Variant report

Variant	esv3416178
Chromosome Location	chr5:179722996-179725694
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:95)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:95 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:179724661-179724980	HepG2	liver:	n/a	n/a
2	CEBPB	chr5:179724956-179725177	IMR90	lung:	n/a	chr5:179725044-179725055
3	CEBPB	chr5:179724872-179725239	Hela-S3	cervix:	n/a	chr5:179725044-179725055
4	CEBPB	chr5:179724757-179725217	HepG2	liver:	n/a	chr5:179725044-179725055
5	CEBPB	chr5:179724801-179725238	MCF-7	breast:	n/a	chr5:179725044-179725055
6	CEBPB	chr5:179724854-179725247	K562	blood:	n/a	chr5:179725044-179725055
7	CEBPB	chr5:179724869-179725199	K562	blood:	n/a	chr5:179725044-179725055
8	CEBPB	chr5:179724929-179725283	HepG2	liver:	n/a	chr5:179725044-179725055
9	CEBPB	chr5:179724959-179725138	K562	blood:	n/a	chr5:179725044-179725055
10	CTCF	chr5:179723960-179724110	A549	lung:	n/a	n/a
11	CTCF	chr5:179723940-179724230	HFF	foreskin:	n/a	n/a
12	CTCF	chr5:179723940-179724090	HCM	heart:	n/a	n/a
13	CTCF	chr5:179723979-179724058	K562	blood:	n/a	n/a
14	CTCF	chr5:179723980-179724130	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr5:179724040-179724190	BE2_C	brain:	n/a	n/a
16	CTCF	chr5:179723960-179724110	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr5:179723980-179724130	HCFaa	heart:	n/a	n/a
18	CTCF	chr5:179723900-179724050	GM12873	blood:	n/a	n/a
19	CTCF	chr5:179723940-179724090	BE2_C	brain:	n/a	n/a
20	CTCF	chr5:179723980-179724130	HA-sp	spinal cord:	n/a	n/a
21	CTCF	chr5:179724000-179724150	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr5:179723900-179724050	GM12868	blood:	n/a	n/a
23	CTCF	chr5:179724000-179724150	GM12878	blood:	n/a	n/a
24	CTCF	chr5:179724000-179724150	HPF	lung:	n/a	n/a
25	CTCF	chr5:179723980-179724130	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr5:179723940-179724090	GM12864	blood:	n/a	n/a
27	CTCF	chr5:179723980-179724130	AG10803	skin:	n/a	n/a
28	CTCF	chr5:179723960-179724110	GM12869	blood:	n/a	n/a
29	CTCF	chr5:179723980-179724130	HVMF	connective:	n/a	n/a
30	CTCF	chr5:179723900-179724050	HEK293	kidney:	n/a	n/a
31	CTCF	chr5:179724020-179724170	HCT-116	colon:	n/a	n/a
32	CTCF	chr5:179724000-179724150	GM12874	blood:	n/a	n/a
33	CTCF	chr5:179723940-179724090	HMF	breast:	n/a	n/a
34	CTCF	chr5:179723940-179724090	GM12871	blood:	n/a	n/a
35	CTCF	chr5:179724000-179724150	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr5:179723899-179724125	IMR90	lung:	n/a	n/a
37	CTCF	chr5:179723940-179724090	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr5:179723880-179724030	GM12873	blood:	n/a	n/a
39	CTCF	chr5:179723980-179724130	HPF	lung:	n/a	n/a
40	CTCF	chr5:179723967-179724142	K562	blood:	n/a	n/a
41	CTCF	chr5:179723980-179724130	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr5:179723980-179724130	HCT-116	colon:	n/a	n/a
43	CTCF	chr5:179723960-179724110	GM12872	blood:	n/a	n/a
44	CTCF	chr5:179723920-179724070	GM12865	blood:	n/a	n/a
45	CTCF	chr5:179723960-179724110	GM12874	blood:	n/a	n/a
46	CTCF	chr5:179723980-179724130	GM12878	blood:	n/a	n/a
47	CTCF	chr5:179723980-179724130	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:179723960-179724110	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr5:179723920-179724070	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr5:179723982-179724056	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179723634-179723684	SK-N-SH_RA	brain:	n/a
2	chr5:179723634-179723684	ProgFib	skin:	n/a
3	chr5:179723634-179723684	AG10803	skin:	n/a
4	chr5:179723634-179723684	GM12878	blood:	n/a
5	chr5:179723634-179723684	NHBE	bronchial:	n/a
6	chr5:179723634-179723684	AoSMC	blood vessel:	n/a
7	chr5:179723634-179723684	PrEC	prostate:	n/a
8	chr5:179723634-179723684	CMK	blood:	n/a
9	chr5:179723634-179723684	A549	lung:	n/a
10	chr5:179723634-179723684	H1-hESC	embryonic stem cell:	embryo
11	chr5:179723634-179723684	HL-60	blood:	n/a
12	chr5:179723634-179723684	HRPEpiC	eye:	n/a
13	chr5:179723634-179723684	Caco-2	colon:	n/a
14	chr5:179723634-179723684	HPAEpiC	pulmonary alveolar:	n/a
15	chr5:179723634-179723684	IMR90	lung:	fetal
16	chr5:179723634-179723684	AG04449	skin:	fetal
17	chr5:179723634-179723684	HCM	heart:	n/a
18	chr5:179723634-179723684	HCPEpiC	choroid plexus:	n/a
19	chr5:179723634-179723684	Jurkat	blood:	n/a
20	chr5:179723634-179723684	MCF-7	breast:	n/a
21	chr5:179723634-179723684	PFSK-1	brain:	n/a
22	chr5:179723634-179723684	NT2-D1	testis:	n/a
23	chr5:179723634-179723684	HepG2	liver:	n/a
24	chr5:179723634-179723684	GM12892	blood:	n/a
25	chr5:179723634-179723684	HMEC	breast:	n/a
26	chr5:179723634-179723684	AG04450	lung:	fetal
27	chr5:179723634-179723684	HCT-116	colon:	n/a
28	chr5:179723634-179723684	HIPEpiC	eye:	n/a
29	chr5:179723634-179723684	HRCEpiC	kidney:	n/a
30	chr5:179723634-179723684	K562	blood:	n/a
31	chr5:179723634-179723684	HUVEC	blood vessel:	n/a
32	chr5:179723634-179723684	NH-A	brain:	n/a
33	chr5:179723634-179723684	GM19239	blood:	n/a
34	chr5:179723634-179723684	BJ	skin:	n/a
35	chr5:179723634-179723684	U87	brain:	n/a
36	chr5:179723634-179723684	HNPCEpiC	eye:	n/a
37	chr5:179723634-179723684	GM06990	blood:	n/a
38	chr5:179723634-179723684	ovcar-3	ovarian:	n/a
39	chr5:179723634-179723684	LNCaP	prostate:	n/a
40	chr5:179723634-179723684	BE2_C	brain:	n/a
41	chr5:179723634-179723684	PANC-1	pancreas:	n/a
42	chr5:179723634-179723684	ECC-1	luminal epithelium:	n/a
43	chr5:179723634-179723684	HRE	kidney:	n/a
44	chr5:179723634-179723684	RPTEC	kidney:	n/a
45	chr5:179723634-179723684	NHDF-neo	bronchial:	n/a
46	chr5:179723634-179723684	Hela-S3	cervix:	n/a
47	chr5:179723634-179723684	HEK293	kidney:	embryo
48	chr5:179723634-179723684	Hepatocyte	liver:	n/a
49	chr5:179723634-179723684	HCF	heart:	n/a
50	chr5:179723634-179723684	SK-N-SH	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179723581..179725108-chr5:179754464..179757151,2	MCF-7	breast:
2	chr5:179724952..179726491-chr5:179726777..179728319,2	MCF-7	breast:
3	chr5:179724591..179726786-chr5:179739258..179741473,3	MCF-7	breast:
4	chr5:179716629..179721643-chr5:179722540..179727897,10	K562	blood:
5	chr5:179721389..179723686-chr5:179731790..179733996,2	K562	blood:
6	chr5:179720972..179723069-chr5:179918796..179921248,2	MCF-7	breast:
7	chr5:179718669..179721180-chr5:179723191..179725367,4	K562	blood:
8	chr5:179715674..179717304-chr5:179721521..179723626,2	K562	blood:
9	chr5:179725066..179727186-chr5:179974697..179977225,2	K562	blood:
10	chr5:179724635..179726412-chr5:179729293..179731756,2	MCF-7	breast:
11	chr5:179720624..179723530-chr5:179725711..179728473,2	K562	blood:

No data

Variant related genes	Relation type
MAPK9	TF binding region
MAPK9	CpG island
ENSG00000050748	chromatin interactions
ENSG00000248367	chromatin interactions

Extended variants
information (count: 155 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:155 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575162721	chr5:179722996-179722997	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs537517040	chr5:179723027-179723028	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs386695724	chr5:179723042-179723043	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs77391006	chr5:179723043-179723044	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs540049240	chr5:179723134-179723135	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs187078746	chr5:179723174-179723175	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs191522322	chr5:179723182-179723183	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs545806908	chr5:179723214-179723215	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs78059749	chr5:179723220-179723221	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs531630056	chr5:179723236-179723237	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs149817273	chr5:179723242-179723243	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs373801435	chr5:179723244-179723245	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs560414158	chr5:179723265-179723266	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs531963623	chr5:179723279-179723280	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs548654569	chr5:179723291-179723292	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs6601107	chr5:179723292-179723293	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
17	rs574398531	chr5:179723322-179723323	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs116401373	chr5:179723341-179723342	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs74937301	chr5:179723361-179723362	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs144731495	chr5:179723429-179723430	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs533659527	chr5:179723443-179723444	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs144503373	chr5:179723446-179723447	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs531479962	chr5:179723461-179723462	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs79427708	chr5:179723518-179723519	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs73343431	chr5:179723523-179723524	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs4290978	chr5:179723592-179723593	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs183638920	chr5:179723627-179723628	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs554206357	chr5:179723635-179723636	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs13179475	chr5:179723683-179723684	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs200731681	chr5:179723689-179723690	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs13154847	chr5:179723705-179723706	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs144556939	chr5:179723746-179723747	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs113834360	chr5:179723747-179723748	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs200874582	chr5:179723756-179723757	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs534014175	chr5:179723775-179723776	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs57097171	chr5:179723776-179723777	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs57210104	chr5:179723780-179723781	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs59980951	chr5:179723793-179723794	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs13179345	chr5:179723799-179723800	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs57424772	chr5:179723813-179723814	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs200972720	chr5:179723822-179723823	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs72176454	chr5:179723823-179723824	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs546044831	chr5:179723830-179723831	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs200178814	chr5:179723831-179723832	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs60372633	chr5:179723832-179723833	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs576345052	chr5:179723843-179723844	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs146504779	chr5:179723855-179723856	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs188153685	chr5:179723856-179723857	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs58492909	chr5:179723857-179723858	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs57503045	chr5:179723859-179723860	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179720000-179727400	Weak transcription	Ovary	ovary
2	chr5:179720600-179723000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr5:179720600-179723200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:179720600-179723200	Weak transcription	Fetal Intestine Large	intestine
5	chr5:179720600-179724800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr5:179720600-179725200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr5:179720600-179726800	Weak transcription	Osteobl	bone
8	chr5:179720600-179727200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr5:179720600-179727200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr5:179720600-179727200	Weak transcription	HSMM	muscle
11	chr5:179720600-179727400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr5:179720600-179727400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr5:179720600-179727400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:179720600-179727600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr5:179720600-179727600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr5:179720600-179727600	Weak transcription	NH-A	brain
17	chr5:179720600-179727800	Weak transcription	Aorta	Aorta
18	chr5:179720600-179727800	Weak transcription	Lung	lung
19	chr5:179720600-179728200	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr5:179720600-179729600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr5:179720600-179730400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr5:179720600-179731400	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr5:179720600-179739200	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr5:179720600-179742800	Weak transcription	Right Ventricle	heart
25	chr5:179720600-179743200	Weak transcription	Fetal Lung	lung
26	chr5:179720600-179756800	Weak transcription	NHDF-Ad	bronchial
27	chr5:179720600-179758400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr5:179720800-179724200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:179720800-179727400	Weak transcription	Fetal Brain Female	brain
30	chr5:179720800-179727800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:179720800-179728000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr5:179720800-179730200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr5:179720800-179743600	Weak transcription	Right Atrium	heart
34	chr5:179720800-179747000	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr5:179721000-179723600	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr5:179721000-179723600	Weak transcription	HepG2	liver
37	chr5:179721000-179724600	Weak transcription	Hela-S3	cervix
38	chr5:179721000-179726800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr5:179721000-179727000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr5:179721000-179727000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:179721000-179727200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr5:179721000-179727400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr5:179721000-179727600	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr5:179721000-179727800	Weak transcription	Brain Cingulate Gyrus	brain
45	chr5:179721000-179727800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr5:179721000-179728000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr5:179721000-179728000	Weak transcription	Brain Anterior Caudate	brain
48	chr5:179721000-179728000	Weak transcription	Brain Hippocampus Middle	brain
49	chr5:179721000-179729400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr5:179721000-179730200	Weak transcription	Brain Angular Gyrus	brain

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