Variant report

Variant	esv3412320
Chromosome Location	chr5:179391746-179395144
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	ARID3A	chr5:179394416-179394766	HepG2	liver:	n/a	n/a
2	CTCF	chr5:179395067-179395148	MCF-7	breast:	n/a	n/a
3	CTCF	chr5:179395066-179395135	Fibrobl	skin:	n/a	n/a
4	CTCF	chr5:179395072-179395137	GM12891	blood:	n/a	n/a
5	CTCF	chr5:179395035-179395153	MCF-7	breast:	n/a	n/a
6	CTCF	chr5:179395076-179395126	MCF-7	breast:	n/a	n/a
7	CTCF	chr5:179395032-179395153	ProgFib	skin:	n/a	n/a
8	CTCF	chr5:179395040-179395153	MCF-7	breast:	n/a	n/a
9	EP300	chr5:179395030-179395230	GM12878	blood:	n/a	n/a
10	EP300	chr5:179395059-179395205	GM12878	blood:	n/a	n/a
11	FOXA1	chr5:179394398-179394961	HepG2	liver:	n/a	chr5:179394744-179394756
12	FOXA1	chr5:179394357-179394868	HepG2	liver:	n/a	chr5:179394744-179394756
13	FOXA1	chr5:179394482-179394934	HepG2	liver:	n/a	chr5:179394744-179394756
14	FOXA1	chr5:179394468-179394903	HepG2	liver:	n/a	chr5:179394744-179394756
15	FOXA2	chr5:179394529-179394793	HepG2	liver:	n/a	chr5:179394744-179394756
16	GABPA	chr5:179395068-179395205	GM12878	blood:	n/a	n/a
17	HNF4A	chr5:179394403-179394744	HepG2	liver:	n/a	chr5:179394499-179394517 chr5:179394501-179394516 chr5:179394502-179394515 chr5:179394594-179394609 chr5:179394594-179394608 chr5:179394501-179394515 chr5:179394595-179394608 chr5:179394595-179394607 chr5:179394594-179394609 chr5:179394502-179394514 chr5:179394501-179394514 chr5:179394594-179394609 chr5:179394592-179394610 chr5:179394594-179394609 chr5:179394595-179394607 chr5:179394502-179394514 chr5:179394594-179394609 chr5:179394502-179394514 chr5:179394501-179394516
18	HNF4A	chr5:179394466-179394737	HepG2	liver:	n/a	chr5:179394499-179394517 chr5:179394501-179394516 chr5:179394502-179394515 chr5:179394594-179394609 chr5:179394594-179394608 chr5:179394501-179394515 chr5:179394595-179394608 chr5:179394595-179394607 chr5:179394594-179394609 chr5:179394502-179394514 chr5:179394501-179394514 chr5:179394594-179394609 chr5:179394592-179394610 chr5:179394594-179394609 chr5:179394595-179394607 chr5:179394502-179394514 chr5:179394594-179394609 chr5:179394502-179394514 chr5:179394501-179394516
19	HNF4G	chr5:179394432-179394827	HepG2	liver:	n/a	chr5:179394499-179394517 chr5:179394501-179394516 chr5:179394502-179394515 chr5:179394594-179394609 chr5:179394592-179394607 chr5:179394594-179394608 chr5:179394501-179394515 chr5:179394595-179394608 chr5:179394595-179394607 chr5:179394594-179394609 chr5:179394502-179394514 chr5:179394501-179394514 chr5:179394594-179394609 chr5:179394592-179394610 chr5:179394594-179394609 chr5:179394595-179394607 chr5:179394502-179394514 chr5:179394594-179394609 chr5:179394502-179394514 chr5:179394501-179394516
20	MYC	chr5:179394984-179395153	MCF-7	breast:	n/a	n/a
21	MYC	chr5:179395060-179395115	H1-hESC	embryonic stem cell:	n/a	n/a
22	PAX5	chr5:179391605-179391856	GM12878	blood:	n/a	n/a
23	PBX3	chr5:179395066-179395202	GM12878	blood:	n/a	n/a
24	POLR2A	chr5:179394950-179395155	MCF-7	breast:	n/a	n/a
25	POLR2A	chr5:179394984-179395154	MCF-7	breast:	n/a	n/a
26	POLR2A	chr5:179394955-179395155	A549	lung:	n/a	n/a
27	SRF	chr5:179395074-179395184	GM12878	blood:	n/a	n/a
28	STAT3	chr5:179392452-179392626	MCF10A-Er-Src	breast:	n/a	n/a
29	TCF3	chr5:179395008-179395228	GM12878	blood:	n/a	n/a
30	USF1	chr5:179395069-179395167	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179393940-179393990	GM12878	blood:	n/a
2	chr5:179393940-179393990	SKMC	muscle:	n/a
3	chr5:179393940-179393990	PANC-1	pancreas:	n/a
4	chr5:179393940-179393990	LNCaP	prostate:	n/a
5	chr5:179393917-179393967	NT2-D1	testis:	n/a
6	chr5:179393917-179393967	LNCaP	prostate:	n/a
7	chr5:179393917-179393967	AG04450	lung:	fetal
8	chr5:179393940-179393990	HNPCEpiC	eye:	n/a
9	chr5:179393917-179393967	SKMC	muscle:	n/a
10	chr5:179393917-179393967	SK-N-MC	brain:	n/a
11	chr5:179393940-179393990	IMR90	lung:	fetal
12	chr5:179393940-179393990	NT2-D1	testis:	n/a
13	chr5:179393917-179393967	HNPCEpiC	eye:	n/a
14	chr5:179393917-179393967	ECC-1	luminal epithelium:	n/a
15	chr5:179393940-179393990	ovcar-3	ovarian:	n/a
16	chr5:179393940-179393990	HAEpiC	amniotic membrane:	n/a
17	chr5:179393940-179393990	HEK293	kidney:	embryo
18	chr5:179393940-179393990	NH-A	brain:	n/a
19	chr5:179393940-179393990	AG09319	gingival:	n/a
20	chr5:179393940-179393990	ProgFib	skin:	n/a
21	chr5:179393940-179393990	SK-N-SH	brain:	n/a
22	chr5:179393940-179393990	HCT-116	colon:	n/a
23	chr5:179393917-179393967	HPAEpiC	pulmonary alveolar:	n/a
24	chr5:179393917-179393967	HEEpiC	esophagus:	n/a
25	chr5:179393940-179393990	ECC-1	luminal epithelium:	n/a
26	chr5:179393917-179393967	GM12891	blood:	n/a
27	chr5:179393917-179393967	NH-A	brain:	n/a
28	chr5:179393940-179393990	U87	brain:	n/a
29	chr5:179393917-179393967	ovcar-3	ovarian:	n/a
30	chr5:179393917-179393967	HEK293	kidney:	embryo
31	chr5:179393940-179393990	AoSMC	blood vessel:	n/a
32	chr5:179393940-179393990	AG10803	skin:	n/a
33	chr5:179393917-179393967	H1-hESC	embryonic stem cell:	embryo
34	chr5:179393940-179393990	HMEC	breast:	n/a
35	chr5:179393917-179393967	CMK	blood:	n/a
36	chr5:179393917-179393967	GM12892	blood:	n/a
37	chr5:179393940-179393990	BE2_C	brain:	n/a
38	chr5:179393940-179393990	RPTEC	kidney:	n/a
39	chr5:179393940-179393990	HL-60	blood:	n/a
40	chr5:179393940-179393990	A549	lung:	n/a
41	chr5:179393917-179393967	GM19239	blood:	n/a
42	chr5:179393940-179393990	K562	blood:	n/a
43	chr5:179393917-179393967	HCT-116	colon:	n/a
44	chr5:179393940-179393990	GM06990	blood:	n/a
45	chr5:179393940-179393990	NHBE	bronchial:	n/a
46	chr5:179393940-179393990	HCF	heart:	n/a
47	chr5:179393917-179393967	HCPEpiC	choroid plexus:	n/a
48	chr5:179393940-179393990	Hepatocyte	liver:	n/a
49	chr5:179393940-179393990	HPAEpiC	pulmonary alveolar:	n/a
50	chr5:179393917-179393967	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:179389315..179391014-chr5:179392894..179395690,2	K562	blood:
2	chr5:179390256..179392099-chr5:179393364..179396130,2	K562	blood:
3	chr5:179391972..179394797-chr5:179396754..179398934,2	MCF-7	breast:
4	chr5:179394352..179395911-chr5:179396095..179398750,2	K562	blood:

Variant related genes	Relation type
RNF130	TF binding region
RNF130	CpG island
ENSG00000113269	chromatin interactions
ENSG00000249412	chromatin interactions

Extended variants
information (count: 149 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:149 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552809106	chr5:179391749-179391750	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs577702454	chr5:179391779-179391780	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs2162760	chr5:179391811-179391812	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs556966748	chr5:179391812-179391813	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs575123906	chr5:179391836-179391837	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs550645907	chr5:179391898-179391899	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79150913	chr5:179391902-179391903	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201202900	chr5:179391914-179391915	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571721574	chr5:179391945-179391946	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35151349	chr5:179391953-179391954	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562319126	chr5:179391988-179391989	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574309239	chr5:179392072-179392073	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs10061208	chr5:179392075-179392076	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs559677489	chr5:179392077-179392078	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs533496842	chr5:179392081-179392082	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs567287170	chr5:179392113-179392114	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs557819789	chr5:179392129-179392130	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs551581727	chr5:179392132-179392133	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs563742966	chr5:179392148-179392149	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs530774531	chr5:179392192-179392193	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs548886670	chr5:179392194-179392195	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs567189310	chr5:179392203-179392204	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs528353137	chr5:179392289-179392290	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs114362050	chr5:179392303-179392304	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs248216	chr5:179392313-179392314	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs10076682	chr5:179392325-179392326	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs556738922	chr5:179392337-179392338	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs568870332	chr5:179392340-179392341	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs113298248	chr5:179392358-179392359	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs145058472	chr5:179392379-179392380	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs557452193	chr5:179392380-179392381	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs541342301	chr5:179392400-179392401	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs553578775	chr5:179392435-179392436	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs578103836	chr5:179392650-179392651	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs574213962	chr5:179392651-179392652	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs545493692	chr5:179392680-179392681	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs375942701	chr5:179392690-179392691	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs563586316	chr5:179392711-179392712	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs10054685	chr5:179392728-179392729	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs115897957	chr5:179392747-179392748	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs558804944	chr5:179392895-179392896	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs182527803	chr5:179392924-179392925	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs370873938	chr5:179392955-179392956	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs189233862	chr5:179392960-179392961	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs115481256	chr5:179392961-179392962	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs571427134	chr5:179392976-179392977	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs532158078	chr5:179393001-179393002	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs550670265	chr5:179393023-179393024	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs568942074	chr5:179393053-179393054	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs193026785	chr5:179393054-179393055	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	20808228	CNVD
small cell lung cancer	20016488	CNVD
Autism	22543975	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179370200-179392800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr5:179373400-179400600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:179373800-179401600	Weak transcription	Colonic Mucosa	Colon
4	chr5:179375400-179392600	Weak transcription	Fetal Kidney	kidney
5	chr5:179376600-179406600	Weak transcription	Psoas Muscle	Psoas
6	chr5:179380000-179392600	Weak transcription	NH-A	brain
7	chr5:179380000-179410800	Weak transcription	Small Intestine	intestine
8	chr5:179380200-179401200	Weak transcription	Esophagus	oesophagus
9	chr5:179380400-179393600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr5:179381000-179397000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr5:179381000-179397200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr5:179381000-179407800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:179381200-179396600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:179381200-179397200	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr5:179381200-179402200	Weak transcription	Fetal Heart	heart
16	chr5:179381200-179405600	Weak transcription	NHLF	lung
17	chr5:179381600-179393600	Weak transcription	Osteobl	bone
18	chr5:179381600-179411800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:179381800-179392600	Weak transcription	HSMM	muscle
20	chr5:179381800-179402200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr5:179382000-179392600	Weak transcription	Primary B cells from peripheral blood	blood
22	chr5:179382000-179401400	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr5:179382200-179401400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr5:179382800-179400600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr5:179383200-179394600	Weak transcription	Stomach Mucosa	stomach
26	chr5:179383200-179408600	Weak transcription	A549	lung
27	chr5:179384000-179394400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr5:179385200-179397600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr5:179386000-179401000	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr5:179386800-179397600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr5:179386800-179397600	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr5:179387400-179395800	Weak transcription	K562	blood
33	chr5:179387800-179397000	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr5:179387800-179397000	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr5:179388000-179393600	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr5:179388000-179394000	Strong transcription	Left Ventricle	heart
37	chr5:179388000-179395000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr5:179388000-179397200	Strong transcription	Adipose Nuclei	Adipose
39	chr5:179388000-179397400	Strong transcription	H1 Cell Line	embryonic stem cell
40	chr5:179388200-179393000	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr5:179388200-179394400	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr5:179388200-179394800	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr5:179388200-179394800	Strong transcription	Skeletal Muscle Female	skeletal muscle
44	chr5:179388200-179396400	Strong transcription	Primary hematopoietic stem cells	blood
45	chr5:179388200-179397400	Strong transcription	Stomach Smooth Muscle	stomach
46	chr5:179388200-179397600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr5:179388400-179394400	Strong transcription	Primary B cells from cord blood	blood
48	chr5:179388400-179397200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr5:179388400-179397200	Strong transcription	Fetal Muscle Trunk	muscle
50	chr5:179388600-179394400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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