Variant report

Variant	nsv519380
Chromosome Location	chr5:179942395-179951574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:60)
CpG islands
(count:123)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:60 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:179942463-179942560	HepG2	liver:	n/a	n/a
2	CEBPB	chr5:179946180-179946318	Hela-S3	cervix:	n/a	chr5:179946274-179946287 chr5:179946275-179946286
3	CEBPB	chr5:179946221-179946350	A549	lung:	n/a	chr5:179946274-179946287 chr5:179946275-179946286
4	CEBPB	chr5:179942299-179942558	HepG2	liver:	n/a	chr5:179942326-179942337
5	CEBPB	chr5:179946110-179946453	IMR90	lung:	n/a	chr5:179946274-179946287 chr5:179946275-179946286
6	CEBPB	chr5:179946168-179946373	HepG2	liver:	n/a	chr5:179946274-179946287 chr5:179946275-179946286
7	CTCF	chr5:179946140-179946290	AG10803	skin:	n/a	n/a
8	CTCF	chr5:179943182-179943301	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr5:179943194-179943296	MCF-7	breast:	n/a	n/a
10	CTCF	chr5:179946120-179946270	AG10803	skin:	n/a	n/a
11	CTCF	chr5:179943196-179943293	MCF-7	breast:	n/a	n/a
12	CTCF	chr5:179943214-179943269	GM12891	blood:	n/a	n/a
13	CUX1	chr5:179950126-179950346	GM12878	blood:	n/a	n/a
14	EBF1	chr5:179950153-179950599	GM12878	blood:	n/a	chr5:179950416-179950427
15	ELF1	chr5:179942851-179943148	K562	blood:	n/a	chr5:179942995-179943008
16	ESR1	chr5:179943636-179944010	T-47D	breast:	n/a	n/a
17	ESR1	chr5:179943693-179943985	T-47D	breast:	n/a	n/a
18	ESR1	chr5:179943653-179944005	T-47D	breast:	n/a	n/a
19	ESR1	chr5:179943665-179944065	T-47D	breast:	n/a	n/a
20	ESR1	chr5:179943694-179944028	T-47D	breast:	n/a	n/a
21	FAM48A	chr5:179946237-179946437	GM12878	blood:	n/a	n/a
22	FOS	chr5:179948222-179948485	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr5:179948184-179948504	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr5:179948188-179948747	MCF10A-Er-Src	breast:	n/a	n/a
25	FOXA1	chr5:179943537-179943842	T-47D	breast:	n/a	n/a
26	GATA2	chr5:179949114-179950010	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr5:179943679-179943987	T-47D	breast:	n/a	chr5:179943854-179943862
28	GATA3	chr5:179949308-179949810	SK-N-SH	brain:	n/a	n/a
29	GATA3	chr5:179943575-179944088	MCF-7	breast:	n/a	chr5:179943854-179943862
30	GATA3	chr5:179943675-179944023	MCF-7	breast:	n/a	chr5:179943854-179943862
31	GATA3	chr5:179949365-179949837	SH-SY5Y	brain:	n/a	n/a
32	GATA3	chr5:179949272-179949859	SK-N-SH	brain:	n/a	n/a
33	IRF1	chr5:179943654-179943757	K562	blood:	n/a	n/a
34	KAP1	chr5:179944689-179945272	HEK293	kidney:	n/a	n/a
35	MAFK	chr5:179943691-179943883	HepG2	liver:	n/a	n/a
36	MAX	chr5:179945948-179946457	NB4	blood:	n/a	n/a
37	MYC	chr5:179948264-179948430	MCF10A-Er-Src	breast:	n/a	n/a
38	MYC	chr5:179946024-179946444	NB4	blood:	n/a	n/a
39	MYC	chr5:179948262-179948500	MCF10A-Er-Src	breast:	n/a	n/a
40	NFIC	chr5:179950603-179951015	ECC-1	luminal epithelium:	n/a	n/a
41	NFIC	chr5:179950547-179951136	ECC-1	luminal epithelium:	n/a	n/a
42	POLR2A	chr5:179942279-179942421	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr5:179943738-179943835	HUVEC	blood vessel:	n/a	n/a
44	POLR2A	chr5:179945825-179946519	HL-60	blood:	n/a	n/a
45	POLR2A	chr5:179949698-179949747	GM12878	blood:	n/a	n/a
46	SPI1	chr5:179946033-179946269	GM12891	blood:	n/a	n/a
47	SPI1	chr5:179945939-179946442	HL-60	blood:	n/a	n/a
48	SPI1	chr5:179945930-179946546	HL-60	blood:	n/a	n/a
49	SPI1	chr5:179946025-179946276	K562	blood:	n/a	n/a
50	SPI1	chr5:179945992-179946384	GM12891	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179950726-179950776	HAEpiC	amniotic membrane:	n/a
2	chr5:179950726-179950776	HAEpiC	amniotic membrane:	n/a
3	chr5:179943471-179943521	PANC-1	pancreas:	n/a
4	chr5:179950726-179950776	NH-A	brain:	n/a
5	chr5:179950726-179950776	Hela-S3	cervix:	n/a
6	chr5:179950726-179950776	GM12878	blood:	n/a
7	chr5:179950726-179950776	HIPEpiC	eye:	n/a
8	chr5:179950726-179950776	IMR90	lung:	fetal
9	chr5:179943471-179943521	IMR90	lung:	fetal
10	chr5:179950726-179950776	SKMC	muscle:	n/a
11	chr5:179950726-179950776	AG09319	gingival:	n/a
12	chr5:179943471-179943521	NB4	blood:	n/a
13	chr5:179943471-179943521	LNCaP	prostate:	n/a
14	chr5:179943471-179943521	HMEC	breast:	n/a
15	chr5:179950726-179950776	LNCaP	prostate:	n/a
16	chr5:179943471-179943521	NT2-D1	testis:	n/a
17	chr5:179950726-179950776	U87	brain:	n/a
18	chr5:179950726-179950776	SAEC	small airway:	n/a
19	chr5:179943471-179943521	GM06990	blood:	n/a
20	chr5:179943471-179943521	GM19239	blood:	n/a
21	chr5:179943471-179943521	HRE	kidney:	n/a
22	chr5:179943471-179943521	AG04449	skin:	fetal
23	chr5:179943471-179943521	HRCEpiC	kidney:	n/a
24	chr5:179950726-179950776	GM06990	blood:	n/a
25	chr5:179943471-179943521	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:179950726-179950776	GM12891	blood:	n/a
27	chr5:179950726-179950776	AoSMC	blood vessel:	n/a
28	chr5:179943471-179943521	AG10803	skin:	n/a
29	chr5:179950726-179950776	HCPEpiC	choroid plexus:	n/a
30	chr5:179943471-179943521	HRPEpiC	eye:	n/a
31	chr5:179950726-179950776	ProgFib	skin:	n/a
32	chr5:179950726-179950776	ovcar-3	ovarian:	n/a
33	chr5:179943471-179943521	HL-60	blood:	n/a
34	chr5:179943471-179943521	CMK	blood:	n/a
35	chr5:179950726-179950776	Hepatocyte	liver:	n/a
36	chr5:179943471-179943521	HCF	heart:	n/a
37	chr5:179950726-179950776	HepG2	liver:	n/a
38	chr5:179950726-179950776	SK-N-SH_RA	brain:	n/a
39	chr5:179943471-179943521	BJ	skin:	n/a
40	chr5:179950726-179950776	NHDF-neo	bronchial:	n/a
41	chr5:179950726-179950776	AG09309	skin:	n/a
42	chr5:179943471-179943521	Caco-2	colon:	n/a
43	chr5:179950726-179950776	Caco-2	colon:	n/a
44	chr5:179943471-179943521	PFSK-1	brain:	n/a
45	chr5:179943471-179943521	GM12892	blood:	n/a
46	chr5:179943471-179943521	T-47D	breast:	n/a
47	chr5:179950726-179950776	HCT-116	colon:	n/a
48	chr5:179943471-179943521	HCM	heart:	n/a
49	chr5:179950726-179950776	BE2_C	brain:	n/a
50	chr5:179950726-179950776	AG04450	lung:	fetal

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179951354..179953735-chr5:179973821..179976240,2	K562	blood:
2	chr5:179932398..179934837-chr5:179942777..179944702,2	K562	blood:
3	chr5:179748916..179751561-chr5:179940581..179942435,2	K562	blood:
4	chr5:179943961..179945573-chr5:179952586..179955313,2	MCF-7	breast:
5	chr5:179944903..179947278-chr5:179974741..179976598,2	MCF-7	breast:
6	chr5:179946293..179947943-chr5:179949478..179951199,2	MCF-7	breast:
7	chr5:179910027..179911879-chr5:179947833..179949549,2	MCF-7	breast:
8	chr5:179946293..179947943-chr5:179949478..179951199,2	MCF-7	breast:
9	chr5:179937654..179940636-chr5:179942142..179944184,2	K562	blood:
10	chr5:179949366..179951227-chr5:180284274..180286708,2	K562	blood:

No data

Variant related genes	Relation type
CNOT6	TF binding region
CNOT6	CpG island
ENSG00000131459	chromatin interactions

Extended variants
information (count: 345 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2453179	chr5:179942395-179942396	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191107782	chr5:179942397-179942398	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs74509872	chr5:179942452-179942453	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs72022051	chr5:179942453-179942454	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs76546561	chr5:179942456-179942457	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs146264165	chr5:179942459-179942460	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs2662275	chr5:179942464-179942465	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs533971230	chr5:179942507-179942508	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs149438430	chr5:179942548-179942549	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs562112928	chr5:179942579-179942580	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs144831317	chr5:179942623-179942624	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs7704146	chr5:179942660-179942661	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs538249153	chr5:179942678-179942679	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs148576780	chr5:179942687-179942688	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs142934061	chr5:179942692-179942693	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs146595242	chr5:179942714-179942715	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs539118550	chr5:179942724-179942725	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs566972834	chr5:179942735-179942736	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs74663489	chr5:179942762-179942763	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs199938299	chr5:179942772-179942773	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs558901289	chr5:179942795-179942796	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs201937425	chr5:179942901-179942902	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs111651097	chr5:179942903-179942904	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2642164	chr5:179942904-179942905	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569519038	chr5:179942911-179942912	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371739317	chr5:179942914-179942915	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538184566	chr5:179942915-179942916	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74427932	chr5:179942918-179942919	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556538350	chr5:179942941-179942942	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573344208	chr5:179942943-179942944	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568403853	chr5:179942957-179942958	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552605869	chr5:179942962-179942963	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572865987	chr5:179942984-179942985	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545170469	chr5:179942991-179942992	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564957522	chr5:179943007-179943008	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530831270	chr5:179943062-179943063	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186724657	chr5:179943100-179943101	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561175146	chr5:179943106-179943107	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539982913	chr5:179943183-179943184	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77152210	chr5:179943199-179943200	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117185119	chr5:179943205-179943206	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547040621	chr5:179943241-179943242	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575019400	chr5:179943266-179943267	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189571930	chr5:179943291-179943292	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2940546	chr5:179943292-179943293	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs144040861	chr5:179943310-179943311	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569399688	chr5:179943316-179943317	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146432630	chr5:179943329-179943330	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183272980	chr5:179943400-179943401	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570958548	chr5:179943417-179943418	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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	22543975	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179923400-179946000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr5:179923600-179949800	Weak transcription	Gastric	stomach
3	chr5:179923600-179949800	Weak transcription	Psoas Muscle	Psoas
4	chr5:179923600-179957000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr5:179924000-179948000	Weak transcription	A549	lung
6	chr5:179924000-179949800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr5:179924200-179949200	Weak transcription	Pancreas	Pancrea
8	chr5:179924200-179949600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr5:179924200-179950000	Weak transcription	Brain Angular Gyrus	brain
10	chr5:179924600-179944800	Weak transcription	Fetal Brain Male	brain
11	chr5:179924600-179944800	Weak transcription	Fetal Lung	lung
12	chr5:179924600-179949800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr5:179924600-179957000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr5:179925600-179943800	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr5:179925600-179945600	Weak transcription	Lung	lung
16	chr5:179925800-179949200	Weak transcription	Left Ventricle	heart
17	chr5:179926000-179947600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:179926800-179948600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr5:179927000-179946000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:179927000-179947800	Weak transcription	NHEK	skin
21	chr5:179927000-179948000	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr5:179927000-179954400	Weak transcription	Hela-S3	cervix
23	chr5:179927400-179945800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr5:179927400-179948200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr5:179927400-179948200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:179927400-179949200	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr5:179927400-179949200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr5:179927400-179949600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:179928600-179945800	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr5:179929000-179959200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr5:179929200-179945800	Weak transcription	Fetal Brain Female	brain
32	chr5:179931400-179946000	Weak transcription	Osteobl	bone
33	chr5:179933800-179950000	Weak transcription	Colon Smooth Muscle	Colon
34	chr5:179933800-179959000	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr5:179934200-179948400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:179934200-179949600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr5:179934200-179956600	Weak transcription	Rectal Smooth Muscle	rectum
38	chr5:179935000-179943000	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr5:179935000-179945000	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr5:179935000-179951000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr5:179935200-179943800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr5:179935200-179951400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr5:179935400-179946000	Weak transcription	Primary hematopoietic stem cells	blood
44	chr5:179935400-179948000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr5:179935400-179948200	Weak transcription	Primary T cells from cord blood	blood
46	chr5:179935800-179945600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr5:179936800-179949200	Weak transcription	Thymus	Thymus
48	chr5:179936800-179949600	Weak transcription	Fetal Muscle Leg	muscle
49	chr5:179936800-179950000	Weak transcription	Fetal Stomach	stomach
50	chr5:179936800-179956200	Weak transcription	Fetal Muscle Trunk	muscle

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