Variant report

Variant	rs547385949
Chromosome Location	chr12:1704130-1704131
allele	-/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:1703311-1704323	K562	blood:	n/a	n/a
2	ZMIZ1	chr12:1703763-1704271	K562	blood:	n/a	n/a
3	BHLHE40	chr12:1703541-1704274	HepG2	liver:	n/a	chr12:1703756-1703772 chr12:1703860-1703876 chr12:1703887-1703903
4	POLR2A	chr12:1703298-1704227	IMR90	lung:	n/a	n/a
5	USF1	chr12:1703875-1704416	HCT-116	colon:	n/a	chr12:1703887-1703903
6	BRCA1	chr12:1704098-1704155	HepG2	liver:	n/a	n/a
7	PAX5	chr12:1703778-1704169	GM12891	blood:	n/a	n/a
8	IRF1	chr12:1703792-1704224	K562	blood:	n/a	n/a
9	POLR2A	chr12:1702979-1704298	HUVEC	blood vessel:	n/a	n/a
10	POLR2A	chr12:1703807-1704173	GM12891	blood:	n/a	n/a
11	CTCF	chr12:1704120-1704270	AG09319	gingival:	n/a	n/a
12	RCOR1	chr12:1703405-1704727	K562	blood:	n/a	n/a
13	MAZ	chr12:1703066-1704776	K562	blood:	n/a	chr12:1703239-1703249 chr12:1704066-1704075 chr12:1703785-1703795
14	POLR2A	chr12:1703830-1704288	SK-N-SH	brain:	n/a	n/a
15	MAZ	chr12:1701409-1704769	IMR90	lung:	n/a	chr12:1703239-1703249 chr12:1704066-1704075 chr12:1703785-1703795
16	ZNF143	chr12:1703782-1704272	GM12878	blood:	n/a	chr12:1703866-1703876
17	GATA3	chr12:1702047-1704421	A549	lung:	n/a	n/a
18	UBTF	chr12:1701676-1704682	K562	blood:	n/a	n/a
19	ZKSCAN1	chr12:1703943-1704310	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr12:1701614-1704251	GM12878	blood:	n/a	n/a
21	CTCF	chr12:1704040-1704190	GM12868	blood:	n/a	n/a
22	POLR2A	chr12:1703678-1704373	GM12892	blood:	n/a	n/a
23	CTCF	chr12:1704090-1704183	K562	blood:	n/a	n/a
24	IRF1	chr12:1703918-1704228	K562	blood:	n/a	n/a
25	ZNF143	chr12:1704012-1704166	H1-hESC	embryonic stem cell:	n/a	n/a
26	HCFC1	chr12:1703269-1704249	K562	blood:	n/a	n/a
27	JUND	chr12:1703379-1704339	K562	blood:	n/a	n/a
28	POLR2A	chr12:1701802-1704293	MCF-7	breast:	n/a	n/a
29	UBTF	chr12:1703080-1704207	K562	blood:	n/a	n/a
30	MAX	chr12:1702649-1704355	NB4	blood:	n/a	chr12:1703239-1703249 chr12:1704066-1704075 chr12:1703785-1703795
31	CTCF	chr12:1704094-1704207	A549	lung:	n/a	n/a
32	MAZ	chr12:1702673-1704275	Hela-S3	cervix:	n/a	chr12:1703239-1703249 chr12:1704066-1704075 chr12:1703785-1703795
33	USF1	chr12:1703970-1704300	SK-N-SH	brain:	n/a	n/a
34	GABPA	chr12:1703876-1704131	HepG2	liver:	n/a	n/a
35	POLR2A	chr12:1703804-1704196	K562	blood:	n/a	n/a
36	POLR2A	chr12:1703055-1704342	HUVEC	blood vessel:	n/a	n/a
37	MAX	chr12:1703844-1704437	SK-N-SH	brain:	n/a	chr12:1704066-1704075
38	MAX	chr12:1703980-1704285	K562	blood:	n/a	chr12:1704066-1704075
39	CTCF	chr12:1704095-1704185	MCF-7	breast:	n/a	n/a
40	TBP	chr12:1703363-1704374	K562	blood:	n/a	n/a
41	MAX	chr12:1701918-1704587	A549	lung:	n/a	chr12:1703239-1703249 chr12:1704066-1704075 chr12:1703785-1703795
42	HDAC2	chr12:1704012-1704258	K562	blood:	n/a	chr12:1704233-1704247
43	E2F6	chr12:1703801-1704283	K562	blood:	n/a	chr12:1704131-1704140
44	GTF2F1	chr12:1703961-1704262	Hela-S3	cervix:	n/a	n/a
45	TAF1	chr12:1703931-1704149	SK-N-SH	brain:	n/a	n/a
46	RFX5	chr12:1703941-1704248	Hela-S3	cervix:	n/a	chr12:1704065-1704080 chr12:1704065-1704080 chr12:1704065-1704080 chr12:1704065-1704078 chr12:1704064-1704081
47	CTCF	chr12:1704020-1704170	WERI-Rb-1	eye:	n/a	n/a
48	BHLHE40	chr12:1703673-1704161	A549	lung:	n/a	chr12:1703756-1703772 chr12:1703860-1703876 chr12:1703887-1703903
49	SREBP1	chr12:1703347-1704797	GM12878	blood:	n/a	chr12:1704368-1704379 chr12:1704065-1704079 chr12:1704066-1704080
50	BACH1	chr12:1704012-1704359	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1704080-1704130	HCPEpiC	choroid plexus:	n/a
2	chr12:1704080-1704130	GM12892	blood:	n/a
3	chr12:1704080-1704130	HRPEpiC	eye:	n/a
4	chr12:1704080-1704130	AG04449	skin:	fetal
5	chr12:1704080-1704130	SKMC	muscle:	n/a
6	chr12:1704080-1704130	GM12878	blood:	n/a
7	chr12:1704080-1704130	NB4	blood:	n/a
8	chr12:1704080-1704130	NHBE	bronchial:	n/a
9	chr12:1704080-1704130	H1-hESC	embryonic stem cell:	embryo
10	chr12:1704080-1704130	ECC-1	luminal epithelium:	n/a
11	chr12:1704080-1704130	HUVEC	blood vessel:	n/a
12	chr12:1704080-1704130	PANC-1	pancreas:	n/a
13	chr12:1704080-1704130	GM12891	blood:	n/a
14	chr12:1704080-1704130	Caco-2	colon:	n/a
15	chr12:1704080-1704130	SK-N-SH	brain:	n/a
16	chr12:1704080-1704130	HPAEpiC	pulmonary alveolar:	n/a
17	chr12:1704080-1704130	K562	blood:	n/a
18	chr12:1704080-1704130	Hepatocyte	liver:	n/a
19	chr12:1704080-1704130	U87	brain:	n/a
20	chr12:1704080-1704130	HL-60	blood:	n/a
21	chr12:1704080-1704130	LNCaP	prostate:	n/a
22	chr12:1704080-1704130	HCT-116	colon:	n/a
23	chr12:1704080-1704130	T-47D	breast:	n/a
24	chr12:1704080-1704130	NT2-D1	testis:	n/a
25	chr12:1704080-1704130	NHDF-neo	bronchial:	n/a
26	chr12:1704080-1704130	MCF10A-Er-Src	breast:	n/a
27	chr12:1704080-1704130	HEK293	kidney:	embryo
28	chr12:1704080-1704130	IMR90	lung:	fetal
29	chr12:1704080-1704130	HRCEpiC	kidney:	n/a
30	chr12:1704080-1704130	ProgFib	skin:	n/a
31	chr12:1704080-1704130	HepG2	liver:	n/a
32	chr12:1704080-1704130	HCF	heart:	n/a
33	chr12:1704080-1704130	SK-N-MC	brain:	n/a
34	chr12:1704080-1704130	HNPCEpiC	eye:	n/a
35	chr12:1704080-1704130	AG09309	skin:	n/a
36	chr12:1704080-1704130	HIPEpiC	eye:	n/a
37	chr12:1704080-1704130	HRE	kidney:	n/a
38	chr12:1704080-1704130	SAEC	small airway:	n/a
39	chr12:1704080-1704130	AG09319	gingival:	n/a
40	chr12:1704080-1704130	CMK	blood:	n/a
41	chr12:1704080-1704130	MCF-7	breast:	n/a
42	chr12:1704080-1704130	AoSMC	blood vessel:	n/a
43	chr12:1704080-1704130	HEEpiC	esophagus:	n/a
44	chr12:1704080-1704130	GM06990	blood:	n/a
45	chr12:1704080-1704130	PrEC	prostate:	n/a
46	chr12:1704080-1704130	BJ	skin:	n/a
47	chr12:1704080-1704130	PFSK-1	brain:	n/a
48	chr12:1704080-1704130	ovcar-3	ovarian:	n/a
49	chr12:1704080-1704130	NH-A	brain:	n/a
50	chr12:1704080-1704130	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr12:1224466..1226137-chr12:1702484..1704918,2	MCF-7	breast:
2	chr12:1700363..1702369-chr12:1703399..1707703,4	K562	blood:
3	chr12:1703565..1707939-chr12:1709383..1712701,6	MCF-7	breast:
4	chr12:1703157..1705505-chr12:1739226..1741204,2	MCF-7	breast:
5	chr12:547432..549780-chr12:1702241..1704941,2	MCF-7	breast:
6	chr12:1703685..1705372-chr12:1898619..1900530,2	K562	blood:
7	chr12:1703426..1704364-chr18:71959175..71959778,2	NB4	blood:
8	chr12:1057714..1059446-chr12:1702277..1704204,2	MCF-7	breast:

Variant related genes	Relation type
FBXL14	TF binding region
FBXL14	CpG island
ENSG00000111186	Chromatin interaction
ENSG00000082805	Chromatin interaction
ENSG00000002016	Chromatin interaction
ENSG00000166347	Chromatin interaction
ENSG00000120647	Chromatin interaction
ENSG00000171823	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529398	chr12:941915-1741311	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv1042863	chr12:1163817-1902302	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv541345	chr12:1163817-1902302	Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	esv3397478	chr12:1535455-1730159	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv898584	chr12:1607390-1783251	Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv826180	chr12:1614395-1759431	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv826181	chr12:1619798-1754941	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv898586	chr12:1690140-1734365	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv556979	chr12:1700134-1704325	Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
10	esv3438770	chr12:1701716-1704664	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
11	nsv556984	chr12:1702470-1704205	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
12	esv1793457	chr12:1702470-1704325	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
13	esv1793746	chr12:1702470-1704325	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
14	esv1799354	chr12:1702470-1704325	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
15	esv1820484	chr12:1702470-1704325	Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
16	esv1834585	chr12:1702470-1704325	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
17	esv1836763	chr12:1702470-1704325	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
18	esv1837561	chr12:1702470-1704325	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
19	esv1839669	chr12:1702470-1704325	Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
20	esv1844404	chr12:1702470-1704325	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
21	nsv556985	chr12:1702470-1704325	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
22	nsv556986	chr12:1702470-1705852	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
23	esv18273	chr12:1702491-1704405	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
24	esv3403028	chr12:1702616-1704989	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
25	nsv556990	chr12:1702707-1704205	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
26	nsv556992	chr12:1702913-1704205	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
27	nsv556993	chr12:1703070-1704325	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
28	esv1834423	chr12:1703324-1727170	Active TSS Weak transcription Genic enhancers Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1700600-1704400	Active TSS	Brain Germinal Matrix	brain
2	chr12:1700800-1704600	Active TSS	Ovary	ovary
3	chr12:1701000-1704800	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr12:1701200-1704200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr12:1701800-1704400	Active TSS	Fetal Kidney	kidney
6	chr12:1701800-1704600	Active TSS	Small Intestine	intestine
7	chr12:1702400-1704200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr12:1702400-1704400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
9	chr12:1702400-1705000	Active TSS	Right Atrium	heart
10	chr12:1702600-1704200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:1702600-1704200	Active TSS	Primary T helper naive cells from peripheral blood	blood
12	chr12:1702600-1704200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
13	chr12:1702600-1704200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr12:1702600-1704200	Active TSS	Rectal Smooth Muscle	rectum
15	chr12:1702600-1704400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr12:1702600-1704400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
17	chr12:1702600-1704400	Active TSS	Primary T cells from cord blood	blood
18	chr12:1702600-1704400	Active TSS	Brain Angular Gyrus	brain
19	chr12:1702600-1704400	Active TSS	Brain Anterior Caudate	brain
20	chr12:1702600-1704400	Active TSS	Colon Smooth Muscle	Colon
21	chr12:1702600-1704400	Active TSS	Lung	lung
22	chr12:1702600-1704400	Active TSS	Thymus	Thymus
23	chr12:1702600-1704400	Active TSS	A549	lung
24	chr12:1702600-1704600	Active TSS	Duodenum Smooth Muscle	Duodenum
25	chr12:1702600-1704600	Active TSS	Fetal Brain Female	brain
26	chr12:1702600-1704600	Active TSS	Left Ventricle	heart
27	chr12:1702600-1704600	Active TSS	Psoas Muscle	Psoas
28	chr12:1702600-1705200	Active TSS	Aorta	Aorta
29	chr12:1702800-1704200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:1702800-1704200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
31	chr12:1702800-1704200	Active TSS	Cortex derived primary cultured neurospheres	brain
32	chr12:1702800-1704200	Active TSS	Brain Cingulate Gyrus	brain
33	chr12:1702800-1704200	Active TSS	Fetal Intestine Large	intestine
34	chr12:1702800-1704200	Active TSS	Hela-S3	cervix
35	chr12:1702800-1704200	Active TSS	HSMM	muscle
36	chr12:1702800-1704200	Active TSS	NHLF	lung
37	chr12:1702800-1704400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr12:1702800-1704400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr12:1702800-1704400	Active TSS	Fetal Intestine Small	intestine
40	chr12:1702800-1704400	Active TSS	Sigmoid Colon	Sigmoid Colon
41	chr12:1702800-1704600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:1702800-1704600	Active TSS	Brain Substantia Nigra	brain
43	chr12:1702800-1704600	Active TSS	Esophagus	oesophagus
44	chr12:1702800-1705000	Active TSS	HSMMtube	muscle
45	chr12:1703000-1704200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr12:1703000-1704200	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr12:1703000-1704200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr12:1703000-1704200	Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr12:1703000-1704200	Active TSS	Primary monocytes fromperipheralblood	blood
50	chr12:1703000-1704200	Active TSS	Primary B cells from peripheral blood	blood

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