906..51610842,2	K562	blood:
11	chr12:51554454..51555957-chr12:51556560..51559304,2	K562	blood:
12	chr12:51546648..51549311-chr12:51552488..51556215,3	K562	blood:
13	chr12:51475941..51478644-chr12:51537858..51540533,2	K562	blood:
14	chr12:51475866..51477468-chr12:51532284..51535126,3	MCF-7	breast:
15	chr12:51534963..51537834-chr12:51539860..51541619,2	K562	blood:
16	chr12:51475882..51478954-chr12:51542218..51546767,4	K562	blood:
17	chr12:51476729..51479140-chr12:51545338..51548033,3	MCF-7	breast:
18	chr12:51475785..51477461-chr12:51525771..51529395,3	MCF-7	breast:
19	chr12:51477465..51479681-chr12:51531530..51534326,2	K562	blood:
20	chr12:51511756..51514256-chr12:51530375..51532854,2	K562	blood:
21	chr12:51529565..51532298-chr12:51637533..51640310,2	K562	blood:
22	chr12:51475915..51477479-chr12:51552231..51555145,2	MCF-7	breast:
23	chr12:51476008..51478537-chr12:51543091..51546002,4	K562	blood:
24	chr12:51474440..51477306-chr12:51528704..51531045,2	K562	blood:
25	chr12:51515480..51517726-chr12:51526699..51529552,2	K562	blood:
26	chr12:51476081..51477615-chr12:51555734..51558069,2	MCF-7	breast:
27	chr12:51546648..51549311-chr12:51552488..51556215,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000200953	TF binding region
RNU6-199P	TF binding region
ENSG00000135457	chromatin interactions
ENSG00000200953	chromatin interactions
ENSG00000183283	chromatin interactions
ENSG00000110925	chromatin interactions
ENSG00000199824	chromatin interactions

Extended variants
information (count: 1233 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1233 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140640969	chr12:51527997-51527998	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574491192	chr12:51528013-51528014	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs73305715	chr12:51528036-51528037	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs553578258	chr12:51528160-51528161	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs576906637	chr12:51528205-51528206	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs531545033	chr12:51528228-51528229	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565496691	chr12:51528231-51528232	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs531076140	chr12:51528280-51528281	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550871636	chr12:51528307-51528308	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs114127158	chr12:51528445-51528446	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374839099	chr12:51528449-51528450	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530026455	chr12:51528457-51528458	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs547005473	chr12:51528476-51528477	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566829109	chr12:51528491-51528492	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs539493805	chr12:51528523-51528524	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs368625715	chr12:51528576-51528577	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs199539266	chr12:51528629-51528630	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs116440481	chr12:51528717-51528718	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs115738387	chr12:51528854-51528855	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534051970	chr12:51528855-51528856	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs199772285	chr12:51528896-51528897	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs200710987	chr12:51528897-51528898	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs398019546	chr12:51528908-51528909	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs187883863	chr12:51528947-51528948	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375493552	chr12:51528975-51528976	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs568407193	chr12:51528976-51528977	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533755798	chr12:51528980-51528981	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs191470454	chr12:51529007-51529008	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576835886	chr12:51529036-51529037	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs542434623	chr12:51529048-51529049	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs183212577	chr12:51529075-51529076	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575430723	chr12:51529089-51529090	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs544442833	chr12:51529109-51529110	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs201750538	chr12:51529113-51529114	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555806317	chr12:51529116-51529117	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112783660	chr12:51529136-51529137	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs187898855	chr12:51529137-51529138	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201840147	chr12:51529217-51529218	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs5798157	chr12:51529219-51529220	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs548961647	chr12:51529220-51529221	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs386376508	chr12:51529221-51529222	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs565877863	chr12:51529223-51529224	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs368045571	chr12:51529226-51529227	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371220551	chr12:51529227-51529228	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs199742063	chr12:51529228-51529229	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs12811508	chr12:51529231-51529232	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs560548321	chr12:51529299-51529300	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532457050	chr12:51529305-51529306	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs79025394	chr12:51529309-51529310	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs552646340	chr12:51529350-51529351	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Seminomas	18059402	CNVD
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
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	21858162	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21509527	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	20409316	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:51477800-51550200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:51502800-51531800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:51503200-51560200	Weak transcription	Right Ventricle	heart
4	chr12:51503600-51532000	Weak transcription	Brain Angular Gyrus	brain
5	chr12:51504800-51563400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr12:51507800-51532200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr12:51507800-51539800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr12:51508000-51543000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr12:51510200-51536200	Weak transcription	Brain Hippocampus Middle	brain
10	chr12:51510200-51554400	Weak transcription	K562	blood
11	chr12:51511400-51531400	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr12:51511400-51558800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr12:51512800-51535600	Weak transcription	Brain Cingulate Gyrus	brain
14	chr12:51513000-51532200	Weak transcription	Primary B cells from peripheral blood	blood
15	chr12:51513000-51565400	Weak transcription	Fetal Lung	lung
16	chr12:51513200-51531600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr12:51514400-51532200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr12:51517200-51547600	Weak transcription	Fetal Kidney	kidney
19	chr12:51517200-51554600	Weak transcription	HepG2	liver
20	chr12:51519000-51529400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr12:51519000-51529400	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr12:51519000-51530200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:51519000-51530400	Weak transcription	Ovary	ovary
24	chr12:51519000-51531600	Weak transcription	Adipose Nuclei	Adipose
25	chr12:51519000-51533800	Weak transcription	Gastric	stomach
26	chr12:51519000-51541000	Weak transcription	Brain Substantia Nigra	brain
27	chr12:51519000-51561600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr12:51519000-51565000	Weak transcription	Colon Smooth Muscle	Colon
29	chr12:51519000-51565200	Weak transcription	Left Ventricle	heart
30	chr12:51519000-51565200	Weak transcription	Pancreas	Pancrea
31	chr12:51519000-51565800	Weak transcription	Esophagus	oesophagus
32	chr12:51519200-51529000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr12:51519200-51529400	Weak transcription	Placenta	Placenta
34	chr12:51519200-51529400	Weak transcription	Fetal Thymus	thymus
35	chr12:51519200-51529600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:51519200-51530000	Weak transcription	Hela-S3	cervix
37	chr12:51519200-51530200	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr12:51519200-51530400	Weak transcription	Aorta	Aorta
39	chr12:51519200-51531400	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr12:51519200-51531600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr12:51519200-51531600	Weak transcription	Brain Anterior Caudate	brain
42	chr12:51519200-51531600	Weak transcription	Duodenum Mucosa	Duodenum
43	chr12:51519200-51531800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:51519200-51531800	Weak transcription	Fetal Intestine Large	intestine
45	chr12:51519200-51532000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr12:51519200-51532000	Weak transcription	Fetal Muscle Trunk	muscle
47	chr12:51519200-51532400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:51519200-51532400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr12:51519200-51533800	Weak transcription	Spleen	Spleen
50	chr12:51519200-51534000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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