Variant report

Variant	nsv470897
Chromosome Location	chr21:28196045-28216066
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:719)
CpG islands
(count:305)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr21:28214484-28216519	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr21:28215029-28217093	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr21:28213211-28213582	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr21:28215168-28216372	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr21:28206498-28206857	IMR90	lung:	n/a	chr21:28206823-28206840
6	CEBPB	chr21:28213214-28213519	HepG2	liver:	n/a	n/a
7	CEBPB	chr21:28207861-28208577	Hela-S3	cervix:	n/a	chr21:28208501-28208512
8	CEBPB	chr21:28213149-28213652	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr21:28213234-28213516	A549	lung:	n/a	n/a
10	CEBPB	chr21:28207349-28208646	IMR90	lung:	n/a	chr21:28208501-28208512
11	CEBPB	chr21:28205773-28206239	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr21:28200947-28201221	HepG2	liver:	n/a	chr21:28201052-28201063 chr21:28200984-28200992
13	CEBPB	chr21:28215241-28215568	IMR90	lung:	n/a	n/a
14	CEBPB	chr21:28213161-28213578	IMR90	lung:	n/a	n/a
15	CEBPB	chr21:28206514-28206957	Hela-S3	cervix:	n/a	chr21:28206823-28206840
16	CHD1	chr21:28205434-28219742	IMR90	lung:	n/a	chr21:28216173-28216180 chr21:28218579-28218589
17	CHD1	chr21:28215007-28215233	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr21:28215177-28218577	Hela-S3	cervix:	n/a	chr21:28216173-28216180
19	CHD2	chr21:28213192-28213540	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr21:28206992-28208227	Hela-S3	cervix:	n/a	n/a
21	CTBP2	chr21:28215279-28216250	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr21:28215800-28215950	HMF	breast:	n/a	n/a
23	CTCF	chr21:28214700-28214850	AG10803	skin:	n/a	n/a
24	CTCF	chr21:28207540-28207690	AG09319	gingival:	n/a	chr21:28207652-28207673 chr21:28207651-28207667
25	CTCF	chr21:28214740-28214890	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr21:28206560-28206710	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr21:28206560-28206710	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr21:28215800-28215950	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr21:28215840-28215990	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr21:28207600-28207750	BJ	skin:	n/a	chr21:28207652-28207673 chr21:28207651-28207667
31	CTCF	chr21:28215766-28215969	Lung_OC	lung:	n/a	n/a
32	CTCF	chr21:28215804-28215955	MCF-7	breast:	n/a	n/a
33	CTCF	chr21:28213340-28213490	RPTEC	kidney:	n/a	n/a
34	CTCF	chr21:28213340-28213490	BE2_C	brain:	n/a	n/a
35	CTCF	chr21:28206581-28206749	Gliobla	brain:	n/a	n/a
36	CTCF	chr21:28215660-28215810	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr21:28206640-28206790	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr21:28206540-28206690	HRE	kidney:	n/a	n/a
39	CTCF	chr21:28206325-28206327	Fibrobl	skin:	n/a	n/a
40	CTCF	chr21:28213220-28213370	SAEC	small airway:	n/a	n/a
41	CTCF	chr21:28215360-28215510	BE2_C	brain:	n/a	n/a
42	CTCF	chr21:28215860-28216010	AG04450	lung:	n/a	n/a
43	CTCF	chr21:28215800-28215950	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr21:28215820-28215970	NHEK	skin:	n/a	n/a
45	CTCF	chr21:28215860-28216010	BJ	skin:	n/a	n/a
46	CTCF	chr21:28215920-28216070	A549	lung:	n/a	n/a
47	CTCF	chr21:28209940-28210090	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr21:28206560-28206710	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr21:28215801-28215960	ProgFib	skin:	n/a	n/a
50	CTCF	chr21:28207620-28207770	HAc	cerebellar:	n/a	chr21:28207652-28207673 chr21:28207651-28207667

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:28215206-28215256	AG04450	lung:	fetal
2	chr21:28214928-28214978	LNCaP	prostate:	n/a
3	chr21:28212803-28212853	PFSK-1	brain:	n/a
4	chr21:28214928-28214978	HMEC	breast:	n/a
5	chr21:28209018-28209068	AG10803	skin:	n/a
6	chr21:28209018-28209068	AG04450	lung:	fetal
7	chr21:28215972-28216022	NT2-D1	testis:	n/a
8	chr21:28209018-28209068	HCM	heart:	n/a
9	chr21:28215206-28215256	GM06990	blood:	n/a
10	chr21:28215972-28216022	MCF10A-Er-Src	breast:	n/a
11	chr21:28212803-28212853	BJ	skin:	n/a
12	chr21:28212803-28212853	HNPCEpiC	eye:	n/a
13	chr21:28212803-28212853	MCF10A-Er-Src	breast:	n/a
14	chr21:28212803-28212853	NHDF-neo	bronchial:	n/a
15	chr21:28215206-28215256	SK-N-SH	brain:	n/a
16	chr21:28214928-28214978	AG09309	skin:	n/a
17	chr21:28215206-28215256	HAEpiC	amniotic membrane:	n/a
18	chr21:28209018-28209068	HMEC	breast:	n/a
19	chr21:28215206-28215256	RPTEC	kidney:	n/a
20	chr21:28215972-28216022	ProgFib	skin:	n/a
21	chr21:28212803-28212853	SK-N-SH	brain:	n/a
22	chr21:28215206-28215256	NT2-D1	testis:	n/a
23	chr21:28214928-28214978	H1-hESC	embryonic stem cell:	embryo
24	chr21:28212803-28212853	ECC-1	luminal epithelium:	n/a
25	chr21:28214928-28214978	HCF	heart:	n/a
26	chr21:28215972-28216022	GM06990	blood:	n/a
27	chr21:28214928-28214978	PANC-1	pancreas:	n/a
28	chr21:28215206-28215256	LNCaP	prostate:	n/a
29	chr21:28215972-28216022	CMK	blood:	n/a
30	chr21:28212803-28212853	HCPEpiC	choroid plexus:	n/a
31	chr21:28214928-28214978	GM12892	blood:	n/a
32	chr21:28215206-28215256	NHDF-neo	bronchial:	n/a
33	chr21:28212803-28212853	GM12892	blood:	n/a
34	chr21:28212803-28212853	HMEC	breast:	n/a
35	chr21:28212803-28212853	AG09309	skin:	n/a
36	chr21:28215972-28216022	PANC-1	pancreas:	n/a
37	chr21:28215206-28215256	BJ	skin:	n/a
38	chr21:28212803-28212853	HIPEpiC	eye:	n/a
39	chr21:28209018-28209068	AG09309	skin:	n/a
40	chr21:28214928-28214978	PrEC	prostate:	n/a
41	chr21:28215206-28215256	HEK293	kidney:	embryo
42	chr21:28209018-28209068	SK-N-MC	brain:	n/a
43	chr21:28215206-28215256	HepG2	liver:	n/a
44	chr21:28209018-28209068	HepG2	liver:	n/a
45	chr21:28214928-28214978	IMR90	lung:	fetal
46	chr21:28209018-28209068	NHBE	bronchial:	n/a
47	chr21:28215206-28215256	SAEC	small airway:	n/a
48	chr21:28209018-28209068	GM12891	blood:	n/a
49	chr21:28215206-28215256	K562	blood:	n/a
50	chr21:28212803-28212853	ProgFib	skin:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:21457560..21458554-chr21:28215410..28216217,2	Hela-S3	cervix:
2	chr21:28193660..28195884-chr21:28196743..28198905,2	K562	blood:
3	chr21:28204050..28205550-chr21:28209063..28211233,2	K562	blood:
4	chr21:28204050..28205550-chr21:28209063..28211233,2	K562	blood:
5	chr21:28208531..28212361-chr21:28215546..28220151,4	MCF-7	breast:
6	chr21:28204779..28207131-chr21:28215983..28217765,2	MCF-7	breast:

No data

Variant related genes	Relation type
ADAMTS1	TF binding region
ADAMTS1	CpG island
ENSG00000165792	chromatin interactions
ENSG00000154734	chromatin interactions

Extended variants
information (count: 845 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs459210	chr21:28196045-28196046	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550976344	chr21:28196128-28196129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567515702	chr21:28196129-28196130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536671355	chr21:28196138-28196139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553152515	chr21:28196147-28196148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs80025667	chr21:28196163-28196164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538855123	chr21:28196223-28196224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138186239	chr21:28196244-28196245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56145711	chr21:28196251-28196252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143921227	chr21:28196254-28196255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73185840	chr21:28196258-28196259	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs561270563	chr21:28196263-28196264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75392587	chr21:28196282-28196283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188565980	chr21:28196327-28196328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540230265	chr21:28196336-28196337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559980766	chr21:28196359-28196360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377647606	chr21:28196360-28196361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs67458608	chr21:28196392-28196393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112656630	chr21:28196394-28196395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs397748370	chr21:28196397-28196398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200749861	chr21:28196398-28196399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532278913	chr21:28196402-28196403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552376436	chr21:28196540-28196541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562706198	chr21:28196547-28196548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532279599	chr21:28196550-28196551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368345257	chr21:28196602-28196603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531552212	chr21:28196640-28196641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192875151	chr21:28196686-28196687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568345468	chr21:28196692-28196693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183155500	chr21:28196722-28196723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147292195	chr21:28196782-28196783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs60964152	chr21:28196791-28196792	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs75501695	chr21:28196798-28196799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538785124	chr21:28196804-28196805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186665745	chr21:28196825-28196826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575408736	chr21:28196829-28196830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538053986	chr21:28196881-28196882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74549510	chr21:28196904-28196905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575116001	chr21:28196925-28196926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539842669	chr21:28196972-28196973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560118527	chr21:28196981-28196982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541918619	chr21:28197019-28197020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79747011	chr21:28197023-28197024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529625659	chr21:28197024-28197025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112769838	chr21:28197031-28197032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376911500	chr21:28197062-28197063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs468919	chr21:28197071-28197072	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs566604425	chr21:28197079-28197080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144914578	chr21:28197132-28197133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531485860	chr21:28197135-28197136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	21251322	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	22174824	CNVD
Renal cell carcinoma	18765545	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Hypoplastic left heart syndrome	22349727	CNVD

Chromatin state (count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:28188400-28198600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr21:28192600-28199800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr21:28195200-28198400	Weak transcription	Dnd41	blood
4	chr21:28198400-28198800	ZNF genes & repeats	Dnd41	blood
5	chr21:28198600-28198800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr21:28198600-28198800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr21:28198600-28199000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr21:28198600-28199400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr21:28198800-28199000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr21:28198800-28199200	Enhancers	NHDF-Ad	bronchial
11	chr21:28198800-28199400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr21:28198800-28199800	Weak transcription	Dnd41	blood
13	chr21:28198800-28200600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr21:28199000-28199200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr21:28199000-28200600	Enhancers	HMEC	breast
16	chr21:28199000-28208400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr21:28199200-28199800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr21:28199200-28200600	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr21:28199200-28200600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr21:28199200-28208800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr21:28199400-28200600	Enhancers	NHEK	skin
22	chr21:28199400-28203600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr21:28199400-28205600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr21:28199600-28199800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr21:28199800-28200600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr21:28199800-28200600	Enhancers	Dnd41	blood
27	chr21:28199800-28205200	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr21:28199800-28208800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr21:28200600-28203200	Weak transcription	Dnd41	blood
30	chr21:28200600-28205000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr21:28200600-28205400	Weak transcription	NHEK	skin
32	chr21:28200600-28205800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr21:28200600-28205800	Weak transcription	HMEC	breast
34	chr21:28200600-28208800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr21:28203200-28209000	Enhancers	Dnd41	blood
36	chr21:28203600-28207800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr21:28203800-28204200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr21:28204000-28210000	Weak transcription	HUVEC	blood vessel
39	chr21:28204200-28204600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr21:28204200-28206400	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr21:28204400-28204800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr21:28204600-28205400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr21:28204600-28209000	Weak transcription	Brain Angular Gyrus	brain
44	chr21:28204800-28205200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr21:28205000-28205600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr21:28205000-28206600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr21:28205200-28206000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr21:28205200-28206400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr21:28205200-28206800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr21:28205400-28205600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood

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