Variant report

Variant	nsv4736
Chromosome Location	chr5:16393955-16439055
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:351)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:16418417-16419114	K562	blood:	n/a	n/a
2	ARID3A	chr5:16430911-16431092	K562	blood:	n/a	n/a
3	ATF1	chr5:16418451-16419026	K562	blood:	n/a	n/a
4	BACH1	chr5:16432552-16432560	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr5:16418500-16419100	K562	blood:	n/a	n/a
6	BHLHE40	chr5:16418484-16419156	K562	blood:	n/a	n/a
7	CBX3	chr5:16418499-16418874	K562	blood:	n/a	n/a
8	CBX3	chr5:16418402-16419100	K562	blood:	n/a	n/a
9	CCNT2	chr5:16418527-16419263	K562	blood:	n/a	n/a
10	CEBPB	chr5:16406041-16406414	Hela-S3	cervix:	n/a	chr5:16406181-16406192 chr5:16406183-16406194
11	CEBPB	chr5:16419933-16420058	K562	blood:	n/a	n/a
12	CEBPB	chr5:16423358-16423483	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr5:16409891-16409913	K562	blood:	n/a	n/a
14	CEBPB	chr5:16406925-16407033	K562	blood:	n/a	chr5:16406987-16406998
15	CEBPB	chr5:16423214-16423560	HepG2	liver:	n/a	n/a
16	CEBPB	chr5:16406051-16406389	H1-hESC	embryonic stem cell:	n/a	chr5:16406181-16406192 chr5:16406183-16406194
17	CEBPB	chr5:16406048-16406368	HepG2	liver:	n/a	chr5:16406181-16406192 chr5:16406183-16406194
18	CEBPB	chr5:16435715-16435789	Hela-S3	cervix:	n/a	chr5:16435773-16435784
19	CEBPB	chr5:16409893-16410144	HepG2	liver:	n/a	chr5:16409985-16409996
20	CEBPB	chr5:16418523-16419085	K562	blood:	n/a	n/a
21	CEBPB	chr5:16423319-16423473	MCF-7	breast:	n/a	n/a
22	CEBPB	chr5:16406024-16406388	MCF-7	breast:	n/a	chr5:16406181-16406192 chr5:16406183-16406194
23	CEBPB	chr5:16423241-16423555	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:16423191-16423582	K562	blood:	n/a	n/a
25	CEBPB	chr5:16410305-16410826	MCF-7	breast:	n/a	chr5:16410519-16410532
26	CEBPB	chr5:16394158-16394358	K562	blood:	n/a	chr5:16394176-16394188 chr5:16394229-16394240
27	CEBPB	chr5:16423309-16423506	K562	blood:	n/a	n/a
28	CEBPB	chr5:16423228-16423501	A549	lung:	n/a	n/a
29	CEBPB	chr5:16394210-16394334	HepG2	liver:	n/a	chr5:16394229-16394240
30	CEBPB	chr5:16406041-16406368	A549	lung:	n/a	chr5:16406181-16406192 chr5:16406183-16406194
31	CEBPB	chr5:16410423-16410705	HepG2	liver:	n/a	chr5:16410519-16410532
32	CEBPB	chr5:16406027-16406362	K562	blood:	n/a	chr5:16406181-16406192 chr5:16406183-16406194
33	CEBPB	chr5:16435699-16435869	HepG2	liver:	n/a	chr5:16435773-16435784
34	CEBPB	chr5:16435634-16435931	K562	blood:	n/a	chr5:16435773-16435784
35	CEBPB	chr5:16423231-16423523	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr5:16423213-16423492	K562	blood:	n/a	n/a
37	CEBPB	chr5:16406032-16406430	MCF-7	breast:	n/a	chr5:16406181-16406192 chr5:16406183-16406194
38	CEBPB	chr5:16409885-16410132	A549	lung:	n/a	chr5:16409985-16409996
39	CEBPD	chr5:16418407-16419206	K562	blood:	n/a	n/a
40	CEBPD	chr5:16418398-16419205	K562	blood:	n/a	n/a
41	CHD2	chr5:16418600-16418845	K562	blood:	n/a	n/a
42	CHD2	chr5:16430462-16430463	K562	blood:	n/a	n/a
43	CREB1	chr5:16418456-16419069	K562	blood:	n/a	n/a
44	CREB1	chr5:16418399-16419244	K562	blood:	n/a	n/a
45	CTCF	chr5:16428680-16428830	HCM	heart:	n/a	n/a
46	CTCF	chr5:16438200-16438350	HRE	kidney:	n/a	n/a
47	CTCF	chr5:16428520-16428670	GM12873	blood:	n/a	n/a
48	CTCF	chr5:16438260-16438470	HRE	kidney:	n/a	n/a
49	CTCF	chr5:16438220-16438370	AG04449	skin:	n/a	n/a
50	CTCF	chr5:16438220-16438370	BE2_C	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16436375-16436425	HCT-116	colon:	n/a
2	chr5:16431777-16431827	ProgFib	skin:	n/a
3	chr5:16431777-16431827	HCF	heart:	n/a
4	chr5:16431777-16431827	Caco-2	colon:	n/a
5	chr5:16436375-16436425	ECC-1	luminal epithelium:	n/a
6	chr5:16436375-16436425	CMK	blood:	n/a
7	chr5:16431777-16431827	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:16436375-16436425	Hepatocyte	liver:	n/a
9	chr5:16436375-16436425	Hela-S3	cervix:	n/a
10	chr5:16436375-16436425	HCF	heart:	n/a
11	chr5:16431777-16431827	ECC-1	luminal epithelium:	n/a
12	chr5:16431777-16431827	PANC-1	pancreas:	n/a
13	chr5:16431777-16431827	AG09319	gingival:	n/a
14	chr5:16431777-16431827	GM19239	blood:	n/a
15	chr5:16436375-16436425	RPTEC	kidney:	n/a
16	chr5:16436375-16436425	HMEC	breast:	n/a
17	chr5:16431777-16431827	NT2-D1	testis:	n/a
18	chr5:16431777-16431827	GM12891	blood:	n/a
19	chr5:16436375-16436425	GM12892	blood:	n/a
20	chr5:16431777-16431827	HRPEpiC	eye:	n/a
21	chr5:16436375-16436425	H1-hESC	embryonic stem cell:	embryo
22	chr5:16436375-16436425	GM12878	blood:	n/a
23	chr5:16436375-16436425	HAEpiC	amniotic membrane:	n/a
24	chr5:16436375-16436425	HEEpiC	esophagus:	n/a
25	chr5:16436375-16436425	NB4	blood:	n/a
26	chr5:16431777-16431827	GM12892	blood:	n/a
27	chr5:16436375-16436425	SK-N-SH_RA	brain:	n/a
28	chr5:16431777-16431827	HUVEC	blood vessel:	n/a
29	chr5:16431777-16431827	RPTEC	kidney:	n/a
30	chr5:16431777-16431827	AG04449	skin:	fetal
31	chr5:16431777-16431827	SK-N-MC	brain:	n/a
32	chr5:16436375-16436425	ovcar-3	ovarian:	n/a
33	chr5:16431777-16431827	T-47D	breast:	n/a
34	chr5:16431777-16431827	NHBE	bronchial:	n/a
35	chr5:16436375-16436425	AG09309	skin:	n/a
36	chr5:16436375-16436425	Caco-2	colon:	n/a
37	chr5:16436375-16436425	MCF-7	breast:	n/a
38	chr5:16436375-16436425	AG04449	skin:	fetal
39	chr5:16436375-16436425	HL-60	blood:	n/a
40	chr5:16436375-16436425	Jurkat	blood:	n/a
41	chr5:16431777-16431827	NH-A	brain:	n/a
42	chr5:16436375-16436425	HepG2	liver:	n/a
43	chr5:16436375-16436425	PrEC	prostate:	n/a
44	chr5:16431777-16431827	SK-N-SH	brain:	n/a
45	chr5:16431777-16431827	NB4	blood:	n/a
46	chr5:16436375-16436425	NH-A	brain:	n/a
47	chr5:16431777-16431827	Jurkat	blood:	n/a
48	chr5:16431777-16431827	Hela-S3	cervix:	n/a
49	chr5:16436375-16436425	PANC-1	pancreas:	n/a
50	chr5:16431777-16431827	Hepatocyte	liver:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:16416919..16420001-chr5:16462576..16465755,4	K562	blood:
2	chr5:16431085..16433776-chr5:16465183..16467258,2	K562	blood:
3	chr5:16428340..16430964-chr5:16464329..16467198,2	K562	blood:
4	chr5:16431881..16434075-chr5:16434927..16437760,2	K562	blood:
5	chr5:16431005..16433615-chr5:16438912..16441485,2	K562	blood:
6	chr5:16417923..16420482-chr5:16527282..16529023,2	K562	blood:
7	chr5:16412596..16415009-chr5:16416995..16418758,3	K562	blood:
8	chr5:16431881..16434075-chr5:16434927..16437760,2	K562	blood:
9	chr5:16437658..16439177-chr5:16439808..16441731,2	K562	blood:
10	chr5:16429539..16431653-chr5:16465262..16467825,2	MCF-7	breast:
11	chr5:16427275..16429815-chr5:16430365..16433352,2	K562	blood:
12	chr5:16433331..16435190-chr5:16462896..16465890,2	MCF-7	breast:
13	chr15:59223945..59226551-chr5:16431073..16432986,2	MCF-7	breast:
14	chr5:16412596..16414928-chr5:16416995..16418758,2	K562	blood:
15	chr5:16412596..16415009-chr5:16416995..16418758,3	K562	blood:
16	chr5:16412596..16414928-chr5:16416995..16418758,2	K562	blood:
17	chr5:16262076..16264265-chr5:16432783..16434475,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXL7-3	chr5:16432313-16432545	NONHSAT100602
2	lnc-ZNF622-1	chr5:16430500-16430713	XLOC_004743
3	lnc-ZNF622-1	chr5:16437483-16438024	XLOC_004743
4	lnc-ZNF622-1	chr5:16431157-16431221	NR_104625
5	lnc-ZNF622-1	chr5:16430500-16430713	XLOC_004743
6	lnc-FBXL7-3	chr5:16428645-16428809	XLOC_004302
7	lnc-FBXL7-3	chr5:16431947-16432008	NONHSAT100602
8	lnc-ZNF622-1	chr5:16430895-16431087	NR_104625
9	lnc-ZNF622-1	chr5:16430895-16431297	XLOC_004743
10	lnc-ZNF622-1	chr5:16431157-16431221	XLOC_004743
11	lnc-FBXL7-3	chr5:16428644-16428809	NONHSAT100602
12	lnc-FBXL7-3	chr5:16432314-16432545	XLOC_004302
13	lnc-ZNF622-1	chr5:16430895-16431087	XLOC_004743
14	lnc-ZNF622-1	chr5:16430500-16430713	XLOC_004743
15	lnc-ZNF622-1	chr5:16430895-16431087	XLOC_004743
16	lnc-ZNF622-1	chr5:16430500-16430713	NR_104625
17	lnc-FBXL7-3	chr5:16431948-16432008	XLOC_004302
18	lnc-ZNF622-1	chr5:16437483-16438024	NR_104625
19	lnc-ZNF622-1	chr5:16418997-16419040	XLOC_004743

No data

Variant related genes	Relation type
ENSG00000249737	TF binding region
ENSG00000249737	CpG island
ENSG00000137776	chromatin interactions
ENSG00000173545	chromatin interactions
ENSG00000248150	chromatin interactions
ENSG00000249737	chromatin interactions

Extended variants
information (count: 1399 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1399 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192789319	chr5:16405646-16405647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs80326742	chr5:16405647-16405648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201851355	chr5:16405713-16405714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147448603	chr5:16405726-16405727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539756041	chr5:16405750-16405751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557736241	chr5:16405759-16405760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576006908	chr5:16405779-16405780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184014212	chr5:16405833-16405834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189095715	chr5:16405859-16405860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538502704	chr5:16405871-16405872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573390611	chr5:16405935-16405936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542063728	chr5:16405936-16405937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10520839	chr5:16405957-16405958	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs538920710	chr5:16406028-16406029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs16868571	chr5:16406092-16406093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs200176337	chr5:16406223-16406224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181484066	chr5:16406233-16406234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564602920	chr5:16406240-16406241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531766855	chr5:16406247-16406248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549899182	chr5:16406288-16406289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78001250	chr5:16406297-16406298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184460648	chr5:16406324-16406325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547872801	chr5:16406328-16406329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190492060	chr5:16406342-16406343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76871412	chr5:16406352-16406353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551679941	chr5:16406366-16406367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569832036	chr5:16406367-16406368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs163067	chr5:16406374-16406375	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs555063828	chr5:16406411-16406412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73753326	chr5:16406467-16406468	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs373068785	chr5:16406469-16406470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139907583	chr5:16406549-16406550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144494252	chr5:16406580-16406581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576277301	chr5:16406584-16406585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76759465	chr5:16406618-16406619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564840548	chr5:16406650-16406651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147863349	chr5:16406699-16406700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75533991	chr5:16406702-16406703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561951044	chr5:16406705-16406706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114019193	chr5:16406771-16406772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182376926	chr5:16406797-16406798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186111185	chr5:16406852-16406853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559527971	chr5:16406916-16406917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141327726	chr5:16406922-16406923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189290075	chr5:16406944-16406945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9686174	chr5:16406954-16406955	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs386685825	chr5:16406960-16406961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs768163	chr5:16406961-16406962	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs114190630	chr5:16406972-16406973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185353919	chr5:16406982-16406983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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

Chromatin state (count:223 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16405600-16418400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr5:16410000-16410200	Enhancers	Fetal Intestine Large	intestine
3	chr5:16410000-16410200	Enhancers	Sigmoid Colon	Sigmoid Colon
4	chr5:16410000-16412800	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr5:16410000-16415400	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr5:16410200-16411200	Weak transcription	Fetal Intestine Large	intestine
7	chr5:16410200-16411200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr5:16410600-16411600	Weak transcription	Fetal Brain Male	brain
9	chr5:16411000-16411800	Enhancers	Colonic Mucosa	Colon
10	chr5:16411000-16413000	Enhancers	NHDF-Ad	bronchial
11	chr5:16411000-16413800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:16411000-16414400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:16411200-16411800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
14	chr5:16411200-16412000	Enhancers	Fetal Intestine Large	intestine
15	chr5:16411200-16412400	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr5:16411200-16414400	Enhancers	HMEC	breast
17	chr5:16411200-16414400	Enhancers	NHEK	skin
18	chr5:16411400-16411600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr5:16411400-16411800	Enhancers	Brain Angular Gyrus	brain
20	chr5:16411400-16411800	Enhancers	Duodenum Mucosa	Duodenum
21	chr5:16411400-16412600	Enhancers	NH-A	brain
22	chr5:16411400-16413000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr5:16411400-16413000	Enhancers	Fetal Heart	heart
24	chr5:16411400-16414600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr5:16411600-16411800	Bivalent Enhancer	Fetal Brain Male	brain
26	chr5:16411600-16411800	Enhancers	Fetal Lung	lung
27	chr5:16411600-16414400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr5:16412000-16412200	Bivalent Enhancer	K562	blood
29	chr5:16412400-16413400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr5:16412600-16412800	Enhancers	Osteobl	bone
31	chr5:16412800-16415000	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr5:16413000-16413400	Weak transcription	Fetal Heart	heart
33	chr5:16413000-16413600	Weak transcription	NHDF-Ad	bronchial
34	chr5:16413400-16413600	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr5:16413400-16413800	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr5:16413400-16414000	Enhancers	Fetal Heart	heart
37	chr5:16413600-16413800	Enhancers	NHDF-Ad	bronchial
38	chr5:16414000-16414400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr5:16414000-16416400	Weak transcription	Fetal Heart	heart
40	chr5:16414600-16415800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr5:16414600-16416400	Enhancers	Fetal Lung	lung
42	chr5:16414800-16415400	Enhancers	Pancreas	Pancrea
43	chr5:16415000-16415200	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr5:16415400-16417800	Weak transcription	Pancreas	Pancrea
45	chr5:16415800-16417600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr5:16416400-16416600	Enhancers	Fetal Heart	heart
47	chr5:16416400-16418800	Weak transcription	Fetal Lung	lung
48	chr5:16416600-16417000	Weak transcription	Fetal Heart	heart
49	chr5:16417000-16419600	Enhancers	Fetal Heart	heart
50	chr5:16417600-16419200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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