Variant report

Variant	esv2760205
Chromosome Location	chr11:48886523-49006938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1524)
CpG islands
(count:1405)
Chromatin interactive
region (count:1)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1524 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48895975-48896341	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:48892892-48893269	HepG2	liver:	n/a	n/a
3	ATF1	chr11:48940082-48940286	K562	blood:	n/a	n/a
4	ATF1	chr11:48895825-48896343	K562	blood:	n/a	n/a
5	ATF1	chr11:48896850-48897050	K562	blood:	n/a	n/a
6	ATF1	chr11:48892890-48893270	K562	blood:	n/a	n/a
7	ATF3	chr11:48892858-48893151	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:48956270-48956471	K562	blood:	n/a	n/a
9	BACH1	chr11:48961635-48962346	K562	blood:	n/a	n/a
10	BATF	chr11:48985116-48985352	GM12878	blood:	n/a	n/a
11	BATF	chr11:48940420-48940720	GM12878	blood:	n/a	n/a
12	BATF	chr11:48946780-48947152	GM12878	blood:	n/a	n/a
13	BATF	chr11:48906543-48906879	GM12878	blood:	n/a	chr11:48906618-48906628
14	BATF	chr11:48934117-48934343	GM12878	blood:	n/a	n/a
15	BATF	chr11:48894524-48895290	GM12878	blood:	n/a	n/a
16	BATF	chr11:48888085-48888631	GM12878	blood:	n/a	n/a
17	BATF	chr11:48953209-48953631	GM12878	blood:	n/a	n/a
18	BATF	chr11:48916722-48917006	GM12878	blood:	n/a	chr11:48916904-48916914
19	BATF	chr11:48934446-48934684	GM12878	blood:	n/a	n/a
20	BATF	chr11:48976068-48976336	GM12878	blood:	n/a	n/a
21	BATF	chr11:48886811-48887099	GM12878	blood:	n/a	n/a
22	BATF	chr11:48935181-48935425	GM12878	blood:	n/a	n/a
23	BATF	chr11:48945011-48945390	GM12878	blood:	n/a	n/a
24	BATF	chr11:48932107-48932317	GM12878	blood:	n/a	n/a
25	BATF	chr11:48955305-48955628	GM12878	blood:	n/a	n/a
26	BATF	chr11:48934181-48934321	GM12878	blood:	n/a	n/a
27	BATF	chr11:48976038-48976262	GM12878	blood:	n/a	n/a
28	BATF	chr11:48916618-48916954	GM12878	blood:	n/a	chr11:48916904-48916914
29	BATF	chr11:48985042-48985405	GM12878	blood:	n/a	n/a
30	BATF	chr11:48894608-48895288	GM12878	blood:	n/a	n/a
31	BATF	chr11:48887996-48888565	GM12878	blood:	n/a	n/a
32	BATF	chr11:48934428-48934662	GM12878	blood:	n/a	n/a
33	BATF	chr11:48892880-48893156	GM12878	blood:	n/a	n/a
34	BATF	chr11:48906491-48906775	GM12878	blood:	n/a	chr11:48906618-48906628
35	BATF	chr11:48946385-48946719	GM12878	blood:	n/a	n/a
36	BATF	chr11:48898982-48899252	GM12878	blood:	n/a	n/a
37	BATF	chr11:48943793-48944288	GM12878	blood:	n/a	n/a
38	BATF	chr11:48953227-48953611	GM12878	blood:	n/a	n/a
39	BATF	chr11:48945095-48945310	GM12878	blood:	n/a	n/a
40	BATF	chr11:48895948-48896327	GM12878	blood:	n/a	n/a
41	BATF	chr11:48895950-48896265	GM12878	blood:	n/a	n/a
42	BATF	chr11:48931968-48932274	GM12878	blood:	n/a	n/a
43	BATF	chr11:48898958-48899437	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:48953316-48953636	GM12878	blood:	n/a	n/a
45	BCL11A	chr11:48894692-48894878	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:48916622-48916957	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:48932094-48932265	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:48887107-48887441	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:48932090-48932523	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:48955295-48955655	GM12878	blood:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48923668-48923718	NB4	blood:	n/a
2	chr11:48987265-48987315	CMK	blood:	n/a
3	chr11:48923668-48923718	NB4	blood:	n/a
4	chr11:48987265-48987315	CMK	blood:	n/a
5	chr11:48922271-48922321	CMK	blood:	n/a
6	chr11:48923577-48923627	AG04449	skin:	fetal
7	chr11:48922271-48922321	U87	brain:	n/a
8	chr11:48922035-48922085	HNPCEpiC	eye:	n/a
9	chr11:48990484-48990534	GM12891	blood:	n/a
10	chr11:48977527-48977577	PrEC	prostate:	n/a
11	chr11:48924804-48924854	HL-60	blood:	n/a
12	chr11:48990330-48990380	ovcar-3	ovarian:	n/a
13	chr11:48977527-48977577	Caco-2	colon:	n/a
14	chr11:48923668-48923718	HCM	heart:	n/a
15	chr11:48923668-48923718	HAEpiC	amniotic membrane:	n/a
16	chr11:48922741-48922791	HNPCEpiC	eye:	n/a
17	chr11:48994113-48994163	Hela-S3	cervix:	n/a
18	chr11:48902014-48902064	PFSK-1	brain:	n/a
19	chr11:48977834-48977884	HCF	heart:	n/a
20	chr11:48989769-48989819	LNCaP	prostate:	n/a
21	chr11:48987265-48987315	AG04449	skin:	fetal
22	chr11:49003361-49003411	AG04449	skin:	fetal
23	chr11:48990484-48990534	U87	brain:	n/a
24	chr11:48924804-48924854	H1-hESC	embryonic stem cell:	embryo
25	chr11:48922035-48922085	HCT-116	colon:	n/a
26	chr11:48922741-48922791	NHBE	bronchial:	n/a
27	chr11:48987265-48987315	GM12891	blood:	n/a
28	chr11:48924804-48924854	HMEC	breast:	n/a
29	chr11:48923392-48923442	NHBE	bronchial:	n/a
30	chr11:48902014-48902064	LNCaP	prostate:	n/a
31	chr11:48922035-48922085	SK-N-SH_RA	brain:	n/a
32	chr11:48922674-48922724	NB4	blood:	n/a
33	chr11:48923577-48923627	SK-N-MC	brain:	n/a
34	chr11:48977527-48977577	A549	lung:	n/a
35	chr11:48922271-48922321	AG09319	gingival:	n/a
36	chr11:48977527-48977577	NH-A	brain:	n/a
37	chr11:48922269-48922319	ovcar-3	ovarian:	n/a
38	chr11:48902014-48902064	GM12878	blood:	n/a
39	chr11:48922271-48922321	AG09309	skin:	n/a
40	chr11:48989769-48989819	ECC-1	luminal epithelium:	n/a
41	chr11:48901705-48901755	AG10803	skin:	n/a
42	chr11:48924804-48924854	HRCEpiC	kidney:	n/a
43	chr11:48990330-48990380	IMR90	lung:	fetal
44	chr11:48977834-48977884	ECC-1	luminal epithelium:	n/a
45	chr11:48922269-48922319	U87	brain:	n/a
46	chr11:49003361-49003411	PANC-1	pancreas:	n/a
47	chr11:48990484-48990534	Hepatocyte	liver:	n/a
48	chr11:48902014-48902064	HPAEpiC	pulmonary alveolar:	n/a
49	chr11:48977527-48977577	GM19239	blood:	n/a
50	chr11:48924804-48924854	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:121484902..121485419-chr11:48946286..48946806,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC084851.1-5	chr11:48916513-48916636	NONHSAT021301
2	lnc-AC084851.1-5	chr11:48919540-48919822	NONHSAT021301
3	lnc-AC084851.1-4	chr11:48929840-48930498	NONHSAT021302
4	lnc-AC084851.1-5	chr11:48914808-48914900	NONHSAT021301
5	lnc-AC084851.1-2	chr11:48982485-48982577	NONHSAT021303
6	lnc-AC084851.1-4	chr11:48928655-48928750	NONHSAT021302
7	lnc-AC084851.1-5	chr11:48919940-48920255	NONHSAT021301
8	lnc-AC084851.1-2	chr11:48981480-48981636	NONHSAT021303
9	lnc-AC084851.1-2	chr11:48983254-48983362	NONHSAT021303
10	lnc-AC084851.1-2	chr11:48981775-48981855	NONHSAT021303

No data

Variant related genes	Relation type
ENSG00000255551	TF binding region
ENSG00000254920	TF binding region
ENSG00000254517	TF binding region
ENSG00000255527	TF binding region
TRIM51CP	TF binding region
TRIM51GP	TF binding region
ENSG00000254728	TF binding region
ENSG00000255551	CpG island
ENSG00000254920	CpG island
ENSG00000254517	CpG island
ENSG00000255527	CpG island
TRIM51CP	CpG island
TRIM51GP	CpG island
ENSG00000254728	CpG island

Extended variants
information (count: 6361 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:6361 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199557797	chr11:48886551-48886552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530971349	chr11:48886552-48886553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550692064	chr11:48886565-48886566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79926422	chr11:48886571-48886572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12222283	chr11:48886572-48886573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529521243	chr11:48886574-48886575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189937718	chr11:48886575-48886576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141168005	chr11:48886619-48886620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12222299	chr11:48886648-48886649	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs537817998	chr11:48886669-48886670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182788797	chr11:48886714-48886715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs55865155	chr11:48886715-48886716	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs559229905	chr11:48886728-48886729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186601135	chr11:48886732-48886733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11493731	chr11:48886755-48886756	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs201661042	chr11:48886775-48886776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs199951873	chr11:48886782-48886783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191545593	chr11:48886785-48886786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201107783	chr11:48886806-48886807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376788312	chr11:48886808-48886809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368968849	chr11:48886809-48886810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373680401	chr11:48886835-48886836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs57325395	chr11:48886838-48886839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200560091	chr11:48886839-48886840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs72912680	chr11:48886841-48886842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144314935	chr11:48886873-48886874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183776287	chr11:48886883-48886884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532144231	chr11:48886899-48886900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12417708	chr11:48886906-48886907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562844529	chr11:48886936-48886937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs61897839	chr11:48886937-48886938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531507172	chr11:48886951-48886952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76957139	chr11:48886959-48886960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75094542	chr11:48886966-48886967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78031168	chr11:48886967-48886968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78418073	chr11:48886970-48886971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61897840	chr11:48886983-48886984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550958423	chr11:48886987-48886988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143635596	chr11:48886988-48886989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567625056	chr11:48887003-48887004	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs61897841	chr11:48887004-48887005	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs61897842	chr11:48887006-48887007	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs367555132	chr11:48887009-48887010	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs112742654	chr11:48887037-48887038	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs113205863	chr11:48887039-48887040	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs111384051	chr11:48887041-48887042	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs113622984	chr11:48887045-48887046	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs11040103	chr11:48887046-48887047	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs539270853	chr11:48887060-48887061	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs558875023	chr11:48887061-48887062	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48868000-48893000	Weak transcription	K562	blood
2	chr11:48881400-48887000	Weak transcription	NHDF-Ad	bronchial
3	chr11:48883600-48888000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr11:48883600-48892800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr11:48883800-48892800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr11:48884800-48886600	Weak transcription	HSMMtube	muscle
7	chr11:48884800-48887000	Weak transcription	NH-A	brain
8	chr11:48886000-48887000	Weak transcription	HUVEC	blood vessel
9	chr11:48887000-48887200	ZNF genes & repeats	HUVEC	blood vessel
10	chr11:48887000-48887200	ZNF genes & repeats	NH-A	brain
11	chr11:48887000-48887200	ZNF genes & repeats	NHDF-Ad	bronchial
12	chr11:48887200-48888000	Weak transcription	HUVEC	blood vessel
13	chr11:48887200-48888400	Weak transcription	NHDF-Ad	bronchial
14	chr11:48887200-48892800	Weak transcription	NH-A	brain
15	chr11:48887400-48893600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:48887400-48900400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
17	chr11:48887600-48901000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr11:48887800-48889400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
19	chr11:48888000-48888400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr11:48888000-48888600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
21	chr11:48888000-48888600	ZNF genes & repeats	HUVEC	blood vessel
22	chr11:48888000-48888800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
23	chr11:48888200-48888600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:48888200-48888600	ZNF genes & repeats	Fetal Brain Male	brain
25	chr11:48888400-48888600	ZNF genes & repeats	NHDF-Ad	bronchial
26	chr11:48888600-48892800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr11:48888600-48893000	Weak transcription	NHDF-Ad	bronchial
28	chr11:48889600-48889800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr11:48891000-48893200	ZNF genes & repeats	Fetal Brain Male	brain
30	chr11:48891800-48893800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
31	chr11:48892400-48892800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr11:48892400-48899400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
33	chr11:48892600-48893200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
34	chr11:48892600-48893200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr11:48892600-48893600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr11:48892800-48893000	Active TSS	Primary T helper cells PMA-I stimulated	--
37	chr11:48892800-48893000	Active TSS	Aorta	Aorta
38	chr11:48892800-48893000	ZNF genes & repeats	Gastric	stomach
39	chr11:48892800-48893000	Bivalent Enhancer	Rectal Smooth Muscle	rectum
40	chr11:48892800-48893200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
41	chr11:48892800-48893200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:48892800-48893200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr11:48892800-48893200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
44	chr11:48892800-48893200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr11:48892800-48893200	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr11:48892800-48893200	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr11:48892800-48893200	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
48	chr11:48892800-48893200	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
49	chr11:48892800-48893200	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
50	chr11:48892800-48893200	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood

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