Variant report

Variant	nsv595140
Chromosome Location	chr4:110354691-110355483
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	ARID3A	chr4:110354211-110354931	HepG2	liver:	n/a	n/a
2	ATF2	chr4:110354473-110355010	GM12878	blood:	n/a	n/a
3	ATF3	chr4:110354590-110355029	K562	blood:	n/a	n/a
4	ATF3	chr4:110354491-110354811	A549	lung:	n/a	n/a
5	BACH1	chr4:110354432-110355016	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:110354710-110354946	K562	blood:	n/a	n/a
7	BCLAF1	chr4:110354396-110355310	GM12878	blood:	n/a	chr4:110354645-110354658 chr4:110354725-110354738 chr4:110354752-110354765
8	BCLAF1	chr4:110354481-110355062	GM12878	blood:	n/a	chr4:110354645-110354658 chr4:110354725-110354738 chr4:110354752-110354765
9	BHLHE40	chr4:110354627-110354827	A549	lung:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
10	BHLHE40	chr4:110354469-110355120	HepG2	liver:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
11	BHLHE40	chr4:110355440-110355810	HepG2	liver:	n/a	n/a
12	BHLHE40	chr4:110354288-110355032	K562	blood:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
13	BHLHE40	chr4:110354543-110355029	GM12878	blood:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
14	BRCA1	chr4:110354583-110354804	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr4:110354768-110354947	GM12878	blood:	n/a	n/a
16	BRCA1	chr4:110354689-110354889	HepG2	liver:	n/a	n/a
17	CBX3	chr4:110354275-110355033	K562	blood:	n/a	n/a
18	CCNT2	chr4:110354501-110355331	K562	blood:	n/a	n/a
19	CEBPB	chr4:110354588-110355000	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:110354600-110354908	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPD	chr4:110354505-110355207	HepG2	liver:	n/a	n/a
22	CHD1	chr4:110354216-110354720	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr4:110355474-110355809	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr4:110354529-110354915	GM12878	blood:	n/a	n/a
25	CHD2	chr4:110354486-110354971	K562	blood:	n/a	n/a
26	CHD2	chr4:110355466-110355836	GM12878	blood:	n/a	n/a
27	CHD2	chr4:110354553-110355068	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr4:110354323-110355067	HepG2	liver:	n/a	n/a
29	CHD2	chr4:110354399-110355043	GM12878	blood:	n/a	n/a
30	CHD2	chr4:110354495-110354992	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr4:110354488-110355154	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr4:110354409-110355456	HepG2	liver:	n/a	n/a
33	CREB1	chr4:110354509-110355241	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr4:110354551-110355299	A549	lung:	n/a	n/a
35	CREB1	chr4:110354428-110355277	GM12878	blood:	n/a	n/a
36	CREB1	chr4:110354403-110355296	K562	blood:	n/a	n/a
37	CREB1	chr4:110354429-110355267	HepG2	liver:	n/a	n/a
38	CREB1	chr4:110354544-110355262	K562	blood:	n/a	n/a
39	CTBP2	chr4:110354442-110355227	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr4:110354620-110354770	GM12872	blood:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
41	CTCF	chr4:110354532-110354917	Fibrobl	skin:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
42	CTCF	chr4:110355400-110355550	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr4:110354600-110354750	Caco-2	colon:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
44	CTCF	chr4:110354660-110354810	HCFaa	heart:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
45	CTCF	chr4:110354640-110354790	GM12866	blood:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
46	CTCF	chr4:110354590-110354865	LNCaP	prostate:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
47	CTCF	chr4:110354140-110355238	SK-N-SH	brain:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
48	CTCF	chr4:110354660-110354810	GM12870	blood:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
49	CTCF	chr4:110354391-110354935	H1-hESC	embryonic stem cell:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
50	CTCF	chr4:110354640-110354790	SAEC	small airway:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:110354896-110354946	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:110355447-110355497	HRCEpiC	kidney:	n/a
3	chr4:110355447-110355497	HRPEpiC	eye:	n/a
4	chr4:110354896-110354946	GM12878	blood:	n/a
5	chr4:110355447-110355497	A549	lung:	n/a
6	chr4:110355447-110355497	NB4	blood:	n/a
7	chr4:110355447-110355497	HEK293	kidney:	embryo
8	chr4:110355447-110355497	BE2_C	brain:	n/a
9	chr4:110355447-110355497	NHBE	bronchial:	n/a
10	chr4:110354820-110354870	AoSMC	blood vessel:	n/a
11	chr4:110355447-110355497	GM12891	blood:	n/a
12	chr4:110354896-110354946	HL-60	blood:	n/a
13	chr4:110354820-110354870	PFSK-1	brain:	n/a
14	chr4:110354820-110354870	HUVEC	blood vessel:	n/a
15	chr4:110355472-110355522	GM19239	blood:	n/a
16	chr4:110354896-110354946	ovcar-3	ovarian:	n/a
17	chr4:110354923-110354973	Hepatocyte	liver:	n/a
18	chr4:110355447-110355497	CMK	blood:	n/a
19	chr4:110354923-110354973	HCT-116	colon:	n/a
20	chr4:110354923-110354973	SK-N-SH	brain:	n/a
21	chr4:110355472-110355522	Hela-S3	cervix:	n/a
22	chr4:110355472-110355522	ProgFib	skin:	n/a
23	chr4:110354820-110354870	AG10803	skin:	n/a
24	chr4:110355472-110355522	HRE	kidney:	n/a
25	chr4:110354820-110354870	HL-60	blood:	n/a
26	chr4:110355472-110355522	IMR90	lung:	fetal
27	chr4:110354923-110354973	GM12878	blood:	n/a
28	chr4:110354820-110354870	SK-N-SH_RA	brain:	n/a
29	chr4:110354923-110354973	HCF	heart:	n/a
30	chr4:110355447-110355497	HCT-116	colon:	n/a
31	chr4:110355472-110355522	AG09319	gingival:	n/a
32	chr4:110354923-110354973	HAEpiC	amniotic membrane:	n/a
33	chr4:110354896-110354946	AG09319	gingival:	n/a
34	chr4:110354820-110354870	IMR90	lung:	fetal
35	chr4:110355472-110355522	HEK293	kidney:	embryo
36	chr4:110355447-110355497	HEEpiC	esophagus:	n/a
37	chr4:110354923-110354973	U87	brain:	n/a
38	chr4:110354923-110354973	PANC-1	pancreas:	n/a
39	chr4:110355447-110355497	AG04450	lung:	fetal
40	chr4:110354820-110354870	SAEC	small airway:	n/a
41	chr4:110354896-110354946	AG09309	skin:	n/a
42	chr4:110354896-110354946	SK-N-MC	brain:	n/a
43	chr4:110355472-110355522	AG04449	skin:	fetal
44	chr4:110355472-110355522	PANC-1	pancreas:	n/a
45	chr4:110354896-110354946	AG04450	lung:	fetal
46	chr4:110355447-110355497	HMEC	breast:	n/a
47	chr4:110354896-110354946	Caco-2	colon:	n/a
48	chr4:110355447-110355497	ProgFib	skin:	n/a
49	chr4:110354923-110354973	NH-A	brain:	n/a
50	chr4:110354896-110354946	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:110354421..110354923-chr7:44084218..44084744,2	Hela-S3	cervix:
2	chr4:110353826..110356085-chr4:110735938..110738635,3	MCF-7	breast:
3	chr4:110353269..110354820-chr4:110577196..110580148,2	MCF-7	breast:
4	chr4:110351870..110353542-chr4:110355047..110357946,2	MCF-7	breast:
5	chr4:110352891..110355275-chr4:110649929..110651520,2	MCF-7	breast:
6	chr4:110354680..110356371-chr4:110650734..110652526,2	MCF-7	breast:
7	chr4:109540362..109542277-chr4:110353620..110356489,2	K562	blood:
8	chr4:110353323..110356452-chr4:110478874..110481567,4	MCF-7	breast:
9	chr14:105261712..105263242-chr4:110355266..110356786,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL25A1-1	chr4:110354890-110354920	ENSG00000247950
2	lnc-COL25A1-1	chr4:110354890-110354939	ENSG00000247950
3	lnc-COL25A1-1	chr4:110354890-110354973	ENSG00000247950

Variant related genes	Relation type
SEC24B-AS1	TF binding region
SEC24B	TF binding region
SEC24B-AS1	CpG island
SEC24B	CpG island
ENSG00000109475	chromatin interactions
ENSG00000234492	chromatin interactions
ENSG00000123739	chromatin interactions
ENSG00000005059	chromatin interactions
ENSG00000109534	chromatin interactions
ENSG00000136279	chromatin interactions
ENSG00000142208	chromatin interactions
ENSG00000272795	chromatin interactions
G3BP1	miRNA target sites
ATP6V1C1	miRNA target sites
CCNG1	miRNA target sites

Extended variants
information (count: 19 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567551528	chr4:110354721-110354722	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs536423717	chr4:110354739-110354740	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs180697394	chr4:110354790-110354791	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs567063509	chr4:110354793-110354794	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs185054241	chr4:110354819-110354820	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs371131199	chr4:110354821-110354822	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs534049793	chr4:110354873-110354874	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs71603023	chr4:110354889-110354890	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs575677521	chr4:110354899-110354900	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
10	rs538377411	chr4:110354966-110354967	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
11	rs72896632	chr4:110354973-110354974	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs570129880	chr4:110355097-110355098	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs574733736	chr4:110355129-110355130	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs540044361	chr4:110355136-110355137	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs553890452	chr4:110355176-110355177	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs577065985	chr4:110355305-110355306	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs13103419	chr4:110355351-110355352	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs546049130	chr4:110355410-110355411	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs115096670	chr4:110355463-110355464	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Schizophrenia	19546859	CNVD
Colorectal cancer	16272173	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:138 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110353400-110356600	Active TSS	K562	blood
2	chr4:110353600-110354800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:110353600-110357000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:110353800-110356000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:110353800-110356000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:110353800-110356000	Active TSS	Fetal Intestine Large	intestine
7	chr4:110353800-110356400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:110353800-110356400	Active TSS	HSMM	muscle
9	chr4:110353800-110356600	Active TSS	H1 Cell Line	embryonic stem cell
10	chr4:110353800-110356800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr4:110353800-110357000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr4:110354000-110355600	Active TSS	Primary T cells fromperipheralblood	blood
13	chr4:110354000-110355600	Active TSS	Fetal Muscle Trunk	muscle
14	chr4:110354000-110355600	Active TSS	Rectal Mucosa Donor 29	rectum
15	chr4:110354000-110355800	Active TSS	Thymus	Thymus
16	chr4:110354000-110356000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr4:110354000-110356000	Active TSS	Esophagus	oesophagus
18	chr4:110354000-110356000	Active TSS	Fetal Brain Female	brain
19	chr4:110354000-110356000	Active TSS	Fetal Stomach	stomach
20	chr4:110354000-110356200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr4:110354000-110356200	Active TSS	H9 Cell Line	embryonic stem cell
22	chr4:110354000-110356200	Bivalent/Poised TSS	HepG2	liver
23	chr4:110354000-110356400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
24	chr4:110354000-110356400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr4:110354000-110356400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr4:110354000-110356400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr4:110354000-110356400	Active TSS	Brain Germinal Matrix	brain
28	chr4:110354000-110356400	Active TSS	Right Ventricle	heart
29	chr4:110354000-110356600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:110354000-110356800	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr4:110354000-110356800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:110354000-110356800	Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr4:110354000-110356800	Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr4:110354000-110356800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:110354000-110356800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:110354000-110356800	Active TSS	Colonic Mucosa	Colon
37	chr4:110354000-110356800	Active TSS	Right Atrium	heart
38	chr4:110354000-110356800	Active TSS	A549	lung
39	chr4:110354000-110356800	Active TSS	NHDF-Ad	bronchial
40	chr4:110354000-110357000	Active TSS	HMEC	breast
41	chr4:110354200-110355000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
42	chr4:110354200-110355800	Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr4:110354200-110355800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr4:110354200-110355800	Active TSS	Fetal Muscle Leg	muscle
45	chr4:110354200-110355800	Active TSS	Placenta	Placenta
46	chr4:110354200-110356000	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr4:110354200-110356000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:110354200-110356000	Active TSS	Brain Anterior Caudate	brain
49	chr4:110354200-110356000	Active TSS	Fetal Intestine Small	intestine
50	chr4:110354200-110356000	Active TSS	Fetal Lung	lung

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