Variant report

Variant	nsv882413
Chromosome Location	chr5:97918829-98022320
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	BACH1	chr5:97971338-97971564	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr5:97992250-97992404	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr5:97992216-97992462	H1-hESC	embryonic stem cell:	n/a	chr5:97992446-97992455
4	CCNT2	chr5:97987369-97987559	K562	blood:	n/a	n/a
5	CEBPB	chr5:97934752-97935098	H1-hESC	embryonic stem cell:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
6	CEBPB	chr5:97993823-97994160	HepG2	liver:	n/a	n/a
7	CEBPB	chr5:97934734-97935106	HepG2	liver:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97935095-97935103 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
8	CEBPB	chr5:97934775-97935102	K562	blood:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
9	CEBPB	chr5:97934745-97935054	A549	lung:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
10	CEBPB	chr5:97934743-97935117	IMR90	lung:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97935095-97935103 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
11	CEBPB	chr5:97934750-97935110	A549	lung:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97935095-97935103 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
12	CEBPB	chr5:97934761-97935081	Hela-S3	cervix:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
13	CEBPB	chr5:97974512-97974899	IMR90	lung:	n/a	n/a
14	CEBPB	chr5:97958537-97958740	HepG2	liver:	n/a	chr5:97958669-97958680 chr5:97958669-97958678 chr5:97958667-97958678
15	CEBPB	chr5:97934708-97935043	MCF-7	breast:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
16	CEBPB	chr5:97939819-97940054	HepG2	liver:	n/a	chr5:97939901-97939912
17	CTCF	chr5:98015880-98016030	HMF	breast:	n/a	n/a
18	CTCF	chr5:97948520-97948670	HCFaa	heart:	n/a	n/a
19	CTCF	chr5:97940960-97941110	HCFaa	heart:	n/a	chr5:97941006-97941024 chr5:97941008-97941029 chr5:97941009-97941017
20	CTCF	chr5:97948520-97948670	NHDF-neo	bronchial:	n/a	n/a
21	CTCF	chr5:97948600-97948750	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr5:98015486-98015572	LNCaP	prostate:	n/a	n/a
23	CTCF	chr5:97981390-97981459	Lung_OC	lung:	n/a	n/a
24	CTCF	chr5:97919720-97919870	HPAF	blood vessel:	n/a	chr5:97919817-97919824
25	CTCF	chr5:97992240-97992390	BE2_C	brain:	n/a	n/a
26	CTCF	chr5:97992560-97992710	NHLF	lung:	n/a	n/a
27	CTCF	chr5:97940920-97941070	HCPEpiC	choroid plexus:	n/a	chr5:97941006-97941024 chr5:97941008-97941029 chr5:97941009-97941017
28	CTCF	chr5:98015960-98016110	HMF	breast:	n/a	n/a
29	CTCF	chr5:97976280-97976430	BE2_C	brain:	n/a	n/a
30	CTCF	chr5:97949460-97949610	AG04449	skin:	n/a	n/a
31	CTCF	chr5:97984640-97984790	AG10803	skin:	n/a	n/a
32	CTCF	chr5:97998060-97998210	HRE	kidney:	n/a	n/a
33	CTCF	chr5:98021648-98021666	Lung_OC	lung:	n/a	n/a
34	CTCF	chr5:98015880-98016030	RPTEC	kidney:	n/a	n/a
35	CTCF	chr5:97940840-97940990	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr5:97958331-97958344	Fibrobl	skin:	n/a	n/a
37	CTCF	chr5:98015994-98016044	NHEK	skin:	n/a	n/a
38	CTCF	chr5:97940980-97941130	HCPEpiC	choroid plexus:	n/a	chr5:97941006-97941024 chr5:97941008-97941029 chr5:97941009-97941017
39	CTCF	chr5:97936801-97936931	Lung_OC	lung:	n/a	n/a
40	E2F4	chr5:97932621-97932875	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr5:97937697-97937912	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr5:97929817-97930175	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr5:97931337-97931768	MCF10A-Er-Src	breast:	n/a	n/a
44	EBF1	chr5:97963022-97963168	GM12878	blood:	n/a	n/a
45	EBF1	chr5:97962327-97962654	GM12878	blood:	n/a	n/a
46	EP300	chr5:97967317-97967833	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr5:97921348-97921644	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr5:97967419-97967862	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr5:97965928-97965946	K562	blood:	n/a	n/a
50	EP300	chr5:97967077-97968028	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97992865-97992915	PrEC	prostate:	n/a
2	chr5:97992865-97992915	PrEC	prostate:	n/a
3	chr5:97971808-97971858	HCF	heart:	n/a
4	chr5:97970899-97970949	LNCaP	prostate:	n/a
5	chr5:97971808-97971858	HMEC	breast:	n/a
6	chr5:97971808-97971858	AG04449	skin:	fetal
7	chr5:97949352-97949402	A549	lung:	n/a
8	chr5:97970899-97970949	GM06990	blood:	n/a
9	chr5:97949352-97949402	PrEC	prostate:	n/a
10	chr5:97992865-97992915	AG09309	skin:	n/a
11	chr5:97949352-97949402	AG09309	skin:	n/a
12	chr5:97970899-97970949	RPTEC	kidney:	n/a
13	chr5:97992865-97992915	CMK	blood:	n/a
14	chr5:97971808-97971858	AG09319	gingival:	n/a
15	chr5:97970899-97970949	AoSMC	blood vessel:	n/a
16	chr5:97970899-97970949	AG10803	skin:	n/a
17	chr5:97971808-97971858	MCF-7	breast:	n/a
18	chr5:97970899-97970949	HCF	heart:	n/a
19	chr5:97992865-97992915	HAEpiC	amniotic membrane:	n/a
20	chr5:97949352-97949402	BJ	skin:	n/a
21	chr5:97971808-97971858	HCM	heart:	n/a
22	chr5:97949352-97949402	ECC-1	luminal epithelium:	n/a
23	chr5:97992865-97992915	SAEC	small airway:	n/a
24	chr5:97970899-97970949	NH-A	brain:	n/a
25	chr5:97970899-97970949	HRPEpiC	eye:	n/a
26	chr5:97949352-97949402	NHDF-neo	bronchial:	n/a
27	chr5:97970899-97970949	HEEpiC	esophagus:	n/a
28	chr5:97949352-97949402	AG10803	skin:	n/a
29	chr5:97992865-97992915	NHDF-neo	bronchial:	n/a
30	chr5:97970899-97970949	HRCEpiC	kidney:	n/a
31	chr5:97992865-97992915	HCT-116	colon:	n/a
32	chr5:97992865-97992915	HepG2	liver:	n/a
33	chr5:97971808-97971858	SK-N-SH_RA	brain:	n/a
34	chr5:97949352-97949402	NHBE	bronchial:	n/a
35	chr5:97949352-97949402	HRCEpiC	kidney:	n/a
36	chr5:97949352-97949402	PANC-1	pancreas:	n/a
37	chr5:97992865-97992915	AG04449	skin:	fetal
38	chr5:97949352-97949402	HAEpiC	amniotic membrane:	n/a
39	chr5:97949352-97949402	HIPEpiC	eye:	n/a
40	chr5:97949352-97949402	SK-N-MC	brain:	n/a
41	chr5:97949352-97949402	SKMC	muscle:	n/a
42	chr5:97971808-97971858	Hepatocyte	liver:	n/a
43	chr5:97949352-97949402	GM06990	blood:	n/a
44	chr5:97971808-97971858	HUVEC	blood vessel:	n/a
45	chr5:97970899-97970949	HIPEpiC	eye:	n/a
46	chr5:97971808-97971858	AG09309	skin:	n/a
47	chr5:97970899-97970949	U87	brain:	n/a
48	chr5:97992865-97992915	SK-N-SH	brain:	n/a
49	chr5:97949352-97949402	LNCaP	prostate:	n/a
50	chr5:97970899-97970949	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:97947803..97949307-chr5:97953669..97956460,2	K562	blood:
2	chr1:114624344..114625029-chr5:97973309..97973944,2	MCF-7	breast:
3	chr5:97960709..97962831-chr5:97972137..97973848,2	K562	blood:
4	chr5:97947803..97949307-chr5:97953669..97956460,2	K562	blood:
5	chr5:97927782..97929943-chr5:97931809..97933564,2	K562	blood:
6	chr5:97960709..97962831-chr5:97972137..97973848,2	K562	blood:
7	chr5:97966444..97968012-chr5:98368423..98370387,2	K562	blood:
8	chr5:97927404..97929282-chr5:97932064..97934664,2	K562	blood:
9	chr5:97980901..97982903-chr5:97985969..97988620,2	K562	blood:
10	chr5:97927404..97929282-chr5:97932064..97934664,2	K562	blood:
11	chr5:98006117..98008420-chr5:98011449..98013351,2	MCF-7	breast:
12	chr5:97927782..97929943-chr5:97931809..97933564,2	K562	blood:
13	chr5:98006117..98008420-chr5:98011449..98013351,2	MCF-7	breast:
14	chr5:97980901..97982903-chr5:97985969..97988620,2	K562	blood:

Variant related genes	Relation type
ENSG00000223053	TF binding region
ENSG00000251553	TF binding region
ENSG00000223053	CpG island
ENSG00000251553	CpG island

Extended variants
information (count: 3899 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3899 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs29661	chr5:97918829-97918830	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560465216	chr5:97918887-97918888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs3853247	chr5:97918906-97918907	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs56202622	chr5:97918953-97918954	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs552347485	chr5:97918979-97918980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186930632	chr5:97919020-97919021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192128020	chr5:97919060-97919061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375663553	chr5:97919134-97919135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537708947	chr5:97919198-97919199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs58568877	chr5:97919199-97919200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs397963400	chr5:97919212-97919213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs17166168	chr5:97919290-97919291	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs183869940	chr5:97919356-97919357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187634649	chr5:97919406-97919407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370889677	chr5:97919450-97919451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116814145	chr5:97919459-97919460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12187587	chr5:97919466-97919467	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs548627383	chr5:97919490-97919491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147260396	chr5:97919523-97919524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191152870	chr5:97919626-97919627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576323700	chr5:97919633-97919634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537585991	chr5:97919671-97919672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555558222	chr5:97919672-97919673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182620343	chr5:97919700-97919701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568382923	chr5:97919709-97919710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74379769	chr5:97919748-97919749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17166171	chr5:97919791-97919792	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs572377037	chr5:97919797-97919798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187137499	chr5:97919829-97919830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139035773	chr5:97919835-97919836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531190469	chr5:97919841-97919842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543530676	chr5:97919855-97919856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76093481	chr5:97919931-97919932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545748343	chr5:97919958-97919959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534149536	chr5:97919984-97919985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374069667	chr5:97920010-97920011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35890082	chr5:97920038-97920039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113250773	chr5:97920040-97920041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529485650	chr5:97920044-97920045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142967147	chr5:97920091-97920092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150908707	chr5:97920112-97920113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577199632	chr5:97920131-97920132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551643292	chr5:97920132-97920133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551336123	chr5:97920140-97920141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs17166173	chr5:97920164-97920165	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs17166174	chr5:97920203-97920204	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs555872310	chr5:97920228-97920229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191606750	chr5:97920235-97920236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185319797	chr5:97920253-97920254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556371894	chr5:97920326-97920327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97916000-97919000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:97916600-97921600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:97917600-97921400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr5:97917600-97921400	Weak transcription	NHLF	lung
5	chr5:97917800-97921400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:97917800-97921400	Weak transcription	NHDF-Ad	bronchial
7	chr5:97917800-97921400	Weak transcription	Osteobl	bone
8	chr5:97918000-97921400	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr5:97919000-97921200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr5:97921200-97922800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr5:97921400-97921600	Enhancers	Fetal Stomach	stomach
12	chr5:97921400-97921800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:97921400-97921800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr5:97921400-97921800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr5:97921400-97922200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr5:97921400-97922200	Enhancers	Osteobl	bone
17	chr5:97921400-97922800	Enhancers	NHLF	lung
18	chr5:97921400-97923000	Enhancers	NHDF-Ad	bronchial
19	chr5:97921600-97921800	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr5:97921600-97922800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:97921600-97923800	Weak transcription	Fetal Stomach	stomach
22	chr5:97921800-97922600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:97921800-97924200	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr5:97921800-97925200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr5:97921800-97927000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr5:97922000-97922800	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr5:97922400-97923600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr5:97922600-97922800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:97922800-97923200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:97922800-97923600	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr5:97922800-97923600	Weak transcription	NHLF	lung
32	chr5:97922800-97923800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr5:97922800-97923800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr5:97923000-97923400	Weak transcription	NHDF-Ad	bronchial
35	chr5:97923200-97924800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr5:97923400-97924800	Enhancers	NHDF-Ad	bronchial
37	chr5:97923600-97923800	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr5:97923600-97924000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr5:97923600-97924800	Enhancers	NHLF	lung
40	chr5:97923800-97924000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:97923800-97924200	Enhancers	Fetal Stomach	stomach
42	chr5:97923800-97924400	Enhancers	HSMM	muscle
43	chr5:97923800-97925200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:97924000-97924200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr5:97924000-97924800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr5:97924200-97924400	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr5:97924200-97925200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr5:97924400-97924800	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr5:97924800-97925200	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr5:97925200-97925400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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