Variant report

Variant	esv4896
Chromosome Location	chr17:45223249-45233036
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr17:45231864-45232246	GM12878	blood:	n/a	n/a
2	CTCF	chr17:45231920-45232070	GM12801	blood:	n/a	n/a
3	CTCF	chr17:45231940-45232090	GM12871	blood:	n/a	n/a
4	CTCF	chr17:45231900-45232050	HPF	lung:	n/a	chr17:45231908-45231916
5	CTCF	chr17:45231920-45232070	AG09319	gingival:	n/a	n/a
6	CTCF	chr17:45232040-45232190	HPF	lung:	n/a	n/a
7	CTCF	chr17:45228640-45228790	HepG2	liver:	n/a	n/a
8	CTCF	chr17:45231940-45232090	GM12870	blood:	n/a	n/a
9	ELK1	chr17:45231872-45232242	GM12878	blood:	n/a	n/a
10	ELK1	chr17:45231870-45232243	Hela-S3	cervix:	n/a	n/a
11	FOXP2	chr17:45231957-45232208	SK-N-MC	brain:	n/a	n/a
12	GATA3	chr17:45232039-45232296	SH-SY5Y	brain:	n/a	n/a
13	GTF2F1	chr17:45231869-45232242	H1-hESC	embryonic stem cell:	n/a	n/a
14	IRF3	chr17:45231870-45232245	GM12878	blood:	n/a	chr17:45232236-45232245
15	MAFK	chr17:45231870-45232245	Hela-S3	cervix:	n/a	n/a
16	MAFK	chr17:45229271-45229456	Hela-S3	cervix:	n/a	n/a
17	MAZ	chr17:45231868-45232244	Hela-S3	cervix:	n/a	n/a
18	MXI1	chr17:45229082-45229281	Hela-S3	cervix:	n/a	n/a
19	NRF1	chr17:45231868-45232240	GM12878	blood:	n/a	n/a
20	POLR2A	chr17:45230367-45230711	K562	blood:	n/a	n/a
21	POLR2A	chr17:45229270-45229283	MCF-7	breast:	n/a	n/a
22	POLR2A	chr17:45227653-45227901	K562	blood:	n/a	n/a
23	POLR2A	chr17:45226642-45226768	HepG2	liver:	n/a	n/a
24	POLR2A	chr17:45227112-45227302	HepG2	liver:	n/a	n/a
25	POLR2A	chr17:45229215-45229222	MCF-7	breast:	n/a	n/a
26	POLR2A	chr17:45230337-45230342	K562	blood:	n/a	n/a
27	POLR2A	chr17:45228291-45228369	A549	lung:	n/a	n/a
28	POLR2A	chr17:45226139-45226502	HepG2	liver:	n/a	n/a
29	PRDM1	chr17:45231734-45232246	Hela-S3	cervix:	n/a	n/a
30	RFX5	chr17:45231867-45232244	GM12878	blood:	n/a	n/a
31	SMC3	chr17:45231869-45232245	GM12878	blood:	n/a	n/a
32	TAL1	chr17:45231870-45232241	K562	blood:	n/a	n/a
33	TBP	chr17:45231869-45232237	K562	blood:	n/a	n/a
34	TCF7L2	chr17:45231871-45232240	Hela-S3	cervix:	n/a	n/a
35	UBTF	chr17:45232040-45232070	K562	blood:	n/a	n/a
36	UBTF	chr17:45232036-45232072	K562	blood:	n/a	n/a
37	USF2	chr17:45231869-45232243	HepG2	liver:	n/a	n/a
38	ZNF143	chr17:45231868-45232244	Hela-S3	cervix:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr17:45227215..45229474-chr17:45232975..45235463,2	K562	blood:
2	chr17:45221635..45223977-chr17:45273349..45275137,2	K562	blood:
3	chr17:45229066..45231948-chr17:45400564..45402346,2	K562	blood:
4	chr17:45223999..45225599-chr17:45315426..45317942,2	K562	blood:
5	chr17:45230921..45233379-chr17:45247997..45250446,2	K562	blood:
6	chr1:25269703..25270473-chr17:45231357..45232201,2	MCF-7	breast:
7	chr17:45201078..45204476-chr17:45221979..45225273,3	K562	blood:
8	chr17:45230921..45233018-chr17:45247997..45250625,2	K562	blood:
9	chr17:45230648..45232405-chr17:45259040..45262576,3	K562	blood:
10	chr17:45231539..45232062-chr2:133019343..133019865,2	MCF-7	breast:
11	chr17:45229552..45231900-chr17:45241796..45244433,2	K562	blood:
12	chr17:45215729..45220383-chr17:45221997..45225323,4	MCF-7	breast:

No data

Variant related genes	Relation type
CDC27	TF binding region
ENSG00000263293	chromatin interactions
ENSG00000178852	chromatin interactions
ENSG00000004897	chromatin interactions

Extended variants
information (count: 391 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113176853	chr17:45223251-45223252	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs75856059	chr17:45223276-45223277	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538319107	chr17:45223290-45223291	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs558627086	chr17:45223325-45223326	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs572069541	chr17:45223335-45223336	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs541069776	chr17:45223348-45223349	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs148098429	chr17:45223367-45223368	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs66518624	chr17:45223405-45223406	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs543762585	chr17:45223408-45223409	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs545812411	chr17:45223429-45223430	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs117791230	chr17:45223466-45223467	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs553894446	chr17:45223539-45223540	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs532346155	chr17:45223589-45223590	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs34867397	chr17:45223590-45223591	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552343101	chr17:45223600-45223601	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559844735	chr17:45223602-45223603	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs141784185	chr17:45223658-45223659	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs146208684	chr17:45223710-45223711	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs538372534	chr17:45223763-45223764	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs568391611	chr17:45223778-45223779	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs138810713	chr17:45223805-45223806	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs112120512	chr17:45223909-45223910	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs34804720	chr17:45223976-45223977	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528229881	chr17:45223995-45223996	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112106760	chr17:45224003-45224004	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551270080	chr17:45224059-45224060	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546373045	chr17:45224094-45224095	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs142785535	chr17:45224100-45224101	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs529012454	chr17:45224114-45224115	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs147410397	chr17:45224137-45224138	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs137957553	chr17:45224189-45224190	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs556399147	chr17:45224191-45224192	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs572206752	chr17:45224222-45224223	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs550475180	chr17:45224267-45224268	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs531197141	chr17:45224300-45224301	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs111256526	chr17:45224322-45224323	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs574501428	chr17:45224342-45224343	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543312822	chr17:45224362-45224363	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557225754	chr17:45224405-45224406	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs115931975	chr17:45224488-45224489	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs117594331	chr17:45224489-45224490	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
42	rs559575789	chr17:45224495-45224496	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201416822	chr17:45224504-45224505	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs571689174	chr17:45224505-45224506	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs201746835	chr17:45224511-45224512	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs149486294	chr17:45224519-45224520	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
47	rs201218251	chr17:45224529-45224530	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs561710471	chr17:45224532-45224533	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs530821131	chr17:45224537-45224538	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs370555651	chr17:45224562-45224563	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	17142309	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45194800-45234200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr17:45214600-45229200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr17:45214800-45234200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr17:45214800-45234200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr17:45215200-45229400	Strong transcription	Brain Germinal Matrix	brain
6	chr17:45216400-45228800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr17:45216400-45232600	Strong transcription	Osteobl	bone
8	chr17:45219000-45225200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr17:45219400-45233400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr17:45220000-45232800	Strong transcription	A549	lung
11	chr17:45221400-45223400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr17:45221400-45223400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr17:45221400-45223600	Weak transcription	Hela-S3	cervix
14	chr17:45221400-45224200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr17:45221400-45224400	Strong transcription	Primary B cells from cord blood	blood
16	chr17:45221400-45225000	Weak transcription	Right Atrium	heart
17	chr17:45221400-45225400	Weak transcription	Psoas Muscle	Psoas
18	chr17:45221400-45225600	Weak transcription	Brain Hippocampus Middle	brain
19	chr17:45221400-45225800	Weak transcription	NHEK	skin
20	chr17:45221400-45227400	Weak transcription	Brain Substantia Nigra	brain
21	chr17:45221400-45227600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr17:45221400-45227600	Weak transcription	Brain Anterior Caudate	brain
23	chr17:45221400-45227800	Weak transcription	Brain Angular Gyrus	brain
24	chr17:45221400-45228000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr17:45221400-45228200	Weak transcription	Gastric	stomach
26	chr17:45221400-45228600	Weak transcription	Fetal Kidney	kidney
27	chr17:45221400-45229000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr17:45221400-45229000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr17:45221400-45230400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr17:45221400-45230400	Weak transcription	Spleen	Spleen
31	chr17:45221400-45231800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr17:45221400-45231800	Weak transcription	Brain Cingulate Gyrus	brain
33	chr17:45221400-45231800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr17:45221400-45232600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr17:45221400-45232800	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr17:45221400-45232800	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr17:45221400-45233000	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr17:45221400-45233000	Strong transcription	NH-A	brain
39	chr17:45221400-45233200	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr17:45221400-45233200	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr17:45221400-45233400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr17:45221400-45233400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr17:45221400-45233400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr17:45221400-45233400	Strong transcription	Liver	Liver
45	chr17:45221400-45233400	Strong transcription	Fetal Thymus	thymus
46	chr17:45221400-45233600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr17:45221400-45233600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr17:45221400-45234200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr17:45221400-45234200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr17:45221400-45234200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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