Variant report

Variant	nsv1018076
Chromosome Location	chr8:58408947-58548970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1046)
CpG islands
(count:0)
Chromatin interactive
region (count:25)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58499788-58500142	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:58462919-58463233	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:58492647-58493411	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:58476520-58477283	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:58500894-58501389	HepG2	liver:	n/a	n/a
6	ATF2	chr8:58492953-58493463	GM12878	blood:	n/a	n/a
7	BACH1	chr8:58428447-58428496	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr8:58493059-58493347	GM12878	blood:	n/a	chr8:58493204-58493215
9	BATF	chr8:58431541-58431841	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:58510285-58510560	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr8:58431714-58432065	GM12878	blood:	n/a	chr8:58431723-58431732
12	BCL3	chr8:58476576-58477390	A549	lung:	n/a	n/a
13	BHLHE40	chr8:58431585-58431909	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:58500849-58501230	HepG2	liver:	n/a	n/a
15	CBX3	chr8:58510232-58510480	HCT-116	colon:	n/a	n/a
16	CBX3	chr8:58510249-58510452	K562	blood:	n/a	n/a
17	CEBPB	chr8:58494550-58494740	HepG2	liver:	n/a	chr8:58494697-58494708
18	CEBPB	chr8:58528378-58528615	A549	lung:	n/a	chr8:58528492-58528503
19	CEBPB	chr8:58471381-58471619	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:58471379-58471748	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr8:58449165-58449365	A549	lung:	n/a	n/a
22	CEBPB	chr8:58463015-58463318	MCF-7	breast:	n/a	n/a
23	CEBPB	chr8:58499687-58500231	MCF-7	breast:	n/a	n/a
24	CEBPB	chr8:58499731-58500732	MCF-7	breast:	n/a	chr8:58500451-58500464
25	CEBPB	chr8:58463050-58463218	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:58449571-58449863	MCF-7	breast:	n/a	n/a
27	CEBPB	chr8:58500565-58500597	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr8:58500276-58500614	HepG2	liver:	n/a	chr8:58500451-58500464
29	CEBPB	chr8:58476753-58477143	HCT-116	colon:	n/a	n/a
30	CEBPB	chr8:58500915-58501211	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:58476582-58477291	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:58518966-58519006	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:58540717-58540946	A549	lung:	n/a	chr8:58540781-58540792
34	CEBPB	chr8:58506312-58506591	A549	lung:	n/a	chr8:58506491-58506504 chr8:58506397-58506408
35	CEBPB	chr8:58492944-58493340	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:58540627-58540916	HepG2	liver:	n/a	chr8:58540781-58540792
37	CEBPB	chr8:58510239-58510577	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:58476611-58477352	A549	lung:	n/a	n/a
39	CEBPB	chr8:58528410-58528618	HepG2	liver:	n/a	chr8:58528492-58528503
40	CEBPB	chr8:58476786-58477197	A549	lung:	n/a	n/a
41	CEBPB	chr8:58500390-58500522	A549	lung:	n/a	chr8:58500451-58500464
42	CEBPB	chr8:58514301-58514448	A549	lung:	n/a	n/a
43	CEBPB	chr8:58495747-58495758	K562	blood:	n/a	n/a
44	CEBPB	chr8:58510291-58510461	MCF-7	breast:	n/a	n/a
45	CEBPB	chr8:58500963-58501204	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:58442628-58442636	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr8:58506299-58506568	HepG2	liver:	n/a	chr8:58506491-58506504 chr8:58506397-58506408
48	CEBPB	chr8:58472080-58472400	A549	lung:	n/a	n/a
49	CEBPB	chr8:58471399-58471681	HepG2	liver:	n/a	n/a
50	CEBPB	chr8:58463011-58463359	HepG2	liver:	n/a	n/a

No data

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58487534..58488381-chr8:59156649..59157508,2	MCF-7	breast:
2	chr8:58462603..58464504-chr8:58491631..58493379,2	K562	blood:
3	chr8:58499798..58502598-chr8:59323213..59325065,2	MCF-7	breast:
4	chr3:27395027..27395631-chr8:58500130..58500818,2	MCF-7	breast:
5	chr8:58462603..58464504-chr8:58491631..58493379,2	K562	blood:
6	chr8:58504798..58506738-chr8:58508959..58511696,2	MCF-7	breast:
7	chr8:58489621..58490358-chr8:58651676..58652569,4	MCF-7	breast:
8	chr8:58489495..58490193-chr8:58651461..58652081,3	MCF-7	breast:
9	chr8:58512585..58515336-chr8:58516943..58518859,2	K562	blood:
10	chr8:58458453..58461364-chr8:58462477..58464451,2	MCF-7	breast:
11	chr8:58458453..58461364-chr8:58462477..58464451,2	MCF-7	breast:
12	chr8:58487590..58488096-chr8:59301318..59302266,2	MCF-7	breast:
13	chr4:139291348..139291947-chr8:58507526..58508108,2	MCF-7	breast:
14	chr8:58460821..58463332-chr8:58465089..58467286,2	K562	blood:
15	chr8:58460821..58463332-chr8:58465089..58467286,2	K562	blood:
16	chr8:58332657..58333329-chr8:58487609..58488171,2	MCF-7	breast:
17	chr8:58487606..58488471-chr8:58651601..58652426,3	MCF-7	breast:
18	chr8:58537334..58539259-chr8:58545738..58547653,2	K562	blood:
19	chr8:58487549..58488499-chr8:59307870..59308447,3	MCF-7	breast:
20	chr8:58504798..58506738-chr8:58508959..58511696,2	MCF-7	breast:
21	chr8:58489820..58490346-chr8:59307522..59308461,2	MCF-7	breast:
22	chr8:58404877..58405459-chr8:58487377..58488213,3	MCF-7	breast:
23	chr8:58537334..58539259-chr8:58545738..58547653,2	K562	blood:
24	chr8:58489931..58492018-chr8:58907170..58909246,2	MCF-7	breast:
25	chr8:58512585..58515336-chr8:58516943..58518859,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-4	chr8:58458029-58463564	NONHSAT126757
2	lnc-FAM110B-10	chr8:58421807-58422176	ucscGeneNc_uc003xth_2
3	lnc-FAM110B-10	chr8:58439655-58439967	ucscGeneNc_uc003xth_2
4	lnc-FAM110B-10	chr8:58427573-58427690	ucscGeneNc_uc003xth_2
5	lnc-IMPAD1-2	chr8:58506725-58507021	ENSG00000253322
6	lnc-FAM110B-10	chr8:58418900-58419128	ucscGeneNc_uc003xth_2
7	lnc-FAM110B-10	chr8:58422335-58422521	ucscGeneNc_uc003xth_2
8	lnc-FAM110B-10	chr8:58428384-58428521	ucscGeneNc_uc003xth_2
9	lnc-FAM110B-10	chr8:58423482-58423699	ucscGeneNc_uc003xth_2
10	lnc-FAM110B-10	chr8:58432559-58432637	ucscGeneNc_uc003xth_2
11	lnc-FAM110B-4	chr8:58504039-58504118	ENSG00000253821
12	lnc-FAM110B-10	chr8:58420077-58420253	ucscGeneNc_uc003xth_2
13	lnc-FAM110B-4	chr8:58458028-58458502	ENSG00000253821

No data

Variant related genes	Relation type
RNU7-174P	TF binding region
ENSG00000215114	chromatin interactions
ENSG00000253821	chromatin interactions

Extended variants
information (count: 3849 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:3849 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16922252	chr8:58408947-58408948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs17820995	chr8:58408961-58408962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529275688	chr8:58409046-58409047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556987138	chr8:58409088-58409089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559832883	chr8:58409091-58409092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528779037	chr8:58409097-58409098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551686577	chr8:58409107-58409108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs386725835	chr8:58409135-58409136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181119087	chr8:58409164-58409165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550668871	chr8:58409166-58409167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536387239	chr8:58409172-58409173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553310600	chr8:58409182-58409183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111442636	chr8:58409236-58409237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184358241	chr8:58409241-58409242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567348997	chr8:58409246-58409247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188275399	chr8:58409267-58409268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377492598	chr8:58409283-58409284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6471619	chr8:58409288-58409289	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs111687318	chr8:58409314-58409315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558483742	chr8:58409337-58409338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7833638	chr8:58409377-58409378	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs575862785	chr8:58409383-58409384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543978986	chr8:58409432-58409433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142367112	chr8:58409490-58409491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573783603	chr8:58409502-58409503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542699815	chr8:58409509-58409510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146507037	chr8:58409518-58409519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182051878	chr8:58409532-58409533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545646967	chr8:58409568-58409569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544832081	chr8:58409655-58409656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115521380	chr8:58409661-58409662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551181490	chr8:58409692-58409693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561006027	chr8:58409693-58409694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs980200	chr8:58409726-58409727	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs546284885	chr8:58409750-58409751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115080321	chr8:58409762-58409763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186370083	chr8:58409795-58409796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552421615	chr8:58409806-58409807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35913613	chr8:58409820-58409821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539979634	chr8:58409894-58409895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372658565	chr8:58409912-58409913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568794341	chr8:58409946-58409947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114039514	chr8:58409959-58409960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139192118	chr8:58409970-58409971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573799592	chr8:58409986-58409987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs980201	chr8:58410034-58410035	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs553107249	chr8:58410075-58410076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573162466	chr8:58410165-58410166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1545451	chr8:58410190-58410191	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs565613927	chr8:58410258-58410259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58407000-58418000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr8:58407600-58409400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr8:58407800-58409000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr8:58408000-58409200	Enhancers	HSMM	muscle
5	chr8:58409400-58414800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr8:58411400-58411800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr8:58411400-58412400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr8:58413600-58423200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr8:58413800-58415200	Enhancers	HSMMtube	muscle
10	chr8:58414000-58416800	Enhancers	HSMM	muscle
11	chr8:58414600-58414800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:58414600-58416400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr8:58414600-58416400	Enhancers	NHDF-Ad	bronchial
14	chr8:58414800-58415400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr8:58414800-58416000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr8:58415000-58416000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr8:58415200-58415600	Flanking Active TSS	HSMMtube	muscle
18	chr8:58415200-58416000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr8:58415400-58415800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr8:58415600-58416600	Enhancers	HSMMtube	muscle
21	chr8:58415800-58416000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr8:58416000-58418800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr8:58416400-58416800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr8:58416400-58418600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr8:58416600-58418400	Weak transcription	HSMMtube	muscle
26	chr8:58418000-58418400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
27	chr8:58418400-58419000	Enhancers	HSMMtube	muscle
28	chr8:58418400-58419400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr8:58418600-58418800	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr8:58418600-58419400	Enhancers	Muscle Satellite Cultured Cells	--
31	chr8:58419000-58424000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr8:58419000-58424400	Weak transcription	HSMMtube	muscle
33	chr8:58419400-58423200	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr8:58423200-58423400	Enhancers	Rectal Smooth Muscle	rectum
35	chr8:58423200-58424000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr8:58423400-58423600	Enhancers	Ovary	ovary
37	chr8:58423400-58423800	Enhancers	Fetal Stomach	stomach
38	chr8:58423400-58424000	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr8:58423400-58424400	Enhancers	HSMM	muscle
40	chr8:58423400-58424400	Enhancers	NHDF-Ad	bronchial
41	chr8:58423400-58424600	Weak transcription	Rectal Smooth Muscle	rectum
42	chr8:58423600-58423800	Enhancers	Colon Smooth Muscle	Colon
43	chr8:58423800-58424200	Enhancers	HepG2	liver
44	chr8:58423800-58425400	Weak transcription	Fetal Stomach	stomach
45	chr8:58424000-58424200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr8:58424000-58424200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
47	chr8:58424000-58424200	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr8:58424000-58424600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr8:58424000-58425200	Weak transcription	Colon Smooth Muscle	Colon
50	chr8:58424000-58426400	Enhancers	Osteobl	bone

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