Variant report

Variant	nsv1060275
Chromosome Location	chr20:15084485-15327541
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1149)
CpG islands
(count:183)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1149 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:15139111-15139485	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:15144336-15144711	HepG2	liver:	n/a	n/a
3	ATF2	chr20:15142645-15143351	GM12878	blood:	n/a	n/a
4	ATF2	chr20:15297929-15299020	GM12878	blood:	n/a	n/a
5	ATF2	chr20:15180601-15181187	GM12878	blood:	n/a	n/a
6	ATF2	chr20:15298201-15298708	GM12878	blood:	n/a	n/a
7	ATF2	chr20:15142556-15143423	GM12878	blood:	n/a	n/a
8	ATF2	chr20:15299152-15299756	GM12878	blood:	n/a	n/a
9	ATF2	chr20:15313045-15313880	GM12878	blood:	n/a	chr20:15313332-15313343
10	ATF2	chr20:15180324-15181228	GM12878	blood:	n/a	n/a
11	ATF2	chr20:15299899-15300572	GM12878	blood:	n/a	n/a
12	ATF2	chr20:15299283-15299738	GM12878	blood:	n/a	n/a
13	BACH1	chr20:15144468-15144534	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr20:15299346-15299710	GM12878	blood:	n/a	n/a
15	BATF	chr20:15142631-15143004	GM12878	blood:	n/a	n/a
16	BATF	chr20:15298174-15298614	GM12878	blood:	n/a	n/a
17	BATF	chr20:15217496-15217756	GM12878	blood:	n/a	n/a
18	BATF	chr20:15142669-15143382	GM12878	blood:	n/a	n/a
19	BATF	chr20:15298206-15298537	GM12878	blood:	n/a	n/a
20	BATF	chr20:15229264-15229547	GM12878	blood:	n/a	n/a
21	BATF	chr20:15313268-15313752	GM12878	blood:	n/a	n/a
22	BATF	chr20:15143005-15143338	GM12878	blood:	n/a	n/a
23	BATF	chr20:15299357-15299730	GM12878	blood:	n/a	n/a
24	BATF	chr20:15180351-15181277	GM12878	blood:	n/a	chr20:15180905-15180913
25	BATF	chr20:15298652-15298919	GM12878	blood:	n/a	n/a
26	BATF	chr20:15180677-15181088	GM12878	blood:	n/a	chr20:15180905-15180913
27	BCL11A	chr20:15180758-15180983	GM12878	blood:	n/a	n/a
28	BCL11A	chr20:15180658-15181150	GM12878	blood:	n/a	n/a
29	BCL3	chr20:15180753-15181061	GM12878	blood:	n/a	n/a
30	BCLAF1	chr20:15142637-15143439	GM12878	blood:	n/a	n/a
31	BCLAF1	chr20:15298185-15298626	GM12878	blood:	n/a	n/a
32	BCLAF1	chr20:15313142-15313783	GM12878	blood:	n/a	n/a
33	BCLAF1	chr20:15298111-15298900	GM12878	blood:	n/a	n/a
34	BHLHE40	chr20:15313573-15313619	GM12878	blood:	n/a	n/a
35	BHLHE40	chr20:15313971-15314073	GM12878	blood:	n/a	n/a
36	BHLHE40	chr20:15298187-15298590	GM12878	blood:	n/a	n/a
37	BHLHE40	chr20:15307828-15307979	K562	blood:	n/a	n/a
38	BHLHE40	chr20:15180594-15181323	GM12878	blood:	n/a	n/a
39	BRCA1	chr20:15217541-15217700	HepG2	liver:	n/a	n/a
40	CBX3	chr20:15217421-15217751	HCT-116	colon:	n/a	n/a
41	CEBPB	chr20:15323545-15323781	A549	lung:	n/a	n/a
42	CEBPB	chr20:15169103-15169442	Hela-S3	cervix:	n/a	chr20:15169267-15169284
43	CEBPB	chr20:15274199-15274343	HepG2	liver:	n/a	n/a
44	CEBPB	chr20:15169144-15169403	H1-hESC	embryonic stem cell:	n/a	chr20:15169267-15169284
45	CEBPB	chr20:15127751-15128049	MCF-7	breast:	n/a	chr20:15127917-15127930 chr20:15128000-15128013 chr20:15127917-15127930 chr20:15127919-15127930 chr20:15127917-15127928 chr20:15127919-15127930
46	CEBPB	chr20:15252432-15252620	A549	lung:	n/a	n/a
47	CEBPB	chr20:15146524-15146700	HepG2	liver:	n/a	n/a
48	CEBPB	chr20:15239247-15239316	A549	lung:	n/a	n/a
49	CEBPB	chr20:15237312-15237381	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr20:15151692-15151964	A549	lung:	n/a	chr20:15151830-15151841

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:15176557-15176607	AG10803	skin:	n/a
2	chr20:15176557-15176607	Hela-S3	cervix:	n/a
3	chr20:15176830-15176880	A549	lung:	n/a
4	chr20:15176830-15176880	NHBE	bronchial:	n/a
5	chr20:15176557-15176607	GM06990	blood:	n/a
6	chr20:15176557-15176607	HCM	heart:	n/a
7	chr20:15176830-15176880	HEEpiC	esophagus:	n/a
8	chr20:15176830-15176880	Caco-2	colon:	n/a
9	chr20:15177509-15177559	Caco-2	colon:	n/a
10	chr20:15176557-15176607	Hepatocyte	liver:	n/a
11	chr20:15176830-15176880	IMR90	lung:	fetal
12	chr20:15176557-15176607	MCF10A-Er-Src	breast:	n/a
13	chr20:15176557-15176607	BE2_C	brain:	n/a
14	chr20:15177509-15177559	CMK	blood:	n/a
15	chr20:15176557-15176607	HCT-116	colon:	n/a
16	chr20:15177509-15177559	BJ	skin:	n/a
17	chr20:15177509-15177559	NT2-D1	testis:	n/a
18	chr20:15176557-15176607	NHDF-neo	bronchial:	n/a
19	chr20:15176557-15176607	HL-60	blood:	n/a
20	chr20:15177509-15177559	NHBE	bronchial:	n/a
21	chr20:15176557-15176607	ProgFib	skin:	n/a
22	chr20:15177509-15177559	MCF-7	breast:	n/a
23	chr20:15177509-15177559	HCT-116	colon:	n/a
24	chr20:15177509-15177559	ECC-1	luminal epithelium:	n/a
25	chr20:15177509-15177559	AG04450	lung:	fetal
26	chr20:15177509-15177559	GM12878	blood:	n/a
27	chr20:15176830-15176880	GM19239	blood:	n/a
28	chr20:15176830-15176880	SKMC	muscle:	n/a
29	chr20:15176557-15176607	H1-hESC	embryonic stem cell:	embryo
30	chr20:15177509-15177559	Hela-S3	cervix:	n/a
31	chr20:15176830-15176880	LNCaP	prostate:	n/a
32	chr20:15177509-15177559	Jurkat	blood:	n/a
33	chr20:15176830-15176880	GM06990	blood:	n/a
34	chr20:15177509-15177559	PANC-1	pancreas:	n/a
35	chr20:15176557-15176607	HAEpiC	amniotic membrane:	n/a
36	chr20:15176830-15176880	RPTEC	kidney:	n/a
37	chr20:15176830-15176880	HMEC	breast:	n/a
38	chr20:15176557-15176607	IMR90	lung:	fetal
39	chr20:15177509-15177559	BE2_C	brain:	n/a
40	chr20:15176830-15176880	ProgFib	skin:	n/a
41	chr20:15177509-15177559	ProgFib	skin:	n/a
42	chr20:15176830-15176880	HepG2	liver:	n/a
43	chr20:15177509-15177559	A549	lung:	n/a
44	chr20:15177509-15177559	GM19239	blood:	n/a
45	chr20:15176830-15176880	SK-N-SH	brain:	n/a
46	chr20:15176830-15176880	HCPEpiC	choroid plexus:	n/a
47	chr20:15176557-15176607	MCF-7	breast:	n/a
48	chr20:15176830-15176880	BE2_C	brain:	n/a
49	chr20:15176557-15176607	AoSMC	blood vessel:	n/a
50	chr20:15176830-15176880	PANC-1	pancreas:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
2	chr20:15280200..15282422-chr20:15286811..15288380,2	MCF-7	breast:
3	chr20:15293454..15295061-chr20:15304426..15306908,2	MCF-7	breast:
4	chr20:15222565..15225391-chr20:15228675..15231649,2	MCF-7	breast:
5	chr20:15293454..15295061-chr20:15304426..15306908,2	MCF-7	breast:
6	chr20:15279663..15281630-chr20:15285386..15287786,2	MCF-7	breast:
7	chr20:15222565..15225391-chr20:15228675..15231649,2	MCF-7	breast:
8	chr20:15280200..15282422-chr20:15286811..15288380,2	MCF-7	breast:
9	chr20:15279663..15281630-chr20:15285386..15287786,2	MCF-7	breast:
10	chr20:14335576..14337791-chr20:15315333..15317078,2	MCF-7	breast:
11	chr20:15213744..15214594-chr5:107680986..107681674,2	MCF-7	breast:
12	chr20:14316387..14318274-chr20:15215878..15217670,2	MCF-7	breast:

No data

Variant related genes	Relation type
MACROD2	TF binding region
RNA5SP475	TF binding region
MACROD2	CpG island
RNA5SP475	CpG island
ENSG00000125848	chromatin interactions

Extended variants
information (count: 6944 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:6944 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs137866310	chr20:15087210-15087211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373622863	chr20:15087218-15087219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189722509	chr20:15087219-15087220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544209310	chr20:15087240-15087241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80091564	chr20:15087264-15087265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182643536	chr20:15087274-15087275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548176394	chr20:15087275-15087276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372610377	chr20:15087284-15087285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6110519	chr20:15087285-15087286	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs527742768	chr20:15087288-15087289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552366014	chr20:15087314-15087315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7272732	chr20:15087330-15087331	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs411338	chr20:15087332-15087333	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs142481768	chr20:15087338-15087339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568726457	chr20:15087412-15087413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536301017	chr20:15087439-15087440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188937382	chr20:15087448-15087449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572984177	chr20:15087509-15087510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549408942	chr20:15087538-15087539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540303064	chr20:15087661-15087662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145978622	chr20:15087667-15087668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576997572	chr20:15087675-15087676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139858191	chr20:15087701-15087702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566406232	chr20:15087702-15087703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6043093	chr20:15087720-15087721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549067092	chr20:15087749-15087750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375667985	chr20:15087879-15087880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6043094	chr20:15087977-15087978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562685071	chr20:15088026-15088027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73096060	chr20:15088027-15088028	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs442314	chr20:15088031-15088032	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs560084881	chr20:15088039-15088040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6043095	chr20:15088074-15088075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527805480	chr20:15088164-15088165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376806724	chr20:15088176-15088177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs193232274	chr20:15088206-15088207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570911407	chr20:15088300-15088301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185307786	chr20:15088348-15088349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550347495	chr20:15088428-15088429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571744828	chr20:15088435-15088436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568774495	chr20:15088451-15088452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536115315	chr20:15088518-15088519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78526672	chr20:15088584-15088585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs17357522	chr20:15088585-15088586	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs533753728	chr20:15088611-15088612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560192912	chr20:15088629-15088630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542689395	chr20:15088630-15088631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76186415	chr20:15088632-15088633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558408123	chr20:15088658-15088659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576866529	chr20:15088665-15088666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Glaucoma	21310917	CNVD
Alagille syndrome	22470819	CNVD
Lung cancer	16773561	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelofibrosis	22110671	CNVD
Kabuki syndrome	21720541	CNVD
Glioblastoma multiforme	22286061	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neurocytoma	17123091	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
Multiple sclerosis	20663923	CNVD
Schizophrenia	20663923	CNVD
brain infarct	20663923	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Esophageal adenocarcinoma	18519675	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21272361	CNVD
Schizophrenia	19805367	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15087200-15087400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr20:15087400-15092200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr20:15088400-15089200	Enhancers	Stomach Mucosa	stomach
4	chr20:15089000-15089600	Enhancers	Fetal Intestine Small	intestine
5	chr20:15090800-15091000	Enhancers	Thymus	Thymus
6	chr20:15091000-15092200	Weak transcription	Thymus	Thymus
7	chr20:15091000-15093400	Enhancers	Fetal Thymus	thymus
8	chr20:15091200-15094000	Enhancers	Dnd41	blood
9	chr20:15092200-15092600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr20:15092200-15093000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr20:15092200-15093000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr20:15092200-15093600	Enhancers	Thymus	Thymus
13	chr20:15092200-15094000	Enhancers	Primary T cells from cord blood	blood
14	chr20:15092400-15092800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr20:15092400-15092800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr20:15093000-15094800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr20:15093400-15095000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr20:15093400-15096000	Weak transcription	Fetal Thymus	thymus
19	chr20:15093600-15094200	Weak transcription	Thymus	Thymus
20	chr20:15093600-15095200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr20:15093800-15094200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr20:15093800-15094600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr20:15093800-15095000	Enhancers	Brain Hippocampus Middle	brain
24	chr20:15093800-15095200	Enhancers	Brain Substantia Nigra	brain
25	chr20:15094000-15094400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr20:15094000-15094600	Enhancers	Fetal Brain Male	brain
27	chr20:15094000-15094800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr20:15094000-15094800	Enhancers	Brain Angular Gyrus	brain
29	chr20:15094000-15095400	Weak transcription	Dnd41	blood
30	chr20:15094000-15096400	Weak transcription	Primary T cells from cord blood	blood
31	chr20:15094200-15094400	Enhancers	Thymus	Thymus
32	chr20:15094400-15095800	Weak transcription	Thymus	Thymus
33	chr20:15094600-15094800	Enhancers	Aorta	Aorta
34	chr20:15094800-15095000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr20:15095400-15097200	Enhancers	Dnd41	blood
36	chr20:15095800-15097000	Enhancers	Thymus	Thymus
37	chr20:15096000-15096200	Enhancers	Fetal Thymus	thymus
38	chr20:15096200-15096600	Weak transcription	Fetal Thymus	thymus
39	chr20:15096400-15096600	Enhancers	Primary T cells from cord blood	blood
40	chr20:15096600-15097200	Enhancers	Fetal Thymus	thymus
41	chr20:15102800-15104400	Enhancers	Dnd41	blood
42	chr20:15103000-15103800	Enhancers	Stomach Mucosa	stomach
43	chr20:15108200-15108400	Enhancers	Aorta	Aorta
44	chr20:15111600-15112000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr20:15119000-15119600	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr20:15119000-15120200	Enhancers	Liver	Liver
47	chr20:15119200-15119800	Enhancers	Fetal Kidney	kidney
48	chr20:15119200-15120000	Enhancers	A549	lung
49	chr20:15119200-15120000	Enhancers	HepG2	liver
50	chr20:15119200-15120200	Enhancers	Stomach Mucosa	stomach

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