Variant report

Variant	nsv597241
Chromosome Location	chr5:14581556-14582435
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	BACH1	chr5:14581450-14582638	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr5:14582372-14582588	Hela-S3	cervix:	n/a	n/a
3	CHD2	chr5:14581431-14582614	Hela-S3	cervix:	n/a	chr5:14581877-14581887 chr5:14582100-14582110
4	CHD2	chr5:14581658-14581933	GM12878	blood:	n/a	chr5:14581877-14581887
5	CHD2	chr5:14581607-14582538	H1-hESC	embryonic stem cell:	n/a	chr5:14581877-14581887 chr5:14582100-14582110
6	CHD2	chr5:14581645-14581935	K562	blood:	n/a	chr5:14581877-14581887
7	CREB1	chr5:14581572-14582063	HepG2	liver:	n/a	n/a
8	CREB1	chr5:14581492-14582060	A549	lung:	n/a	n/a
9	CREB1	chr5:14582246-14582531	A549	lung:	n/a	n/a
10	CTCF	chr5:14582420-14582570	HVMF	connective:	n/a	n/a
11	CTCF	chr5:14582435-14582597	MCF-7	breast:	n/a	n/a
12	CTCF	chr5:14582400-14582550	GM12865	blood:	n/a	n/a
13	CTCF	chr5:14582430-14582662	Spleen_OC	spleen:	n/a	n/a
14	CTCF	chr5:14582360-14582510	GM12868	blood:	n/a	n/a
15	CTCF	chr5:14582420-14582570	HPF	lung:	n/a	n/a
16	CTCF	chr5:14582420-14582570	HEK293	kidney:	n/a	n/a
17	CTCF	chr5:14582429-14582620	GM12878	blood:	n/a	n/a
18	CTCF	chr5:14582420-14582570	HCM	heart:	n/a	n/a
19	CTCF	chr5:14582420-14582570	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr5:14582420-14582570	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr5:14582000-14582150	GM12865	blood:	n/a	n/a
22	CTCF	chr5:14582420-14582570	BJ	skin:	n/a	n/a
23	CTCF	chr5:14582400-14582550	GM12864	blood:	n/a	n/a
24	CTCF	chr5:14582420-14582570	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr5:14582400-14582550	HEK293	kidney:	n/a	n/a
26	CTCF	chr5:14582420-14582570	HepG2	liver:	n/a	n/a
27	CTCF	chr5:14582420-14582570	GM12866	blood:	n/a	n/a
28	CTCF	chr5:14582360-14582510	HAc	cerebellar:	n/a	n/a
29	CTCF	chr5:14582380-14582530	GM12867	blood:	n/a	n/a
30	CTCF	chr5:14582120-14582270	AG04449	skin:	n/a	n/a
31	CTCF	chr5:14582420-14582570	AG04449	skin:	n/a	n/a
32	CTCF	chr5:14582420-14582570	GM12865	blood:	n/a	n/a
33	CTCF	chr5:14582400-14582550	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr5:14582420-14582570	GM12864	blood:	n/a	n/a
35	CTCF	chr5:14582420-14582642	MCF-7	breast:	n/a	n/a
36	CTCF	chr5:14581500-14581650	HEK293	kidney:	n/a	n/a
37	CTCF	chr5:14582395-14582709	GM12878	blood:	n/a	n/a
38	CTCF	chr5:14582300-14582450	GM12875	blood:	n/a	n/a
39	CTCF	chr5:14582080-14582230	GM12869	blood:	n/a	n/a
40	CTCF	chr5:14582420-14582570	GM12875	blood:	n/a	n/a
41	CTCF	chr5:14582020-14582170	GM12866	blood:	n/a	n/a
42	CTCF	chr5:14582420-14582570	GM12872	blood:	n/a	n/a
43	E2F4	chr5:14582378-14582640	MCF10A-Er-Src	breast:	n/a	chr5:14582521-14582532 chr5:14582521-14582528 chr5:14582521-14582528 chr5:14582520-14582529 chr5:14582520-14582531 chr5:14582521-14582528 chr5:14582516-14582531
44	E2F4	chr5:14581742-14581999	MCF10A-Er-Src	breast:	n/a	chr5:14581833-14581842
45	E2F6	chr5:14582320-14582738	A549	lung:	n/a	chr5:14582521-14582532 chr5:14582521-14582528 chr5:14582521-14582528 chr5:14582520-14582529 chr5:14582520-14582531 chr5:14582521-14582528 chr5:14582516-14582531
46	E2F6	chr5:14582142-14582815	A549	lung:	n/a	chr5:14582521-14582532 chr5:14582521-14582528 chr5:14582521-14582528 chr5:14582520-14582529 chr5:14582520-14582531 chr5:14582521-14582528 chr5:14582516-14582531
47	E2F6	chr5:14581783-14582139	K562	blood:	n/a	chr5:14582122-14582131 chr5:14581833-14581842
48	E2F6	chr5:14581385-14582204	H1-hESC	embryonic stem cell:	n/a	chr5:14582122-14582131 chr5:14581720-14581732 chr5:14581833-14581842
49	E2F6	chr5:14582365-14582765	H1-hESC	embryonic stem cell:	n/a	chr5:14582521-14582532 chr5:14582521-14582528 chr5:14582521-14582528 chr5:14582520-14582529 chr5:14582520-14582531 chr5:14582521-14582528 chr5:14582516-14582531
50	E2F6	chr5:14581829-14582163	K562	blood:	n/a	chr5:14582122-14582131 chr5:14581833-14581842

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:14582133-14582183	LNCaP	prostate:	n/a
2	chr5:14581826-14581876	BE2_C	brain:	n/a
3	chr5:14581529-14581579	IMR90	lung:	fetal
4	chr5:14582133-14582183	LNCaP	prostate:	n/a
5	chr5:14581826-14581876	BE2_C	brain:	n/a
6	chr5:14581529-14581579	IMR90	lung:	fetal
7	chr5:14581651-14581701	GM06990	blood:	n/a
8	chr5:14581942-14581992	AG10803	skin:	n/a
9	chr5:14581771-14581821	U87	brain:	n/a
10	chr5:14581699-14581749	U87	brain:	n/a
11	chr5:14581620-14581670	T-47D	breast:	n/a
12	chr5:14582133-14582183	HCM	heart:	n/a
13	chr5:14582133-14582183	HAEpiC	amniotic membrane:	n/a
14	chr5:14581651-14581701	PFSK-1	brain:	n/a
15	chr5:14581529-14581579	MCF10A-Er-Src	breast:	n/a
16	chr5:14581771-14581821	HUVEC	blood vessel:	n/a
17	chr5:14581699-14581749	HRCEpiC	kidney:	n/a
18	chr5:14581620-14581670	AG10803	skin:	n/a
19	chr5:14581651-14581701	SK-N-SH_RA	brain:	n/a
20	chr5:14581699-14581749	HIPEpiC	eye:	n/a
21	chr5:14581620-14581670	HRE	kidney:	n/a
22	chr5:14581529-14581579	K562	blood:	n/a
23	chr5:14581699-14581749	AG09319	gingival:	n/a
24	chr5:14581651-14581701	AG09309	skin:	n/a
25	chr5:14581771-14581821	ProgFib	skin:	n/a
26	chr5:14581699-14581749	K562	blood:	n/a
27	chr5:14581642-14581692	NT2-D1	testis:	n/a
28	chr5:14581942-14581992	IMR90	lung:	fetal
29	chr5:14581942-14581992	AG04450	lung:	fetal
30	chr5:14581699-14581749	AoSMC	blood vessel:	n/a
31	chr5:14581699-14581749	HCF	heart:	n/a
32	chr5:14581620-14581670	H1-hESC	embryonic stem cell:	embryo
33	chr5:14581699-14581749	SAEC	small airway:	n/a
34	chr5:14581699-14581749	RPTEC	kidney:	n/a
35	chr5:14581651-14581701	SK-N-MC	brain:	n/a
36	chr5:14581620-14581670	IMR90	lung:	fetal
37	chr5:14581642-14581692	K562	blood:	n/a
38	chr5:14581699-14581749	HRPEpiC	eye:	n/a
39	chr5:14581651-14581701	HPAEpiC	pulmonary alveolar:	n/a
40	chr5:14581620-14581670	HRPEpiC	eye:	n/a
41	chr5:14581620-14581670	HNPCEpiC	eye:	n/a
42	chr5:14582133-14582183	AoSMC	blood vessel:	n/a
43	chr5:14581826-14581876	AG09309	skin:	n/a
44	chr5:14581699-14581749	HepG2	liver:	n/a
45	chr5:14581942-14581992	HUVEC	blood vessel:	n/a
46	chr5:14581642-14581692	T-47D	breast:	n/a
47	chr5:14581942-14581992	BE2_C	brain:	n/a
48	chr5:14581529-14581579	HIPEpiC	eye:	n/a
49	chr5:14581642-14581692	PrEC	prostate:	n/a
50	chr5:14581529-14581579	HAEpiC	amniotic membrane:	n/a

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

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

Extended variants
information (count: 31 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs31978	chr5:14581556-14581557	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368312800	chr5:14581569-14581570	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs530518366	chr5:14581613-14581614	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs546649033	chr5:14581621-14581622	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs552106960	chr5:14581655-14581656	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs190879224	chr5:14581670-14581671	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs571729727	chr5:14581734-14581735	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs561185572	chr5:14581791-14581792	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs538711784	chr5:14581803-14581804	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs557578507	chr5:14581804-14581805	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs575898906	chr5:14581812-14581813	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs536977379	chr5:14581818-14581819	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs555277801	chr5:14581819-14581820	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs373342436	chr5:14581823-14581824	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs573546500	chr5:14581883-14581884	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs540246203	chr5:14581897-14581898	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558228835	chr5:14581900-14581901	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370882613	chr5:14581955-14581956	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576878445	chr5:14581961-14581962	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543970385	chr5:14581980-14581981	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs375610503	chr5:14582020-14582021	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs116803888	chr5:14582058-14582059	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs368129063	chr5:14582098-14582099	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541751119	chr5:14582119-14582120	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560038055	chr5:14582205-14582206	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs527549107	chr5:14582256-14582257	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546975480	chr5:14582258-14582259	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs528151732	chr5:14582259-14582260	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs182928074	chr5:14582275-14582276	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs532678241	chr5:14582329-14582330	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs371703437	chr5:14582402-14582403	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	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:252 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14580800-14581600	Enhancers	Fetal Brain Male	brain
2	chr5:14580800-14581600	Flanking Active TSS	Hela-S3	cervix
3	chr5:14580800-14581600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr5:14580800-14583400	Active TSS	Brain Inferior Temporal Lobe	brain
5	chr5:14580800-14583400	Active TSS	Colonic Mucosa	Colon
6	chr5:14581000-14581600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
7	chr5:14581000-14581600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
8	chr5:14581000-14581600	Bivalent Enhancer	Stomach Mucosa	stomach
9	chr5:14581000-14583200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr5:14581000-14583400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
11	chr5:14581200-14581600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
12	chr5:14581200-14581600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
13	chr5:14581200-14581600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr5:14581200-14581600	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr5:14581200-14581600	Flanking Active TSS	Primary T cells from cord blood	blood
16	chr5:14581200-14581600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
17	chr5:14581200-14581600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr5:14581200-14581600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr5:14581200-14581600	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr5:14581200-14581600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr5:14581200-14581600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr5:14581200-14581600	Flanking Active TSS	Duodenum Mucosa	Duodenum
23	chr5:14581200-14581600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
24	chr5:14581200-14581600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
25	chr5:14581200-14581600	Flanking Bivalent TSS/Enh	NHDF-Ad	bronchial
26	chr5:14581200-14581800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr5:14581200-14581800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr5:14581200-14581800	Flanking Active TSS	Primary hematopoietic stem cells	blood
29	chr5:14581200-14581800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr5:14581200-14581800	Flanking Active TSS	Adipose Nuclei	Adipose
31	chr5:14581200-14581800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
32	chr5:14581200-14581800	Flanking Active TSS	Placenta	Placenta
33	chr5:14581200-14581800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
34	chr5:14581200-14582200	Active TSS	Stomach Smooth Muscle	stomach
35	chr5:14581200-14582600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:14581200-14582800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr5:14581200-14582800	Active TSS	Brain Hippocampus Middle	brain
38	chr5:14581200-14582800	Active TSS	Brain Substantia Nigra	brain
39	chr5:14581200-14582800	Active TSS	Right Atrium	heart
40	chr5:14581200-14583000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr5:14581200-14583000	Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr5:14581200-14583000	Bivalent/Poised TSS	NHEK	skin
43	chr5:14581200-14583200	Active TSS	H9 Cell Line	embryonic stem cell
44	chr5:14581200-14583200	Active TSS	Brain Anterior Caudate	brain
45	chr5:14581200-14583200	Active TSS	Fetal Brain Female	brain
46	chr5:14581200-14583400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
47	chr5:14581200-14583400	Active TSS	Brain Angular Gyrus	brain
48	chr5:14581400-14581600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr5:14581400-14581600	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr5:14581400-14581600	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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