Variant report

Variant	nsv1022160
Chromosome Location	chr5:58645805-58689010
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:951)
CpG islands
(count:122)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:951 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:58676085-58676588	GM12878	blood:	n/a	n/a
2	ATF2	chr5:58667352-58667796	GM12878	blood:	n/a	n/a
3	ATF2	chr5:58667411-58667779	GM12878	blood:	n/a	n/a
4	ATF2	chr5:58663693-58663944	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:58676057-58676572	GM12878	blood:	n/a	n/a
6	ATF3	chr5:58652777-58654067	A549	lung:	n/a	n/a
7	BATF	chr5:58676201-58676554	GM12878	blood:	n/a	n/a
8	BATF	chr5:58667359-58667749	GM12878	blood:	n/a	chr5:58667586-58667597 chr5:58667587-58667597
9	BATF	chr5:58667396-58667737	GM12878	blood:	n/a	chr5:58667586-58667597 chr5:58667587-58667597
10	BATF	chr5:58676204-58676489	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:58676193-58676445	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:58676120-58676482	GM12878	blood:	n/a	chr5:58676143-58676152
13	BCL3	chr5:58655859-58656666	A549	lung:	n/a	n/a
14	BCL3	chr5:58657154-58657767	A549	lung:	n/a	n/a
15	BCL3	chr5:58652380-58654882	A549	lung:	n/a	chr5:58654065-58654072
16	BCL3	chr5:58653155-58654805	A549	lung:	n/a	chr5:58654065-58654072
17	BCL3	chr5:58676156-58676940	A549	lung:	n/a	n/a
18	BCLAF1	chr5:58676088-58676598	GM12878	blood:	n/a	chr5:58676143-58676152
19	BCLAF1	chr5:58676236-58676535	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:58676155-58676534	GM12878	blood:	n/a	n/a
21	CBX3	chr5:58663710-58664021	HCT-116	colon:	n/a	n/a
22	CEBPB	chr5:58658453-58658601	A549	lung:	n/a	n/a
23	CEBPB	chr5:58653216-58653932	A549	lung:	n/a	chr5:58653463-58653476
24	CEBPB	chr5:58659381-58659514	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:58652378-58654781	A549	lung:	n/a	chr5:58654387-58654404 chr5:58653463-58653476
26	CEBPB	chr5:58655870-58656886	A549	lung:	n/a	chr5:58656328-58656341 chr5:58656201-58656214
27	CEBPB	chr5:58655968-58656493	A549	lung:	n/a	chr5:58656328-58656341 chr5:58656201-58656214
28	CEBPB	chr5:58653597-58653845	MCF-7	breast:	n/a	n/a
29	CEBPB	chr5:58663663-58664162	A549	lung:	n/a	n/a
30	CEBPB	chr5:58657316-58657613	MCF-7	breast:	n/a	n/a
31	CEBPB	chr5:58648680-58648832	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr5:58658471-58658649	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:58648218-58648500	A549	lung:	n/a	chr5:58648345-58648356
34	CEBPB	chr5:58654293-58654492	A549	lung:	n/a	chr5:58654387-58654404
35	CEBPB	chr5:58648274-58648474	Hela-S3	cervix:	n/a	chr5:58648345-58648356
36	CEBPB	chr5:58676221-58676517	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr5:58655980-58656547	A549	lung:	n/a	chr5:58656328-58656341 chr5:58656201-58656214
38	CEBPB	chr5:58652711-58653861	A549	lung:	n/a	chr5:58653463-58653476
39	CHD2	chr5:58652971-58652987	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr5:58676237-58676498	GM12878	blood:	n/a	n/a
41	CREB1	chr5:58654387-58654602	A549	lung:	n/a	n/a
42	CREB1	chr5:58663700-58663957	A549	lung:	n/a	n/a
43	CREB1	chr5:58653258-58653846	A549	lung:	n/a	n/a
44	CREB1	chr5:58653318-58653866	A549	lung:	n/a	n/a
45	CREB1	chr5:58676076-58676698	GM12878	blood:	n/a	n/a
46	CREB1	chr5:58667434-58667800	GM12878	blood:	n/a	n/a
47	CREB1	chr5:58667475-58667763	GM12878	blood:	n/a	n/a
48	CREB1	chr5:58676157-58676565	GM12878	blood:	n/a	n/a
49	CTCF	chr5:58676360-58676510	HUVEC	blood vessel:	n/a	chr5:58676465-58676486 chr5:58676471-58676487 chr5:58676470-58676488 chr5:58676475-58676483
50	CTCF	chr5:58663740-58663890	GM12867	blood:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:58653624-58653674	IMR90	lung:	fetal
2	chr5:58653624-58653674	Hepatocyte	liver:	n/a
3	chr5:58653624-58653674	K562	blood:	n/a
4	chr5:58652808-58652858	HL-60	blood:	n/a
5	chr5:58653624-58653674	GM12891	blood:	n/a
6	chr5:58652808-58652858	HCPEpiC	choroid plexus:	n/a
7	chr5:58652808-58652858	AG09309	skin:	n/a
8	chr5:58653624-58653674	SK-N-SH	brain:	n/a
9	chr5:58652808-58652858	GM12892	blood:	n/a
10	chr5:58652808-58652858	Caco-2	colon:	n/a
11	chr5:58652808-58652858	AG04449	skin:	fetal
12	chr5:58653624-58653674	AG04450	lung:	fetal
13	chr5:58652808-58652858	SK-N-SH	brain:	n/a
14	chr5:58653624-58653674	NB4	blood:	n/a
15	chr5:58652808-58652858	K562	blood:	n/a
16	chr5:58653624-58653674	CMK	blood:	n/a
17	chr5:58653624-58653674	ProgFib	skin:	n/a
18	chr5:58652808-58652858	NHDF-neo	bronchial:	n/a
19	chr5:58652808-58652858	NH-A	brain:	n/a
20	chr5:58653624-58653674	AoSMC	blood vessel:	n/a
21	chr5:58652808-58652858	HIPEpiC	eye:	n/a
22	chr5:58653624-58653674	BE2_C	brain:	n/a
23	chr5:58652808-58652858	AoSMC	blood vessel:	n/a
24	chr5:58653624-58653674	T-47D	breast:	n/a
25	chr5:58653624-58653674	MCF-7	breast:	n/a
26	chr5:58653624-58653674	NH-A	brain:	n/a
27	chr5:58652808-58652858	PrEC	prostate:	n/a
28	chr5:58653624-58653674	NT2-D1	testis:	n/a
29	chr5:58653624-58653674	SKMC	muscle:	n/a
30	chr5:58652808-58652858	HepG2	liver:	n/a
31	chr5:58652808-58652858	HNPCEpiC	eye:	n/a
32	chr5:58653624-58653674	HUVEC	blood vessel:	n/a
33	chr5:58653624-58653674	SK-N-MC	brain:	n/a
34	chr5:58653624-58653674	U87	brain:	n/a
35	chr5:58653624-58653674	HRCEpiC	kidney:	n/a
36	chr5:58653624-58653674	GM06990	blood:	n/a
37	chr5:58653624-58653674	BJ	skin:	n/a
38	chr5:58653624-58653674	AG04449	skin:	fetal
39	chr5:58653624-58653674	HPAEpiC	pulmonary alveolar:	n/a
40	chr5:58652808-58652858	HRPEpiC	eye:	n/a
41	chr5:58652808-58652858	HPAEpiC	pulmonary alveolar:	n/a
42	chr5:58652808-58652858	CMK	blood:	n/a
43	chr5:58652808-58652858	AG10803	skin:	n/a
44	chr5:58652808-58652858	SK-N-SH_RA	brain:	n/a
45	chr5:58653624-58653674	AG09319	gingival:	n/a
46	chr5:58652808-58652858	HUVEC	blood vessel:	n/a
47	chr5:58653624-58653674	HAEpiC	amniotic membrane:	n/a
48	chr5:58653624-58653674	SAEC	small airway:	n/a
49	chr5:58653624-58653674	GM12878	blood:	n/a
50	chr5:58652808-58652858	PFSK-1	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:58483931..58484785-chr5:58663381..58664456,4	MCF-7	breast:
2	chr5:58631024..58631593-chr5:58663326..58663872,2	MCF-7	breast:
3	chr5:58514307..58514912-chr5:58675986..58677121,4	MCF-7	breast:
4	chr5:58517841..58518362-chr5:58663716..58664223,2	MCF-7	breast:
5	chr5:58513952..58514913-chr5:58663432..58664673,5	MCF-7	breast:
6	chr5:58657123..58657869-chr5:58676349..58676935,2	MCF-7	breast:
7	chr5:58657123..58657869-chr5:58676349..58676935,2	MCF-7	breast:
8	chr5:58484203..58484779-chr5:58676055..58676926,3	MCF-7	breast:
9	chr5:58651518..58653116-chr5:58654954..58657664,2	K562	blood:
10	chr5:58484022..58484971-chr5:58675909..58676491,2	MCF-7	breast:
11	chr5:58645161..58647091-chr5:58651070..58653977,2	K562	blood:
12	chr5:58685998..58686505-chr5:58956311..58957192,2	MCF-7	breast:
13	chr5:58685562..58686590-chr5:58792342..58793267,6	MCF-7	breast:

No data

Variant related genes	Relation type
PDE4D	TF binding region
PDE4D	CpG island
ENSG00000113448	chromatin interactions

Extended variants
information (count: 1534 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1534 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35274	chr5:58645805-58645806	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544093163	chr5:58645865-58645866	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529714888	chr5:58645898-58645899	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144243670	chr5:58645906-58645907	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs76615409	chr5:58645923-58645924	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs192652518	chr5:58645927-58645928	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs184206064	chr5:58645991-58645992	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs189530524	chr5:58646025-58646026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs549091380	chr5:58646064-58646065	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs40125	chr5:58646112-58646113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs181955899	chr5:58646123-58646124	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185090887	chr5:58646154-58646155	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs571907254	chr5:58646232-58646233	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs552299225	chr5:58646247-58646248	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs6450516	chr5:58646353-58646354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs146580969	chr5:58646373-58646374	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572903727	chr5:58646374-58646375	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149129920	chr5:58646397-58646398	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs555469491	chr5:58646411-58646412	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs189022626	chr5:58646452-58646453	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs143249994	chr5:58646461-58646462	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564171616	chr5:58646518-58646519	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs13359805	chr5:58646567-58646568	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs151255889	chr5:58646596-58646597	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200973180	chr5:58646703-58646704	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371893612	chr5:58646722-58646723	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs140873925	chr5:58646794-58646795	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146238743	chr5:58646803-58646804	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548979018	chr5:58646807-58646808	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs138822549	chr5:58646846-58646847	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs142805561	chr5:58646852-58646853	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs73092960	chr5:58646898-58646899	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs181702938	chr5:58646921-58646922	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs531490739	chr5:58646929-58646930	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs116736364	chr5:58646955-58646956	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs547745523	chr5:58646988-58646989	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs567975658	chr5:58647055-58647056	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs376248600	chr5:58647168-58647169	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs185608749	chr5:58647314-58647315	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs35275	chr5:58647328-58647329	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs537581331	chr5:58647351-58647352	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs552564393	chr5:58647472-58647473	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs577787064	chr5:58647491-58647492	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs146946474	chr5:58647579-58647580	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs137990587	chr5:58647581-58647582	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs573605812	chr5:58647610-58647611	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs542610790	chr5:58647638-58647639	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs537229146	chr5:58647804-58647805	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs536663297	chr5:58647819-58647820	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs554700094	chr5:58647820-58647821	Enhancers Weak transcription Flanking Active TSS	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	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58634400-58647800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:58635200-58652600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr5:58637200-58646000	Weak transcription	Psoas Muscle	Psoas
4	chr5:58640200-58646000	Weak transcription	Right Ventricle	heart
5	chr5:58641200-58648000	Enhancers	A549	lung
6	chr5:58641800-58646600	Weak transcription	Fetal Brain Female	brain
7	chr5:58642200-58653200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr5:58642600-58646800	Weak transcription	Brain Angular Gyrus	brain
9	chr5:58642600-58647000	Weak transcription	Fetal Stomach	stomach
10	chr5:58642600-58652600	Weak transcription	Fetal Brain Male	brain
11	chr5:58642600-58652600	Weak transcription	Small Intestine	intestine
12	chr5:58643200-58646600	Weak transcription	Brain Substantia Nigra	brain
13	chr5:58643200-58646600	Weak transcription	Fetal Lung	lung
14	chr5:58643200-58647000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr5:58643200-58647000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr5:58643600-58652400	Weak transcription	Fetal Kidney	kidney
17	chr5:58643800-58646000	Weak transcription	Brain Hippocampus Middle	brain
18	chr5:58643800-58646000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr5:58644200-58650400	Enhancers	Fetal Heart	heart
20	chr5:58644400-58646600	Weak transcription	Rectal Smooth Muscle	rectum
21	chr5:58644800-58648600	Weak transcription	Hela-S3	cervix
22	chr5:58645000-58646000	Weak transcription	Left Ventricle	heart
23	chr5:58645000-58646600	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr5:58645800-58646000	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr5:58645800-58647600	Enhancers	Colon Smooth Muscle	Colon
26	chr5:58646000-58646200	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr5:58646000-58646400	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr5:58646000-58646800	Enhancers	Right Ventricle	heart
29	chr5:58646000-58647200	Enhancers	Left Ventricle	heart
30	chr5:58646000-58647400	Enhancers	Right Atrium	heart
31	chr5:58646000-58648400	Enhancers	Brain Hippocampus Middle	brain
32	chr5:58646000-58648400	Enhancers	Psoas Muscle	Psoas
33	chr5:58646200-58654400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr5:58646400-58646600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr5:58646600-58646800	Flanking Active TSS	Rectal Smooth Muscle	rectum
36	chr5:58646600-58646800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
37	chr5:58646600-58647000	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr5:58646600-58648000	Enhancers	Fetal Brain Female	brain
39	chr5:58646600-58648000	Enhancers	Fetal Muscle Leg	muscle
40	chr5:58646600-58648000	Enhancers	Ovary	ovary
41	chr5:58646600-58648600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr5:58646600-58649400	Enhancers	Brain Substantia Nigra	brain
43	chr5:58646600-58649400	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr5:58646600-58650000	Enhancers	Fetal Lung	lung
45	chr5:58646800-58647000	Enhancers	Rectal Smooth Muscle	rectum
46	chr5:58646800-58647000	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr5:58646800-58647800	Weak transcription	Right Ventricle	heart
48	chr5:58646800-58648600	Enhancers	Brain Angular Gyrus	brain
49	chr5:58647000-58647200	Flanking Active TSS	Rectal Smooth Muscle	rectum
50	chr5:58647000-58647200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle

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