Variant report

Variant	esv1848638
Chromosome Location	chr5:16150721-16180167
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	chr5:16172018-16172145	K562	blood:	n/a	n/a
2	ATF2	chr5:16178853-16179248	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr5:16160992-16161105	K562	blood:	n/a	n/a
4	CBX3	chr5:16178898-16179206	K562	blood:	n/a	n/a
5	CEBPB	chr5:16158619-16158913	IMR90	lung:	n/a	chr5:16158763-16158774
6	CEBPB	chr5:16152640-16152641	HepG2	liver:	n/a	n/a
7	CEBPB	chr5:16158661-16158803	A549	lung:	n/a	chr5:16158763-16158774
8	CEBPB	chr5:16158641-16158925	HepG2	liver:	n/a	chr5:16158763-16158774
9	CEBPB	chr5:16158666-16158909	K562	blood:	n/a	chr5:16158763-16158774
10	CHD1	chr5:16178992-16179348	H1-hESC	embryonic stem cell:	n/a	chr5:16179097-16179107
11	CHD2	chr5:16178920-16179263	H1-hESC	embryonic stem cell:	n/a	chr5:16179097-16179107
12	CREB1	chr5:16160883-16161149	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr5:16160898-16161131	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr5:16178961-16179519	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr5:16161020-16161170	WI-38	lung:	n/a	chr5:16161023-16161031 chr5:16161020-16161041
16	CTCF	chr5:16160960-16161110	HA-sp	spinal cord:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
17	CTCF	chr5:16179016-16179460	MCF-7	breast:	n/a	chr5:16179111-16179124
18	CTCF	chr5:16160856-16161177	K562	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
19	CTCF	chr5:16160960-16161110	HepG2	liver:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
20	CTCF	chr5:16160903-16161147	LNCaP	prostate:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
21	CTCF	chr5:16160940-16161090	HPF	lung:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
22	CTCF	chr5:16160980-16161130	BE2_C	brain:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
23	CTCF	chr5:16160920-16161147	A549	lung:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
24	CTCF	chr5:16160960-16161110	BJ	skin:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
25	CTCF	chr5:16160960-16161110	AoAF	blood vessel:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
26	CTCF	chr5:16179240-16179390	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr5:16160980-16161130	GM06990	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
28	CTCF	chr5:16179010-16179444	MCF-7	breast:	n/a	chr5:16179111-16179124
29	CTCF	chr5:16160920-16161070	HBMEC	blood vessel:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
30	CTCF	chr5:16160940-16161090	HCT-116	colon:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
31	CTCF	chr5:16179047-16179173	MCF-7	breast:	n/a	chr5:16179111-16179124
32	CTCF	chr5:16160960-16161110	HPAF	blood vessel:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
33	CTCF	chr5:16160940-16161090	HVMF	connective:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
34	CTCF	chr5:16160960-16161110	Hela-S3	cervix:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
35	CTCF	chr5:16160940-16161090	MCF-7	breast:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
36	CTCF	chr5:16160769-16161173	MCF-7	breast:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
37	CTCF	chr5:16179200-16179350	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr5:16160980-16161130	GM12864	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
39	CTCF	chr5:16160820-16160970	HCM	heart:	n/a	n/a
40	CTCF	chr5:16160905-16161141	GM10248	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
41	CTCF	chr5:16179280-16179430	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:16160916-16161145	Fibrobl	skin:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
43	CTCF	chr5:16160912-16161149	SK-N-SH_RA	brain:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
44	CTCF	chr5:16179258-16179441	LNCaP	prostate:	n/a	n/a
45	CTCF	chr5:16160911-16161146	NHEK	skin:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
46	CTCF	chr5:16160899-16161120	GM20000	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
47	CTCF	chr5:16179020-16179170	HBMEC	blood vessel:	n/a	chr5:16179111-16179124
48	CTCF	chr5:16160960-16161110	GM12873	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
49	CTCF	chr5:16160840-16160990	HCT-116	colon:	n/a	n/a
50	CTCF	chr5:16160900-16161050	HFF-Myc	foreskin:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16179135-16179185	HCF	heart:	n/a
2	chr5:16179135-16179185	HCF	heart:	n/a
3	chr5:16179660-16179710	HCT-116	colon:	n/a
4	chr5:16180048-16180098	T-47D	breast:	n/a
5	chr5:16179873-16179923	AG04450	lung:	fetal
6	chr5:16179660-16179710	AG04450	lung:	fetal
7	chr5:16180055-16180105	HEEpiC	esophagus:	n/a
8	chr5:16179660-16179710	LNCaP	prostate:	n/a
9	chr5:16175867-16175917	A549	lung:	n/a
10	chr5:16175867-16175917	ProgFib	skin:	n/a
11	chr5:16180062-16180112	PANC-1	pancreas:	n/a
12	chr5:16175867-16175917	SK-N-MC	brain:	n/a
13	chr5:16180048-16180098	GM19239	blood:	n/a
14	chr5:16179210-16179260	HNPCEpiC	eye:	n/a
15	chr5:16180076-16180126	HCPEpiC	choroid plexus:	n/a
16	chr5:16179012-16179062	Caco-2	colon:	n/a
17	chr5:16179633-16179683	PANC-1	pancreas:	n/a
18	chr5:16180076-16180126	HRCEpiC	kidney:	n/a
19	chr5:16180033-16180083	ProgFib	skin:	n/a
20	chr5:16180033-16180083	HCM	heart:	n/a
21	chr5:16179660-16179710	HCF	heart:	n/a
22	chr5:16175867-16175917	T-47D	breast:	n/a
23	chr5:16179210-16179260	SK-N-SH	brain:	n/a
24	chr5:16180062-16180112	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:16180068-16180118	HRCEpiC	kidney:	n/a
26	chr5:16180033-16180083	AoSMC	blood vessel:	n/a
27	chr5:16180076-16180126	ProgFib	skin:	n/a
28	chr5:16180076-16180126	SAEC	small airway:	n/a
29	chr5:16179660-16179710	PrEC	prostate:	n/a
30	chr5:16175867-16175917	H1-hESC	embryonic stem cell:	embryo
31	chr5:16179873-16179923	HCT-116	colon:	n/a
32	chr5:16175867-16175917	LNCaP	prostate:	n/a
33	chr5:16175867-16175917	AoSMC	blood vessel:	n/a
34	chr5:16180033-16180083	RPTEC	kidney:	n/a
35	chr5:16180048-16180098	SK-N-SH	brain:	n/a
36	chr5:16179012-16179062	HMEC	breast:	n/a
37	chr5:16180068-16180118	AG09309	skin:	n/a
38	chr5:16179012-16179062	HCT-116	colon:	n/a
39	chr5:16180055-16180105	HUVEC	blood vessel:	n/a
40	chr5:16180068-16180118	HCF	heart:	n/a
41	chr5:16180076-16180126	AoSMC	blood vessel:	n/a
42	chr5:16179873-16179923	Caco-2	colon:	n/a
43	chr5:16180072-16180122	LNCaP	prostate:	n/a
44	chr5:16179873-16179923	NHDF-neo	bronchial:	n/a
45	chr5:16180062-16180112	ECC-1	luminal epithelium:	n/a
46	chr5:16179873-16179923	ovcar-3	ovarian:	n/a
47	chr5:16179135-16179185	BE2_C	brain:	n/a
48	chr5:16180068-16180118	BJ	skin:	n/a
49	chr5:16180055-16180105	SAEC	small airway:	n/a
50	chr5:16180076-16180126	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:16160155..16161946-chr5:16453809..16456643,2	K562	blood:
2	chr5:16160527..16161482-chr5:16456070..16456876,5	MCF-7	breast:
3	chr5:15898065..15900379-chr5:16172599..16174745,2	K562	blood:
4	chr5:16160550..16161095-chr5:16456058..16456643,2	MCF-7	breast:
5	chr5:16168738..16170646-chr5:16177300..16179499,2	MCF-7	breast:
6	chr5:16177598..16179739-chr5:16465554..16467569,2	MCF-7	breast:

Variant related genes	Relation type
MARCH11	TF binding region
ENSG00000250448	TF binding region
MARCH11	CpG island
ENSG00000250448	CpG island
ENSG00000183654	chromatin interactions
ENSG00000173545	chromatin interactions

Extended variants
information (count: 1023 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1023 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2591983	chr5:16150721-16150722	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs2591984	chr5:16150723-16150724	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs146955047	chr5:16150775-16150776	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551030144	chr5:16150905-16150906	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569001633	chr5:16150939-16150940	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536026742	chr5:16150991-16150992	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs3910978	chr5:16151004-16151005	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559224849	chr5:16151017-16151018	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577266709	chr5:16151021-16151022	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs76836761	chr5:16151081-16151082	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559808924	chr5:16151089-16151090	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558232634	chr5:16151159-16151160	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576756370	chr5:16151160-16151161	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188418908	chr5:16151164-16151165	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556220610	chr5:16151237-16151238	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs146885845	chr5:16151301-16151302	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs79830066	chr5:16151348-16151349	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs555308094	chr5:16151373-16151374	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs145808380	chr5:16151375-16151376	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs540648994	chr5:16151392-16151393	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs11955448	chr5:16151496-16151497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565161475	chr5:16151603-16151604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75290131	chr5:16151614-16151615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111683651	chr5:16151668-16151669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145242773	chr5:16151693-16151694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371044597	chr5:16151709-16151710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs180780847	chr5:16151725-16151726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148381429	chr5:16151730-16151731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529842405	chr5:16151742-16151743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184958307	chr5:16151745-16151746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189800110	chr5:16151748-16151749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113095621	chr5:16151759-16151760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs70938045	chr5:16151798-16151799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs58891017	chr5:16151801-16151802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552547940	chr5:16151848-16151849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9312907	chr5:16151881-16151882	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552427547	chr5:16151897-16151898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7726990	chr5:16151976-16151977	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs112407988	chr5:16151992-16151993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs66468106	chr5:16151993-16151994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181747265	chr5:16152036-16152037	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs555994712	chr5:16152089-16152090	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs370066922	chr5:16152136-16152137	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs530126391	chr5:16152162-16152163	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs1561637	chr5:16152168-16152169	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs567161927	chr5:16152201-16152202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531589110	chr5:16152280-16152281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs367871075	chr5:16152317-16152318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368353463	chr5:16152372-16152373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149177621	chr5:16152382-16152383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16149600-16151200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:16150200-16153200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:16150600-16151200	Enhancers	Fetal Heart	heart
4	chr5:16151200-16151400	Flanking Active TSS	Fetal Heart	heart
5	chr5:16151200-16154000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:16151400-16152000	Enhancers	Fetal Heart	heart
7	chr5:16152000-16152200	Flanking Active TSS	Fetal Heart	heart
8	chr5:16152200-16152400	Enhancers	Fetal Heart	heart
9	chr5:16152400-16152600	Flanking Active TSS	Fetal Heart	heart
10	chr5:16152600-16153200	Enhancers	Fetal Heart	heart
11	chr5:16153000-16153400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr5:16153200-16153600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:16153200-16153600	Flanking Active TSS	Fetal Heart	heart
14	chr5:16153200-16153600	Enhancers	Placenta	Placenta
15	chr5:16153600-16156800	Enhancers	Fetal Heart	heart
16	chr5:16154000-16154800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:16154800-16157600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:16155800-16156800	Enhancers	Fetal Lung	lung
19	chr5:16156800-16157000	Flanking Active TSS	Fetal Heart	heart
20	chr5:16157000-16157600	Enhancers	Fetal Heart	heart
21	chr5:16157600-16158600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:16157600-16158600	Active TSS	Fetal Heart	heart
23	chr5:16158600-16158800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:16158600-16159000	Weak transcription	Fetal Heart	heart
25	chr5:16158800-16163400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:16159000-16159400	Enhancers	Fetal Heart	heart
27	chr5:16159400-16159600	Genic enhancers	Fetal Heart	heart
28	chr5:16159600-16160800	Weak transcription	Fetal Heart	heart
29	chr5:16160800-16164400	Enhancers	Fetal Heart	heart
30	chr5:16163400-16164200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:16164200-16166000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:16164400-16165200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr5:16164400-16166800	Weak transcription	Fetal Heart	heart
34	chr5:16165200-16166400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr5:16166000-16166400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr5:16166400-16166800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:16166800-16167600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:16166800-16168400	Enhancers	Fetal Heart	heart
39	chr5:16167600-16171400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:16168400-16169400	Weak transcription	Fetal Heart	heart
41	chr5:16169400-16174600	Enhancers	Fetal Heart	heart
42	chr5:16171400-16176600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:16174600-16176000	Genic enhancers	Fetal Heart	heart
44	chr5:16175600-16175800	Enhancers	HMEC	breast
45	chr5:16176000-16177000	Enhancers	Fetal Heart	heart
46	chr5:16176600-16177200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:16177000-16177400	Flanking Active TSS	Fetal Heart	heart
48	chr5:16177200-16178400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:16177400-16177800	Enhancers	Fetal Heart	heart
50	chr5:16177800-16178200	Flanking Active TSS	Fetal Heart	heart

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