Variant report

Variant	esv3320079
Chromosome Location	chr1:62765252-62770865
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	E2F6	chr1:62767306-62768019	H1-hESC	embryonic stem cell:	n/a	n/a
2	FOS	chr1:62765464-62765546	MCF10A-Er-Src	breast:	n/a	n/a
3	FOXA2	chr1:62765439-62765717	HepG2	liver:	n/a	n/a
4	KAP1	chr1:62765453-62765879	U2OS	brain:	n/a	n/a
5	MAX	chr1:62765381-62765938	HepG2	liver:	n/a	n/a
6	MAX	chr1:62767417-62767940	H1-hESC	embryonic stem cell:	n/a	chr1:62767575-62767586 chr1:62767574-62767587 chr1:62767575-62767585 chr1:62767576-62767585 chr1:62767576-62767586 chr1:62767576-62767586 chr1:62767574-62767589 chr1:62767567-62767583 chr1:62767576-62767586 chr1:62767575-62767586 chr1:62767577-62767586
7	MAX	chr1:62767387-62767805	H1-hESC	embryonic stem cell:	n/a	chr1:62767575-62767586 chr1:62767574-62767587 chr1:62767575-62767585 chr1:62767576-62767585 chr1:62767576-62767586 chr1:62767576-62767586 chr1:62767574-62767589 chr1:62767567-62767583 chr1:62767576-62767586 chr1:62767575-62767586 chr1:62767577-62767586
8	MAX	chr1:62767435-62767721	NB4	blood:	n/a	chr1:62767575-62767586 chr1:62767574-62767587 chr1:62767575-62767585 chr1:62767576-62767585 chr1:62767576-62767586 chr1:62767576-62767586 chr1:62767574-62767589 chr1:62767567-62767583 chr1:62767576-62767586 chr1:62767575-62767586 chr1:62767577-62767586
9	MAX	chr1:62767412-62767698	K562	blood:	n/a	chr1:62767575-62767586 chr1:62767574-62767587 chr1:62767575-62767585 chr1:62767576-62767585 chr1:62767576-62767586 chr1:62767576-62767586 chr1:62767574-62767589 chr1:62767567-62767583 chr1:62767576-62767586 chr1:62767575-62767586 chr1:62767577-62767586
10	MAX	chr1:62767331-62768008	H1-hESC	embryonic stem cell:	n/a	chr1:62767575-62767586 chr1:62767574-62767587 chr1:62767575-62767585 chr1:62767576-62767585 chr1:62767576-62767586 chr1:62767576-62767586 chr1:62767574-62767589 chr1:62767567-62767583 chr1:62767576-62767586 chr1:62767575-62767586 chr1:62767577-62767586
11	MYC	chr1:62765532-62765754	HepG2	liver:	n/a	n/a
12	MYC	chr1:62765513-62765715	MCF10A-Er-Src	breast:	n/a	n/a
13	MYC	chr1:62767508-62767734	H1-hESC	embryonic stem cell:	n/a	chr1:62767575-62767586 chr1:62767574-62767587 chr1:62767575-62767585 chr1:62767576-62767585 chr1:62767576-62767586 chr1:62767576-62767586 chr1:62767574-62767589 chr1:62767567-62767583 chr1:62767576-62767586 chr1:62767575-62767586 chr1:62767577-62767586
14	MYC	chr1:62765447-62765661	MCF10A-Er-Src	breast:	n/a	n/a
15	NFIC	chr1:62765227-62765866	ECC-1	luminal epithelium:	n/a	chr1:62765620-62765648
16	NFIC	chr1:62765292-62765855	ECC-1	luminal epithelium:	n/a	chr1:62765620-62765648
17	POLR2A	chr1:62766532-62766947	H1-neurons	neurons:	n/a	n/a
18	TAL1	chr1:62770478-62770709	K562	blood:	n/a	n/a
19	USF1	chr1:62767428-62767766	H1-hESC	embryonic stem cell:	n/a	n/a
20	USF1	chr1:62767393-62767711	H1-hESC	embryonic stem cell:	n/a	n/a

Variant related genes	Relation type
RNU6-371P	TF binding region

Extended variants
information (count: 206 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:206 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544417423	chr1:62765313-62765314	Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs184336634	chr1:62765368-62765369	Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs374353395	chr1:62765389-62765390	Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs10889318	chr1:62765461-62765462	Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs79306000	chr1:62765478-62765479	Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs537892062	chr1:62765507-62765508	Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs186895536	chr1:62765525-62765526	Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs368745768	chr1:62765570-62765571	Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs556529762	chr1:62765622-62765623	Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs527689542	chr1:62765698-62765699	Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs12063531	chr1:62765738-62765739	Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs568281778	chr1:62765745-62765746	Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs529073026	chr1:62765766-62765767	Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs550825054	chr1:62765815-62765816	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs75829160	chr1:62765827-62765828	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs539579917	chr1:62765846-62765847	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs557781322	chr1:62765866-62765867	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs566414185	chr1:62765885-62765886	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs192732144	chr1:62765976-62765977	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560276749	chr1:62765992-62765993	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116307158	chr1:62765999-62766000	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10493319	chr1:62766001-62766002	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs544377057	chr1:62766029-62766030	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185011804	chr1:62766033-62766034	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577713045	chr1:62766038-62766039	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148260464	chr1:62766049-62766050	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189082078	chr1:62766072-62766073	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527652987	chr1:62766086-62766087	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140452761	chr1:62766094-62766095	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114336143	chr1:62766189-62766190	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529241549	chr1:62766235-62766236	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116468198	chr1:62766259-62766260	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569116991	chr1:62766312-62766313	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1325740	chr1:62766316-62766317	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs531299962	chr1:62766379-62766380	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145442926	chr1:62766398-62766399	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10493320	chr1:62766406-62766407	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533752256	chr1:62766407-62766408	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181074481	chr1:62766430-62766431	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs115771447	chr1:62766445-62766446	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114046745	chr1:62766449-62766450	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556442294	chr1:62766475-62766476	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577776413	chr1:62766498-62766499	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1325741	chr1:62766508-62766509	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547549396	chr1:62766509-62766510	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1325742	chr1:62766527-62766528	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs572479272	chr1:62766535-62766536	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs542995550	chr1:62766547-62766548	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs184872591	chr1:62766554-62766555	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs568818349	chr1:62766590-62766591	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62754400-62773400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:62759800-62765400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr1:62759800-62770800	Enhancers	Fetal Muscle Leg	muscle
4	chr1:62761800-62767200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:62762000-62765400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:62762000-62765600	Weak transcription	Stomach Smooth Muscle	stomach
7	chr1:62762000-62766000	Weak transcription	Brain Angular Gyrus	brain
8	chr1:62762000-62767000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr1:62762200-62765400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr1:62762200-62765600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:62762200-62765600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr1:62762200-62767200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr1:62762200-62773200	Weak transcription	Fetal Lung	lung
14	chr1:62762400-62765400	Weak transcription	Brain Germinal Matrix	brain
15	chr1:62762600-62765600	Weak transcription	Brain Cingulate Gyrus	brain
16	chr1:62763200-62765800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr1:62764800-62765800	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr1:62764800-62768000	Enhancers	Pancreas	Pancrea
19	chr1:62765000-62765400	Enhancers	Aorta	Aorta
20	chr1:62765000-62765800	Enhancers	Fetal Thymus	thymus
21	chr1:62765000-62765800	Enhancers	Lung	lung
22	chr1:62765000-62765800	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr1:62765000-62765800	Enhancers	Right Atrium	heart
24	chr1:62765000-62765800	Enhancers	Hela-S3	cervix
25	chr1:62765000-62766000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:62765000-62766000	Enhancers	Fetal Muscle Trunk	muscle
27	chr1:62765000-62766200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:62765000-62766200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr1:62765000-62766200	Enhancers	Gastric	stomach
30	chr1:62765000-62766200	Enhancers	HMEC	breast
31	chr1:62765000-62766400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:62765000-62766400	Enhancers	Fetal Kidney	kidney
33	chr1:62765000-62766400	Enhancers	Left Ventricle	heart
34	chr1:62765000-62766400	Enhancers	Stomach Mucosa	stomach
35	chr1:62765000-62766400	Enhancers	HSMM	muscle
36	chr1:62765000-62767000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:62765000-62767600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:62765000-62768000	Enhancers	Fetal Stomach	stomach
39	chr1:62765200-62765600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr1:62765200-62765600	Weak transcription	Brain Substantia Nigra	brain
41	chr1:62765200-62765800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr1:62765200-62765800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
43	chr1:62765200-62765800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr1:62765200-62766000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr1:62765200-62766000	Enhancers	Adipose Nuclei	Adipose
46	chr1:62765200-62766200	Enhancers	Fetal Heart	heart
47	chr1:62765200-62766400	Enhancers	Brain Anterior Caudate	brain
48	chr1:62765200-62766400	Enhancers	HSMMtube	muscle
49	chr1:62765200-62766600	Enhancers	Brain Hippocampus Middle	brain
50	chr1:62765200-62767600	Genic enhancers	HepG2	liver

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