Variant report

Variant	nsv525475
Chromosome Location	chr22:22195075-22205611
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:22018749..22020328-chr22:22203244..22205660,2	K562	blood:
2	chr22:22018828..22021785-chr22:22203115..22205660,2	K562	blood:
3	chr22:22065544..22067322-chr22:22204712..22206990,2	K562	blood:
4	chr22:22133123..22135559-chr22:22203142..22206068,3	K562	blood:
5	chr22:22198089..22199852-chr22:22294992..22297541,2	K562	blood:
6	chr22:22094397..22096556-chr22:22202913..22204728,2	K562	blood:
7	chr22:22195671..22198608-chr22:22219400..22221487,2	MCF-7	breast:
8	chr22:22151815..22154124-chr22:22193537..22196414,2	K562	blood:
9	chr22:22081612..22083911-chr22:22197531..22199059,2	K562	blood:
10	chr22:22203415..22205330-chr22:22291423..22293151,2	K562	blood:
11	chr22:22156400..22158214-chr22:22194352..22196591,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000100034	chromatin interactions
ENSG00000100023	chromatin interactions
ENSG00000224086	chromatin interactions

Extended variants
information (count: 432 )
Associated
traits (count: 220 )

Variant overlapped rSNPs/rCNVs (count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12172554	chr22:22195075-22195076	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535031575	chr22:22195083-22195084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs199810094	chr22:22195104-22195105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376204416	chr22:22195113-22195114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377191296	chr22:22195115-22195116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558100123	chr22:22195116-22195117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138967398	chr22:22195136-22195137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576604574	chr22:22195175-22195176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370630532	chr22:22195195-22195196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542156312	chr22:22195237-22195238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs377675935	chr22:22195306-22195307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369852600	chr22:22195319-22195320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141550246	chr22:22195404-22195405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs9610400	chr22:22195406-22195407	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs550702153	chr22:22195516-22195517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561294583	chr22:22195578-22195579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200773426	chr22:22195579-22195580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530174259	chr22:22195603-22195604	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192080584	chr22:22195620-22195621	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183007241	chr22:22195633-22195634	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139234566	chr22:22195670-22195671	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs78104334	chr22:22195690-22195691	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs35907379	chr22:22195739-22195740	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377742022	chr22:22195792-22195793	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569577438	chr22:22195805-22195806	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538494074	chr22:22195833-22195834	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370086900	chr22:22195836-22195837	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188098030	chr22:22195837-22195838	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557035737	chr22:22195894-22195895	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115579413	chr22:22195982-22195983	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116775559	chr22:22196006-22196007	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113077215	chr22:22196010-22196011	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553433834	chr22:22196023-22196024	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76351455	chr22:22196101-22196102	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147908844	chr22:22196253-22196254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192409780	chr22:22196265-22196266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562295473	chr22:22196279-22196280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575939462	chr22:22196288-22196289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184598125	chr22:22196289-22196290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561155080	chr22:22196326-22196327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188226217	chr22:22196355-22196356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192661701	chr22:22196394-22196395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs5999785	chr22:22196404-22196405	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs113263302	chr22:22196438-22196439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189097646	chr22:22196520-22196521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560672056	chr22:22196525-22196526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572275289	chr22:22196529-22196530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376467144	chr22:22196531-22196532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62235149	chr22:22196532-22196533	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs567996474	chr22:22196539-22196540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:220)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Emanuel syndrome	21549014	CNVD
Digeorge syndrome	22283845	CNVD
Schizophrenia	17504246	CNVD
Digeorge syndrome	18033723	CNVD
22q11 deletion syndrome	17034021	CNVD
22q11 deletion syndrome	22511897	CNVD
22q11 deletion syndrome	16829213	CNVD
Autism	22067053	CNVD
Autism	19218893	CNVD
Biliary cancer	22067053	CNVD
Congenital heart defect	21390462	CNVD
Digeorge syndrome	16617304	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Obsessive-compulsive disorder	22067053	CNVD
Psychosis	22067053	CNVD
Schizophrenia	19415332	CNVD
Schizophrenia	20587603	CNVD
Shprintzen syndrome	19443537	CNVD
absent pulmonary valve syndrome	16795129	CNVD
language delay	22067053	CNVD
periventricular nodular heterotopia	20648244	CNVD
renal disease	17924346	CNVD
Schizophrenia	20433910	CNVD
22q11 deletion syndrome	17028864	CNVD
Schizophrenia	16969581	CNVD
Non-syndromic sensorineural hearing loss	17135275	CNVD
velo-cardio-facial syndrome	17135275	CNVD
Digeorge syndrome	18787571	CNVD
Autism	18925931	CNVD
Non-small cell lung cancer	21829676	CNVD
22q11.2 microdeletion syndrome	21547621	CNVD
Congenital heart defect	21308838	CNVD
Digeorge syndrome	16512914	CNVD
Digeorge syndrome	20954168	CNVD
Nuchal translucency	21837766	CNVD
Right aortic arch in the fetus	17066500	CNVD
Shprintzen syndrome	17117043	CNVD
Tetralogy of fallot	17405110	CNVD
Velocardiofacial syndrome	20140301	CNVD
Velocardiofacial syndrome	16512914	CNVD
bone mass and metabolism	20516202	CNVD
choanal atresia	18209138	CNVD
extracardiac malformations	17086578	CNVD
fetal heart defects	21308838	CNVD
parathyroid gland dysfunction	16793949	CNVD
prenatal diagnosis	20453657	CNVD
velopharyngeal insufficiency	19620585	CNVD
Prader-willi syndrome	20942916	CNVD
22q11 deletion syndrome	17653112	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Cat eye syndrome	21549014	CNVD
Digeorge syndrome	21549014	CNVD
22q11.2 microdeletion syndrome	22051516	CNVD
22q11.2 microdeletion syndrome	18483005	CNVD
22q11.2 microdeletion syndrome	19565140	CNVD
22q11.2 microdeletion syndrome	20396437	CNVD
22q11.2 microdeletion syndrome	21390462	CNVD
22q11.2 microdeletion syndrome	21573985	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Congenital heart defect	21257016	CNVD
Developmental delay	18414209	CNVD
DiGeorge-Velo cardiofacial	19284877	CNVD
Epilepsy	20970697	CNVD
Heart disease	20551144	CNVD
Hughes'' syndrome	16595601	CNVD
Mental retardation	18414209	CNVD
Okamoto syndrome	19046188	CNVD
Primary immunodeficiency	22566803	CNVD
Schizophrenia	20877625	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Tetralogy of Fallot	22912587	CNVD
Velocardiofacial syndrome	17556857	CNVD
Velocardiofacial syndrome	20206275	CNVD
Velocardiofacial syndrome	20970697	CNVD
delayed speech development	21274400	CNVD
velo-cardio-facial syndrome	16511839	CNVD
velo-cardio-facial syndrome	21763005	CNVD
22q11.2 microdeletion syndrome	18799940	CNVD
Digeorge syndrome	20877625	CNVD
22q11.2 microdeletion syndrome	18923514	CNVD
Congenital heart defect	22185286	CNVD
DiGeorge-Velo cardiofacial	16773131	CNVD
Digeorge syndrome	20186050	CNVD
velo-cardio-facial conotruncal-face syndrome	20186050	CNVD
22q11.2 microdeletion syndrome	22116936	CNVD
Disorders of sex development	22290220	CNVD
22q11.2 duplication syndrome	18923514	CNVD
Autism	22095694	CNVD
Mental retardation	19951919	CNVD
Honadal dysgenesis	21048976	CNVD
Mental retardation	16773131	CNVD
22q11.2 microdeletion syndrome	22395003	CNVD
22q11.2 microdeletion syndrome	18691436	CNVD
22q11.2 microdeletion syndrome	18053182	CNVD
22q11.2 microdeletion syndrome	18324686	CNVD
22q11.2 microdeletion syndrome	20074913	CNVD
Congenital heart defect	20802965	CNVD
Congenital heart defect	21134246	CNVD
DiGeorge syndrome	19040613	CNVD
DiGeorge-Velo cardiofacial	18179902	CNVD
Digeorge syndrome	18172682	CNVD
Digeorge syndrome	22470819	CNVD
Digeorge syndrome	21364285	CNVD
Neuroendocrine carcinoma	22470819	CNVD
Non-syndromic sensorineural hearing loss	20069674	CNVD
Smith-Magenis syndrome	18301319	CNVD
Tetralogy of fallot	19144126	CNVD
Velo-cardio-facial syndrome	21364285	CNVD
Velocardiofacial syndrome	18788013	CNVD
cardiac malformation	20573211	CNVD
cardiac malformation	18172682	CNVD
velo-cardio-facial syndrome	18636631	CNVD
Schizophrenia	21822266	CNVD
synaptic plasticity	21368174	CNVD
Schizophrenia	18043741	CNVD
sporadic birth defects	19047251	CNVD
Autism	19046189	CNVD
DiGeorge-Velo cardiofacial	19047251	CNVD
Hypernasal speech	21968682	CNVD
Mental retardation	17339581	CNVD
diverse phenotype	16760730	CNVD
Mental retardation	20152051	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Autism	19521722	CNVD
Digeorge syndrome	19521722	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Mental retardation	17124404	CNVD
Tourette syndrome	20069037	CNVD
Williams-beuren syndrome	18553513	CNVD
Emphysema	19352772	CNVD
Schizophrenia	17160897	CNVD
Cancer	17160897	CNVD
Neuropsychiatric disorder	20069037	CNVD
DiGeorge-Velo cardiofacial	17597781	CNVD
Digeorge syndrome	17576883	CNVD
Schizophrenia	18806272	CNVD
Schizophrenia	18990708	CNVD
Velocardiofacial syndrome	17576883	CNVD
Schizophrenia	20075378	CNVD
Neurodevelopmental disorder	17015230	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Disease	21346257	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Developmental delay	21147756	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Asthma	21956041	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	21128281	CNVD
Systemic lupus erythematosus	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
22q11.23 microdeletion syndrome	19193630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Autism	20841430	CNVD

Chromatin state (count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:22182600-22210400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr22:22185400-22200400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr22:22187200-22198200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr22:22187200-22198400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr22:22187200-22200200	Weak transcription	Spleen	Spleen
6	chr22:22187800-22211000	Weak transcription	Dnd41	blood
7	chr22:22189200-22196000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr22:22189600-22197400	Weak transcription	Esophagus	oesophagus
9	chr22:22189600-22198600	Weak transcription	Thymus	Thymus
10	chr22:22189600-22200600	Weak transcription	Ovary	ovary
11	chr22:22190000-22197600	Weak transcription	Lung	lung
12	chr22:22190000-22201200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr22:22190200-22197200	Weak transcription	Primary T cells from cord blood	blood
14	chr22:22190400-22200600	Weak transcription	Brain Germinal Matrix	brain
15	chr22:22191000-22197400	Weak transcription	Primary B cells from cord blood	blood
16	chr22:22192000-22197200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr22:22192000-22197600	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr22:22192000-22198000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr22:22192200-22195600	Weak transcription	K562	blood
20	chr22:22192200-22195800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr22:22192200-22195800	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr22:22192200-22197200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr22:22192200-22197200	Weak transcription	Aorta	Aorta
24	chr22:22192200-22197200	Weak transcription	Fetal Thymus	thymus
25	chr22:22192200-22197400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr22:22192200-22197400	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr22:22192200-22197600	Weak transcription	Stomach Smooth Muscle	stomach
28	chr22:22192200-22197800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr22:22192200-22198000	Weak transcription	Primary hematopoietic stem cells	blood
30	chr22:22192200-22198000	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr22:22192200-22198200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr22:22192200-22198200	Weak transcription	Fetal Intestine Large	intestine
33	chr22:22192200-22198200	Weak transcription	Fetal Intestine Small	intestine
34	chr22:22192200-22198400	Weak transcription	Right Ventricle	heart
35	chr22:22192200-22198600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr22:22192200-22198600	Weak transcription	Duodenum Mucosa	Duodenum
37	chr22:22192200-22198800	Weak transcription	Brain Substantia Nigra	brain
38	chr22:22192200-22200200	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr22:22192200-22200400	Weak transcription	Fetal Brain Female	brain
40	chr22:22192200-22200600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr22:22192200-22200800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr22:22192200-22201200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr22:22192200-22202600	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr22:22192200-22203800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr22:22192200-22203800	Weak transcription	NHLF	lung
46	chr22:22192200-22204000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr22:22192200-22204200	Weak transcription	Small Intestine	intestine
48	chr22:22192200-22209000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr22:22192200-22210000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr22:22192200-22210000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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