Variant report

Variant	nsv904298
Chromosome Location	chr15:62218689-62338797
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:474)
CpG islands
(count:0)
Chromatin interactive
region (count:44)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:62281922-62282216	K562	blood:	n/a	n/a
2	BACH1	chr15:62234203-62234206	K562	blood:	n/a	n/a
3	BACH1	chr15:62281967-62282167	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr15:62281910-62282262	K562	blood:	n/a	n/a
5	BCL3	chr15:62255882-62256211	GM12878	blood:	n/a	n/a
6	BCLAF1	chr15:62319158-62319771	GM12878	blood:	n/a	chr15:62319715-62319724 chr15:62319302-62319311
7	BHLHE40	chr15:62338355-62338604	GM12878	blood:	n/a	n/a
8	CEBPB	chr15:62275362-62275602	HepG2	liver:	n/a	chr15:62275465-62275476
9	CEBPB	chr15:62301289-62301563	A549	lung:	n/a	chr15:62301426-62301437 chr15:62301424-62301437 chr15:62301424-62301435
10	CEBPB	chr15:62281886-62282169	K562	blood:	n/a	n/a
11	CEBPB	chr15:62265849-62266044	K562	blood:	n/a	chr15:62265887-62265898 chr15:62265886-62265897 chr15:62265888-62265897
12	CEBPB	chr15:62275367-62275598	MCF-7	breast:	n/a	chr15:62275465-62275476
13	CEBPB	chr15:62265786-62266041	A549	lung:	n/a	chr15:62265887-62265898 chr15:62265886-62265897 chr15:62265888-62265897
14	CEBPB	chr15:62232985-62233209	HepG2	liver:	n/a	n/a
15	CEBPB	chr15:62266744-62266785	HepG2	liver:	n/a	n/a
16	CEBPB	chr15:62275283-62275661	Hela-S3	cervix:	n/a	chr15:62275465-62275476
17	CEBPB	chr15:62301294-62301592	K562	blood:	n/a	chr15:62301426-62301437 chr15:62301424-62301437 chr15:62301424-62301435
18	CEBPB	chr15:62225483-62225689	K562	blood:	n/a	chr15:62225584-62225597 chr15:62225586-62225597 chr15:62225531-62225544 chr15:62225584-62225597 chr15:62225584-62225597 chr15:62225586-62225597
19	CEBPB	chr15:62227818-62228070	A549	lung:	n/a	chr15:62227893-62227904
20	CEBPB	chr15:62302620-62302823	Hela-S3	cervix:	n/a	chr15:62302710-62302721
21	CEBPB	chr15:62227701-62228189	K562	blood:	n/a	chr15:62227893-62227904
22	CEBPB	chr15:62239060-62239292	IMR90	lung:	n/a	n/a
23	CEBPB	chr15:62312273-62312326	K562	blood:	n/a	n/a
24	CEBPB	chr15:62227747-62228056	Hela-S3	cervix:	n/a	chr15:62227893-62227904
25	CEBPB	chr15:62302567-62302836	IMR90	lung:	n/a	chr15:62302710-62302721
26	CEBPB	chr15:62301279-62301591	HepG2	liver:	n/a	chr15:62301426-62301437 chr15:62301424-62301437 chr15:62301424-62301435
27	CEBPB	chr15:62265777-62266054	HepG2	liver:	n/a	chr15:62265887-62265898 chr15:62265886-62265897 chr15:62265888-62265897
28	CEBPB	chr15:62275251-62275629	MCF-7	breast:	n/a	chr15:62275465-62275476
29	CEBPB	chr15:62302565-62302878	HepG2	liver:	n/a	chr15:62302710-62302721
30	CHD1	chr15:62338325-62338537	GM12878	blood:	n/a	n/a
31	CHD2	chr15:62221823-62221825	GM12878	blood:	n/a	n/a
32	CHD2	chr15:62338367-62338529	GM12878	blood:	n/a	n/a
33	CTCF	chr15:62314300-62314442	MCF-7	breast:	n/a	n/a
34	CTCF	chr15:62314280-62314430	GM12872	blood:	n/a	n/a
35	CTCF	chr15:62314280-62314430	HMEC	breast:	n/a	n/a
36	CTCF	chr15:62314379-62314413	LNCaP	prostate:	n/a	n/a
37	CTCF	chr15:62314300-62314450	HPF	lung:	n/a	n/a
38	CTCF	chr15:62240716-62240764	GM20000	blood:	n/a	n/a
39	CTCF	chr15:62314360-62314510	HVMF	connective:	n/a	n/a
40	CTCF	chr15:62289900-62290050	HCM	heart:	n/a	n/a
41	CTCF	chr15:62314380-62314530	GM12878	blood:	n/a	n/a
42	CTCF	chr15:62314290-62314457	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr15:62314196-62314505	MCF-7	breast:	n/a	n/a
44	CTCF	chr15:62314220-62314370	NB4	blood:	n/a	n/a
45	CTCF	chr15:62314220-62314370	HVMF	connective:	n/a	n/a
46	CTCF	chr15:62314170-62314566	HepG2	liver:	n/a	n/a
47	CTCF	chr15:62321160-62321310	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr15:62314320-62314470	K562	blood:	n/a	n/a
49	CTCF	chr15:62314365-62314430	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr15:62314400-62314550	RPTEC	kidney:	n/a	n/a

No data

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:62316405..62318620-chr15:62326377..62328272,2	MCF-7	breast:
2	chr15:62304589..62306825-chr15:62320734..62322432,2	K562	blood:
3	chr15:62248426..62250802-chr15:62259693..62261364,2	K562	blood:
4	chr15:62304589..62306825-chr15:62320734..62322432,2	K562	blood:
5	chr15:62268988..62271189-chr15:62273485..62276457,2	MCF-7	breast:
6	chr15:62231542..62233712-chr15:62238622..62240411,2	K562	blood:
7	chr15:62242750..62243662-chr5:173738637..173739199,2	MCF-7	breast:
8	chr15:62334378..62336089-chr15:62337603..62339508,2	K562	blood:
9	chr15:62266682..62269656-chr15:62302600..62304271,2	K562	blood:
10	chr15:62299637..62301994-chr15:62304316..62306759,2	K562	blood:
11	chr15:62316405..62318620-chr15:62326377..62328272,2	MCF-7	breast:
12	chr15:62223179..62225292-chr15:62226281..62228642,2	K562	blood:
13	chr15:62266682..62269656-chr15:62302600..62304271,2	K562	blood:
14	chr15:62248426..62250802-chr15:62259693..62261364,2	K562	blood:
15	chr15:62236123..62237658-chr15:62241444..62244261,2	K562	blood:
16	chr15:62231542..62233712-chr15:62238622..62240411,2	K562	blood:
17	chr15:62311499..62313000-chr16:85836919..85839810,2	K562	blood:
18	chr15:62235589..62237658-chr15:62241156..62242944,2	K562	blood:
19	chr15:62275008..62277065-chr15:62352447..62354062,2	MCF-7	breast:
20	chr15:62280133..62283452-chr15:62316207..62318715,3	K562	blood:
21	chr15:62236123..62237658-chr15:62241444..62244261,2	K562	blood:
22	chr15:62334378..62336089-chr15:62337603..62339508,2	K562	blood:
23	chr15:62328623..62331543-chr15:62331564..62333336,2	MCF-7	breast:
24	chr15:62279274..62280986-chr15:62358759..62361498,2	MCF-7	breast:
25	chr15:62222450..62224583-chr15:62247796..62249719,2	MCF-7	breast:
26	chr15:62283744..62286045-chr15:62287984..62289712,2	K562	blood:
27	chr15:62280133..62283452-chr15:62316207..62318715,3	K562	blood:
28	chr15:62252284..62254348-chr15:62257141..62258725,2	K562	blood:
29	chr15:62320983..62322579-chr15:62345142..62347207,2	K562	blood:
30	chr15:62299637..62301994-chr15:62304316..62306759,2	K562	blood:
31	chr15:62268988..62271189-chr15:62273485..62276457,2	MCF-7	breast:
32	chr15:62241235..62242799-chr15:62250211..62252735,2	K562	blood:
33	chr15:62283890..62286224-chr15:62350363..62353063,2	K562	blood:
34	chr15:62222450..62224583-chr15:62247796..62249719,2	MCF-7	breast:
35	chr15:62241235..62242799-chr15:62250211..62252735,2	K562	blood:
36	chr15:62223179..62225292-chr15:62226281..62228642,2	K562	blood:
37	chr15:62249551..62252071-chr15:62252647..62254754,2	MCF-7	breast:
38	chr15:62259986..62262200-chr15:62266004..62268197,2	K562	blood:
39	chr11:22957855..22958444-chr15:62239142..62239729,2	MCF-7	breast:
40	chr15:62328623..62331543-chr15:62331564..62333336,2	MCF-7	breast:
41	chr15:62270934..62272587-chr15:62351243..62353224,2	MCF-7	breast:
42	chr15:62213296..62215607-chr15:62227904..62230544,2	K562	blood:
43	chr15:62259986..62262200-chr15:62266004..62268197,2	K562	blood:
44	chr15:62235589..62237658-chr15:62241156..62242944,2	K562	blood:

No data

Variant related genes	Relation type
VPS13C	TF binding region
ENSG00000259251	chromatin interactions
ENSG00000198535	chromatin interactions
ENSG00000131143	chromatin interactions
ENSG00000129003	chromatin interactions

Extended variants
information (count: 5055 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5055 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10459634	chr15:62218689-62218690	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564201001	chr15:62218696-62218697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377601910	chr15:62218700-62218701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183930077	chr15:62218706-62218707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189100713	chr15:62218819-62218820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538132503	chr15:62218866-62218867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9788739	chr15:62218872-62218873	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs373150186	chr15:62218902-62218903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148322729	chr15:62218909-62218910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536268756	chr15:62218921-62218922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554609201	chr15:62218933-62218934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115478969	chr15:62218984-62218985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28440175	chr15:62218992-62218993	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs371331874	chr15:62219004-62219005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559098427	chr15:62219058-62219059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192964161	chr15:62219065-62219066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184858220	chr15:62219091-62219092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111448115	chr15:62219121-62219122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189715257	chr15:62219152-62219153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74642348	chr15:62219196-62219197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs62009109	chr15:62219231-62219232	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs181580403	chr15:62219242-62219243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150162293	chr15:62219245-62219246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369800639	chr15:62219271-62219272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373951857	chr15:62219335-62219336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75341202	chr15:62219337-62219338	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200812869	chr15:62219347-62219348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138875838	chr15:62219349-62219350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143892807	chr15:62219356-62219357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568279338	chr15:62219377-62219378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187060746	chr15:62219390-62219391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200162212	chr15:62219394-62219395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200965872	chr15:62219402-62219403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369302453	chr15:62219427-62219428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150220235	chr15:62219432-62219433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138853397	chr15:62219449-62219450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs202146413	chr15:62219491-62219492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142801465	chr15:62219512-62219513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144073158	chr15:62219513-62219514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185692367	chr15:62219538-62219539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373361801	chr15:62219546-62219547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376542266	chr15:62219569-62219570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189521181	chr15:62219596-62219597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374490074	chr15:62219621-62219622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs58216278	chr15:62219645-62219646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549926495	chr15:62219655-62219656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557141550	chr15:62219666-62219667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538074579	chr15:62219678-62219679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181848153	chr15:62219695-62219696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575166226	chr15:62219772-62219773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Mental retardation	17124404	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:2481 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:62142400-62253000	Weak transcription	Spleen	Spleen
2	chr15:62143800-62235600	Weak transcription	Fetal Brain Male	brain
3	chr15:62146800-62230000	Weak transcription	Pancreas	Pancrea
4	chr15:62150000-62276200	Weak transcription	Psoas Muscle	Psoas
5	chr15:62184600-62236800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr15:62185000-62221000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr15:62185600-62262200	Weak transcription	Gastric	stomach
8	chr15:62185600-62333600	Weak transcription	Right Ventricle	heart
9	chr15:62185800-62300000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr15:62187200-62246000	Weak transcription	A549	lung
11	chr15:62188600-62309400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr15:62194600-62235400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr15:62194600-62266800	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr15:62194800-62225600	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr15:62195000-62219800	Strong transcription	Primary B cells from cord blood	blood
16	chr15:62195400-62234200	Strong transcription	Primary B cells from peripheral blood	blood
17	chr15:62195400-62235800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr15:62195600-62285400	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr15:62196400-62225200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr15:62197000-62225400	Weak transcription	Esophagus	oesophagus
21	chr15:62197000-62236200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr15:62198800-62223600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr15:62205000-62236600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr15:62205400-62219800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr15:62206600-62242600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:62207600-62220800	Weak transcription	Small Intestine	intestine
27	chr15:62207800-62226000	Weak transcription	Stomach Mucosa	stomach
28	chr15:62207800-62263200	Weak transcription	Fetal Brain Female	brain
29	chr15:62208200-62226000	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr15:62208200-62263200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr15:62208200-62290200	Weak transcription	Aorta	Aorta
32	chr15:62208400-62253200	Weak transcription	Thymus	Thymus
33	chr15:62208600-62220800	Weak transcription	HSMMtube	muscle
34	chr15:62208600-62222400	Weak transcription	Fetal Heart	heart
35	chr15:62208600-62236800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:62209800-62219000	Weak transcription	K562	blood
37	chr15:62209800-62219200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr15:62209800-62220800	Weak transcription	NHEK	skin
39	chr15:62209800-62223800	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr15:62209800-62236200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr15:62209800-62236600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr15:62209800-62236600	Weak transcription	Lung	lung
43	chr15:62209800-62236600	Weak transcription	Ovary	ovary
44	chr15:62209800-62250600	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr15:62209800-62252400	Weak transcription	Brain Cingulate Gyrus	brain
46	chr15:62210000-62225000	Weak transcription	Brain Germinal Matrix	brain
47	chr15:62210000-62237000	Weak transcription	Colonic Mucosa	Colon
48	chr15:62210000-62242800	Weak transcription	Brain Substantia Nigra	brain
49	chr15:62211400-62223400	Strong transcription	Fetal Intestine Large	intestine
50	chr15:62212000-62220800	Weak transcription	NHLF	lung

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