Variant report

Variant	esv1793388
Chromosome Location	chr5:16159343-16179704
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	CHD1	chr5:16178992-16179348	H1-hESC	embryonic stem cell:	n/a	chr5:16179097-16179107
6	CHD2	chr5:16178920-16179263	H1-hESC	embryonic stem cell:	n/a	chr5:16179097-16179107
7	CREB1	chr5:16160898-16161131	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr5:16160883-16161149	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTBP2	chr5:16178961-16179519	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr5:16160680-16160830	GM12801	blood:	n/a	n/a
11	CTCF	chr5:16160920-16161070	GM12878	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
12	CTCF	chr5:16160900-16161050	GM12866	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
13	CTCF	chr5:16160897-16161155	Hela-S3	cervix:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
14	CTCF	chr5:16160782-16161125	HepG2	liver:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
15	CTCF	chr5:16179020-16179170	HBMEC	blood vessel:	n/a	chr5:16179111-16179124
16	CTCF	chr5:16160940-16161090	GM12864	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
17	CTCF	chr5:16160942-16161131	GM19238	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
18	CTCF	chr5:16160980-16161130	BJ	skin:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
19	CTCF	chr5:16160940-16161090	RPTEC	kidney:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
20	CTCF	chr5:16160980-16161130	GM06990	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
21	CTCF	chr5:16160960-16161110	NHEK	skin:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
22	CTCF	chr5:16160920-16161070	GM12868	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
23	CTCF	chr5:16179258-16179441	LNCaP	prostate:	n/a	n/a
24	CTCF	chr5:16160980-16161130	HUVEC	blood vessel:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
25	CTCF	chr5:16160920-16161070	HAc	cerebellar:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
26	CTCF	chr5:16160783-16161160	H1-hESC	embryonic stem cell:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
27	CTCF	chr5:16160930-16161128	GM19239	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
28	CTCF	chr5:16160804-16161179	K562	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
29	CTCF	chr5:16179243-16179405	MCF-7	breast:	n/a	n/a
30	CTCF	chr5:16160940-16161090	K562	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
31	CTCF	chr5:16160980-16161130	HepG2	liver:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
32	CTCF	chr5:16160940-16161090	HPF	lung:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
33	CTCF	chr5:16160609-16161630	SK-N-SH	brain:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
34	CTCF	chr5:16160920-16161070	HUVEC	blood vessel:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
35	CTCF	chr5:16160937-16161094	SK-N-SH_RA	brain:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
36	CTCF	chr5:16160915-16161143	HepG2	liver:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
37	CTCF	chr5:16160940-16161090	GM12865	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
38	CTCF	chr5:16160960-16161110	BJ	skin:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
39	CTCF	chr5:16160960-16161110	GM12878	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
40	CTCF	chr5:16160893-16161138	GM13977	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
41	CTCF	chr5:16160856-16161177	K562	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
42	CTCF	chr5:16160903-16161147	LNCaP	prostate:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
43	CTCF	chr5:16160960-16161110	GM12874	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
44	CTCF	chr5:16160940-16161090	GM12867	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
45	CTCF	chr5:16179200-16179350	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr5:16160960-16161110	GM12865	blood:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
47	CTCF	chr5:16160980-16161130	NHEK	skin:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
48	CTCF	chr5:16160980-16161130	AG09319	gingival:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
49	CTCF	chr5:16160921-16161077	A549	lung:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035
50	CTCF	chr5:16160960-16161110	AoAF	blood vessel:	n/a	chr5:16161018-16161036 chr5:16161023-16161031 chr5:16161020-16161041 chr5:16161019-16161035

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16179633-16179683	HPAEpiC	pulmonary alveolar:	n/a
2	chr5:16179633-16179683	HPAEpiC	pulmonary alveolar:	n/a
3	chr5:16178784-16178834	AG09309	skin:	n/a
4	chr5:16179660-16179710	A549	lung:	n/a
5	chr5:16178784-16178834	HepG2	liver:	n/a
6	chr5:16179660-16179710	BJ	skin:	n/a
7	chr5:16179633-16179683	Caco-2	colon:	n/a
8	chr5:16175867-16175917	K562	blood:	n/a
9	chr5:16179012-16179062	SK-N-SH	brain:	n/a
10	chr5:16178784-16178834	GM19239	blood:	n/a
11	chr5:16179012-16179062	PANC-1	pancreas:	n/a
12	chr5:16179210-16179260	NB4	blood:	n/a
13	chr5:16179210-16179260	HAEpiC	amniotic membrane:	n/a
14	chr5:16179633-16179683	NH-A	brain:	n/a
15	chr5:16178784-16178834	HRE	kidney:	n/a
16	chr5:16179660-16179710	HAEpiC	amniotic membrane:	n/a
17	chr5:16178784-16178834	HUVEC	blood vessel:	n/a
18	chr5:16179135-16179185	Jurkat	blood:	n/a
19	chr5:16179135-16179185	HCT-116	colon:	n/a
20	chr5:16175867-16175917	PFSK-1	brain:	n/a
21	chr5:16179210-16179260	PFSK-1	brain:	n/a
22	chr5:16179012-16179062	HCM	heart:	n/a
23	chr5:16179633-16179683	HCM	heart:	n/a
24	chr5:16179660-16179710	RPTEC	kidney:	n/a
25	chr5:16178784-16178834	PrEC	prostate:	n/a
26	chr5:16179210-16179260	SK-N-SH	brain:	n/a
27	chr5:16179012-16179062	K562	blood:	n/a
28	chr5:16179012-16179062	HRCEpiC	kidney:	n/a
29	chr5:16175867-16175917	HEK293	kidney:	embryo
30	chr5:16178784-16178834	HCF	heart:	n/a
31	chr5:16179210-16179260	NHDF-neo	bronchial:	n/a
32	chr5:16178784-16178834	NHDF-neo	bronchial:	n/a
33	chr5:16175867-16175917	U87	brain:	n/a
34	chr5:16179660-16179710	HUVEC	blood vessel:	n/a
35	chr5:16179210-16179260	NHBE	bronchial:	n/a
36	chr5:16178784-16178834	HAEpiC	amniotic membrane:	n/a
37	chr5:16179660-16179710	GM19239	blood:	n/a
38	chr5:16179012-16179062	A549	lung:	n/a
39	chr5:16179135-16179185	SAEC	small airway:	n/a
40	chr5:16179633-16179683	HEEpiC	esophagus:	n/a
41	chr5:16179135-16179185	HEEpiC	esophagus:	n/a
42	chr5:16178784-16178834	RPTEC	kidney:	n/a
43	chr5:16179633-16179683	MCF10A-Er-Src	breast:	n/a
44	chr5:16179660-16179710	HCT-116	colon:	n/a
45	chr5:16179660-16179710	PANC-1	pancreas:	n/a
46	chr5:16179633-16179683	HepG2	liver:	n/a
47	chr5:16175867-16175917	PrEC	prostate:	n/a
48	chr5:16179135-16179185	NT2-D1	testis:	n/a
49	chr5:16179012-16179062	AoSMC	blood vessel:	n/a
50	chr5:16179210-16179260	K562	blood:	n/a

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

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: 703 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6880397	chr5:16159343-16159344	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34844382	chr5:16159363-16159364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs398093209	chr5:16159364-16159365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142407709	chr5:16159376-16159377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184176796	chr5:16159381-16159382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534554153	chr5:16159444-16159445	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188772667	chr5:16159467-16159468	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576835151	chr5:16159476-16159477	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192802159	chr5:16159483-16159484	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182077741	chr5:16159502-16159503	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556260619	chr5:16159532-16159533	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574558115	chr5:16159595-16159596	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147900175	chr5:16159616-16159617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35536004	chr5:16159629-16159630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553961337	chr5:16159665-16159666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4608920	chr5:16159683-16159684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2582678	chr5:16159724-16159725	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs187034731	chr5:16159733-16159734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564333717	chr5:16159759-16159760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531339036	chr5:16159767-16159768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543416510	chr5:16159814-16159815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560132425	chr5:16159849-16159850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561784789	chr5:16159856-16159857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141694155	chr5:16159885-16159886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191569436	chr5:16159950-16159951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567092352	chr5:16159982-16159983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527839035	chr5:16160041-16160042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552836991	chr5:16160053-16160054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536943055	chr5:16160065-16160066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10475074	chr5:16160092-16160093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs537864563	chr5:16160121-16160122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184391131	chr5:16160122-16160123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190376760	chr5:16160131-16160132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568092013	chr5:16160185-16160186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35725012	chr5:16160201-16160202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs173176	chr5:16160216-16160217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs553966351	chr5:16160243-16160244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562063927	chr5:16160275-16160276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572217024	chr5:16160384-16160385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61131990	chr5:16160438-16160439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377251417	chr5:16160439-16160440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545634945	chr5:16160442-16160443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376996924	chr5:16160450-16160451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192858417	chr5:16160493-16160494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147676965	chr5:16160554-16160555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561710927	chr5:16160578-16160579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185872030	chr5:16160649-16160650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2402097	chr5:16160686-16160687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539029570	chr5:16160802-16160803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551033648	chr5:16160902-16160903	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:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16158800-16163400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:16159000-16159400	Enhancers	Fetal Heart	heart
3	chr5:16159400-16159600	Genic enhancers	Fetal Heart	heart
4	chr5:16159600-16160800	Weak transcription	Fetal Heart	heart
5	chr5:16160800-16164400	Enhancers	Fetal Heart	heart
6	chr5:16163400-16164200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:16164200-16166000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:16164400-16165200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:16164400-16166800	Weak transcription	Fetal Heart	heart
10	chr5:16165200-16166400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr5:16166000-16166400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:16166400-16166800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:16166800-16167600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:16166800-16168400	Enhancers	Fetal Heart	heart
15	chr5:16167600-16171400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:16168400-16169400	Weak transcription	Fetal Heart	heart
17	chr5:16169400-16174600	Enhancers	Fetal Heart	heart
18	chr5:16171400-16176600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:16174600-16176000	Genic enhancers	Fetal Heart	heart
20	chr5:16175600-16175800	Enhancers	HMEC	breast
21	chr5:16176000-16177000	Enhancers	Fetal Heart	heart
22	chr5:16176600-16177200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:16177000-16177400	Flanking Active TSS	Fetal Heart	heart
24	chr5:16177200-16178400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:16177400-16177800	Enhancers	Fetal Heart	heart
26	chr5:16177800-16178200	Flanking Active TSS	Fetal Heart	heart
27	chr5:16178000-16179400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr5:16178200-16179000	Active TSS	Fetal Heart	heart
29	chr5:16178200-16179200	Active TSS	Brain Angular Gyrus	brain
30	chr5:16178200-16179400	Active TSS	Brain Anterior Caudate	brain
31	chr5:16178400-16179000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
32	chr5:16178400-16179400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:16178400-16179400	Active TSS	Brain Cingulate Gyrus	brain
34	chr5:16178400-16179400	Active TSS	Brain Inferior Temporal Lobe	brain
35	chr5:16178600-16178800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr5:16178600-16178800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
37	chr5:16178600-16178800	Bivalent Enhancer	Fetal Brain Male	brain
38	chr5:16178600-16179000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr5:16178600-16179400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
40	chr5:16178600-16179600	Enhancers	Gastric	stomach
41	chr5:16178600-16180200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr5:16178600-16181000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
43	chr5:16178800-16179000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr5:16178800-16179000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr5:16178800-16179000	Enhancers	H9 Cell Line	embryonic stem cell
46	chr5:16178800-16179000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
47	chr5:16178800-16179000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
48	chr5:16178800-16179000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
49	chr5:16178800-16179000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr5:16178800-16179000	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain

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