Variant report

Variant	nsv1018555
Chromosome Location	chr5:97719032-97873906
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	chr5:97840348-97840659	HepG2	liver:	n/a	n/a
2	BACH1	chr5:97793840-97793961	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr5:97746502-97746660	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:97746518-97746652	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:97746451-97746723	GM12878	blood:	n/a	n/a
6	BHLHE40	chr5:97746497-97746672	HepG2	liver:	n/a	n/a
7	CEBPB	chr5:97769459-97769707	IMR90	lung:	n/a	n/a
8	CEBPB	chr5:97810520-97810893	MCF-7	breast:	n/a	chr5:97810648-97810659
9	CEBPB	chr5:97810486-97810835	K562	blood:	n/a	chr5:97810648-97810659
10	CEBPB	chr5:97797272-97797669	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:97810464-97810843	IMR90	lung:	n/a	chr5:97810648-97810659
12	CEBPB	chr5:97797235-97797557	IMR90	lung:	n/a	n/a
13	CEBPB	chr5:97810441-97810814	HepG2	liver:	n/a	chr5:97810648-97810659
14	CEBPB	chr5:97790192-97790497	Hela-S3	cervix:	n/a	chr5:97790323-97790334
15	CEBPB	chr5:97807160-97807430	HepG2	liver:	n/a	chr5:97807290-97807301
16	CEBPB	chr5:97790219-97790451	A549	lung:	n/a	chr5:97790323-97790334
17	CEBPB	chr5:97807135-97807430	IMR90	lung:	n/a	chr5:97807290-97807301
18	CEBPB	chr5:97795449-97795657	HepG2	liver:	n/a	n/a
19	CEBPB	chr5:97810486-97810851	ECC-1	luminal epithelium:	n/a	chr5:97810648-97810659
20	CEBPB	chr5:97750006-97750503	HepG2	liver:	n/a	chr5:97750380-97750391
21	CEBPB	chr5:97810499-97810836	H1-hESC	embryonic stem cell:	n/a	chr5:97810648-97810659
22	CEBPB	chr5:97810475-97810832	A549	lung:	n/a	chr5:97810648-97810659
23	CEBPB	chr5:97749852-97751208	IMR90	lung:	n/a	chr5:97750380-97750391
24	CEBPB	chr5:97795418-97795680	IMR90	lung:	n/a	n/a
25	CEBPB	chr5:97752620-97752745	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:97790707-97790974	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:97793793-97794619	IMR90	lung:	n/a	n/a
28	CEBPB	chr5:97810486-97810843	Hela-S3	cervix:	n/a	chr5:97810648-97810659
29	CEBPB	chr5:97810464-97810846	HepG2	liver:	n/a	chr5:97810648-97810659
30	CEBPB	chr5:97801334-97801412	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:97768051-97768595	H1-hESC	embryonic stem cell:	n/a	chr5:97768584-97768595
32	CEBPB	chr5:97810456-97810914	A549	lung:	n/a	chr5:97810648-97810659
33	CEBPB	chr5:97797189-97797660	A549	lung:	n/a	n/a
34	CEBPB	chr5:97790230-97790466	HepG2	liver:	n/a	chr5:97790323-97790334
35	CEBPB	chr5:97790141-97791027	IMR90	lung:	n/a	chr5:97790323-97790334
36	CEBPB	chr5:97810587-97810749	HepG2	liver:	n/a	chr5:97810648-97810659
37	CHD2	chr5:97725871-97725896	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr5:97777920-97778070	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr5:97824448-97824550	Fibrobl	skin:	n/a	n/a
40	CTCF	chr5:97790660-97790810	HA-sp	spinal cord:	n/a	chr5:97790741-97790759
41	CTCF	chr5:97790680-97790830	RPTEC	kidney:	n/a	chr5:97790741-97790759
42	CTCF	chr5:97793740-97793890	HMF	breast:	n/a	n/a
43	CTCF	chr5:97742660-97742810	GM12873	blood:	n/a	chr5:97742741-97742750
44	CTCF	chr5:97790600-97790750	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr5:97742644-97742747	Fibrobl	skin:	n/a	n/a
46	CTCF	chr5:97742663-97742753	MCF-7	breast:	n/a	chr5:97742741-97742750
47	CTCF	chr5:97831931-97832025	LNCaP	prostate:	n/a	n/a
48	CTCF	chr5:97742620-97742770	HRPEpiC	eye:	n/a	chr5:97742741-97742750
49	CTCF	chr5:97742620-97742770	GM12864	blood:	n/a	chr5:97742741-97742750
50	CTCF	chr5:97793680-97793830	AG04450	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97745972-97746022	GM19239	blood:	n/a
2	chr5:97761216-97761266	HCPEpiC	choroid plexus:	n/a
3	chr5:97745972-97746022	GM19239	blood:	n/a
4	chr5:97761216-97761266	HCPEpiC	choroid plexus:	n/a
5	chr5:97833812-97833862	AG04449	skin:	fetal
6	chr5:97745972-97746022	NHDF-neo	bronchial:	n/a
7	chr5:97839561-97839611	HepG2	liver:	n/a
8	chr5:97728181-97728231	AG09309	skin:	n/a
9	chr5:97873389-97873439	RPTEC	kidney:	n/a
10	chr5:97873389-97873439	U87	brain:	n/a
11	chr5:97873389-97873439	AG10803	skin:	n/a
12	chr5:97833812-97833862	HIPEpiC	eye:	n/a
13	chr5:97833812-97833862	ovcar-3	ovarian:	n/a
14	chr5:97833812-97833862	A549	lung:	n/a
15	chr5:97839561-97839611	HNPCEpiC	eye:	n/a
16	chr5:97728038-97728088	HCM	heart:	n/a
17	chr5:97745972-97746022	HEK293	kidney:	embryo
18	chr5:97727913-97727963	PANC-1	pancreas:	n/a
19	chr5:97839561-97839611	AG04450	lung:	fetal
20	chr5:97728038-97728088	HEEpiC	esophagus:	n/a
21	chr5:97746735-97746785	K562	blood:	n/a
22	chr5:97725789-97725839	HRCEpiC	kidney:	n/a
23	chr5:97727913-97727963	HCT-116	colon:	n/a
24	chr5:97728181-97728231	HCPEpiC	choroid plexus:	n/a
25	chr5:97833812-97833862	MCF-7	breast:	n/a
26	chr5:97761216-97761266	A549	lung:	n/a
27	chr5:97725789-97725839	Caco-2	colon:	n/a
28	chr5:97873389-97873439	PrEC	prostate:	n/a
29	chr5:97761216-97761266	SK-N-SH_RA	brain:	n/a
30	chr5:97746735-97746785	A549	lung:	n/a
31	chr5:97728038-97728088	MCF-7	breast:	n/a
32	chr5:97873389-97873439	AG09319	gingival:	n/a
33	chr5:97839561-97839611	U87	brain:	n/a
34	chr5:97833812-97833862	PrEC	prostate:	n/a
35	chr5:97839561-97839611	HCT-116	colon:	n/a
36	chr5:97746735-97746785	Caco-2	colon:	n/a
37	chr5:97839561-97839611	NB4	blood:	n/a
38	chr5:97833812-97833862	H1-hESC	embryonic stem cell:	embryo
39	chr5:97833812-97833862	RPTEC	kidney:	n/a
40	chr5:97833812-97833862	HCPEpiC	choroid plexus:	n/a
41	chr5:97873389-97873439	GM12892	blood:	n/a
42	chr5:97727913-97727963	HMEC	breast:	n/a
43	chr5:97761216-97761266	HEEpiC	esophagus:	n/a
44	chr5:97725789-97725839	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:97725789-97725839	IMR90	lung:	fetal
46	chr5:97727913-97727963	HRCEpiC	kidney:	n/a
47	chr5:97839561-97839611	HRCEpiC	kidney:	n/a
48	chr5:97873389-97873439	NHBE	bronchial:	n/a
49	chr5:97746735-97746785	HepG2	liver:	n/a
50	chr5:97839561-97839611	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:97849489..97851225-chr5:97851628..97853211,2	MCF-7	breast:
2	chr5:97849489..97851225-chr5:97851628..97853211,2	MCF-7	breast:
3	chr5:97701474..97704049-chr5:97723105..97724886,2	K562	blood:

Variant related genes	Relation type
ENSG00000249448	TF binding region
KRT8P32	TF binding region
MRPS35P2	TF binding region
ENSG00000249990	TF binding region
ENSG00000249448	CpG island
KRT8P32	CpG island
MRPS35P2	CpG island
ENSG00000249990	CpG island

Extended variants
information (count: 5701 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:5701 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558559517	chr5:97719051-97719052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547371300	chr5:97719098-97719099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369446735	chr5:97719100-97719101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544006096	chr5:97719149-97719150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372644775	chr5:97719171-97719172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144555403	chr5:97719172-97719173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184943007	chr5:97719174-97719175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188521188	chr5:97719177-97719178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375810944	chr5:97719264-97719265	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs369981102	chr5:97719265-97719266	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs560424859	chr5:97719276-97719277	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs527934515	chr5:97719335-97719336	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs146150393	chr5:97719341-97719342	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs192169687	chr5:97719344-97719345	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs76219849	chr5:97719370-97719371	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs531716773	chr5:97719424-97719425	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs373511144	chr5:97719440-97719441	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs369543453	chr5:97719450-97719451	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs536492798	chr5:97719468-97719469	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs184426399	chr5:97719494-97719495	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs113724866	chr5:97719495-97719496	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs544053606	chr5:97719507-97719508	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs558873359	chr5:97719509-97719510	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs567551249	chr5:97719515-97719516	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs56032123	chr5:97719518-97719519	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs556279280	chr5:97719556-97719557	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs199930992	chr5:97719586-97719587	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs140161076	chr5:97719635-97719636	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs542022874	chr5:97719685-97719686	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs560285643	chr5:97719750-97719751	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs371177423	chr5:97719753-97719754	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs550064244	chr5:97719762-97719763	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs572420827	chr5:97719765-97719766	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs546122928	chr5:97719820-97719821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578047705	chr5:97719839-97719840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564781869	chr5:97719844-97719845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531658106	chr5:97719861-97719862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374490550	chr5:97719862-97719863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531600730	chr5:97719873-97719874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375251033	chr5:97719878-97719879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528398434	chr5:97719881-97719882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144315413	chr5:97719882-97719883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs3034697	chr5:97719891-97719892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377337016	chr5:97719902-97719903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189538263	chr5:97719929-97719930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549718812	chr5:97719957-97719958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370332555	chr5:97719967-97719968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370275765	chr5:97719986-97719987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554151768	chr5:97720047-97720048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376367348	chr5:97720103-97720104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97707200-97719200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:97713800-97722200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr5:97714200-97725800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr5:97719200-97719800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:97721400-97733600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:97721800-97727800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:97722200-97723000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr5:97722400-97722800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:97722400-97722800	Enhancers	Fetal Muscle Trunk	muscle
10	chr5:97722400-97723200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr5:97723200-97725600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr5:97723600-97724200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:97724400-97727400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:97724600-97725000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr5:97725200-97727800	Enhancers	Stomach Mucosa	stomach
16	chr5:97725400-97725600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr5:97725400-97725800	Enhancers	Small Intestine	intestine
18	chr5:97725400-97726600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr5:97725400-97726800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:97725600-97725800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr5:97725600-97726600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:97725600-97726800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr5:97725800-97726200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr5:97725800-97726800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr5:97725800-97727000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:97726000-97726600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr5:97726000-97727200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr5:97726200-97726800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr5:97726600-97727200	Enhancers	NHDF-Ad	bronchial
30	chr5:97727400-97728200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:97727600-97727800	Enhancers	Gastric	stomach
32	chr5:97727600-97728200	Enhancers	Pancreas	Pancrea
33	chr5:97727800-97728200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:97727800-97728800	Weak transcription	Gastric	stomach
35	chr5:97728200-97730200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr5:97728200-97734400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:97730200-97731000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:97731000-97731400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:97731400-97732600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:97732600-97733200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:97732600-97733800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:97732600-97734600	Enhancers	NHDF-Ad	bronchial
43	chr5:97732600-97735000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr5:97732800-97733200	Enhancers	HMEC	breast
45	chr5:97732800-97733400	Enhancers	Osteobl	bone
46	chr5:97733000-97734600	Enhancers	Brain Cingulate Gyrus	brain
47	chr5:97733200-97735200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:97733400-97737200	Weak transcription	Osteobl	bone
49	chr5:97733600-97734000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr5:97733800-97734000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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