Variant report

Variant	nsv830217
Chromosome Location	chr5:16004704-16225229
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:842)
CpG islands
(count:1406)
Chromatin interactive
region (count:29)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:842 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:16187942-16187963	HepG2	liver:	n/a	n/a
2	ATF1	chr5:16078251-16078371	K562	blood:	n/a	n/a
3	ATF1	chr5:16172018-16172145	K562	blood:	n/a	n/a
4	ATF2	chr5:16178853-16179248	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:16134461-16134531	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:16221325-16221582	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr5:16090408-16090698	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr5:16067593-16067849	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:16067544-16067879	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:16067524-16067875	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:16160992-16161105	K562	blood:	n/a	n/a
12	BHLHE40	chr5:16067488-16068063	GM12878	blood:	n/a	n/a
13	BRCA1	chr5:16208066-16208104	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr5:16118562-16118564	GM12878	blood:	n/a	n/a
15	CBX3	chr5:16178898-16179206	K562	blood:	n/a	n/a
16	CEBPB	chr5:16017858-16018183	HepG2	liver:	n/a	chr5:16018017-16018028
17	CEBPB	chr5:16140782-16140887	K562	blood:	n/a	chr5:16140833-16140844
18	CEBPB	chr5:16140717-16140949	IMR90	lung:	n/a	chr5:16140833-16140844
19	CEBPB	chr5:16017853-16018196	IMR90	lung:	n/a	chr5:16018017-16018028
20	CEBPB	chr5:16124683-16124734	HepG2	liver:	n/a	chr5:16124714-16124725
21	CEBPB	chr5:16090639-16090849	IMR90	lung:	n/a	chr5:16090755-16090764 chr5:16090755-16090766 chr5:16090753-16090764
22	CEBPB	chr5:16021667-16021751	H1-hESC	embryonic stem cell:	n/a	chr5:16021704-16021715 chr5:16021702-16021713 chr5:16021704-16021713
23	CEBPB	chr5:16079604-16079786	HepG2	liver:	n/a	chr5:16079658-16079669
24	CEBPB	chr5:16124051-16124228	HepG2	liver:	n/a	chr5:16124110-16124121
25	CEBPB	chr5:16021589-16021859	A549	lung:	n/a	chr5:16021704-16021715 chr5:16021702-16021713 chr5:16021704-16021713
26	CEBPB	chr5:16090602-16090895	HepG2	liver:	n/a	chr5:16090755-16090764 chr5:16090755-16090766 chr5:16090753-16090764
27	CEBPB	chr5:16021527-16021865	IMR90	lung:	n/a	chr5:16021704-16021715 chr5:16021702-16021713 chr5:16021704-16021713
28	CEBPB	chr5:16090522-16090823	K562	blood:	n/a	chr5:16090755-16090764 chr5:16090755-16090766 chr5:16090753-16090764
29	CEBPB	chr5:16152640-16152641	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:16197748-16197902	HepG2	liver:	n/a	chr5:16197853-16197864
31	CEBPB	chr5:16158619-16158913	IMR90	lung:	n/a	chr5:16158763-16158774
32	CEBPB	chr5:16090700-16090704	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:16017886-16018126	Hela-S3	cervix:	n/a	chr5:16018017-16018028
34	CEBPB	chr5:16158666-16158909	K562	blood:	n/a	chr5:16158763-16158774
35	CEBPB	chr5:16140751-16140975	HepG2	liver:	n/a	chr5:16140833-16140844
36	CEBPB	chr5:16086466-16086494	A549	lung:	n/a	n/a
37	CEBPB	chr5:16186943-16187161	HepG2	liver:	n/a	chr5:16187059-16187070
38	CEBPB	chr5:16158641-16158925	HepG2	liver:	n/a	chr5:16158763-16158774
39	CEBPB	chr5:16021529-16021878	HepG2	liver:	n/a	chr5:16021704-16021715 chr5:16021702-16021713 chr5:16021704-16021713
40	CEBPB	chr5:16158661-16158803	A549	lung:	n/a	chr5:16158763-16158774
41	CEBPB	chr5:16219317-16219504	HepG2	liver:	n/a	chr5:16219411-16219422
42	CEBPB	chr5:16017882-16018169	A549	lung:	n/a	chr5:16018017-16018028
43	CEBPB	chr5:16090579-16090758	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr5:16017923-16018188	K562	blood:	n/a	chr5:16018017-16018028
45	CHD1	chr5:16178992-16179348	H1-hESC	embryonic stem cell:	n/a	chr5:16179097-16179107
46	CHD2	chr5:16066472-16066757	GM12878	blood:	n/a	n/a
47	CHD2	chr5:16178920-16179263	H1-hESC	embryonic stem cell:	n/a	chr5:16179097-16179107
48	CHD2	chr5:16067476-16067959	GM12878	blood:	n/a	n/a
49	CREB1	chr5:16160898-16161131	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr5:16160883-16161149	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16180076-16180126	ECC-1	luminal epithelium:	n/a
2	chr5:16181039-16181089	AoSMC	blood vessel:	n/a
3	chr5:16178784-16178834	NT2-D1	testis:	n/a
4	chr5:16180076-16180126	ECC-1	luminal epithelium:	n/a
5	chr5:16181039-16181089	AoSMC	blood vessel:	n/a
6	chr5:16178784-16178834	NT2-D1	testis:	n/a
7	chr5:16180076-16180126	PrEC	prostate:	n/a
8	chr5:16180048-16180098	BJ	skin:	n/a
9	chr5:16179660-16179710	GM12891	blood:	n/a
10	chr5:16179660-16179710	RPTEC	kidney:	n/a
11	chr5:16180315-16180365	BJ	skin:	n/a
12	chr5:16180068-16180118	LNCaP	prostate:	n/a
13	chr5:16179012-16179062	HEK293	kidney:	embryo
14	chr5:16180048-16180098	HL-60	blood:	n/a
15	chr5:16179012-16179062	A549	lung:	n/a
16	chr5:16180055-16180105	AG09319	gingival:	n/a
17	chr5:16180068-16180118	SK-N-SH	brain:	n/a
18	chr5:16180062-16180112	HEEpiC	esophagus:	n/a
19	chr5:16180419-16180469	NB4	blood:	n/a
20	chr5:16179660-16179710	GM19239	blood:	n/a
21	chr5:16180055-16180105	HEEpiC	esophagus:	n/a
22	chr5:16180419-16180469	Hepatocyte	liver:	n/a
23	chr5:16180072-16180122	SKMC	muscle:	n/a
24	chr5:16179012-16179062	MCF-7	breast:	n/a
25	chr5:16178784-16178834	HIPEpiC	eye:	n/a
26	chr5:16180315-16180365	GM06990	blood:	n/a
27	chr5:16181039-16181089	HCM	heart:	n/a
28	chr5:16179633-16179683	CMK	blood:	n/a
29	chr5:16180068-16180118	PrEC	prostate:	n/a
30	chr5:16180062-16180112	NHDF-neo	bronchial:	n/a
31	chr5:16179210-16179260	GM12891	blood:	n/a
32	chr5:16180072-16180122	GM12891	blood:	n/a
33	chr5:16180072-16180122	HUVEC	blood vessel:	n/a
34	chr5:16179210-16179260	HUVEC	blood vessel:	n/a
35	chr5:16182882-16182932	ECC-1	luminal epithelium:	n/a
36	chr5:16180055-16180105	HepG2	liver:	n/a
37	chr5:16178784-16178834	SK-N-SH	brain:	n/a
38	chr5:16180033-16180083	Jurkat	blood:	n/a
39	chr5:16179012-16179062	U87	brain:	n/a
40	chr5:16180393-16180443	AG09309	skin:	n/a
41	chr5:16180055-16180105	PFSK-1	brain:	n/a
42	chr5:16180033-16180083	ProgFib	skin:	n/a
43	chr5:16179012-16179062	NHDF-neo	bronchial:	n/a
44	chr5:16180033-16180083	Hepatocyte	liver:	n/a
45	chr5:16180072-16180122	SAEC	small airway:	n/a
46	chr5:16179873-16179923	AG09309	skin:	n/a
47	chr5:16180259-16180309	GM12891	blood:	n/a
48	chr5:16179210-16179260	ECC-1	luminal epithelium:	n/a
49	chr5:16180068-16180118	HEEpiC	esophagus:	n/a
50	chr5:16180076-16180126	NT2-D1	testis:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:16184562..16186282-chr5:16187209..16189140,2	K562	blood:
2	chr5:16129063..16131920-chr5:16133489..16135923,2	K562	blood:
3	chr5:16224922..16226598-chr5:16244028..16246781,2	K562	blood:
4	chr5:16001947..16004680-chr5:16004715..16007542,2	K562	blood:
5	chr5:16160527..16161482-chr5:16456070..16456876,5	MCF-7	breast:
6	chr5:16067708..16069576-chr5:16071311..16074069,2	MCF-7	breast:
7	chr5:16168738..16170646-chr5:16177300..16179499,2	MCF-7	breast:
8	chr5:16090699..16092377-chr5:16094611..16097490,2	K562	blood:
9	chr5:16160155..16161946-chr5:16453809..16456643,2	K562	blood:
10	chr5:16184562..16186282-chr5:16187209..16189140,2	K562	blood:
11	chr5:16083769..16085725-chr5:16085859..16088630,2	MCF-7	breast:
12	chr5:16090699..16092377-chr5:16094611..16097490,2	K562	blood:
13	chr5:16187691..16190038-chr5:16191837..16194176,2	MCF-7	breast:
14	chr12:93336335..93337122-chr5:16068355..16069020,2	MCF-7	breast:
15	chr5:16067708..16069576-chr5:16071311..16074069,2	MCF-7	breast:
16	chr5:16056969..16059021-chr5:16061126..16062953,2	MCF-7	breast:
17	chr5:16075594..16077567-chr5:16078597..16080753,2	MCF-7	breast:
18	chr5:16083769..16085725-chr5:16085859..16088630,2	MCF-7	breast:
19	chr5:16126552..16128505-chr5:16129062..16130884,2	MCF-7	breast:
20	chr5:16049675..16052943-chr5:16053892..16056326,3	K562	blood:
21	chr5:16178511..16180394-chr5:16183166..16185235,2	K562	blood:
22	chr5:16036693..16039245-chr5:16041131..16043734,2	K562	blood:
23	chr5:16049675..16052943-chr5:16053892..16056326,3	K562	blood:
24	chr5:16177598..16179739-chr5:16465554..16467569,2	MCF-7	breast:
25	chr5:16160550..16161095-chr5:16456058..16456643,2	MCF-7	breast:
26	chr5:16036693..16039245-chr5:16041131..16043734,2	K562	blood:
27	chr5:16056969..16059021-chr5:16061126..16062953,2	MCF-7	breast:
28	chr5:16075594..16077567-chr5:16078597..16080753,2	MCF-7	breast:
29	chr5:15898065..15900379-chr5:16172599..16174745,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARCH11-3	chr5:16192197-16192818	NONHSAT100595
2	lnc-FBXL7-2	chr5:16180347-16180549	ENSG00000250448
3	lnc-FBXL7-2	chr5:16183832-16185694	ENSG00000250448

No data

Variant related genes	Relation type
NACAP6	TF binding region
RNA5SP178	TF binding region
ENSG00000250981	TF binding region
MARCH11	TF binding region
ENSG00000250448	TF binding region
NACAP6	CpG island
RNA5SP178	CpG island
ENSG00000250981	CpG island
MARCH11	CpG island
ENSG00000250448	CpG island
ENSG00000173545	chromatin interactions
ENSG00000183654	chromatin interactions
ENSG00000248403	chromatin interactions
ENSG00000250981	chromatin interactions
ENSG00000250448	chromatin interactions
PTEN	miRNA target sites
CRKL	miRNA target sites

Extended variants
information (count: 7309 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:7309 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144360529	chr5:16004721-16004722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576135695	chr5:16004740-16004741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549879446	chr5:16004745-16004746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547574308	chr5:16004757-16004758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs367914402	chr5:16004777-16004778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574951748	chr5:16004787-16004788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147825784	chr5:16004788-16004789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371832733	chr5:16004795-16004796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs32827	chr5:16004804-16004805	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs527674574	chr5:16004845-16004846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs193024609	chr5:16004852-16004853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564324946	chr5:16004918-16004919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114829961	chr5:16004932-16004933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550021964	chr5:16004943-16004944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568219478	chr5:16004984-16004985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183407635	chr5:16005078-16005079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187952298	chr5:16005102-16005103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565678677	chr5:16005130-16005131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192415968	chr5:16005133-16005134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183750311	chr5:16005146-16005147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575960381	chr5:16005148-16005149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537117284	chr5:16005155-16005156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555196801	chr5:16005194-16005195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373374226	chr5:16005209-16005210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188020924	chr5:16005221-16005222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192749205	chr5:16005250-16005251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566545204	chr5:16005266-16005267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112947443	chr5:16005332-16005333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546527671	chr5:16005384-16005385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372974695	chr5:16005447-16005448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564471336	chr5:16005458-16005459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531629942	chr5:16005472-16005473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76348393	chr5:16005486-16005487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562075420	chr5:16005526-16005527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529046335	chr5:16005534-16005535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547237012	chr5:16005563-16005564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375235708	chr5:16005635-16005636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565543607	chr5:16005704-16005705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533019063	chr5:16005722-16005723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs551404875	chr5:16005731-16005732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141217384	chr5:16005745-16005746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113707202	chr5:16005754-16005755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184697115	chr5:16005777-16005778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534346810	chr5:16005783-16005784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146965413	chr5:16005785-16005786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547324469	chr5:16005806-16005807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567120756	chr5:16005809-16005810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567414283	chr5:16005835-16005836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534708832	chr5:16005836-16005837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189531444	chr5:16005851-16005852	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	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
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16004200-16005400	Enhancers	Fetal Kidney	kidney
2	chr5:16005200-16006000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr5:16005200-16007400	Enhancers	Fetal Heart	heart
4	chr5:16006000-16006400	Enhancers	Left Ventricle	heart
5	chr5:16006400-16007800	Weak transcription	Left Ventricle	heart
6	chr5:16007400-16008200	Flanking Active TSS	Fetal Heart	heart
7	chr5:16007800-16008200	Enhancers	Left Ventricle	heart
8	chr5:16008200-16008600	Enhancers	Fetal Heart	heart
9	chr5:16008600-16009000	Flanking Active TSS	Fetal Heart	heart
10	chr5:16009000-16009200	Enhancers	Fetal Heart	heart
11	chr5:16009200-16009600	Weak transcription	Fetal Heart	heart
12	chr5:16009600-16010200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:16009600-16010400	ZNF genes & repeats	Fetal Heart	heart
14	chr5:16010400-16011400	Active TSS	Fetal Heart	heart
15	chr5:16011400-16013000	Weak transcription	Fetal Heart	heart
16	chr5:16012400-16012800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:16012800-16013200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:16013000-16013800	Enhancers	Fetal Heart	heart
19	chr5:16013200-16014400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:16013800-16020400	Weak transcription	Fetal Heart	heart
21	chr5:16014000-16014600	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr5:16014400-16014600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:16014600-16015600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:16019000-16019400	Enhancers	Dnd41	blood
25	chr5:16020400-16020800	Enhancers	Fetal Heart	heart
26	chr5:16020800-16021800	Weak transcription	Fetal Heart	heart
27	chr5:16021400-16022000	Enhancers	Adipose Nuclei	Adipose
28	chr5:16021800-16022400	Enhancers	Fetal Heart	heart
29	chr5:16022000-16025800	Weak transcription	Adipose Nuclei	Adipose
30	chr5:16022400-16025400	Weak transcription	Fetal Heart	heart
31	chr5:16025400-16026800	Enhancers	Fetal Heart	heart
32	chr5:16025600-16026600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:16025800-16026200	Enhancers	Adipose Nuclei	Adipose
34	chr5:16026000-16026600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr5:16026800-16033600	Weak transcription	Fetal Heart	heart
36	chr5:16033400-16035600	Enhancers	Adipose Nuclei	Adipose
37	chr5:16033600-16033800	Enhancers	Fetal Heart	heart
38	chr5:16033800-16034200	Enhancers	Brain Germinal Matrix	brain
39	chr5:16033800-16034200	Weak transcription	Fetal Heart	heart
40	chr5:16034000-16035200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr5:16034200-16035200	Enhancers	Fetal Heart	heart
42	chr5:16034200-16035400	Enhancers	Fetal Lung	lung
43	chr5:16035200-16038800	Weak transcription	Fetal Heart	heart
44	chr5:16036800-16039800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr5:16038800-16039400	Enhancers	Fetal Heart	heart
46	chr5:16039400-16044000	Weak transcription	Fetal Heart	heart
47	chr5:16039800-16041600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr5:16041600-16043800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr5:16043800-16047800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr5:16044000-16044800	Enhancers	Fetal Heart	heart

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