Variant report

Variant	nsv562777
Chromosome Location	chr13:95962120-96027507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:386)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:95969693-95970101	K562	blood:	n/a	n/a
2	ARID3A	chr13:95966627-95967073	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
4	BACH1	chr13:95969790-95969856	K562	blood:	n/a	n/a
5	BACH1	chr13:96001635-96001886	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr13:95966774-95966999	K562	blood:	n/a	n/a
7	BHLHE40	chr13:96012862-96013164	K562	blood:	n/a	n/a
8	BHLHE40	chr13:95969437-95969892	K562	blood:	n/a	n/a
9	BRCA1	chr13:95972005-95972368	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr13:95966541-95967031	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr13:96008953-96009226	K562	blood:	n/a	n/a
12	CBX3	chr13:96015553-96015829	K562	blood:	n/a	n/a
13	CCNT2	chr13:95969690-95969892	K562	blood:	n/a	n/a
14	CEBPB	chr13:95966767-95966976	HepG2	liver:	n/a	n/a
15	CEBPB	chr13:96022472-96022715	IMR90	lung:	n/a	chr13:96022629-96022640
16	CEBPB	chr13:96022569-96022728	HepG2	liver:	n/a	chr13:96022629-96022640
17	CEBPB	chr13:95973519-95973677	HepG2	liver:	n/a	n/a
18	CEBPB	chr13:95971922-95972499	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr13:96001631-96001874	K562	blood:	n/a	n/a
20	CEBPB	chr13:95966710-95967200	MCF-7	breast:	n/a	n/a
21	CEBPB	chr13:95966781-95967036	K562	blood:	n/a	n/a
22	CEBPB	chr13:95966626-95967127	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr13:95966797-95966979	K562	blood:	n/a	n/a
24	CEBPB	chr13:95966667-95967172	MCF-7	breast:	n/a	n/a
25	CEBPB	chr13:95966736-95967046	IMR90	lung:	n/a	n/a
26	CEBPB	chr13:95969679-95969976	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr13:95966676-95967088	HepG2	liver:	n/a	n/a
28	CEBPB	chr13:95966696-95967048	HepG2	liver:	n/a	n/a
29	CEBPB	chr13:96022480-96022768	K562	blood:	n/a	chr13:96022629-96022640
30	CEBPB	chr13:95966589-95967162	HCT-116	colon:	n/a	n/a
31	CEBPB	chr13:95966693-95967096	HepG2	liver:	n/a	n/a
32	CEBPB	chr13:95966527-95967229	HCT-116	colon:	n/a	n/a
33	CEBPB	chr13:95966713-95967073	A549	lung:	n/a	n/a
34	CEBPB	chr13:96004765-96005063	Hela-S3	cervix:	n/a	n/a
35	CEBPD	chr13:95966782-95967001	HepG2	liver:	n/a	n/a
36	CEBPD	chr13:95966717-95966976	HepG2	liver:	n/a	n/a
37	CHD2	chr13:95966767-95966967	HepG2	liver:	n/a	n/a
38	CHD2	chr13:95966711-95967026	Hela-S3	cervix:	n/a	n/a
39	CREB1	chr13:95966624-95967070	HepG2	liver:	n/a	n/a
40	CREB1	chr13:95966585-95967155	HepG2	liver:	n/a	n/a
41	CTCF	chr13:96006540-96006690	HMEC	breast:	n/a	n/a
42	CTCF	chr13:96004700-96004850	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr13:96012942-96013126	K562	blood:	n/a	n/a
44	CTCF	chr13:96004693-96004848	MCF-7	breast:	n/a	n/a
45	CTCF	chr13:96004692-96004867	NHEK	skin:	n/a	n/a
46	CTCF	chr13:96006484-96006517	LNCaP	prostate:	n/a	n/a
47	CTCF	chr13:96004700-96004850	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr13:96006337-96006441	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr13:96004720-96004870	RPTEC	kidney:	n/a	n/a
50	CTCF	chr13:96004740-96004890	RPTEC	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96008021-96008071	GM06990	blood:	n/a
2	chr13:96008021-96008071	AG04450	lung:	fetal
3	chr13:96008021-96008071	NHDF-neo	bronchial:	n/a
4	chr13:96008021-96008071	SAEC	small airway:	n/a
5	chr13:96008021-96008071	CMK	blood:	n/a
6	chr13:96008021-96008071	SK-N-SH	brain:	n/a
7	chr13:96008021-96008071	MCF10A-Er-Src	breast:	n/a
8	chr13:96008021-96008071	AG04449	skin:	fetal
9	chr13:96008021-96008071	SK-N-SH_RA	brain:	n/a
10	chr13:96008021-96008071	A549	lung:	n/a
11	chr13:96008021-96008071	HRE	kidney:	n/a
12	chr13:96008021-96008071	HCF	heart:	n/a
13	chr13:96008021-96008071	BE2_C	brain:	n/a
14	chr13:96008021-96008071	HMEC	breast:	n/a
15	chr13:96008021-96008071	HRPEpiC	eye:	n/a
16	chr13:96008021-96008071	Jurkat	blood:	n/a
17	chr13:96008021-96008071	HepG2	liver:	n/a
18	chr13:96008021-96008071	NB4	blood:	n/a
19	chr13:96008021-96008071	BJ	skin:	n/a
20	chr13:96008021-96008071	GM19239	blood:	n/a
21	chr13:96008021-96008071	HEK293	kidney:	embryo
22	chr13:96008021-96008071	HIPEpiC	eye:	n/a
23	chr13:96008021-96008071	SK-N-MC	brain:	n/a
24	chr13:96008021-96008071	HAEpiC	amniotic membrane:	n/a
25	chr13:96008021-96008071	PrEC	prostate:	n/a
26	chr13:96008021-96008071	HCM	heart:	n/a
27	chr13:96008021-96008071	Hela-S3	cervix:	n/a
28	chr13:96008021-96008071	GM12892	blood:	n/a
29	chr13:96008021-96008071	HL-60	blood:	n/a
30	chr13:96008021-96008071	HCPEpiC	choroid plexus:	n/a
31	chr13:96008021-96008071	ProgFib	skin:	n/a
32	chr13:96008021-96008071	AG10803	skin:	n/a
33	chr13:96008021-96008071	ovcar-3	ovarian:	n/a
34	chr13:96008021-96008071	HEEpiC	esophagus:	n/a
35	chr13:96008021-96008071	NT2-D1	testis:	n/a
36	chr13:96008021-96008071	H1-hESC	embryonic stem cell:	embryo
37	chr13:96008021-96008071	AoSMC	blood vessel:	n/a
38	chr13:96008021-96008071	AG09309	skin:	n/a
39	chr13:96008021-96008071	RPTEC	kidney:	n/a
40	chr13:96008021-96008071	T-47D	breast:	n/a
41	chr13:96008021-96008071	HPAEpiC	pulmonary alveolar:	n/a
42	chr13:96008021-96008071	Caco-2	colon:	n/a
43	chr13:96008021-96008071	NHBE	bronchial:	n/a
44	chr13:96008021-96008071	AG09319	gingival:	n/a
45	chr13:96008021-96008071	GM12891	blood:	n/a
46	chr13:96008021-96008071	HCT-116	colon:	n/a
47	chr13:96008021-96008071	K562	blood:	n/a
48	chr13:96008021-96008071	ECC-1	luminal epithelium:	n/a
49	chr13:96008021-96008071	SKMC	muscle:	n/a
50	chr13:96008021-96008071	LNCaP	prostate:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
2	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
3	chr13:95952688..95955357-chr13:95971303..95973623,2	K562	blood:
4	chr13:95953151..95954875-chr13:95967251..95970117,3	K562	blood:
5	chr13:95953151..95954875-chr13:95967251..95969604,2	K562	blood:
6	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
7	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCC4-2	chr13:96003796-96003967	NONHSAT034758

No data

Variant related genes	Relation type
RNY4P27	TF binding region
RNY3P8	TF binding region
RNY4P27	CpG island
RNY3P8	CpG island
ENSG00000125257	chromatin interactions

Extended variants
information (count: 2396 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2396 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9524901	chr13:95962120-95962121	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532886425	chr13:95962124-95962125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546070926	chr13:95962146-95962147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562773628	chr13:95962171-95962172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563096689	chr13:95962173-95962174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531282737	chr13:95962175-95962176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547899982	chr13:95962190-95962191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2992910	chr13:95962216-95962217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs2992911	chr13:95962220-95962221	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs547625979	chr13:95962241-95962242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570654553	chr13:95962276-95962277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs60107625	chr13:95962319-95962320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs397691581	chr13:95962322-95962323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138383995	chr13:95962402-95962403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs59108692	chr13:95962424-95962425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs189308717	chr13:95962427-95962428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371770100	chr13:95962443-95962444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538314079	chr13:95962476-95962477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562513545	chr13:95962477-95962478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374803010	chr13:95962494-95962495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533779853	chr13:95962518-95962519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555117923	chr13:95962525-95962526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574728804	chr13:95962535-95962536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9516558	chr13:95962573-95962574	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs373991090	chr13:95962577-95962578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2993586	chr13:95962578-95962579	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs546502282	chr13:95962621-95962622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs56974411	chr13:95962635-95962636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs397761549	chr13:95962644-95962645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs202212148	chr13:95962645-95962646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374985352	chr13:95962675-95962676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191489962	chr13:95962706-95962707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576241991	chr13:95962758-95962759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs386773579	chr13:95962790-95962791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561454319	chr13:95962791-95962792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147435319	chr13:95962820-95962821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139736076	chr13:95962821-95962822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2993587	chr13:95962878-95962879	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs533056429	chr13:95962879-95962880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550121962	chr13:95962891-95962892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183687840	chr13:95962906-95962907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535648998	chr13:95962907-95962908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549246122	chr13:95962912-95962913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568451221	chr13:95962923-95962924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547602485	chr13:95962940-95962941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188791428	chr13:95962963-95962964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35372225	chr13:95962965-95962966	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs1764409	chr13:95963029-95963030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs75222834	chr13:95963057-95963058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71823160	chr13:95963071-95963072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:195 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95954800-95968800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr13:95956800-95968800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:95957800-95967000	Weak transcription	Fetal Intestine Small	intestine
4	chr13:95961600-95963800	Weak transcription	K562	blood
5	chr13:95963200-95963600	Enhancers	Rectal Smooth Muscle	rectum
6	chr13:95963800-95964000	Enhancers	K562	blood
7	chr13:95964000-95964600	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr13:95964000-95968600	Weak transcription	K562	blood
9	chr13:95964600-95966600	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr13:95966200-95967400	Enhancers	Hela-S3	cervix
11	chr13:95966200-95967600	Enhancers	Liver	Liver
12	chr13:95966200-95967800	Enhancers	HepG2	liver
13	chr13:95966600-95967000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr13:95966600-95967000	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr13:95966600-95967000	Enhancers	HMEC	breast
16	chr13:95966600-95967200	Enhancers	Fetal Intestine Large	intestine
17	chr13:95966600-95967400	Enhancers	Stomach Mucosa	stomach
18	chr13:95966800-95967200	Enhancers	Fetal Thymus	thymus
19	chr13:95966800-95967200	Enhancers	Gastric	stomach
20	chr13:95966800-95967200	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr13:95966800-95967200	Enhancers	Thymus	Thymus
22	chr13:95967000-95967200	Enhancers	Fetal Intestine Small	intestine
23	chr13:95967000-95967200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
24	chr13:95967200-95967400	Enhancers	Lung	lung
25	chr13:95967200-95967400	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr13:95967200-95968600	Weak transcription	Gastric	stomach
27	chr13:95967400-95968600	Weak transcription	Lung	lung
28	chr13:95967400-95968800	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr13:95967400-95968800	Weak transcription	Hela-S3	cervix
30	chr13:95967600-95970800	Weak transcription	Liver	Liver
31	chr13:95967800-95969600	Weak transcription	HepG2	liver
32	chr13:95968600-95968800	Enhancers	Gastric	stomach
33	chr13:95968600-95969600	Enhancers	K562	blood
34	chr13:95968600-95970200	Enhancers	Lung	lung
35	chr13:95968800-95969000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr13:95968800-95969000	Weak transcription	Gastric	stomach
37	chr13:95968800-95969600	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr13:95968800-95969800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr13:95968800-95969800	Enhancers	HUVEC	blood vessel
40	chr13:95968800-95970000	Enhancers	Hela-S3	cervix
41	chr13:95968800-95970200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr13:95969600-95969800	Enhancers	HepG2	liver
43	chr13:95969600-95969800	Flanking Active TSS	K562	blood
44	chr13:95969600-95970200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr13:95969800-95970000	Enhancers	K562	blood
46	chr13:95969800-95971400	Weak transcription	HUVEC	blood vessel
47	chr13:95970000-95970200	Flanking Active TSS	K562	blood
48	chr13:95970000-95971400	Weak transcription	Hela-S3	cervix
49	chr13:95970200-95971000	Enhancers	K562	blood
50	chr13:95970800-95972600	Enhancers	Liver	Liver

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