Variant report

Variant	nsv949596
Chromosome Location	chr5:152343943-152548821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:579)
CpG islands
(count:305)
Chromatin interactive
region (count:11)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:152515158-152515217	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr5:152527977-152528226	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr5:152460935-152461295	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:152364298-152364669	IMR90	lung:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
5	CEBPB	chr5:152508396-152508656	HepG2	liver:	n/a	chr5:152508487-152508498
6	CEBPB	chr5:152460961-152461275	A549	lung:	n/a	n/a
7	CEBPB	chr5:152364298-152364651	HepG2	liver:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
8	CEBPB	chr5:152374246-152374450	HepG2	liver:	n/a	chr5:152374363-152374374
9	CEBPB	chr5:152417076-152417380	IMR90	lung:	n/a	n/a
10	CEBPB	chr5:152397705-152398057	K562	blood:	n/a	n/a
11	CEBPB	chr5:152407673-152407928	IMR90	lung:	n/a	n/a
12	CEBPB	chr5:152397708-152398049	HepG2	liver:	n/a	n/a
13	CEBPB	chr5:152416959-152417413	HepG2	liver:	n/a	n/a
14	CEBPB	chr5:152461004-152461275	K562	blood:	n/a	n/a
15	CEBPB	chr5:152402341-152402642	IMR90	lung:	n/a	n/a
16	CEBPB	chr5:152426684-152426884	HepG2	liver:	n/a	chr5:152426744-152426755 chr5:152426761-152426772
17	CEBPB	chr5:152433601-152433807	A549	lung:	n/a	n/a
18	CEBPB	chr5:152460940-152461296	IMR90	lung:	n/a	n/a
19	CEBPB	chr5:152460961-152461274	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr5:152364398-152364644	K562	blood:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
21	CEBPB	chr5:152547105-152547298	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:152417165-152417346	K562	blood:	n/a	n/a
23	CEBPB	chr5:152460914-152461345	MCF-7	breast:	n/a	n/a
24	CEBPB	chr5:152460930-152461293	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:152416917-152417321	A549	lung:	n/a	n/a
26	CEBPB	chr5:152397697-152398071	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr5:152397710-152398025	A549	lung:	n/a	n/a
28	CEBPB	chr5:152364302-152364664	A549	lung:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
29	CEBPB	chr5:152397695-152398058	IMR90	lung:	n/a	n/a
30	CHD2	chr5:152541505-152541527	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr5:152528060-152528210	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr5:152528020-152528170	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr5:152528080-152528230	A549	lung:	n/a	n/a
34	CTCF	chr5:152528080-152528230	GM12873	blood:	n/a	n/a
35	CTCF	chr5:152528044-152528213	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr5:152528060-152528210	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr5:152528060-152528210	BJ	skin:	n/a	n/a
38	CTCF	chr5:152528000-152528150	RPTEC	kidney:	n/a	n/a
39	CTCF	chr5:152528040-152528190	AG09309	skin:	n/a	n/a
40	CTCF	chr5:152447543-152447703	NHEK	skin:	n/a	n/a
41	CTCF	chr5:152447500-152447650	HRE	kidney:	n/a	n/a
42	CTCF	chr5:152528004-152528228	HepG2	liver:	n/a	n/a
43	CTCF	chr5:152538200-152538350	HMEC	breast:	n/a	n/a
44	CTCF	chr5:152528040-152528190	HRE	kidney:	n/a	n/a
45	CTCF	chr5:152499640-152499790	GM12871	blood:	n/a	n/a
46	CTCF	chr5:152515180-152515330	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr5:152527972-152528209	A549	lung:	n/a	n/a
48	CTCF	chr5:152528060-152528210	GM12871	blood:	n/a	n/a
49	CTCF	chr5:152528100-152528250	GM12872	blood:	n/a	n/a
50	CTCF	chr5:152528040-152528190	WERI-Rb-1	eye:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:152374989-152375039	SK-N-SH_RA	brain:	n/a
2	chr5:152502171-152502221	MCF-7	breast:	n/a
3	chr5:152374989-152375039	HEEpiC	esophagus:	n/a
4	chr5:152502171-152502221	LNCaP	prostate:	n/a
5	chr5:152352697-152352747	HRCEpiC	kidney:	n/a
6	chr5:152374989-152375039	IMR90	lung:	fetal
7	chr5:152502171-152502221	HMEC	breast:	n/a
8	chr5:152374989-152375039	AoSMC	blood vessel:	n/a
9	chr5:152352468-152352518	ovcar-3	ovarian:	n/a
10	chr5:152352697-152352747	HepG2	liver:	n/a
11	chr5:152352468-152352518	GM06990	blood:	n/a
12	chr5:152502171-152502221	HRPEpiC	eye:	n/a
13	chr5:152376702-152376752	HEK293	kidney:	embryo
14	chr5:152352468-152352518	MCF-7	breast:	n/a
15	chr5:152502171-152502221	HCPEpiC	choroid plexus:	n/a
16	chr5:152376702-152376752	NH-A	brain:	n/a
17	chr5:152352697-152352747	AG04449	skin:	fetal
18	chr5:152374989-152375039	HCM	heart:	n/a
19	chr5:152352697-152352747	PrEC	prostate:	n/a
20	chr5:152376702-152376752	HCPEpiC	choroid plexus:	n/a
21	chr5:152376702-152376752	K562	blood:	n/a
22	chr5:152502171-152502221	HCM	heart:	n/a
23	chr5:152502171-152502221	GM12891	blood:	n/a
24	chr5:152374989-152375039	HEK293	kidney:	embryo
25	chr5:152376702-152376752	PFSK-1	brain:	n/a
26	chr5:152502171-152502221	AG04449	skin:	fetal
27	chr5:152352697-152352747	HMEC	breast:	n/a
28	chr5:152352468-152352518	Jurkat	blood:	n/a
29	chr5:152376702-152376752	HepG2	liver:	n/a
30	chr5:152374989-152375039	PFSK-1	brain:	n/a
31	chr5:152502171-152502221	AG10803	skin:	n/a
32	chr5:152502171-152502221	SAEC	small airway:	n/a
33	chr5:152352697-152352747	NHBE	bronchial:	n/a
34	chr5:152352468-152352518	K562	blood:	n/a
35	chr5:152374989-152375039	Hepatocyte	liver:	n/a
36	chr5:152374989-152375039	NH-A	brain:	n/a
37	chr5:152374989-152375039	HUVEC	blood vessel:	n/a
38	chr5:152352468-152352518	HRCEpiC	kidney:	n/a
39	chr5:152352697-152352747	SKMC	muscle:	n/a
40	chr5:152374989-152375039	SK-N-MC	brain:	n/a
41	chr5:152502171-152502221	AG09309	skin:	n/a
42	chr5:152352697-152352747	T-47D	breast:	n/a
43	chr5:152376702-152376752	SK-N-MC	brain:	n/a
44	chr5:152376702-152376752	HL-60	blood:	n/a
45	chr5:152352697-152352747	IMR90	lung:	fetal
46	chr5:152376702-152376752	BE2_C	brain:	n/a
47	chr5:152374989-152375039	NB4	blood:	n/a
48	chr5:152352697-152352747	NHDF-neo	bronchial:	n/a
49	chr5:152374989-152375039	ECC-1	luminal epithelium:	n/a
50	chr5:152374989-152375039	HMEC	breast:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:152472931..152474977-chr5:152475321..152477555,2	MCF-7	breast:
2	chr5:152354651..152356569-chr5:152358890..152361095,2	K562	blood:
3	chr5:152484555..152486992-chr5:152492317..152495243,3	K562	blood:
4	chr5:152472931..152474977-chr5:152475321..152477555,2	MCF-7	breast:
5	chr5:152463300..152464864-chr5:152488382..152490078,2	K562	blood:
6	chr5:152354651..152356569-chr5:152358890..152361095,2	K562	blood:
7	chr5:151939767..151940736-chr5:152527629..152528599,7	MCF-7	breast:
8	chr5:151971696..151972663-chr5:152527730..152528402,3	MCF-7	breast:
9	chr5:152463300..152464864-chr5:152488382..152490078,2	K562	blood:
10	chr5:152484555..152486992-chr5:152492317..152495243,3	K562	blood:
11	chr20:26189300..26190278-chr5:152422915..152423415,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMUR2-1	chr5:152351826-152351909	XLOC_005056
2	lnc-NMUR2-1	chr5:152351274-152351343	XLOC_005056
3	lnc-NMUR2-1	chr5:152345801-152345894	XLOC_005056
4	lnc-NMUR2-1	chr5:152351274-152351346	XLOC_005056
5	lnc-NMUR2-1	chr5:152345801-152345909	XLOC_005056
6	lnc-NMUR2-1	chr5:152351274-152351346	ENSG00000249484.4
7	lnc-NMUR2-1	chr5:152345801-152345894	XLOC_005056
8	lnc-NMUR2-1	chr5:152346653-152346666	ENSG00000249484.4
9	lnc-NMUR2-1	chr5:152345801-152345894	ENSG00000249484.4
10	lnc-NMUR2-1	chr5:152352638-152352763	XLOC_005056
11	lnc-NMUR2-1	chr5:152351574-152351793	XLOC_005056
12	lnc-NMUR2-1	chr5:152352638-152352763	ENSG00000249484.4
13	lnc-NMUR2-1	chr5:152351826-152351909	ENSG00000249484
14	lnc-NMUR2-1	chr5:152345801-152345894	ENSG00000249484
15	lnc-NMUR2-1	chr5:152448272-152448373	XLOC_005056
16	lnc-NMUR2-1	chr5:152351574-152351793	ENSG00000249484.4

No data

Variant related genes	Relation type
ENSG00000249484	TF binding region
ENSG00000249484	CpG island
ENSG00000227195	chromatin interactions
FAM122A	miRNA target sites
DICER1	miRNA target sites

Extended variants
information (count: 4616 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4616 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561829668	chr5:152345822-152345823	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs190116279	chr5:152345830-152345831	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs529408302	chr5:152345859-152345860	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs182586311	chr5:152345865-152345866	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs575837099	chr5:152345877-152345878	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs374790983	chr5:152346037-152346038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142386812	chr5:152346067-152346068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113239714	chr5:152346098-152346099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188394390	chr5:152346103-152346104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs28649893	chr5:152346158-152346159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536104503	chr5:152346164-152346165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569561236	chr5:152346179-152346180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72806776	chr5:152346227-152346228	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs538066440	chr5:152346239-152346240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533368634	chr5:152346245-152346246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148342908	chr5:152346252-152346253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576461079	chr5:152346269-152346270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552066640	chr5:152346298-152346299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78749638	chr5:152346325-152346326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562488288	chr5:152346363-152346364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529796717	chr5:152346367-152346368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372261496	chr5:152346375-152346376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138353554	chr5:152346653-152346654	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs542256626	chr5:152351280-152351281	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs148668004	chr5:152351290-152351291	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs373737887	chr5:152351300-152351301	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs201032721	chr5:152351540-152351541	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs537737520	chr5:152351551-152351552	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs560152294	chr5:152351565-152351566	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs549430657	chr5:152351574-152351575	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs567639155	chr5:152351576-152351577	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs144483925	chr5:152351601-152351602	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs72806784	chr5:152351711-152351712	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs73282467	chr5:152351732-152351733	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs538505462	chr5:152351747-152351748	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs557111152	chr5:152351775-152351776	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs184871170	chr5:152351861-152351862	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs189626558	chr5:152351862-152351863	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs556906443	chr5:152352132-152352133	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs536660796	chr5:152352226-152352227	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs73799169	chr5:152352242-152352243	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs536156546	chr5:152352279-152352280	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs186120587	chr5:152352355-152352356	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs572507083	chr5:152352380-152352381	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs539886757	chr5:152352402-152352403	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs558514527	chr5:152352429-152352430	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs576896168	chr5:152352435-152352436	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs544271503	chr5:152352461-152352462	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs563747671	chr5:152352514-152352515	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs191042651	chr5:152352521-152352522	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
Crohn''s disease	20106866	CNVD
Breast cancer	20409316	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Deafness	19353646	CNVD
Developmental delay	19353646	CNVD
dysmorphism	19353646	CNVD
feeding difficulties	19353646	CNVD
strabismus	19353646	CNVD
Gastric adenocarcinoma	19115996	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:152346000-152346400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:152354200-152355600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:152357200-152357400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:152357800-152358200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:152357800-152358400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:152357800-152358800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:152358000-152358400	Enhancers	Stomach Mucosa	stomach
8	chr5:152358200-152358600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:152359800-152361200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:152362200-152362800	ZNF genes & repeats	Aorta	Aorta
11	chr5:152362800-152367000	Weak transcription	Aorta	Aorta
12	chr5:152364600-152364800	Enhancers	Fetal Brain Female	brain
13	chr5:152364800-152367200	Weak transcription	Fetal Brain Female	brain
14	chr5:152365400-152366000	Enhancers	Fetal Brain Male	brain
15	chr5:152365400-152368000	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr5:152366000-152367000	Weak transcription	Fetal Brain Male	brain
17	chr5:152366600-152367400	Enhancers	Stomach Mucosa	stomach
18	chr5:152367000-152367200	Enhancers	Aorta	Aorta
19	chr5:152367000-152367400	Enhancers	Fetal Brain Male	brain
20	chr5:152367200-152367800	Enhancers	Fetal Brain Female	brain
21	chr5:152367400-152370200	Weak transcription	Stomach Mucosa	stomach
22	chr5:152367400-152373000	Weak transcription	Fetal Brain Male	brain
23	chr5:152367800-152371800	Weak transcription	Fetal Brain Female	brain
24	chr5:152368000-152369400	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr5:152369400-152370200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr5:152370200-152371000	Enhancers	Stomach Mucosa	stomach
27	chr5:152373000-152374400	Enhancers	Fetal Brain Male	brain
28	chr5:152373400-152374200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:152373400-152374200	Enhancers	Gastric	stomach
30	chr5:152373400-152374200	Enhancers	HMEC	breast
31	chr5:152373600-152374000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr5:152373600-152374000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr5:152373600-152374200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr5:152373600-152375400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr5:152373800-152374000	Enhancers	Fetal Brain Female	brain
36	chr5:152373800-152375600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr5:152374000-152374600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr5:152374200-152375400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr5:152374600-152375000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:152375000-152375400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr5:152375000-152375600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr5:152377200-152377800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:152377600-152377800	Enhancers	H9 Cell Line	embryonic stem cell
44	chr5:152378400-152378600	Enhancers	H9 Cell Line	embryonic stem cell
45	chr5:152383800-152387400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr5:152386200-152386600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:152386400-152386600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr5:152386600-152387200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr5:152387400-152388000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:152388000-152388200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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