Variant report

Variant	nsv1017812
Chromosome Location	chr5:152220845-152467431
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	CEBPB	chr5:152332003-152332331	HepG2	liver:	n/a	chr5:152332151-152332162
2	CEBPB	chr5:152460940-152461296	IMR90	lung:	n/a	n/a
3	CEBPB	chr5:152433601-152433807	A549	lung:	n/a	n/a
4	CEBPB	chr5:152460935-152461295	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr5:152417165-152417346	K562	blood:	n/a	n/a
6	CEBPB	chr5:152364298-152364651	HepG2	liver:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
7	CEBPB	chr5:152336872-152337072	MCF-7	breast:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
8	CEBPB	chr5:152460930-152461293	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:152336837-152337081	IMR90	lung:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
10	CEBPB	chr5:152364398-152364644	K562	blood:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
11	CEBPB	chr5:152332017-152332290	A549	lung:	n/a	chr5:152332151-152332162
12	CEBPB	chr5:152397705-152398057	K562	blood:	n/a	n/a
13	CEBPB	chr5:152402341-152402642	IMR90	lung:	n/a	n/a
14	CEBPB	chr5:152397695-152398058	IMR90	lung:	n/a	n/a
15	CEBPB	chr5:152374246-152374450	HepG2	liver:	n/a	chr5:152374363-152374374
16	CEBPB	chr5:152460961-152461275	A549	lung:	n/a	n/a
17	CEBPB	chr5:152416959-152417413	HepG2	liver:	n/a	n/a
18	CEBPB	chr5:152407673-152407928	IMR90	lung:	n/a	n/a
19	CEBPB	chr5:152336869-152337086	K562	blood:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
20	CEBPB	chr5:152460961-152461274	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr5:152397697-152398071	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:152397708-152398049	HepG2	liver:	n/a	n/a
23	CEBPB	chr5:152250975-152251178	A549	lung:	n/a	chr5:152251072-152251083
24	CEBPB	chr5:152460914-152461345	MCF-7	breast:	n/a	n/a
25	CEBPB	chr5:152336825-152337119	Hela-S3	cervix:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
26	CEBPB	chr5:152364298-152364669	IMR90	lung:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
27	CEBPB	chr5:152417076-152417380	IMR90	lung:	n/a	n/a
28	CEBPB	chr5:152332064-152332264	H1-hESC	embryonic stem cell:	n/a	chr5:152332151-152332162
29	CEBPB	chr5:152342360-152342457	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:152250941-152251175	HepG2	liver:	n/a	chr5:152251072-152251083
31	CEBPB	chr5:152426684-152426884	HepG2	liver:	n/a	chr5:152426744-152426755 chr5:152426761-152426772
32	CEBPB	chr5:152336818-152337158	HepG2	liver:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
33	CEBPB	chr5:152416917-152417321	A549	lung:	n/a	n/a
34	CEBPB	chr5:152332005-152332335	IMR90	lung:	n/a	chr5:152332151-152332162
35	CEBPB	chr5:152397710-152398025	A549	lung:	n/a	n/a
36	CEBPB	chr5:152336825-152337124	A549	lung:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
37	CEBPB	chr5:152461004-152461275	K562	blood:	n/a	n/a
38	CEBPB	chr5:152364302-152364664	A549	lung:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
39	CEBPB	chr5:152333400-152333656	HepG2	liver:	n/a	n/a
40	CTCF	chr5:152283080-152283138	GM13976	blood:	n/a	n/a
41	CTCF	chr5:152385260-152385410	HMEC	breast:	n/a	n/a
42	CTCF	chr5:152287665-152287712	Kidney_OC	kidney:	n/a	chr5:152287696-152287704 chr5:152287680-152287696
43	CTCF	chr5:152345185-152345249	GM13976	blood:	n/a	n/a
44	CTCF	chr5:152440620-152440770	HepG2	liver:	n/a	n/a
45	CTCF	chr5:152447543-152447703	NHEK	skin:	n/a	n/a
46	CTCF	chr5:152413164-152413297	Lung_OC	lung:	n/a	n/a
47	CTCF	chr5:152416840-152416990	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr5:152416840-152416990	HMEC	breast:	n/a	n/a
49	CTCF	chr5:152383240-152383390	GM12869	blood:	n/a	n/a
50	CTCF	chr5:152400036-152400055	Spleen_OC	spleen:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:152279040-152279090	Caco-2	colon:	n/a
2	chr5:152279040-152279090	Caco-2	colon:	n/a
3	chr5:152376702-152376752	Jurkat	blood:	n/a
4	chr5:152376702-152376752	SK-N-SH	brain:	n/a
5	chr5:152352697-152352747	HNPCEpiC	eye:	n/a
6	chr5:152309662-152309712	AG09309	skin:	n/a
7	chr5:152234077-152234127	GM06990	blood:	n/a
8	chr5:152234077-152234127	PFSK-1	brain:	n/a
9	chr5:152352697-152352747	HIPEpiC	eye:	n/a
10	chr5:152352697-152352747	ovcar-3	ovarian:	n/a
11	chr5:152352697-152352747	HEK293	kidney:	embryo
12	chr5:152279040-152279090	IMR90	lung:	fetal
13	chr5:152352697-152352747	PrEC	prostate:	n/a
14	chr5:152374989-152375039	U87	brain:	n/a
15	chr5:152352697-152352747	RPTEC	kidney:	n/a
16	chr5:152234077-152234127	T-47D	breast:	n/a
17	chr5:152352697-152352747	GM12891	blood:	n/a
18	chr5:152309662-152309712	AG10803	skin:	n/a
19	chr5:152376702-152376752	HRPEpiC	eye:	n/a
20	chr5:152376702-152376752	GM12892	blood:	n/a
21	chr5:152376702-152376752	GM19239	blood:	n/a
22	chr5:152279040-152279090	T-47D	breast:	n/a
23	chr5:152352468-152352518	AG10803	skin:	n/a
24	chr5:152352468-152352518	HUVEC	blood vessel:	n/a
25	chr5:152352468-152352518	BJ	skin:	n/a
26	chr5:152309662-152309712	SK-N-MC	brain:	n/a
27	chr5:152279040-152279090	ovcar-3	ovarian:	n/a
28	chr5:152374989-152375039	NHBE	bronchial:	n/a
29	chr5:152352468-152352518	GM12892	blood:	n/a
30	chr5:152352468-152352518	GM12878	blood:	n/a
31	chr5:152279040-152279090	GM19239	blood:	n/a
32	chr5:152352697-152352747	ProgFib	skin:	n/a
33	chr5:152352468-152352518	SK-N-MC	brain:	n/a
34	chr5:152352697-152352747	LNCaP	prostate:	n/a
35	chr5:152279040-152279090	PANC-1	pancreas:	n/a
36	chr5:152352697-152352747	PANC-1	pancreas:	n/a
37	chr5:152352697-152352747	HCM	heart:	n/a
38	chr5:152376702-152376752	ECC-1	luminal epithelium:	n/a
39	chr5:152309662-152309712	GM19239	blood:	n/a
40	chr5:152234077-152234127	AG09309	skin:	n/a
41	chr5:152234077-152234127	HepG2	liver:	n/a
42	chr5:152376702-152376752	AG09309	skin:	n/a
43	chr5:152374989-152375039	HMEC	breast:	n/a
44	chr5:152352697-152352747	BE2_C	brain:	n/a
45	chr5:152309662-152309712	MCF-7	breast:	n/a
46	chr5:152376702-152376752	HCF	heart:	n/a
47	chr5:152352468-152352518	HEK293	kidney:	embryo
48	chr5:152352468-152352518	GM12891	blood:	n/a
49	chr5:152309662-152309712	U87	brain:	n/a
50	chr5:152352697-152352747	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:152247556..152250256-chr5:152250400..152252605,2	K562	blood:
2	chr5:152247556..152250256-chr5:152250400..152252605,2	K562	blood:
3	chr5:152463300..152464864-chr5:152488382..152490078,2	K562	blood:
4	chr20:26189300..26190278-chr5:152422915..152423415,2	MCF-7	breast:
5	chr5:152354651..152356569-chr5:152358890..152361095,2	K562	blood:
6	chr5:152354651..152356569-chr5:152358890..152361095,2	K562	blood:

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

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: 3987 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3987 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561915369	chr5:152231463-152231464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs367974899	chr5:152231519-152231520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7722574	chr5:152231526-152231527	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs563251549	chr5:152231621-152231622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117721677	chr5:152231655-152231656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187698365	chr5:152231656-152231657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567135549	chr5:152231663-152231664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534191441	chr5:152231711-152231712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142158359	chr5:152231724-152231725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71970560	chr5:152231725-152231726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs55811518	chr5:152231755-152231756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559221573	chr5:152231767-152231768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs151062042	chr5:152231854-152231855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192662782	chr5:152231960-152231961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs367766453	chr5:152231997-152231998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184336338	chr5:152232068-152232069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574637954	chr5:152232113-152232114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541602926	chr5:152232147-152232148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553720048	chr5:152232169-152232170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375362046	chr5:152232170-152232171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146367713	chr5:152232188-152232189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201765465	chr5:152232189-152232190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113492944	chr5:152232191-152232192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35069511	chr5:152232193-152232194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10038949	chr5:152232195-152232196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs67993892	chr5:152232197-152232198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs62400587	chr5:152232199-152232200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35302973	chr5:152232227-152232228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs56065344	chr5:152232228-152232229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545751582	chr5:152232248-152232249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200674783	chr5:152232270-152232271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs72802864	chr5:152232297-152232298	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs531295609	chr5:152232332-152232333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375847309	chr5:152232353-152232354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543484981	chr5:152232396-152232397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548784417	chr5:152232407-152232408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76280371	chr5:152232469-152232470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189497212	chr5:152232514-152232515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567617864	chr5:152232531-152232532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs13161486	chr5:152232533-152232534	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs145113760	chr5:152232562-152232563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546658861	chr5:152232600-152232601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192583915	chr5:152232639-152232640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539334375	chr5:152232640-152232641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4533946	chr5:152232645-152232646	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs141318365	chr5:152232658-152232659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75723307	chr5:152232662-152232663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570850239	chr5:152232684-152232685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537844413	chr5:152232712-152232713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4364437	chr5:152232725-152232726	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:269 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:152231400-152232000	Enhancers	Stomach Mucosa	stomach
2	chr5:152232000-152235200	Weak transcription	Stomach Mucosa	stomach
3	chr5:152232800-152235200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr5:152233000-152233400	Enhancers	H9 Cell Line	embryonic stem cell
5	chr5:152233000-152233800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr5:152233000-152234600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr5:152233000-152235400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr5:152233000-152236200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr5:152233200-152235600	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr5:152233200-152235800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr5:152233400-152233800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr5:152233400-152235800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr5:152233800-152234200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr5:152234000-152236400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr5:152234200-152236000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr5:152234800-152235200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr5:152235200-152235800	Enhancers	Stomach Mucosa	stomach
18	chr5:152235800-152237000	Weak transcription	Stomach Mucosa	stomach
19	chr5:152236000-152237000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr5:152236400-152236800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr5:152236800-152238400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr5:152237000-152237400	Enhancers	Stomach Mucosa	stomach
23	chr5:152237200-152237400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr5:152237200-152237400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:152237200-152237600	Enhancers	Gastric	stomach
26	chr5:152237400-152240400	Weak transcription	Stomach Mucosa	stomach
27	chr5:152237600-152238200	Weak transcription	Gastric	stomach
28	chr5:152238200-152238400	Enhancers	Gastric	stomach
29	chr5:152240000-152240600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:152240200-152240800	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr5:152240400-152241200	Enhancers	Stomach Mucosa	stomach
32	chr5:152241000-152241600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr5:152243200-152245200	Enhancers	HSMM	muscle
34	chr5:152246000-152247400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr5:152247200-152247400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr5:152247400-152247800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr5:152247400-152248400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr5:152248400-152248600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr5:152253400-152253600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:152253400-152253600	ZNF genes & repeats	Gastric	stomach
41	chr5:152261400-152262800	Enhancers	Fetal Brain Male	brain
42	chr5:152262000-152263200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr5:152262200-152264800	Enhancers	Brain Germinal Matrix	brain
44	chr5:152262400-152263200	Enhancers	Fetal Brain Female	brain
45	chr5:152279800-152280200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr5:152279800-152280600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr5:152279800-152280800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr5:152280000-152280600	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr5:152280000-152280800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr5:152281200-152282200	Enhancers	Liver	Liver

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