Variant report

Variant	nsv550665
Chromosome Location	chr10:42664952-42711436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1272)
CpG islands
(count:305)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1272 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr10:42677087-42677277	GM12878	blood:	n/a	n/a
2	BATF	chr10:42673879-42674402	GM12878	blood:	n/a	n/a
3	BATF	chr10:42661279-42666179	GM12878	blood:	n/a	chr10:42665305-42665316
4	BATF	chr10:42666306-42667023	GM12878	blood:	n/a	n/a
5	BATF	chr10:42691041-42691261	GM12878	blood:	n/a	n/a
6	BATF	chr10:42683465-42683803	GM12878	blood:	n/a	n/a
7	BATF	chr10:42681054-42681429	GM12878	blood:	n/a	n/a
8	BATF	chr10:42683418-42684038	GM12878	blood:	n/a	n/a
9	BATF	chr10:42697926-42698033	GM12878	blood:	n/a	n/a
10	BATF	chr10:42676194-42676528	GM12878	blood:	n/a	n/a
11	BATF	chr10:42676678-42677222	GM12878	blood:	n/a	n/a
12	BATF	chr10:42696631-42696866	GM12878	blood:	n/a	n/a
13	BATF	chr10:42678782-42679680	GM12878	blood:	n/a	n/a
14	BATF	chr10:42664499-42666109	GM12878	blood:	n/a	chr10:42665305-42665316
15	BATF	chr10:42678393-42678733	GM12878	blood:	n/a	n/a
16	BATF	chr10:42704442-42704772	GM12878	blood:	n/a	chr10:42704640-42704651
17	BATF	chr10:42684802-42685128	GM12878	blood:	n/a	n/a
18	BATF	chr10:42684572-42684848	GM12878	blood:	n/a	n/a
19	BATF	chr10:42684889-42685225	GM12878	blood:	n/a	n/a
20	BATF	chr10:42704531-42704782	GM12878	blood:	n/a	chr10:42704640-42704651
21	BATF	chr10:42678896-42679605	GM12878	blood:	n/a	n/a
22	BATF	chr10:42667213-42667659	GM12878	blood:	n/a	n/a
23	BATF	chr10:42676274-42676463	GM12878	blood:	n/a	n/a
24	BATF	chr10:42666434-42667002	GM12878	blood:	n/a	n/a
25	BATF	chr10:42667064-42667644	GM12878	blood:	n/a	n/a
26	BATF	chr10:42681006-42681427	GM12878	blood:	n/a	n/a
27	BATF	chr10:42671037-42671253	GM12878	blood:	n/a	n/a
28	BATF	chr10:42673852-42674316	GM12878	blood:	n/a	n/a
29	BCL11A	chr10:42664523-42666119	GM12878	blood:	n/a	n/a
30	BCL11A	chr10:42679981-42680151	GM12878	blood:	n/a	n/a
31	BCL11A	chr10:42684721-42685144	GM12878	blood:	n/a	n/a
32	BCL11A	chr10:42678728-42679747	GM12878	blood:	n/a	n/a
33	BCL11A	chr10:42703088-42703254	GM12878	blood:	n/a	n/a
34	BCL11A	chr10:42676208-42676416	GM12878	blood:	n/a	n/a
35	BCL11A	chr10:42704553-42704791	GM12878	blood:	n/a	n/a
36	BCL11A	chr10:42704506-42704681	GM12878	blood:	n/a	n/a
37	BCL11A	chr10:42683453-42683798	GM12878	blood:	n/a	n/a
38	BCL11A	chr10:42677046-42677285	GM12878	blood:	n/a	n/a
39	BCL11A	chr10:42678781-42679602	GM12878	blood:	n/a	n/a
40	BCL11A	chr10:42666418-42667036	GM12878	blood:	n/a	n/a
41	BCL11A	chr10:42667099-42667656	GM12878	blood:	n/a	n/a
42	BCL11A	chr10:42677828-42678108	GM12878	blood:	n/a	n/a
43	BCL11A	chr10:42705685-42705867	GM12878	blood:	n/a	n/a
44	BCL11A	chr10:42674588-42674874	GM12878	blood:	n/a	n/a
45	BCL11A	chr10:42698731-42698923	GM12878	blood:	n/a	n/a
46	BCL11A	chr10:42677876-42678057	GM12878	blood:	n/a	n/a
47	BCL11A	chr10:42682187-42682422	GM12878	blood:	n/a	n/a
48	BCL11A	chr10:42676707-42676961	GM12878	blood:	n/a	n/a
49	BCL11A	chr10:42674640-42674904	GM12878	blood:	n/a	n/a
50	BCL11A	chr10:42667269-42667681	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:42672859-42672909	HepG2	liver:	n/a
2	chr10:42677108-42677158	HAEpiC	amniotic membrane:	n/a
3	chr10:42677108-42677158	HL-60	blood:	n/a
4	chr10:42673902-42673952	BJ	skin:	n/a
5	chr10:42673902-42673952	HRE	kidney:	n/a
6	chr10:42677108-42677158	AG09309	skin:	n/a
7	chr10:42673902-42673952	Caco-2	colon:	n/a
8	chr10:42677108-42677158	ECC-1	luminal epithelium:	n/a
9	chr10:42672859-42672909	ProgFib	skin:	n/a
10	chr10:42672589-42672639	MCF-7	breast:	n/a
11	chr10:42672589-42672639	BE2_C	brain:	n/a
12	chr10:42672589-42672639	PFSK-1	brain:	n/a
13	chr10:42677108-42677158	SAEC	small airway:	n/a
14	chr10:42670961-42671011	AG10803	skin:	n/a
15	chr10:42672859-42672909	NH-A	brain:	n/a
16	chr10:42672589-42672639	NHBE	bronchial:	n/a
17	chr10:42672859-42672909	GM12891	blood:	n/a
18	chr10:42672859-42672909	T-47D	breast:	n/a
19	chr10:42672859-42672909	AG04450	lung:	fetal
20	chr10:42677108-42677158	NHBE	bronchial:	n/a
21	chr10:42670961-42671011	ECC-1	luminal epithelium:	n/a
22	chr10:42673902-42673952	PANC-1	pancreas:	n/a
23	chr10:42672589-42672639	GM06990	blood:	n/a
24	chr10:42672859-42672909	AoSMC	blood vessel:	n/a
25	chr10:42670961-42671011	HMEC	breast:	n/a
26	chr10:42673902-42673952	RPTEC	kidney:	n/a
27	chr10:42670961-42671011	BE2_C	brain:	n/a
28	chr10:42670961-42671011	SK-N-MC	brain:	n/a
29	chr10:42670961-42671011	NB4	blood:	n/a
30	chr10:42672589-42672639	GM12891	blood:	n/a
31	chr10:42670961-42671011	PrEC	prostate:	n/a
32	chr10:42670961-42671011	Hela-S3	cervix:	n/a
33	chr10:42672589-42672639	ECC-1	luminal epithelium:	n/a
34	chr10:42673902-42673952	PrEC	prostate:	n/a
35	chr10:42673902-42673952	ProgFib	skin:	n/a
36	chr10:42672589-42672639	HL-60	blood:	n/a
37	chr10:42673902-42673952	BE2_C	brain:	n/a
38	chr10:42677108-42677158	HepG2	liver:	n/a
39	chr10:42673902-42673952	LNCaP	prostate:	n/a
40	chr10:42677108-42677158	HEK293	kidney:	embryo
41	chr10:42670961-42671011	HL-60	blood:	n/a
42	chr10:42670961-42671011	PFSK-1	brain:	n/a
43	chr10:42672859-42672909	Caco-2	colon:	n/a
44	chr10:42672589-42672639	H1-hESC	embryonic stem cell:	embryo
45	chr10:42672589-42672639	Caco-2	colon:	n/a
46	chr10:42670961-42671011	ProgFib	skin:	n/a
47	chr10:42672859-42672909	HMEC	breast:	n/a
48	chr10:42672589-42672639	HCM	heart:	n/a
49	chr10:42672589-42672639	PrEC	prostate:	n/a
50	chr10:42672589-42672639	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:42673929..42674445-chr10:43600657..43601190,2	K562	blood:
2	chr10:42673795..42674377-chr10:42765091..42765784,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMS1-9	chr10:42686975-42687136	NONHSAT012855
2	lnc-BMS1-8	chr10:42705438-42705831	NONHSAT012856
3	lnc-BMS1-9	chr10:42687963-42689514	NONHSAT012855

No data

Variant related genes	Relation type
ENSG00000271650	TF binding region
IGKV1OR10-1	TF binding region
ENSG00000271650	CpG island
IGKV1OR10-1	CpG island

Extended variants
information (count: 1557 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1557 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573497963	chr10:42664952-42664953	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs139564617	chr10:42664966-42664967	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542112872	chr10:42664972-42664973	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377359601	chr10:42664986-42664987	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561971673	chr10:42664990-42664991	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111217447	chr10:42664991-42664992	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150975419	chr10:42665012-42665013	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111209087	chr10:42665034-42665035	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200091918	chr10:42665038-42665039	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146920163	chr10:42665050-42665051	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201641610	chr10:42665051-42665052	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530976407	chr10:42665053-42665054	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141520129	chr10:42665061-42665062	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs118192555	chr10:42665070-42665071	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564378802	chr10:42665080-42665081	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533372410	chr10:42665087-42665088	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140086658	chr10:42665089-42665090	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546720560	chr10:42665095-42665096	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370944642	chr10:42665100-42665101	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs151224333	chr10:42665123-42665124	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149705637	chr10:42665124-42665125	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566857977	chr10:42665127-42665128	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375319054	chr10:42665131-42665132	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535778061	chr10:42665145-42665146	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12413004	chr10:42665146-42665147	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569086524	chr10:42665151-42665152	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs202008579	chr10:42665153-42665154	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200156912	chr10:42665156-42665157	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200991087	chr10:42665171-42665172	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141394177	chr10:42665181-42665182	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138185521	chr10:42665199-42665200	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538008445	chr10:42665202-42665203	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147218416	chr10:42665223-42665224	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140167867	chr10:42665224-42665225	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111217000	chr10:42665227-42665228	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557835530	chr10:42665229-42665230	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571211170	chr10:42665233-42665234	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533877319	chr10:42665239-42665240	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553533219	chr10:42665247-42665248	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573278691	chr10:42665264-42665265	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188890035	chr10:42665266-42665267	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542149140	chr10:42665270-42665271	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555614619	chr10:42665279-42665280	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575437150	chr10:42665292-42665293	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544360494	chr10:42665295-42665296	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546126732	chr10:42665296-42665297	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371563253	chr10:42665304-42665305	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564694153	chr10:42665309-42665310	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138157991	chr10:42665318-42665319	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144425148	chr10:42665324-42665325	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Obesity	20622171	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:42655800-42668200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
2	chr10:42660000-42668200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr10:42660400-42668000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr10:42660400-42668000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
5	chr10:42660600-42668000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr10:42661000-42667600	ZNF genes & repeats	Primary T cells from cord blood	blood
7	chr10:42661200-42667000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
8	chr10:42661200-42667200	ZNF genes & repeats	Brain Substantia Nigra	brain
9	chr10:42661200-42667400	ZNF genes & repeats	K562	blood
10	chr10:42661200-42667600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
11	chr10:42661200-42667600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr10:42661200-42667600	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
13	chr10:42661200-42667600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
14	chr10:42661200-42667600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
15	chr10:42661200-42667600	ZNF genes & repeats	Fetal Brain Male	brain
16	chr10:42661200-42667600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
17	chr10:42661200-42667800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
18	chr10:42661200-42667800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:42661200-42667800	ZNF genes & repeats	Adipose Nuclei	Adipose
20	chr10:42661200-42667800	ZNF genes & repeats	Fetal Heart	heart
21	chr10:42661200-42667800	ZNF genes & repeats	Fetal Lung	lung
22	chr10:42661200-42668000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
23	chr10:42661200-42668200	ZNF genes & repeats	Liver	Liver
24	chr10:42661400-42667200	ZNF genes & repeats	Primary B cells from cord blood	blood
25	chr10:42661400-42667200	ZNF genes & repeats	GM12878-XiMat	blood
26	chr10:42661400-42667400	ZNF genes & repeats	HepG2	liver
27	chr10:42661400-42667600	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
28	chr10:42661400-42667600	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
29	chr10:42661400-42667600	ZNF genes & repeats	Fetal Kidney	kidney
30	chr10:42661400-42667600	ZNF genes & repeats	HUVEC	blood vessel
31	chr10:42661400-42667800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
32	chr10:42661600-42666800	Weak transcription	NHDF-Ad	bronchial
33	chr10:42666000-42667600	ZNF genes & repeats	Gastric	stomach
34	chr10:42666800-42667400	ZNF genes & repeats	NH-A	brain
35	chr10:42666800-42667600	ZNF genes & repeats	NHDF-Ad	bronchial
36	chr10:42667200-42667600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
37	chr10:42667200-42667600	ZNF genes & repeats	Brain Hippocampus Middle	brain
38	chr10:42667800-42668200	Weak transcription	NHDF-Ad	bronchial
39	chr10:42668000-42668200	Weak transcription	Fetal Lung	lung
40	chr10:42668000-42668400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr10:42668200-42673400	Weak transcription	Liver	Liver
42	chr10:42672400-42672600	Active TSS	Psoas Muscle	Psoas
43	chr10:42672600-42672800	Flanking Active TSS	Primary hematopoietic stem cells	blood
44	chr10:42672600-42672800	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
45	chr10:42672600-42672800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr10:42672600-42672800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr10:42672600-42672800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr10:42672600-42672800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr10:42672600-42673000	Enhancers	Primary B cells from peripheral blood	blood
50	chr10:42672600-42673000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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