Variant report

Variant	nsv1023570
Chromosome Location	chr5:58486384-58537849
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	ATF2	chr5:58534307-58534738	GM12878	blood:	n/a	n/a
2	ATF2	chr5:58534331-58534713	GM12878	blood:	n/a	n/a
3	BATF	chr5:58534243-58534773	GM12878	blood:	n/a	chr5:58534489-58534500
4	BATF	chr5:58496129-58496399	GM12878	blood:	n/a	n/a
5	BATF	chr5:58534293-58534727	GM12878	blood:	n/a	chr5:58534489-58534500
6	BCL11A	chr5:58534325-58534706	GM12878	blood:	n/a	n/a
7	BCL3	chr5:58501799-58502474	A549	lung:	n/a	n/a
8	BCL3	chr5:58534385-58534704	GM12878	blood:	n/a	n/a
9	BCL3	chr5:58489533-58490349	A549	lung:	n/a	chr5:58490204-58490212 chr5:58490054-58490063 chr5:58489885-58489894
10	BCLAF1	chr5:58534282-58534784	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:58515920-58516300	HepG2	liver:	n/a	n/a
12	BHLHE40	chr5:58534398-58534662	GM12878	blood:	n/a	n/a
13	CEBPB	chr5:58494699-58495044	IMR90	lung:	n/a	chr5:58494865-58494874 chr5:58494864-58494875 chr5:58494865-58494874
14	CEBPB	chr5:58529240-58529359	A549	lung:	n/a	chr5:58529263-58529276 chr5:58529265-58529276
15	CEBPB	chr5:58493758-58494092	A549	lung:	n/a	chr5:58493940-58493951
16	CEBPB	chr5:58489721-58490213	Hela-S3	cervix:	n/a	chr5:58490029-58490042 chr5:58490031-58490040 chr5:58490030-58490041 chr5:58490029-58490040
17	CEBPB	chr5:58489465-58490517	A549	lung:	n/a	chr5:58490029-58490042 chr5:58490031-58490040 chr5:58490030-58490041 chr5:58490029-58490040
18	CEBPB	chr5:58489896-58490103	K562	blood:	n/a	chr5:58490029-58490042 chr5:58490031-58490040 chr5:58490030-58490041 chr5:58490029-58490040
19	CEBPB	chr5:58489938-58490113	H1-hESC	embryonic stem cell:	n/a	chr5:58490029-58490042 chr5:58490031-58490040 chr5:58490030-58490041 chr5:58490029-58490040
20	CEBPB	chr5:58493770-58494080	HepG2	liver:	n/a	chr5:58493940-58493951
21	CEBPB	chr5:58532351-58532600	A549	lung:	n/a	n/a
22	CEBPB	chr5:58493699-58494207	A549	lung:	n/a	chr5:58493940-58493951
23	CEBPB	chr5:58493824-58494083	H1-hESC	embryonic stem cell:	n/a	chr5:58493940-58493951
24	CEBPB	chr5:58501855-58502491	A549	lung:	n/a	n/a
25	CEBPB	chr5:58502035-58502341	IMR90	lung:	n/a	n/a
26	CEBPB	chr5:58489869-58490206	HepG2	liver:	n/a	chr5:58490029-58490042 chr5:58490031-58490040 chr5:58490030-58490041 chr5:58490029-58490040
27	CEBPB	chr5:58493916-58493977	Hela-S3	cervix:	n/a	chr5:58493940-58493951
28	CEBPB	chr5:58493793-58494092	K562	blood:	n/a	chr5:58493940-58493951
29	CEBPB	chr5:58494701-58495027	A549	lung:	n/a	chr5:58494865-58494874 chr5:58494864-58494875 chr5:58494865-58494874
30	CEBPB	chr5:58489707-58490296	A549	lung:	n/a	chr5:58490029-58490042 chr5:58490031-58490040 chr5:58490030-58490041 chr5:58490029-58490040
31	CEBPB	chr5:58494733-58494949	Hela-S3	cervix:	n/a	chr5:58494865-58494874 chr5:58494864-58494875 chr5:58494865-58494874
32	CEBPB	chr5:58494589-58495141	A549	lung:	n/a	chr5:58494865-58494874 chr5:58494864-58494875 chr5:58494865-58494874
33	CEBPB	chr5:58500004-58500219	HepG2	liver:	n/a	n/a
34	CEBPB	chr5:58489709-58490443	A549	lung:	n/a	chr5:58490029-58490042 chr5:58490031-58490040 chr5:58490030-58490041 chr5:58490029-58490040
35	CEBPB	chr5:58509937-58510137	A549	lung:	n/a	n/a
36	CEBPB	chr5:58518877-58519197	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr5:58508607-58508626	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:58502036-58502362	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr5:58494702-58495307	H1-hESC	embryonic stem cell:	n/a	chr5:58494865-58494874 chr5:58494864-58494875 chr5:58494865-58494874
40	CEBPB	chr5:58489602-58490461	IMR90	lung:	n/a	chr5:58490029-58490042 chr5:58490031-58490040 chr5:58490030-58490041 chr5:58490029-58490040
41	CEBPB	chr5:58494688-58495044	HepG2	liver:	n/a	chr5:58494865-58494874 chr5:58494864-58494875 chr5:58494865-58494874
42	CEBPB	chr5:58509925-58510196	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:58493766-58494121	IMR90	lung:	n/a	chr5:58493940-58493951
44	CEBPB	chr5:58517362-58517512	A549	lung:	n/a	chr5:58517495-58517506
45	CEBPB	chr5:58502050-58502322	A549	lung:	n/a	n/a
46	CHD2	chr5:58502109-58502216	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr5:58534416-58534548	GM12878	blood:	n/a	n/a
48	CHD2	chr5:58489849-58490104	Hela-S3	cervix:	n/a	n/a
49	CREB1	chr5:58489663-58490172	A549	lung:	n/a	n/a
50	CREB1	chr5:58534260-58534881	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:58535559-58535609	HAEpiC	amniotic membrane:	n/a
2	chr5:58535559-58535609	PANC-1	pancreas:	n/a
3	chr5:58535559-58535609	HUVEC	blood vessel:	n/a
4	chr5:58535559-58535609	NHBE	bronchial:	n/a
5	chr5:58535559-58535609	ovcar-3	ovarian:	n/a
6	chr5:58535559-58535609	HL-60	blood:	n/a
7	chr5:58535559-58535609	AoSMC	blood vessel:	n/a
8	chr5:58535559-58535609	GM12891	blood:	n/a
9	chr5:58535559-58535609	HCM	heart:	n/a
10	chr5:58535559-58535609	ProgFib	skin:	n/a
11	chr5:58535559-58535609	SK-N-SH	brain:	n/a
12	chr5:58535559-58535609	GM19239	blood:	n/a
13	chr5:58535559-58535609	Hepatocyte	liver:	n/a
14	chr5:58535559-58535609	RPTEC	kidney:	n/a
15	chr5:58535559-58535609	LNCaP	prostate:	n/a
16	chr5:58535559-58535609	BE2_C	brain:	n/a
17	chr5:58535559-58535609	CMK	blood:	n/a
18	chr5:58535559-58535609	PFSK-1	brain:	n/a
19	chr5:58535559-58535609	HIPEpiC	eye:	n/a
20	chr5:58535559-58535609	T-47D	breast:	n/a
21	chr5:58535559-58535609	HepG2	liver:	n/a
22	chr5:58535559-58535609	HMEC	breast:	n/a
23	chr5:58535559-58535609	Hela-S3	cervix:	n/a
24	chr5:58535559-58535609	SKMC	muscle:	n/a
25	chr5:58535559-58535609	AG10803	skin:	n/a
26	chr5:58535559-58535609	IMR90	lung:	fetal
27	chr5:58535559-58535609	HPAEpiC	pulmonary alveolar:	n/a
28	chr5:58535559-58535609	Caco-2	colon:	n/a
29	chr5:58535559-58535609	SK-N-SH_RA	brain:	n/a
30	chr5:58535559-58535609	HEEpiC	esophagus:	n/a
31	chr5:58535559-58535609	AG09319	gingival:	n/a
32	chr5:58535559-58535609	HCF	heart:	n/a
33	chr5:58535559-58535609	NH-A	brain:	n/a
34	chr5:58535559-58535609	HRPEpiC	eye:	n/a
35	chr5:58535559-58535609	A549	lung:	n/a
36	chr5:58535559-58535609	ECC-1	luminal epithelium:	n/a
37	chr5:58535559-58535609	HNPCEpiC	eye:	n/a
38	chr5:58535559-58535609	MCF-7	breast:	n/a
39	chr5:58535559-58535609	PrEC	prostate:	n/a
40	chr5:58535559-58535609	Jurkat	blood:	n/a
41	chr5:58535559-58535609	HEK293	kidney:	embryo
42	chr5:58535559-58535609	HCPEpiC	choroid plexus:	n/a
43	chr5:58535559-58535609	AG09309	skin:	n/a
44	chr5:58535559-58535609	BJ	skin:	n/a
45	chr5:58535559-58535609	HRCEpiC	kidney:	n/a
46	chr5:58535559-58535609	HCT-116	colon:	n/a
47	chr5:58535559-58535609	SK-N-MC	brain:	n/a
48	chr5:58535559-58535609	K562	blood:	n/a
49	chr5:58535559-58535609	MCF10A-Er-Src	breast:	n/a
50	chr5:58535559-58535609	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr5:58513952..58514913-chr5:58663432..58664673,5	MCF-7	breast:
2	chr5:58532712..58534586-chr5:58538179..58539997,2	K562	blood:
3	chr5:58529142..58529735-chr6:26031124..26031817,2	Hela-S3	cervix:
4	chr5:58514307..58514912-chr5:58675986..58677121,4	MCF-7	breast:
5	chr1:106991021..106991578-chr5:58515452..58516343,2	MCF-7	breast:
6	chr5:58517841..58518362-chr5:58663716..58664223,2	MCF-7	breast:
7	chr5:58483785..58484780-chr5:58514094..58514743,3	MCF-7	breast:

Variant related genes	Relation type
PDE4D	TF binding region
PDE4D	CpG island

Extended variants
information (count: 2033 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:2033 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72764094	chr5:58486399-58486400	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112487235	chr5:58486402-58486403	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs545307767	chr5:58486440-58486441	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs565280469	chr5:58486446-58486447	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs556843464	chr5:58486472-58486473	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs546218456	chr5:58486495-58486496	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs183039210	chr5:58486548-58486549	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs188243305	chr5:58486627-58486628	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs191336168	chr5:58486632-58486633	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs549133501	chr5:58486661-58486662	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs182766295	chr5:58486677-58486678	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs187685305	chr5:58486717-58486718	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs552761121	chr5:58486738-58486739	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs191366230	chr5:58486769-58486770	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs200423912	chr5:58486790-58486791	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs6882204	chr5:58486827-58486828	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184571514	chr5:58486844-58486845	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187769384	chr5:58486860-58486861	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144009304	chr5:58486887-58486888	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549056512	chr5:58487014-58487015	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146140625	chr5:58487041-58487042	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542775230	chr5:58487046-58487047	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77830843	chr5:58487112-58487113	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74727488	chr5:58487113-58487114	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556678933	chr5:58487162-58487163	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545246562	chr5:58487213-58487214	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113125811	chr5:58487220-58487221	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528011833	chr5:58487222-58487223	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540193142	chr5:58487238-58487239	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577368077	chr5:58487249-58487250	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528936745	chr5:58487289-58487290	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192087958	chr5:58487307-58487308	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537949227	chr5:58487323-58487324	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562643050	chr5:58487324-58487325	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185334134	chr5:58487332-58487333	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2021384	chr5:58487364-58487365	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs571546995	chr5:58487387-58487388	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534093856	chr5:58487413-58487414	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547738974	chr5:58487416-58487417	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189793495	chr5:58487427-58487428	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567554252	chr5:58487488-58487489	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536693502	chr5:58487493-58487494	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571761091	chr5:58487495-58487496	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140181414	chr5:58487513-58487514	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576160181	chr5:58487543-58487544	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199799202	chr5:58487595-58487596	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538832137	chr5:58487612-58487613	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs143768418	chr5:58487619-58487620	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7727032	chr5:58487687-58487688	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541364822	chr5:58487711-58487712	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Hepatocellular carcinoma	16750200	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	17982442	CNVD
Gastric cancer	22315472	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58449800-58489400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:58474400-58520000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr5:58474800-58491000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr5:58479800-58487200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:58479800-58489800	Weak transcription	Gastric	stomach
6	chr5:58480200-58488800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr5:58481000-58486600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr5:58484400-58489200	Weak transcription	Hela-S3	cervix
9	chr5:58484400-58489400	Weak transcription	HSMMtube	muscle
10	chr5:58484400-58489800	Active TSS	Right Ventricle	heart
11	chr5:58484600-58486800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:58484600-58495600	Weak transcription	Fetal Kidney	kidney
13	chr5:58484800-58486600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:58484800-58486600	Enhancers	Colon Smooth Muscle	Colon
15	chr5:58484800-58489400	Weak transcription	NH-A	brain
16	chr5:58484800-58489800	Weak transcription	Fetal Heart	heart
17	chr5:58484800-58491000	Weak transcription	Fetal Stomach	stomach
18	chr5:58484800-58501200	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr5:58485000-58486600	Enhancers	Rectal Smooth Muscle	rectum
20	chr5:58485000-58489000	Weak transcription	Primary B cells from peripheral blood	blood
21	chr5:58485000-58489200	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr5:58485000-58489200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr5:58485000-58489800	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr5:58485000-58491200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr5:58485000-58491800	Weak transcription	Stomach Smooth Muscle	stomach
26	chr5:58485000-58492600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr5:58485000-58499000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr5:58485000-58505200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:58485000-58518800	Weak transcription	Primary hematopoietic stem cells	blood
30	chr5:58485400-58489400	Weak transcription	Osteobl	bone
31	chr5:58485600-58488200	Weak transcription	Left Ventricle	heart
32	chr5:58485600-58491000	Weak transcription	Aorta	Aorta
33	chr5:58485600-58500400	Weak transcription	Psoas Muscle	Psoas
34	chr5:58485600-58501600	Weak transcription	HUVEC	blood vessel
35	chr5:58485600-58512400	Weak transcription	Pancreas	Pancrea
36	chr5:58485600-58518200	Weak transcription	Fetal Muscle Trunk	muscle
37	chr5:58485800-58489600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:58485800-58489600	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr5:58486000-58486400	Enhancers	A549	lung
40	chr5:58486000-58488600	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr5:58486000-58489400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr5:58486000-58489400	Weak transcription	Fetal Intestine Small	intestine
43	chr5:58486000-58489400	Weak transcription	Fetal Muscle Leg	muscle
44	chr5:58486000-58489600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr5:58486000-58494200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr5:58486000-58508600	Weak transcription	Fetal Intestine Large	intestine
47	chr5:58486400-58486800	Flanking Active TSS	A549	lung
48	chr5:58486600-58486800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr5:58486600-58489800	Weak transcription	Colon Smooth Muscle	Colon
50	chr5:58486600-58492000	Weak transcription	Rectal Smooth Muscle	rectum

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