Variant report

Variant	nsv600089
Chromosome Location	chr5:152200109-152488891
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:429)
CpG islands
(count:427)
Chromatin interactive
region (count:10)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:152203895-152204173	GM12878	blood:	n/a	chr5:152204083-152204093 chr5:152204082-152204093
2	BATF	chr5:152203943-152204249	GM12878	blood:	n/a	chr5:152204083-152204093 chr5:152204082-152204093
3	CEBPB	chr5:152397708-152398049	HepG2	liver:	n/a	n/a
4	CEBPB	chr5:152336825-152337119	Hela-S3	cervix:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
5	CEBPB	chr5:152336869-152337086	K562	blood:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
6	CEBPB	chr5:152460940-152461296	IMR90	lung:	n/a	n/a
7	CEBPB	chr5:152397695-152398058	IMR90	lung:	n/a	n/a
8	CEBPB	chr5:152397697-152398071	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr5:152433601-152433807	A549	lung:	n/a	n/a
10	CEBPB	chr5:152342360-152342457	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:152426684-152426884	HepG2	liver:	n/a	chr5:152426744-152426755 chr5:152426761-152426772
12	CEBPB	chr5:152460935-152461295	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:152250975-152251178	A549	lung:	n/a	chr5:152251072-152251083
14	CEBPB	chr5:152332003-152332331	HepG2	liver:	n/a	chr5:152332151-152332162
15	CEBPB	chr5:152364298-152364669	IMR90	lung:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
16	CEBPB	chr5:152364302-152364664	A549	lung:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
17	CEBPB	chr5:152460930-152461293	HepG2	liver:	n/a	n/a
18	CEBPB	chr5:152397710-152398025	A549	lung:	n/a	n/a
19	CEBPB	chr5:152417076-152417380	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:152407673-152407928	IMR90	lung:	n/a	n/a
21	CEBPB	chr5:152397705-152398057	K562	blood:	n/a	n/a
22	CEBPB	chr5:152336825-152337124	A549	lung:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
23	CEBPB	chr5:152460961-152461275	A549	lung:	n/a	n/a
24	CEBPB	chr5:152402341-152402642	IMR90	lung:	n/a	n/a
25	CEBPB	chr5:152364298-152364651	HepG2	liver:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
26	CEBPB	chr5:152336818-152337158	HepG2	liver:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
27	CEBPB	chr5:152416917-152417321	A549	lung:	n/a	n/a
28	CEBPB	chr5:152416959-152417413	HepG2	liver:	n/a	n/a
29	CEBPB	chr5:152332017-152332290	A549	lung:	n/a	chr5:152332151-152332162
30	CEBPB	chr5:152336837-152337081	IMR90	lung:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
31	CEBPB	chr5:152333400-152333656	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:152250941-152251175	HepG2	liver:	n/a	chr5:152251072-152251083
33	CEBPB	chr5:152460961-152461274	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr5:152461004-152461275	K562	blood:	n/a	n/a
35	CEBPB	chr5:152332064-152332264	H1-hESC	embryonic stem cell:	n/a	chr5:152332151-152332162
36	CEBPB	chr5:152364398-152364644	K562	blood:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
37	CEBPB	chr5:152336872-152337072	MCF-7	breast:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
38	CEBPB	chr5:152460914-152461345	MCF-7	breast:	n/a	n/a
39	CEBPB	chr5:152374246-152374450	HepG2	liver:	n/a	chr5:152374363-152374374
40	CEBPB	chr5:152417165-152417346	K562	blood:	n/a	n/a
41	CEBPB	chr5:152332005-152332335	IMR90	lung:	n/a	chr5:152332151-152332162
42	CTCF	chr5:152469448-152469519	ProgFib	skin:	n/a	n/a
43	CTCF	chr5:152447543-152447703	NHEK	skin:	n/a	n/a
44	CTCF	chr5:152205160-152205310	GM06990	blood:	n/a	n/a
45	CTCF	chr5:152227793-152227902	Lung_OC	lung:	n/a	n/a
46	CTCF	chr5:152385260-152385410	HMEC	breast:	n/a	n/a
47	CTCF	chr5:152416924-152416952	Fibrobl	skin:	n/a	n/a
48	CTCF	chr5:152447536-152447715	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr5:152283080-152283138	GM13976	blood:	n/a	n/a
50	CTCF	chr5:152205120-152205270	HEK293	kidney:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:152374989-152375039	AoSMC	blood vessel:	n/a
2	chr5:152374989-152375039	ovcar-3	ovarian:	n/a
3	chr5:152352697-152352747	HRPEpiC	eye:	n/a
4	chr5:152374989-152375039	HIPEpiC	eye:	n/a
5	chr5:152234077-152234127	GM19239	blood:	n/a
6	chr5:152279040-152279090	Jurkat	blood:	n/a
7	chr5:152279040-152279090	RPTEC	kidney:	n/a
8	chr5:152352697-152352747	HPAEpiC	pulmonary alveolar:	n/a
9	chr5:152352697-152352747	HCT-116	colon:	n/a
10	chr5:152352468-152352518	HEEpiC	esophagus:	n/a
11	chr5:152309662-152309712	Caco-2	colon:	n/a
12	chr5:152234077-152234127	A549	lung:	n/a
13	chr5:152352697-152352747	U87	brain:	n/a
14	chr5:152309662-152309712	HAEpiC	amniotic membrane:	n/a
15	chr5:152374989-152375039	HepG2	liver:	n/a
16	chr5:152234077-152234127	Hepatocyte	liver:	n/a
17	chr5:152234077-152234127	MCF10A-Er-Src	breast:	n/a
18	chr5:152279040-152279090	H1-hESC	embryonic stem cell:	embryo
19	chr5:152374989-152375039	HEEpiC	esophagus:	n/a
20	chr5:152279040-152279090	HL-60	blood:	n/a
21	chr5:152374989-152375039	PrEC	prostate:	n/a
22	chr5:152352468-152352518	T-47D	breast:	n/a
23	chr5:152309662-152309712	BJ	skin:	n/a
24	chr5:152376702-152376752	Caco-2	colon:	n/a
25	chr5:152352697-152352747	GM06990	blood:	n/a
26	chr5:152234077-152234127	HCM	heart:	n/a
27	chr5:152352468-152352518	SKMC	muscle:	n/a
28	chr5:152374989-152375039	AG09309	skin:	n/a
29	chr5:152309662-152309712	HIPEpiC	eye:	n/a
30	chr5:152352697-152352747	NH-A	brain:	n/a
31	chr5:152374989-152375039	BJ	skin:	n/a
32	chr5:152352697-152352747	RPTEC	kidney:	n/a
33	chr5:152352468-152352518	PFSK-1	brain:	n/a
34	chr5:152309662-152309712	HNPCEpiC	eye:	n/a
35	chr5:152309662-152309712	HCPEpiC	choroid plexus:	n/a
36	chr5:152376702-152376752	HCM	heart:	n/a
37	chr5:152376702-152376752	HAEpiC	amniotic membrane:	n/a
38	chr5:152352468-152352518	NHBE	bronchial:	n/a
39	chr5:152352468-152352518	NHDF-neo	bronchial:	n/a
40	chr5:152352468-152352518	Caco-2	colon:	n/a
41	chr5:152352468-152352518	GM19239	blood:	n/a
42	chr5:152234077-152234127	AG09309	skin:	n/a
43	chr5:152376702-152376752	AG04449	skin:	fetal
44	chr5:152376702-152376752	GM12891	blood:	n/a
45	chr5:152309662-152309712	HEK293	kidney:	embryo
46	chr5:152234077-152234127	GM12892	blood:	n/a
47	chr5:152374989-152375039	SKMC	muscle:	n/a
48	chr5:152279040-152279090	PrEC	prostate:	n/a
49	chr5:152309662-152309712	NT2-D1	testis:	n/a
50	chr5:152374989-152375039	HRCEpiC	kidney:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:152472931..152474977-chr5:152475321..152477555,2	MCF-7	breast:
2	chr5:152247556..152250256-chr5:152250400..152252605,2	K562	blood:
3	chr20:26189300..26190278-chr5:152422915..152423415,2	MCF-7	breast:
4	chr5:152354651..152356569-chr5:152358890..152361095,2	K562	blood:
5	chr5:152463300..152464864-chr5:152488382..152490078,2	K562	blood:
6	chr5:152354651..152356569-chr5:152358890..152361095,2	K562	blood:
7	chr5:152247556..152250256-chr5:152250400..152252605,2	K562	blood:
8	chr5:152484555..152486992-chr5:152492317..152495243,3	K562	blood:
9	chr5:152463300..152464864-chr5:152488382..152490078,2	K562	blood:
10	chr5:152472931..152474977-chr5:152475321..152477555,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMUR2-1	chr5:152351274-152351346	ENSG00000249484.4
2	lnc-NMUR2-1	chr5:152351574-152351793	ENSG00000249484.4
3	lnc-NMUR2-1	chr5:152351826-152351909	XLOC_005056
4	lnc-NMUR2-1	chr5:152345801-152345894	XLOC_005056
5	lnc-NMUR2-1	chr5:152352638-152352763	ENSG00000249484.4
6	lnc-NMUR2-1	chr5:152346653-152346666	ENSG00000249484.4
7	lnc-NMUR2-1	chr5:152345801-152345894	ENSG00000249484.4
8	lnc-NMUR2-1	chr5:152318398-152318551	ENSG00000249484.4
9	lnc-NMUR2-1	chr5:152351274-152351343	XLOC_005056
10	lnc-NMUR2-1	chr5:152345801-152345909	XLOC_005056
11	lnc-NMUR2-1	chr5:152352638-152352763	XLOC_005056
12	lnc-NMUR2-1	chr5:152345801-152345894	XLOC_005056
13	lnc-NMUR2-1	chr5:152345801-152345894	ENSG00000249484
14	lnc-NMUR2-1	chr5:152448272-152448373	XLOC_005056
15	lnc-NMUR2-1	chr5:152264987-152265188	XLOC_005056
16	lnc-NMUR2-1	chr5:152351274-152351346	XLOC_005056
17	lnc-NMUR2-1	chr5:152318398-152318551	XLOC_005056
18	lnc-NMUR2-1	chr5:152351826-152351909	ENSG00000249484
19	lnc-NMUR2-1	chr5:152351574-152351793	XLOC_005056

No data

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

Extended variants
information (count: 4790 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4790 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555783767	chr5:152213016-152213017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527973689	chr5:152213082-152213083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552871328	chr5:152213144-152213145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114134315	chr5:152213150-152213151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184768125	chr5:152213151-152213152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188048639	chr5:152213190-152213191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563593359	chr5:152213263-152213264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115166783	chr5:152213328-152213329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552417551	chr5:152213336-152213337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13154038	chr5:152213340-152213341	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs560998415	chr5:152213352-152213353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528214764	chr5:152213374-152213375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547966827	chr5:152213407-152213408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556363212	chr5:152213409-152213410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367760716	chr5:152213430-152213431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs180816091	chr5:152213544-152213545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551629087	chr5:152213641-152213642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10043503	chr5:152213681-152213682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537409650	chr5:152213699-152213700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10037923	chr5:152213700-152213701	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs574072838	chr5:152213737-152213738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368335434	chr5:152213749-152213750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534837573	chr5:152213754-152213755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553191555	chr5:152213760-152213761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140812662	chr5:152213831-152213832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545247223	chr5:152213873-152213874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557247097	chr5:152213906-152213907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184480683	chr5:152213944-152213945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189801913	chr5:152214023-152214024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560769604	chr5:152214036-152214037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528173754	chr5:152214039-152214040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73799129	chr5:152214043-152214044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564659909	chr5:152214059-152214060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537606615	chr5:152214074-152214075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533302851	chr5:152214086-152214087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185898535	chr5:152214126-152214127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12188960	chr5:152214214-152214215	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs12186623	chr5:152214254-152214255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs35562264	chr5:152214332-152214333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540147349	chr5:152214391-152214392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549333819	chr5:152214420-152214421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567590268	chr5:152214477-152214478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368403565	chr5:152214495-152214496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535035052	chr5:152214518-152214519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553477584	chr5:152214544-152214545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74550018	chr5:152214545-152214546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201809683	chr5:152214563-152214564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538799646	chr5:152214565-152214566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557234747	chr5:152214604-152214605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575492569	chr5:152214668-152214669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Schizophrenia	23813976	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:152213000-152213200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:152213200-152218000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:152217800-152218600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:152218000-152218200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:152218000-152218400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:152218000-152218600	Active TSS	Liver	Liver
7	chr5:152218000-152218800	Enhancers	Colon Smooth Muscle	Colon
8	chr5:152231400-152232000	Enhancers	Stomach Mucosa	stomach
9	chr5:152232000-152235200	Weak transcription	Stomach Mucosa	stomach
10	chr5:152232800-152235200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr5:152233000-152233400	Enhancers	H9 Cell Line	embryonic stem cell
12	chr5:152233000-152233800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr5:152233000-152234600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr5:152233000-152235400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr5:152233000-152236200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr5:152233200-152235600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr5:152233200-152235800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr5:152233400-152233800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:152233400-152235800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:152233800-152234200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr5:152234000-152236400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr5:152234200-152236000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr5:152234800-152235200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr5:152235200-152235800	Enhancers	Stomach Mucosa	stomach
25	chr5:152235800-152237000	Weak transcription	Stomach Mucosa	stomach
26	chr5:152236000-152237000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr5:152236400-152236800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr5:152236800-152238400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:152237000-152237400	Enhancers	Stomach Mucosa	stomach
30	chr5:152237200-152237400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr5:152237200-152237400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:152237200-152237600	Enhancers	Gastric	stomach
33	chr5:152237400-152240400	Weak transcription	Stomach Mucosa	stomach
34	chr5:152237600-152238200	Weak transcription	Gastric	stomach
35	chr5:152238200-152238400	Enhancers	Gastric	stomach
36	chr5:152240000-152240600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:152240200-152240800	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr5:152240400-152241200	Enhancers	Stomach Mucosa	stomach
39	chr5:152241000-152241600	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr5:152243200-152245200	Enhancers	HSMM	muscle
41	chr5:152246000-152247400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr5:152247200-152247400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr5:152247400-152247800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr5:152247400-152248400	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr5:152248400-152248600	Enhancers	H1 Cell Line	embryonic stem cell
46	chr5:152253400-152253600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:152253400-152253600	ZNF genes & repeats	Gastric	stomach
48	chr5:152261400-152262800	Enhancers	Fetal Brain Male	brain
49	chr5:152262000-152263200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr5:152262200-152264800	Enhancers	Brain Germinal Matrix	brain

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