Variant report

Variant	esv1838635
Chromosome Location	chr6:134269008-134273139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:311)
CpG islands
(count:184)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:134273021-134273329	K562	blood:	n/a	n/a
2	ARID3A	chr6:134272926-134274538	HepG2	liver:	n/a	n/a
3	BACH1	chr6:134273056-134273937	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:134273134-134273398	K562	blood:	n/a	n/a
5	BCLAF1	chr6:134273080-134273855	GM12878	blood:	n/a	chr6:134273461-134273470
6	BCLAF1	chr6:134272983-134274536	GM12878	blood:	n/a	chr6:134273461-134273470 chr6:134274106-134274115 chr6:134274200-134274209 chr6:134274522-134274535
7	BHLHE40	chr6:134272994-134274455	GM12878	blood:	n/a	n/a
8	CHD2	chr6:134273108-134274868	Hela-S3	cervix:	n/a	chr6:134273783-134273792
9	CHD2	chr6:134273044-134274595	GM12878	blood:	n/a	chr6:134273783-134273792
10	CTBP2	chr6:134273033-134274598	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr6:134273080-134273230	AG10803	skin:	n/a	n/a
12	CTCF	chr6:134273100-134273250	GM12865	blood:	n/a	n/a
13	CTCF	chr6:134273111-134273248	Pancreas_OC	pancreas:	n/a	n/a
14	CTCF	chr6:134273120-134273270	HMEC	breast:	n/a	n/a
15	CTCF	chr6:134273087-134273288	GM19240	blood:	n/a	n/a
16	CTCF	chr6:134273120-134273410	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr6:134269980-134270130	GM12869	blood:	n/a	n/a
18	CTCF	chr6:134273023-134273697	GM12878	blood:	n/a	chr6:134273431-134273444
19	CTCF	chr6:134273120-134273270	AG04450	lung:	n/a	n/a
20	CTCF	chr6:134273060-134273210	HMF	breast:	n/a	n/a
21	CTCF	chr6:134273080-134273230	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr6:134273080-134273230	GM12870	blood:	n/a	n/a
23	CTCF	chr6:134273080-134273230	GM12873	blood:	n/a	n/a
24	CTCF	chr6:134273100-134273250	AG04450	lung:	n/a	n/a
25	CTCF	chr6:134273120-134273270	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr6:134272989-134273283	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr6:134273100-134273250	RPTEC	kidney:	n/a	n/a
28	CTCF	chr6:134273080-134273230	HRE	kidney:	n/a	n/a
29	CTCF	chr6:134273087-134273243	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr6:134273100-134273250	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:134273080-134273230	GM12875	blood:	n/a	n/a
32	CTCF	chr6:134273060-134273210	GM12865	blood:	n/a	n/a
33	CTCF	chr6:134273106-134273366	Lung_OC	lung:	n/a	n/a
34	CTCF	chr6:134273120-134273277	GM12878	blood:	n/a	n/a
35	CTCF	chr6:134273100-134273250	HAc	cerebellar:	n/a	n/a
36	CTCF	chr6:134273120-134273270	AG09309	skin:	n/a	n/a
37	CTCF	chr6:134272963-134273351	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr6:134273109-134273231	GM10266	blood:	n/a	n/a
39	CTCF	chr6:134273120-134273270	GM12867	blood:	n/a	n/a
40	CTCF	chr6:134273120-134273270	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr6:134273078-134273509	K562	blood:	n/a	chr6:134273431-134273444
42	CTCF	chr6:134273080-134273230	HepG2	liver:	n/a	n/a
43	CTCF	chr6:134273100-134273250	GM12875	blood:	n/a	n/a
44	CTCF	chr6:134273040-134273190	WI-38	lung:	n/a	n/a
45	CTCF	chr6:134273075-134273636	K562	blood:	n/a	chr6:134273431-134273444
46	CTCF	chr6:134273080-134273230	HCM	heart:	n/a	n/a
47	CTCF	chr6:134273080-134273230	HEK293	kidney:	n/a	n/a
48	CTCF	chr6:134273100-134273250	HPF	lung:	n/a	n/a
49	CTCF	chr6:134273120-134273270	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr6:134273100-134273250	HA-sp	spinal cord:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:134273121-134273171	HAEpiC	amniotic membrane:	n/a
2	chr6:134273121-134273171	HAEpiC	amniotic membrane:	n/a
3	chr6:134272463-134272513	U87	brain:	n/a
4	chr6:134270138-134270188	AoSMC	blood vessel:	n/a
5	chr6:134270138-134270188	HepG2	liver:	n/a
6	chr6:134270138-134270188	GM12878	blood:	n/a
7	chr6:134270138-134270188	MCF10A-Er-Src	breast:	n/a
8	chr6:134272463-134272513	LNCaP	prostate:	n/a
9	chr6:134273121-134273171	A549	lung:	n/a
10	chr6:134273121-134273171	GM12878	blood:	n/a
11	chr6:134273121-134273171	K562	blood:	n/a
12	chr6:134270138-134270188	Jurkat	blood:	n/a
13	chr6:134273121-134273171	HIPEpiC	eye:	n/a
14	chr6:134272463-134272513	SK-N-SH_RA	brain:	n/a
15	chr6:134273121-134273171	SK-N-SH	brain:	n/a
16	chr6:134270138-134270188	HCPEpiC	choroid plexus:	n/a
17	chr6:134272463-134272513	BJ	skin:	n/a
18	chr6:134272463-134272513	Jurkat	blood:	n/a
19	chr6:134270138-134270188	H1-hESC	embryonic stem cell:	embryo
20	chr6:134272463-134272513	MCF-7	breast:	n/a
21	chr6:134273121-134273171	ECC-1	luminal epithelium:	n/a
22	chr6:134272463-134272513	Hela-S3	cervix:	n/a
23	chr6:134273121-134273171	ProgFib	skin:	n/a
24	chr6:134273121-134273171	NH-A	brain:	n/a
25	chr6:134273121-134273171	HCM	heart:	n/a
26	chr6:134270138-134270188	AG10803	skin:	n/a
27	chr6:134270138-134270188	NT2-D1	testis:	n/a
28	chr6:134273121-134273171	HEK293	kidney:	embryo
29	chr6:134272463-134272513	A549	lung:	n/a
30	chr6:134273121-134273171	GM12892	blood:	n/a
31	chr6:134270138-134270188	LNCaP	prostate:	n/a
32	chr6:134272463-134272513	GM12878	blood:	n/a
33	chr6:134272463-134272513	HIPEpiC	eye:	n/a
34	chr6:134272463-134272513	HNPCEpiC	eye:	n/a
35	chr6:134270138-134270188	HCM	heart:	n/a
36	chr6:134273121-134273171	Hepatocyte	liver:	n/a
37	chr6:134272463-134272513	SK-N-MC	brain:	n/a
38	chr6:134273121-134273171	Jurkat	blood:	n/a
39	chr6:134272463-134272513	ECC-1	luminal epithelium:	n/a
40	chr6:134272463-134272513	NT2-D1	testis:	n/a
41	chr6:134272463-134272513	NHBE	bronchial:	n/a
42	chr6:134272463-134272513	SK-N-SH	brain:	n/a
43	chr6:134270138-134270188	GM19239	blood:	n/a
44	chr6:134272463-134272513	AG04449	skin:	fetal
45	chr6:134272463-134272513	K562	blood:	n/a
46	chr6:134272463-134272513	T-47D	breast:	n/a
47	chr6:134273121-134273171	AG10803	skin:	n/a
48	chr6:134272463-134272513	GM12891	blood:	n/a
49	chr6:134273121-134273171	HepG2	liver:	n/a
50	chr6:134272463-134272513	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:134260984..134262645-chr6:134269778..134271680,2	K562	blood:
2	chr6:134259055..134262632-chr6:134266342..134269518,3	K562	blood:

No data

Variant related genes	Relation type
TBPL1	TF binding region
TBPL1	CpG island

Extended variants
information (count: 123 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:123 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541820301	chr6:134269058-134269059	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs561942571	chr6:134269079-134269080	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs77909489	chr6:134269184-134269185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541183390	chr6:134269198-134269199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560269520	chr6:134269313-134269314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187002360	chr6:134269338-134269339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552440355	chr6:134269346-134269347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562764983	chr6:134269391-134269392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6938805	chr6:134269392-134269393	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs78487977	chr6:134269466-134269467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150995831	chr6:134269569-134269570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs80292618	chr6:134269605-134269606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191835577	chr6:134269622-134269623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373585943	chr6:134269724-134269725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142749236	chr6:134269798-134269799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370051933	chr6:134269799-134269800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570246037	chr6:134269825-134269826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539637311	chr6:134269885-134269886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556386085	chr6:134269936-134269937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140816779	chr6:134269939-134269940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149753959	chr6:134269955-134269956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146760338	chr6:134269957-134269958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572372555	chr6:134269960-134269961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541445989	chr6:134270036-134270037	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs543077160	chr6:134270072-134270073	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564411164	chr6:134270074-134270075	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs564618890	chr6:134270131-134270132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs578176193	chr6:134270215-134270216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182163776	chr6:134270276-134270277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562679644	chr6:134270458-134270459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186900361	chr6:134270556-134270557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs193236829	chr6:134270580-134270581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78114420	chr6:134270607-134270608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546986380	chr6:134270619-134270620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs527276249	chr6:134270640-134270641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559339753	chr6:134270686-134270687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547410371	chr6:134270738-134270739	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs185746976	chr6:134270763-134270764	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs539150658	chr6:134270794-134270795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549923151	chr6:134270802-134270803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569932743	chr6:134270811-134270812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4896016	chr6:134270849-134270850	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs527937958	chr6:134270871-134270872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34082514	chr6:134270880-134270881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs55705079	chr6:134271016-134271017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566399985	chr6:134271023-134271024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79787597	chr6:134271042-134271043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
48	rs558182849	chr6:134271067-134271068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs578112586	chr6:134271199-134271200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs9402553	chr6:134271203-134271204	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134266600-134272400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:134266800-134272200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:134267000-134272200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:134267800-134271600	Enhancers	Liver	Liver
5	chr6:134268000-134270200	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr6:134268000-134270400	Enhancers	Duodenum Mucosa	Duodenum
7	chr6:134268000-134270400	Enhancers	Pancreas	Pancrea
8	chr6:134268200-134269200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr6:134268200-134269600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr6:134268200-134270000	Weak transcription	Gastric	stomach
11	chr6:134268200-134270600	Enhancers	Stomach Mucosa	stomach
12	chr6:134268400-134272200	Weak transcription	Aorta	Aorta
13	chr6:134268600-134272400	Weak transcription	Fetal Brain Female	brain
14	chr6:134269000-134272400	Weak transcription	K562	blood
15	chr6:134269200-134270000	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr6:134269600-134270200	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr6:134270000-134270400	Enhancers	Gastric	stomach
18	chr6:134270000-134272400	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr6:134270200-134272400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr6:134270200-134272400	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr6:134270400-134272200	Weak transcription	Duodenum Mucosa	Duodenum
22	chr6:134270400-134272200	Weak transcription	Gastric	stomach
23	chr6:134270400-134272400	Weak transcription	Pancreas	Pancrea
24	chr6:134270600-134272200	Weak transcription	Stomach Mucosa	stomach
25	chr6:134271600-134272000	Weak transcription	Liver	Liver
26	chr6:134272000-134272600	Enhancers	Liver	Liver
27	chr6:134272200-134272400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:134272200-134272400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr6:134272200-134272400	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr6:134272200-134272400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:134272200-134272400	Enhancers	Muscle Satellite Cultured Cells	--
32	chr6:134272200-134272400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:134272200-134272400	Enhancers	Adipose Nuclei	Adipose
34	chr6:134272200-134272400	Flanking Active TSS	Aorta	Aorta
35	chr6:134272200-134272400	Enhancers	Brain Anterior Caudate	brain
36	chr6:134272200-134272400	Enhancers	Brain Cingulate Gyrus	brain
37	chr6:134272200-134272400	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr6:134272200-134272400	Enhancers	Brain Substantia Nigra	brain
39	chr6:134272200-134272400	Enhancers	Duodenum Mucosa	Duodenum
40	chr6:134272200-134272400	Enhancers	Fetal Lung	lung
41	chr6:134272200-134272400	Enhancers	A549	lung
42	chr6:134272200-134272400	Enhancers	GM12878-XiMat	blood
43	chr6:134272200-134272400	Enhancers	HSMM	muscle
44	chr6:134272200-134272400	Enhancers	HSMMtube	muscle
45	chr6:134272200-134272400	Enhancers	NHDF-Ad	bronchial
46	chr6:134272200-134272400	Enhancers	NHEK	skin
47	chr6:134272200-134272600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:134272200-134272600	Enhancers	Primary B cells from peripheral blood	blood
49	chr6:134272200-134272600	Enhancers	Primary T cells fromperipheralblood	blood
50	chr6:134272200-134272600	Enhancers	Primary T killer memory cells from peripheral blood	blood

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