Variant report

Variant	esv1837962
Chromosome Location	chr5:14578546-14582501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:352)
CpG islands
(count:612)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:352 , 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	BACH1	chr5:14581450-14582638	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr5:14580284-14581199	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr5:14582372-14582588	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:14580456-14581171	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr5:14580675-14581099	MCF-7	breast:	n/a	n/a
6	CHD1	chr5:14581346-14581369	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr5:14581645-14581935	K562	blood:	n/a	chr5:14581877-14581887
8	CHD2	chr5:14581607-14582538	H1-hESC	embryonic stem cell:	n/a	chr5:14581877-14581887 chr5:14582100-14582110
9	CHD2	chr5:14581658-14581933	GM12878	blood:	n/a	chr5:14581877-14581887
10	CHD2	chr5:14581431-14582614	Hela-S3	cervix:	n/a	chr5:14581877-14581887 chr5:14582100-14582110
11	CREB1	chr5:14582246-14582531	A549	lung:	n/a	n/a
12	CREB1	chr5:14581572-14582063	HepG2	liver:	n/a	n/a
13	CREB1	chr5:14581492-14582060	A549	lung:	n/a	n/a
14	CTCF	chr5:14582440-14582590	HFF-Myc	foreskin:	n/a	n/a
15	CTCF	chr5:14582420-14582570	GM12872	blood:	n/a	n/a
16	CTCF	chr5:14582480-14582630	NHEK	skin:	n/a	n/a
17	CTCF	chr5:14582080-14582230	GM12869	blood:	n/a	n/a
18	CTCF	chr5:14582020-14582170	GM12866	blood:	n/a	n/a
19	CTCF	chr5:14582360-14582510	HAc	cerebellar:	n/a	n/a
20	CTCF	chr5:14582460-14582610	GM12869	blood:	n/a	n/a
21	CTCF	chr5:14582380-14582530	GM12867	blood:	n/a	n/a
22	CTCF	chr5:14582440-14582590	GM12868	blood:	n/a	n/a
23	CTCF	chr5:14582440-14582590	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr5:14581500-14581650	HEK293	kidney:	n/a	n/a
25	CTCF	chr5:14582444-14582617	NHEK	skin:	n/a	n/a
26	CTCF	chr5:14582480-14582630	HL-60	blood:	n/a	n/a
27	CTCF	chr5:14582480-14582630	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr5:14582446-14582609	GM19239	blood:	n/a	n/a
29	CTCF	chr5:14582480-14582630	AG09319	gingival:	n/a	n/a
30	CTCF	chr5:14582460-14582610	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr5:14582300-14582450	GM12875	blood:	n/a	n/a
32	CTCF	chr5:14582442-14582582	Fibrobl	skin:	n/a	n/a
33	CTCF	chr5:14582480-14582630	GM12872	blood:	n/a	n/a
34	CTCF	chr5:14582480-14582630	GM12869	blood:	n/a	n/a
35	CTCF	chr5:14582460-14582610	SAEC	small airway:	n/a	n/a
36	CTCF	chr5:14582480-14582630	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr5:14582440-14582590	BE2_C	brain:	n/a	n/a
38	CTCF	chr5:14582492-14582595	IMR90	lung:	n/a	n/a
39	CTCF	chr5:14582440-14582590	GM12872	blood:	n/a	n/a
40	CTCF	chr5:14582440-14582613	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:14582460-14582610	HFF	foreskin:	n/a	n/a
42	CTCF	chr5:14582420-14582642	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:14582460-14582610	GM06990	blood:	n/a	n/a
44	CTCF	chr5:14582440-14582590	GM12873	blood:	n/a	n/a
45	CTCF	chr5:14582420-14582570	HepG2	liver:	n/a	n/a
46	CTCF	chr5:14582480-14582630	HRE	kidney:	n/a	n/a
47	CTCF	chr5:14582461-14582592	Gliobla	brain:	n/a	n/a
48	CTCF	chr5:14582451-14582599	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr5:14582472-14582602	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr5:14582498-14582586	GM20000	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:14581529-14581579	AG09309	skin:	n/a
2	chr5:14581826-14581876	U87	brain:	n/a
3	chr5:14581529-14581579	AG09309	skin:	n/a
4	chr5:14581826-14581876	U87	brain:	n/a
5	chr5:14582133-14582183	SKMC	muscle:	n/a
6	chr5:14582133-14582183	AG04450	lung:	fetal
7	chr5:14581942-14581992	ECC-1	luminal epithelium:	n/a
8	chr5:14581771-14581821	HIPEpiC	eye:	n/a
9	chr5:14581620-14581670	HUVEC	blood vessel:	n/a
10	chr5:14581642-14581692	ProgFib	skin:	n/a
11	chr5:14581942-14581992	HCPEpiC	choroid plexus:	n/a
12	chr5:14581642-14581692	SKMC	muscle:	n/a
13	chr5:14581651-14581701	NT2-D1	testis:	n/a
14	chr5:14581699-14581749	GM12892	blood:	n/a
15	chr5:14581404-14581454	BJ	skin:	n/a
16	chr5:14581404-14581454	HCF	heart:	n/a
17	chr5:14581404-14581454	BE2_C	brain:	n/a
18	chr5:14581699-14581749	BJ	skin:	n/a
19	chr5:14581404-14581454	HNPCEpiC	eye:	n/a
20	chr5:14581620-14581670	HL-60	blood:	n/a
21	chr5:14581942-14581992	NHBE	bronchial:	n/a
22	chr5:14581404-14581454	SK-N-SH_RA	brain:	n/a
23	chr5:14581642-14581692	ECC-1	luminal epithelium:	n/a
24	chr5:14582133-14582183	HepG2	liver:	n/a
25	chr5:14581642-14581692	HL-60	blood:	n/a
26	chr5:14581699-14581749	RPTEC	kidney:	n/a
27	chr5:14581771-14581821	NHBE	bronchial:	n/a
28	chr5:14581642-14581692	AoSMC	blood vessel:	n/a
29	chr5:14581699-14581749	Caco-2	colon:	n/a
30	chr5:14581942-14581992	ovcar-3	ovarian:	n/a
31	chr5:14581699-14581749	SK-N-MC	brain:	n/a
32	chr5:14581651-14581701	HEEpiC	esophagus:	n/a
33	chr5:14581651-14581701	MCF-7	breast:	n/a
34	chr5:14581642-14581692	K562	blood:	n/a
35	chr5:14581942-14581992	K562	blood:	n/a
36	chr5:14581529-14581579	ovcar-3	ovarian:	n/a
37	chr5:14581771-14581821	GM12878	blood:	n/a
38	chr5:14581404-14581454	HPAEpiC	pulmonary alveolar:	n/a
39	chr5:14581651-14581701	HEK293	kidney:	embryo
40	chr5:14581642-14581692	AG09309	skin:	n/a
41	chr5:14581642-14581692	HMEC	breast:	n/a
42	chr5:14581642-14581692	MCF10A-Er-Src	breast:	n/a
43	chr5:14581699-14581749	AG04449	skin:	fetal
44	chr5:14582133-14582183	HCPEpiC	choroid plexus:	n/a
45	chr5:14581826-14581876	HEEpiC	esophagus:	n/a
46	chr5:14581529-14581579	ProgFib	skin:	n/a
47	chr5:14582133-14582183	PANC-1	pancreas:	n/a
48	chr5:14581529-14581579	PFSK-1	brain:	n/a
49	chr5:14581771-14581821	CMK	blood:	n/a
50	chr5:14581651-14581701	IMR90	lung:	fetal

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:14582284..14584528-chr5:14622359..14624603,2	MCF-7	breast:
2	chr5:14569029..14571729-chr5:14576984..14579113,2	MCF-7	breast:
3	chr5:14487528..14489858-chr5:14581341..14583372,2	MCF-7	breast:
4	chr5:14582227..14584118-chr5:14585804..14588637,2	K562	blood:
5	chr5:14497681..14499439-chr5:14580941..14582507,2	MCF-7	breast:

No data

Variant related genes	Relation type
FAM105A	TF binding region
FAM105A	CpG island
ENSG00000038382	chromatin interactions

Extended variants
information (count: 222 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:222 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs152787	chr5:14578546-14578547	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77547745	chr5:14578552-14578553	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs199652185	chr5:14578557-14578558	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs553429919	chr5:14578561-14578562	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs142704709	chr5:14578564-14578565	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs79555184	chr5:14578569-14578570	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs181453897	chr5:14578572-14578573	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs55828470	chr5:14578581-14578582	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs186930814	chr5:14578605-14578606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191728552	chr5:14578606-14578607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144153516	chr5:14578607-14578608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530024058	chr5:14578613-14578614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376746664	chr5:14578641-14578642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs32637	chr5:14578648-14578649	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs548725222	chr5:14578673-14578674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566991175	chr5:14578678-14578679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73752126	chr5:14578697-14578698	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs552813326	chr5:14578698-14578699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570909117	chr5:14578700-14578701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183974536	chr5:14578708-14578709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371902266	chr5:14578709-14578710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150972772	chr5:14578725-14578726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139569274	chr5:14578732-14578733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553319310	chr5:14578737-14578738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116631383	chr5:14578764-14578765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573136585	chr5:14578771-14578772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557981377	chr5:14578789-14578790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576150911	chr5:14578791-14578792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543731524	chr5:14578794-14578795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551142129	chr5:14578795-14578796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs152642	chr5:14578799-14578800	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs77401307	chr5:14578815-14578816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187789209	chr5:14578817-14578818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373301559	chr5:14578818-14578819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543487536	chr5:14578829-14578830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114940562	chr5:14578832-14578833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568575308	chr5:14578837-14578838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527788891	chr5:14578839-14578840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116470336	chr5:14578852-14578853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540576401	chr5:14578853-14578854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375187041	chr5:14578854-14578855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550321134	chr5:14578885-14578886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568676540	chr5:14578886-14578887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369429368	chr5:14578892-14578893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535894361	chr5:14578903-14578904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535708590	chr5:14578907-14578908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79452037	chr5:14578909-14578910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565331507	chr5:14578913-14578914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76663938	chr5:14578914-14578915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182132112	chr5:14578921-14578922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
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
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
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14574600-14581200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr5:14575200-14580800	Weak transcription	Fetal Brain Male	brain
3	chr5:14575200-14581200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr5:14575200-14581400	Weak transcription	Pancreas	Pancrea
5	chr5:14575400-14580200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr5:14576200-14580200	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr5:14576400-14580200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr5:14576600-14579000	Weak transcription	Hela-S3	cervix
9	chr5:14576800-14579000	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr5:14576800-14580000	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr5:14579000-14580800	Enhancers	Hela-S3	cervix
12	chr5:14579600-14579800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr5:14579600-14579800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr5:14579600-14581200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr5:14580000-14580400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr5:14580000-14580400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:14580000-14580800	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr5:14580200-14581200	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr5:14580200-14581200	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr5:14580200-14581200	Enhancers	Duodenum Mucosa	Duodenum
21	chr5:14580200-14581200	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr5:14580400-14581200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr5:14580600-14581200	Bivalent Enhancer	Thymus	Thymus
24	chr5:14580600-14581400	Bivalent Enhancer	Colon Smooth Muscle	Colon
25	chr5:14580800-14581000	Bivalent Enhancer	Fetal Kidney	kidney
26	chr5:14580800-14581000	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr5:14580800-14581200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
28	chr5:14580800-14581200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:14580800-14581200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr5:14580800-14581200	Bivalent Enhancer	Primary B cells from cord blood	blood
31	chr5:14580800-14581200	Enhancers	Adipose Nuclei	Adipose
32	chr5:14580800-14581200	Enhancers	Fetal Brain Female	brain
33	chr5:14580800-14581200	Enhancers	Placenta	Placenta
34	chr5:14580800-14581200	Enhancers	Fetal Stomach	stomach
35	chr5:14580800-14581200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
36	chr5:14580800-14581200	Bivalent Enhancer	NHDF-Ad	bronchial
37	chr5:14580800-14581400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr5:14580800-14581400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr5:14580800-14581400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr5:14580800-14581400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr5:14580800-14581400	Enhancers	Fetal Intestine Large	intestine
42	chr5:14580800-14581400	Bivalent Enhancer	Fetal Lung	lung
43	chr5:14580800-14581400	Bivalent Enhancer	Fetal Muscle Leg	muscle
44	chr5:14580800-14581400	Bivalent Enhancer	Fetal Thymus	thymus
45	chr5:14580800-14581400	Bivalent Enhancer	HepG2	liver
46	chr5:14580800-14581600	Enhancers	Fetal Brain Male	brain
47	chr5:14580800-14581600	Flanking Active TSS	Hela-S3	cervix
48	chr5:14580800-14581600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr5:14580800-14583400	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr5:14580800-14583400	Active TSS	Colonic Mucosa	Colon

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