Variant report

Variant	nsv1017504
Chromosome Location	chr5:91092920-91178854
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	ATF1	chr5:91148131-91148258	K562	blood:	n/a	n/a
2	BCL11A	chr5:91171038-91171201	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr5:91093475-91093720	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr5:91144174-91144682	HCT-116	colon:	n/a	n/a
5	CBX3	chr5:91144125-91144870	HCT-116	colon:	n/a	n/a
6	CEBPB	chr5:91119513-91119708	K562	blood:	n/a	chr5:91119640-91119651 chr5:91119642-91119651 chr5:91119642-91119653
7	CEBPB	chr5:91097703-91097916	HepG2	liver:	n/a	chr5:91097854-91097865
8	CEBPB	chr5:91144247-91144583	IMR90	lung:	n/a	n/a
9	CEBPB	chr5:91144205-91144635	A549	lung:	n/a	n/a
10	CEBPB	chr5:91152417-91152693	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr5:91127369-91127575	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:91152497-91152724	HepG2	liver:	n/a	n/a
13	CEBPB	chr5:91144266-91144568	HepG2	liver:	n/a	n/a
14	CEBPB	chr5:91144100-91144745	HCT-116	colon:	n/a	n/a
15	CEBPB	chr5:91144301-91144592	A549	lung:	n/a	n/a
16	CEBPB	chr5:91145762-91146149	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:91143989-91144785	HCT-116	colon:	n/a	n/a
18	CEBPB	chr5:91144946-91145322	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr5:91093081-91093758	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:91144241-91144690	A549	lung:	n/a	n/a
21	CEBPB	chr5:91144102-91144750	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:91119557-91119748	HepG2	liver:	n/a	chr5:91119640-91119651 chr5:91119642-91119651 chr5:91119642-91119653
23	CEBPB	chr5:91144308-91144641	MCF-7	breast:	n/a	n/a
24	CHD2	chr5:91144229-91144697	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr5:91171380-91171530	HPF	lung:	n/a	chr5:91171402-91171423 chr5:91171407-91171425
26	CTCF	chr5:91160880-91161030	A549	lung:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
27	CTCF	chr5:91160860-91161010	MCF-7	breast:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
28	CTCF	chr5:91160760-91160910	RPTEC	kidney:	n/a	chr5:91160902-91160910
29	CTCF	chr5:91160827-91160991	Hela-S3	cervix:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
30	CTCF	chr5:91160768-91161038	SK-N-SH_RA	brain:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
31	CTCF	chr5:91160820-91160970	WERI-Rb-1	eye:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
32	CTCF	chr5:91171360-91171510	HA-sp	spinal cord:	n/a	chr5:91171402-91171423 chr5:91171407-91171425
33	CTCF	chr5:91171377-91171404	LNCaP	prostate:	n/a	n/a
34	CTCF	chr5:91160871-91160950	GM13977	blood:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
35	CTCF	chr5:91171380-91171530	A549	lung:	n/a	chr5:91171402-91171423 chr5:91171407-91171425
36	CTCF	chr5:91171320-91171470	HBMEC	blood vessel:	n/a	chr5:91171402-91171423 chr5:91171407-91171425
37	CTCF	chr5:91160720-91160870	HFF	foreskin:	n/a	n/a
38	CTCF	chr5:91098718-91098846	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr5:91160800-91160950	AG09319	gingival:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
40	CTCF	chr5:91171400-91171550	HMF	breast:	n/a	chr5:91171402-91171423 chr5:91171407-91171425
41	CTCF	chr5:91160880-91161030	RPTEC	kidney:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
42	CTCF	chr5:91160875-91160925	GM10266	blood:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
43	CTCF	chr5:91098764-91098773	A549	lung:	n/a	n/a
44	CTCF	chr5:91160881-91160951	GM12878	blood:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
45	CTCF	chr5:91160866-91160950	HepG2	liver:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
46	CTCF	chr5:91160800-91160950	HMF	breast:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
47	CTCF	chr5:91160780-91161030	HA-sp	spinal cord:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
48	CTCF	chr5:91160859-91160991	Medullo	brain:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
49	CTCF	chr5:91160800-91160950	HCT-116	colon:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920
50	CTCF	chr5:91160800-91160950	HCPEpiC	choroid plexus:	n/a	chr5:91160898-91160914 chr5:91160902-91160910 chr5:91160897-91160915 chr5:91160899-91160920

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:91137099-91137149	HEK293	kidney:	embryo
2	chr5:91137099-91137149	K562	blood:	n/a
3	chr5:91137099-91137149	SK-N-SH_RA	brain:	n/a
4	chr5:91137099-91137149	HRE	kidney:	n/a
5	chr5:91137099-91137149	GM12878	blood:	n/a
6	chr5:91137099-91137149	HIPEpiC	eye:	n/a
7	chr5:91137099-91137149	NHBE	bronchial:	n/a
8	chr5:91137099-91137149	U87	brain:	n/a
9	chr5:91137099-91137149	HCT-116	colon:	n/a
10	chr5:91137099-91137149	SK-N-MC	brain:	n/a
11	chr5:91137099-91137149	AoSMC	blood vessel:	n/a
12	chr5:91137099-91137149	A549	lung:	n/a
13	chr5:91137099-91137149	MCF10A-Er-Src	breast:	n/a
14	chr5:91137099-91137149	HRPEpiC	eye:	n/a
15	chr5:91137099-91137149	AG04449	skin:	fetal
16	chr5:91137099-91137149	GM06990	blood:	n/a
17	chr5:91137099-91137149	CMK	blood:	n/a
18	chr5:91137099-91137149	ProgFib	skin:	n/a
19	chr5:91137099-91137149	RPTEC	kidney:	n/a
20	chr5:91137099-91137149	PFSK-1	brain:	n/a
21	chr5:91137099-91137149	AG09309	skin:	n/a
22	chr5:91137099-91137149	NT2-D1	testis:	n/a
23	chr5:91137099-91137149	GM12892	blood:	n/a
24	chr5:91137099-91137149	GM12891	blood:	n/a
25	chr5:91137099-91137149	BE2_C	brain:	n/a
26	chr5:91137099-91137149	SAEC	small airway:	n/a
27	chr5:91137099-91137149	MCF-7	breast:	n/a
28	chr5:91137099-91137149	SKMC	muscle:	n/a
29	chr5:91137099-91137149	NH-A	brain:	n/a
30	chr5:91137099-91137149	HPAEpiC	pulmonary alveolar:	n/a
31	chr5:91137099-91137149	LNCaP	prostate:	n/a
32	chr5:91137099-91137149	PANC-1	pancreas:	n/a
33	chr5:91137099-91137149	Hela-S3	cervix:	n/a
34	chr5:91137099-91137149	HCM	heart:	n/a
35	chr5:91137099-91137149	HRCEpiC	kidney:	n/a
36	chr5:91137099-91137149	HL-60	blood:	n/a
37	chr5:91137099-91137149	NB4	blood:	n/a
38	chr5:91137099-91137149	HepG2	liver:	n/a
39	chr5:91137099-91137149	HAEpiC	amniotic membrane:	n/a
40	chr5:91137099-91137149	AG04450	lung:	fetal
41	chr5:91137099-91137149	ovcar-3	ovarian:	n/a
42	chr5:91137099-91137149	NHDF-neo	bronchial:	n/a
43	chr5:91137099-91137149	AG09319	gingival:	n/a
44	chr5:91137099-91137149	HUVEC	blood vessel:	n/a
45	chr5:91137099-91137149	HCPEpiC	choroid plexus:	n/a
46	chr5:91137099-91137149	BJ	skin:	n/a
47	chr5:91137099-91137149	Jurkat	blood:	n/a
48	chr5:91137099-91137149	Hepatocyte	liver:	n/a
49	chr5:91137099-91137149	IMR90	lung:	fetal
50	chr5:91137099-91137149	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:91100711..91102288-chr5:91114486..91116676,2	MCF-7	breast:
2	chr5:91165736..91168298-chr5:91169196..91172814,3	K562	blood:
3	chr5:91164822..91166961-chr5:91195203..91197338,2	K562	blood:
4	chr5:91164129..91166638-chr5:91167068..91169772,2	MCF-7	breast:
5	chr5:91148456..91150162-chr5:91156168..91158769,2	K562	blood:
6	chr5:91164129..91166638-chr5:91167068..91169772,2	MCF-7	breast:
7	chr5:91100711..91102288-chr5:91114486..91116676,2	MCF-7	breast:
8	chr5:91164818..91166462-chr5:91169540..91172351,2	MCF-7	breast:
9	chr5:91148456..91150162-chr5:91156168..91158769,2	K562	blood:
10	chr5:91164818..91166462-chr5:91169540..91172351,2	MCF-7	breast:
11	chr5:91165736..91168298-chr5:91169196..91172814,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARRDC3-10	chr5:91139504-91140346	NONHSAT102766

Variant related genes	Relation type
PCBP2P3	TF binding region
PCBP2P3	CpG island

Extended variants
information (count: 2303 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2303 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4244210	chr5:91092920-91092921	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538269040	chr5:91092937-91092938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs13357799	chr5:91092948-91092949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4559033	chr5:91092963-91092964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534226898	chr5:91093034-91093035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553909904	chr5:91093041-91093042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573939372	chr5:91093075-91093076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531123064	chr5:91093090-91093091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111983913	chr5:91093094-91093095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536346465	chr5:91093100-91093101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568697200	chr5:91093174-91093175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9293576	chr5:91093184-91093185	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs187170900	chr5:91093202-91093203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs9293577	chr5:91093210-91093211	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs72773348	chr5:91093223-91093224	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs565301318	chr5:91093224-91093225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577963050	chr5:91093259-91093260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539619294	chr5:91093272-91093273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs199599311	chr5:91093283-91093284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200620071	chr5:91093284-91093285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201646985	chr5:91093287-91093288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540541829	chr5:91093331-91093332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560380219	chr5:91093349-91093350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567731868	chr5:91093394-91093395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537355204	chr5:91093434-91093435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549084619	chr5:91093474-91093475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562410332	chr5:91093492-91093493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531457582	chr5:91093532-91093533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551045061	chr5:91093588-91093589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191874940	chr5:91093646-91093647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115357041	chr5:91093682-91093683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371950412	chr5:91093720-91093721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs4397159	chr5:91093751-91093752	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs536479973	chr5:91093753-91093754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556731679	chr5:91093762-91093763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575718078	chr5:91093825-91093826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4398667	chr5:91093880-91093881	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs539124501	chr5:91093883-91093884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561343391	chr5:91093958-91093959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114669161	chr5:91093962-91093963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs4270726	chr5:91093966-91093967	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs547541631	chr5:91098601-91098602	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs567891851	chr5:91098603-91098604	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs536347118	chr5:91098663-91098664	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs2913452	chr5:91098697-91098698	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs186507412	chr5:91098708-91098709	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs111778066	chr5:91098724-91098725	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs114756754	chr5:91098756-91098757	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs139918868	chr5:91098761-91098762	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs559015054	chr5:91098779-91098780	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	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
Esophageal adenocarcinoma	18519675	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
Ovarian cancer	21720365	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
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91084200-91093200	Weak transcription	Hela-S3	cervix
2	chr5:91092000-91093200	Weak transcription	A549	lung
3	chr5:91093000-91093800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:91093200-91093400	Enhancers	A549	lung
5	chr5:91093200-91093600	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr5:91093200-91093800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:91093200-91094000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:91093200-91094000	Enhancers	Hela-S3	cervix
9	chr5:91093400-91093800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr5:91093400-91093800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr5:91098600-91099200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
12	chr5:91098600-91099200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:91099000-91099200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr5:91099200-91104000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr5:91108600-91108800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
16	chr5:91108800-91110600	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr5:91119800-91120800	Enhancers	Fetal Brain Male	brain
18	chr5:91120800-91121200	Weak transcription	Fetal Brain Male	brain
19	chr5:91121200-91121400	Enhancers	Fetal Brain Male	brain
20	chr5:91121400-91122400	Enhancers	Hela-S3	cervix
21	chr5:91121400-91134000	Weak transcription	Fetal Brain Male	brain
22	chr5:91122200-91122800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr5:91122200-91122800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr5:91122400-91122800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr5:91125200-91128000	Enhancers	Fetal Lung	lung
26	chr5:91128000-91129400	Weak transcription	Fetal Lung	lung
27	chr5:91129400-91130600	Enhancers	Fetal Lung	lung
28	chr5:91129800-91130200	Enhancers	Fetal Stomach	stomach
29	chr5:91129800-91130600	Enhancers	Fetal Heart	heart
30	chr5:91130200-91131200	Weak transcription	Fetal Stomach	stomach
31	chr5:91130600-91134800	Weak transcription	Fetal Heart	heart
32	chr5:91131200-91131400	Enhancers	Fetal Stomach	stomach
33	chr5:91134000-91137200	Enhancers	Fetal Brain Female	brain
34	chr5:91134000-91137600	Enhancers	Fetal Brain Male	brain
35	chr5:91134400-91135200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:91134600-91134800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:91134600-91135400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr5:91134800-91135000	Enhancers	Fetal Heart	heart
39	chr5:91134800-91135400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:91135000-91135200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr5:91135000-91135200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr5:91135000-91135200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr5:91135000-91135400	Flanking Active TSS	Fetal Heart	heart
44	chr5:91135000-91135600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr5:91135000-91136000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr5:91135200-91136200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr5:91135200-91136400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr5:91135200-91136600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr5:91135400-91136200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr5:91135400-91136200	Enhancers	Fetal Heart	heart

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