Variant report

Variant	esv1796116
Chromosome Location	chr5:14572712-14582501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:403)
CpG islands
(count:732)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr5:14576509-14576615	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr5:14580284-14581199	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:14576202-14576652	Hela-S3	cervix:	n/a	chr5:14576207-14576218
5	CEBPB	chr5:14573058-14573258	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:14580675-14581099	MCF-7	breast:	n/a	n/a
7	CEBPB	chr5:14575320-14575597	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:14582372-14582588	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr5:14580456-14581171	Hela-S3	cervix:	n/a	n/a
10	CHD1	chr5:14581346-14581369	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr5:14581607-14582538	H1-hESC	embryonic stem cell:	n/a	chr5:14581877-14581887 chr5:14582100-14582110
12	CHD2	chr5:14581658-14581933	GM12878	blood:	n/a	chr5:14581877-14581887
13	CHD2	chr5:14581431-14582614	Hela-S3	cervix:	n/a	chr5:14581877-14581887 chr5:14582100-14582110
14	CHD2	chr5:14581645-14581935	K562	blood:	n/a	chr5:14581877-14581887
15	CREB1	chr5:14581572-14582063	HepG2	liver:	n/a	n/a
16	CREB1	chr5:14582246-14582531	A549	lung:	n/a	n/a
17	CREB1	chr5:14581492-14582060	A549	lung:	n/a	n/a
18	CTCF	chr5:14582435-14582597	MCF-7	breast:	n/a	n/a
19	CTCF	chr5:14582480-14582630	GM12878	blood:	n/a	n/a
20	CTCF	chr5:14582437-14582629	A549	lung:	n/a	n/a
21	CTCF	chr5:14582420-14582570	HPF	lung:	n/a	n/a
22	CTCF	chr5:14582444-14582617	NHEK	skin:	n/a	n/a
23	CTCF	chr5:14582460-14582610	AG04450	lung:	n/a	n/a
24	CTCF	chr5:14582440-14582590	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr5:14582442-14582582	Fibrobl	skin:	n/a	n/a
26	CTCF	chr5:14582480-14582630	NHEK	skin:	n/a	n/a
27	CTCF	chr5:14582480-14582630	MCF-7	breast:	n/a	n/a
28	CTCF	chr5:14582420-14582570	HepG2	liver:	n/a	n/a
29	CTCF	chr5:14582360-14582510	HAc	cerebellar:	n/a	n/a
30	CTCF	chr5:14582451-14582599	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr5:14582455-14582604	GM19240	blood:	n/a	n/a
32	CTCF	chr5:14582460-14582610	Caco-2	colon:	n/a	n/a
33	CTCF	chr5:14582420-14582570	AG04449	skin:	n/a	n/a
34	CTCF	chr5:14582420-14582570	GM12875	blood:	n/a	n/a
35	CTCF	chr5:14582460-14582610	GM12864	blood:	n/a	n/a
36	CTCF	chr5:14582440-14582590	GM12872	blood:	n/a	n/a
37	CTCF	chr5:14582480-14582591	GM13977	blood:	n/a	n/a
38	CTCF	chr5:14582400-14582550	GM12865	blood:	n/a	n/a
39	CTCF	chr5:14577611-14577759	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr5:14582460-14582610	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr5:14582480-14582630	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr5:14582480-14582630	HVMF	connective:	n/a	n/a
43	CTCF	chr5:14582460-14582610	GM12869	blood:	n/a	n/a
44	CTCF	chr5:14582300-14582450	GM12875	blood:	n/a	n/a
45	CTCF	chr5:14582480-14582630	GM12873	blood:	n/a	n/a
46	CTCF	chr5:14582500-14582650	NB4	blood:	n/a	n/a
47	CTCF	chr5:14582080-14582230	GM12869	blood:	n/a	n/a
48	CTCF	chr5:14582020-14582170	GM12866	blood:	n/a	n/a
49	CTCF	chr5:14582452-14582573	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr5:14582440-14582590	GM12873	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:14581529-14581579	AG04449	skin:	fetal
2	chr5:14577364-14577414	HMEC	breast:	n/a
3	chr5:14581771-14581821	U87	brain:	n/a
4	chr5:14581942-14581992	T-47D	breast:	n/a
5	chr5:14581404-14581454	AG09319	gingival:	n/a
6	chr5:14577586-14577636	NB4	blood:	n/a
7	chr5:14577586-14577636	AG09309	skin:	n/a
8	chr5:14581642-14581692	CMK	blood:	n/a
9	chr5:14581404-14581454	NHDF-neo	bronchial:	n/a
10	chr5:14581651-14581701	NHDF-neo	bronchial:	n/a
11	chr5:14581826-14581876	AG09319	gingival:	n/a
12	chr5:14577586-14577636	Jurkat	blood:	n/a
13	chr5:14581620-14581670	NH-A	brain:	n/a
14	chr5:14581404-14581454	RPTEC	kidney:	n/a
15	chr5:14581826-14581876	NHDF-neo	bronchial:	n/a
16	chr5:14582133-14582183	HPAEpiC	pulmonary alveolar:	n/a
17	chr5:14581404-14581454	ovcar-3	ovarian:	n/a
18	chr5:14581620-14581670	PrEC	prostate:	n/a
19	chr5:14581771-14581821	GM12878	blood:	n/a
20	chr5:14581942-14581992	K562	blood:	n/a
21	chr5:14581771-14581821	Hela-S3	cervix:	n/a
22	chr5:14582133-14582183	GM19239	blood:	n/a
23	chr5:14577586-14577636	SK-N-MC	brain:	n/a
24	chr5:14581620-14581670	MCF10A-Er-Src	breast:	n/a
25	chr5:14581826-14581876	HIPEpiC	eye:	n/a
26	chr5:14582133-14582183	BJ	skin:	n/a
27	chr5:14581620-14581670	PFSK-1	brain:	n/a
28	chr5:14581942-14581992	PFSK-1	brain:	n/a
29	chr5:14582133-14582183	HIPEpiC	eye:	n/a
30	chr5:14581699-14581749	AoSMC	blood vessel:	n/a
31	chr5:14581942-14581992	ProgFib	skin:	n/a
32	chr5:14581642-14581692	AG09319	gingival:	n/a
33	chr5:14577364-14577414	AG10803	skin:	n/a
34	chr5:14581620-14581670	NB4	blood:	n/a
35	chr5:14577364-14577414	HRPEpiC	eye:	n/a
36	chr5:14581699-14581749	GM12892	blood:	n/a
37	chr5:14581651-14581701	GM12891	blood:	n/a
38	chr5:14581642-14581692	HepG2	liver:	n/a
39	chr5:14581651-14581701	HL-60	blood:	n/a
40	chr5:14577586-14577636	AG09319	gingival:	n/a
41	chr5:14581620-14581670	H1-hESC	embryonic stem cell:	embryo
42	chr5:14577364-14577414	U87	brain:	n/a
43	chr5:14581699-14581749	AG09309	skin:	n/a
44	chr5:14582133-14582183	ovcar-3	ovarian:	n/a
45	chr5:14581529-14581579	HNPCEpiC	eye:	n/a
46	chr5:14577364-14577414	NT2-D1	testis:	n/a
47	chr5:14581771-14581821	K562	blood:	n/a
48	chr5:14581404-14581454	MCF10A-Er-Src	breast:	n/a
49	chr5:14581529-14581579	Hela-S3	cervix:	n/a
50	chr5:14577586-14577636	HCF	heart:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:14582227..14584118-chr5:14585804..14588637,2	K562	blood:
2	chr5:14497681..14499439-chr5:14580941..14582507,2	MCF-7	breast:
3	chr5:14487528..14489858-chr5:14581341..14583372,2	MCF-7	breast:
4	chr5:14575023..14577429-chr5:14607385..14610126,2	K562	blood:
5	chr5:14569029..14571729-chr5:14576984..14579113,2	MCF-7	breast:
6	chr5:14566492..14568363-chr5:14571376..14573521,2	MCF-7	breast:
7	chr5:14582284..14584528-chr5:14622359..14624603,2	MCF-7	breast:

No data

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

Extended variants
information (count: 503 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs32635	chr5:14572712-14572713	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141330055	chr5:14572761-14572762	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527470667	chr5:14572873-14572874	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193106059	chr5:14572876-14572877	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577429748	chr5:14572894-14572895	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143572065	chr5:14572902-14572903	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148003245	chr5:14572911-14572912	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538629071	chr5:14572928-14572929	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546578511	chr5:14572941-14572942	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11950740	chr5:14572946-14572947	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569187993	chr5:14572960-14572961	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536395401	chr5:14572963-14572964	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553447200	chr5:14572976-14572977	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555039588	chr5:14572993-14572994	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573389945	chr5:14572994-14572995	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540806085	chr5:14573032-14573033	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140791645	chr5:14573098-14573099	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577625652	chr5:14573099-14573100	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544879112	chr5:14573134-14573135	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184256645	chr5:14573171-14573172	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529688233	chr5:14573178-14573179	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150080041	chr5:14573179-14573180	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560172038	chr5:14573184-14573185	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188470139	chr5:14573185-14573186	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138534607	chr5:14573207-14573208	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs191748715	chr5:14573216-14573217	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs184298896	chr5:14573266-14573267	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs10043690	chr5:14573280-14573281	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs188990767	chr5:14573305-14573306	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs569197925	chr5:14573346-14573347	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs536636046	chr5:14573403-14573404	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs138846736	chr5:14573408-14573409	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs375607038	chr5:14573421-14573422	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs373396055	chr5:14573449-14573450	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs534249325	chr5:14573468-14573469	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs559202517	chr5:14573470-14573471	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs577466689	chr5:14573485-14573486	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs538585706	chr5:14573548-14573549	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs571599537	chr5:14573556-14573557	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs556805534	chr5:14573562-14573563	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs574382071	chr5:14573592-14573593	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs541833073	chr5:14573675-14573676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181518122	chr5:14573698-14573699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185238508	chr5:14573742-14573743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545446476	chr5:14573753-14573754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563988342	chr5:14573756-14573757	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556022799	chr5:14573781-14573782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190484540	chr5:14573782-14573783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561993002	chr5:14573816-14573817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs152623	chr5:14573859-14573860	Enhancers 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:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14560600-14576000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr5:14570200-14576600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr5:14570800-14574200	Weak transcription	A549	lung
4	chr5:14570800-14574400	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr5:14571400-14573200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr5:14571600-14573600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr5:14573000-14575200	Enhancers	Primary B cells from cord blood	blood
8	chr5:14573200-14576200	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr5:14573600-14574200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr5:14573600-14575000	Weak transcription	Gastric	stomach
11	chr5:14573600-14575200	Enhancers	Right Atrium	heart
12	chr5:14574200-14574400	Enhancers	A549	lung
13	chr5:14574200-14574600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr5:14574200-14574600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr5:14574200-14575400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr5:14574200-14575600	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr5:14574400-14574800	Weak transcription	A549	lung
18	chr5:14574400-14575200	Enhancers	Adipose Nuclei	Adipose
19	chr5:14574400-14575200	Enhancers	Fetal Thymus	thymus
20	chr5:14574400-14575200	Enhancers	Pancreas	Pancrea
21	chr5:14574400-14575200	Enhancers	Spleen	Spleen
22	chr5:14574400-14575400	Enhancers	Lung	lung
23	chr5:14574400-14575400	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr5:14574400-14575400	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr5:14574400-14576000	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr5:14574400-14576200	Enhancers	Fetal Muscle Leg	muscle
27	chr5:14574600-14581200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr5:14574800-14575000	Enhancers	Fetal Brain Male	brain
29	chr5:14574800-14575200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr5:14574800-14575200	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr5:14574800-14575200	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr5:14574800-14575400	Enhancers	A549	lung
33	chr5:14574800-14575600	Enhancers	Placenta	Placenta
34	chr5:14574800-14576400	Enhancers	Duodenum Mucosa	Duodenum
35	chr5:14575000-14575200	Enhancers	Fetal Muscle Trunk	muscle
36	chr5:14575000-14575200	Enhancers	Gastric	stomach
37	chr5:14575000-14575200	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr5:14575000-14575400	Enhancers	Fetal Heart	heart
39	chr5:14575000-14575400	Enhancers	Fetal Stomach	stomach
40	chr5:14575000-14576600	Enhancers	Hela-S3	cervix
41	chr5:14575200-14576000	Weak transcription	Adipose Nuclei	Adipose
42	chr5:14575200-14580800	Weak transcription	Fetal Brain Male	brain
43	chr5:14575200-14581200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr5:14575200-14581400	Weak transcription	Pancreas	Pancrea
45	chr5:14575400-14576800	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr5:14575400-14580200	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr5:14576000-14576200	Enhancers	Adipose Nuclei	Adipose
48	chr5:14576200-14580200	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr5:14576400-14580200	Weak transcription	Duodenum Mucosa	Duodenum
50	chr5:14576600-14579000	Weak transcription	Hela-S3	cervix

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