Variant report

Variant	nsv882407
Chromosome Location	chr5:97553255-97783046
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1155)
CpG islands
(count:732)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1155 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:97746502-97746660	GM12878	blood:	n/a	n/a
2	BATF	chr5:97645337-97645915	GM12878	blood:	n/a	n/a
3	BATF	chr5:97645337-97645719	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	BHLHE40	chr5:97628311-97628485	GM12878	blood:	n/a	n/a
8	BRCA1	chr5:97645795-97645833	GM12878	blood:	n/a	n/a
9	BRCA1	chr5:97685433-97685750	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr5:97685443-97685884	HCT-116	colon:	n/a	n/a
11	CBX3	chr5:97685436-97685704	K562	blood:	n/a	n/a
12	CBX3	chr5:97685379-97685899	HCT-116	colon:	n/a	n/a
13	CBX3	chr5:97645411-97646065	HCT-116	colon:	n/a	n/a
14	CBX3	chr5:97685463-97685711	K562	blood:	n/a	n/a
15	CEBPB	chr5:97635212-97636077	IMR90	lung:	n/a	chr5:97635412-97635425
16	CEBPB	chr5:97697523-97697868	HepG2	liver:	n/a	chr5:97697695-97697706 chr5:97697727-97697739
17	CEBPB	chr5:97584522-97585081	IMR90	lung:	n/a	n/a
18	CEBPB	chr5:97676744-97677715	IMR90	lung:	n/a	chr5:97677511-97677524
19	CEBPB	chr5:97597425-97597751	HepG2	liver:	n/a	chr5:97597602-97597615 chr5:97597603-97597614
20	CEBPB	chr5:97608471-97608702	A549	lung:	n/a	n/a
21	CEBPB	chr5:97643902-97644227	MCF-7	breast:	n/a	n/a
22	CEBPB	chr5:97644007-97644208	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr5:97643447-97644305	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:97649774-97650367	IMR90	lung:	n/a	chr5:97649783-97649794
25	CEBPB	chr5:97584633-97584906	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:97749852-97751208	IMR90	lung:	n/a	chr5:97750380-97750391
27	CEBPB	chr5:97697598-97697834	A549	lung:	n/a	chr5:97697695-97697706 chr5:97697727-97697739
28	CEBPB	chr5:97643931-97644180	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr5:97768051-97768595	H1-hESC	embryonic stem cell:	n/a	chr5:97768584-97768595
30	CEBPB	chr5:97597480-97597748	IMR90	lung:	n/a	chr5:97597602-97597615 chr5:97597603-97597614
31	CEBPB	chr5:97697542-97697873	IMR90	lung:	n/a	chr5:97697695-97697706 chr5:97697727-97697739
32	CEBPB	chr5:97645344-97646348	IMR90	lung:	n/a	n/a
33	CEBPB	chr5:97608531-97608770	IMR90	lung:	n/a	n/a
34	CEBPB	chr5:97643930-97644266	A549	lung:	n/a	n/a
35	CEBPB	chr5:97769459-97769707	IMR90	lung:	n/a	n/a
36	CEBPB	chr5:97752620-97752745	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:97643923-97644280	HepG2	liver:	n/a	n/a
38	CEBPB	chr5:97712721-97712774	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr5:97750006-97750503	HepG2	liver:	n/a	chr5:97750380-97750391
40	CEBPB	chr5:97643935-97644279	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:97697601-97697741	H1-hESC	embryonic stem cell:	n/a	chr5:97697695-97697706 chr5:97697727-97697739
42	CHD1	chr5:97684821-97686326	IMR90	lung:	n/a	n/a
43	CHD2	chr5:97725871-97725896	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr5:97685427-97685753	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr5:97645660-97645872	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr5:97742640-97742790	GM12872	blood:	n/a	chr5:97742741-97742750
47	CTCF	chr5:97685460-97685610	SAEC	small airway:	n/a	n/a
48	CTCF	chr5:97742720-97742870	GM12864	blood:	n/a	chr5:97742741-97742750
49	CTCF	chr5:97742620-97742770	GM12875	blood:	n/a	chr5:97742741-97742750
50	CTCF	chr5:97685520-97685670	GM12868	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97676915-97676965	HRPEpiC	eye:	n/a
2	chr5:97728181-97728231	HEEpiC	esophagus:	n/a
3	chr5:97725789-97725839	AG04450	lung:	fetal
4	chr5:97728038-97728088	SK-N-MC	brain:	n/a
5	chr5:97728181-97728231	Caco-2	colon:	n/a
6	chr5:97655532-97655582	Hepatocyte	liver:	n/a
7	chr5:97728181-97728231	PANC-1	pancreas:	n/a
8	chr5:97728181-97728231	ECC-1	luminal epithelium:	n/a
9	chr5:97703334-97703384	GM12878	blood:	n/a
10	chr5:97655532-97655582	HNPCEpiC	eye:	n/a
11	chr5:97703334-97703384	BJ	skin:	n/a
12	chr5:97746735-97746785	HCF	heart:	n/a
13	chr5:97761216-97761266	A549	lung:	n/a
14	chr5:97727913-97727963	GM12878	blood:	n/a
15	chr5:97728181-97728231	AG04450	lung:	fetal
16	chr5:97676915-97676965	PrEC	prostate:	n/a
17	chr5:97678851-97678901	RPTEC	kidney:	n/a
18	chr5:97655532-97655582	CMK	blood:	n/a
19	chr5:97676915-97676965	HIPEpiC	eye:	n/a
20	chr5:97727913-97727963	Hela-S3	cervix:	n/a
21	chr5:97645526-97645576	K562	blood:	n/a
22	chr5:97678851-97678901	U87	brain:	n/a
23	chr5:97703334-97703384	HL-60	blood:	n/a
24	chr5:97703334-97703384	IMR90	lung:	fetal
25	chr5:97676915-97676965	GM06990	blood:	n/a
26	chr5:97703334-97703384	SK-N-SH_RA	brain:	n/a
27	chr5:97655532-97655582	Jurkat	blood:	n/a
28	chr5:97727913-97727963	HRCEpiC	kidney:	n/a
29	chr5:97728181-97728231	Hepatocyte	liver:	n/a
30	chr5:97746735-97746785	ECC-1	luminal epithelium:	n/a
31	chr5:97655532-97655582	AG10803	skin:	n/a
32	chr5:97703334-97703384	AG04450	lung:	fetal
33	chr5:97678851-97678901	GM06990	blood:	n/a
34	chr5:97728181-97728231	HCM	heart:	n/a
35	chr5:97745972-97746022	ovcar-3	ovarian:	n/a
36	chr5:97745972-97746022	NH-A	brain:	n/a
37	chr5:97761216-97761266	Jurkat	blood:	n/a
38	chr5:97745972-97746022	SK-N-SH_RA	brain:	n/a
39	chr5:97728038-97728088	AG09319	gingival:	n/a
40	chr5:97725789-97725839	HCPEpiC	choroid plexus:	n/a
41	chr5:97727913-97727963	PrEC	prostate:	n/a
42	chr5:97727913-97727963	AG10803	skin:	n/a
43	chr5:97703334-97703384	LNCaP	prostate:	n/a
44	chr5:97678851-97678901	NHDF-neo	bronchial:	n/a
45	chr5:97745972-97746022	SAEC	small airway:	n/a
46	chr5:97761216-97761266	HCF	heart:	n/a
47	chr5:97645526-97645576	HCM	heart:	n/a
48	chr5:97678851-97678901	AG04449	skin:	fetal
49	chr5:97645526-97645576	SK-N-MC	brain:	n/a
50	chr5:97728181-97728231	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr5:97701474..97704049-chr5:97723105..97724886,2	K562	blood:
2	chr5:97593547..97596828-chr5:97596937..97599291,3	K562	blood:
3	chr5:97615949..97618290-chr5:97620124..97621957,2	MCF-7	breast:
4	chr5:97701258..97703130-chr5:97705966..97708009,2	K562	blood:
5	chr5:97615949..97618290-chr5:97620124..97621957,2	MCF-7	breast:
6	chr5:97689861..97692016-chr5:97695118..97697823,2	K562	blood:
7	chr5:97689861..97692016-chr5:97695118..97697823,2	K562	blood:
8	chr5:97655512..97657959-chr5:97658277..97660581,2	K562	blood:
9	chr5:97655512..97657959-chr5:97658277..97660581,2	K562	blood:
10	chr5:97593547..97596828-chr5:97596937..97599291,3	K562	blood:
11	chr5:97701258..97703130-chr5:97705966..97708009,2	K562	blood:
12	chr5:97701474..97704049-chr5:97723105..97724886,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHD1-7	chr5:97645844-97646056	NONHSAT102942

No data

Variant related genes	Relation type
ENSG00000176183	TF binding region
ENSG00000249448	TF binding region
KRT8P32	TF binding region
MRPS35P2	TF binding region
ENSG00000249990	TF binding region
ENSG00000176183	CpG island
ENSG00000249448	CpG island
KRT8P32	CpG island
MRPS35P2	CpG island
ENSG00000249990	CpG island

Extended variants
information (count: 8435 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:8435 , 50 per page) page: 1 2 3 4 5 6 7 ... 169

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4398658	chr5:97553255-97553256	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377539991	chr5:97553298-97553299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183720691	chr5:97553332-97553333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4535481	chr5:97553344-97553345	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs549716891	chr5:97553357-97553358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141753452	chr5:97553359-97553360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188194019	chr5:97553395-97553396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554404745	chr5:97553411-97553412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7735474	chr5:97553508-97553509	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs193277918	chr5:97553510-97553511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565712374	chr5:97553515-97553516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75948770	chr5:97553540-97553541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74409820	chr5:97553638-97553639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76417933	chr5:97553679-97553680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78642516	chr5:97553692-97553693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551285166	chr5:97553718-97553719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368287700	chr5:97553719-97553720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185429707	chr5:97553732-97553733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78813219	chr5:97553760-97553761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552943107	chr5:97553792-97553793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139554743	chr5:97553823-97553824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545002643	chr5:97553854-97553855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556992862	chr5:97553907-97553908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554310838	chr5:97553944-97553945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189406519	chr5:97553976-97553977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543575519	chr5:97554014-97554015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7723133	chr5:97554032-97554033	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs529171011	chr5:97554039-97554040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191537862	chr5:97554063-97554064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559690496	chr5:97554089-97554090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10069519	chr5:97554193-97554194	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs375087624	chr5:97554256-97554257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551412372	chr5:97554323-97554324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149799353	chr5:97554365-97554366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73153346	chr5:97554390-97554391	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs549540267	chr5:97554408-97554409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188840530	chr5:97554421-97554422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567806212	chr5:97554465-97554466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550704432	chr5:97554493-97554494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534980350	chr5:97554495-97554496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371075252	chr5:97554542-97554543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181123979	chr5:97554563-97554564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376222993	chr5:97554606-97554607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552449066	chr5:97554607-97554608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553202824	chr5:97554618-97554619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111472334	chr5:97554652-97554653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7727963	chr5:97554712-97554713	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs186976012	chr5:97554719-97554720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111785613	chr5:97554766-97554767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575671220	chr5:97554777-97554778	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Breast cancer	21611746	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:871 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97551800-97553400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:97553400-97554400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:97554400-97555200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:97559800-97560000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:97562800-97563800	Enhancers	Dnd41	blood
6	chr5:97563000-97563400	ZNF genes & repeats	Pancreas	Pancrea
7	chr5:97563200-97563800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
8	chr5:97564000-97567200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:97567200-97572200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:97572200-97572800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:97572800-97576000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:97576000-97577200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:97577200-97581800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:97581800-97582200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr5:97582200-97602400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:97583800-97585600	Enhancers	Osteobl	bone
17	chr5:97584600-97585200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:97584600-97585200	Enhancers	NHEK	skin
19	chr5:97584600-97585400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:97584800-97585200	Enhancers	NH-A	brain
21	chr5:97587800-97588000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:97587800-97588600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr5:97588400-97588800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr5:97588600-97588800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr5:97596600-97597000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr5:97597400-97597800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr5:97597400-97600000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr5:97598000-97598200	Enhancers	Brain Germinal Matrix	brain
29	chr5:97598000-97599000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr5:97598200-97599000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr5:97598200-97599200	Weak transcription	Brain Germinal Matrix	brain
32	chr5:97598800-97599400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr5:97599200-97599800	Enhancers	Brain Germinal Matrix	brain
34	chr5:97599400-97600800	Enhancers	HUVEC	blood vessel
35	chr5:97602400-97602800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr5:97602800-97603000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:97603000-97603200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:97603200-97634200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:97603600-97604600	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr5:97608200-97609000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr5:97608400-97609000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr5:97608600-97609200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr5:97608800-97609400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr5:97612000-97613200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr5:97612200-97612600	Enhancers	Stomach Mucosa	stomach
46	chr5:97612200-97612800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr5:97612200-97612800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr5:97612200-97613000	Enhancers	NHDF-Ad	bronchial
49	chr5:97612400-97613000	Enhancers	Osteobl	bone
50	chr5:97613000-97622800	Weak transcription	NHDF-Ad	bronchial

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