Variant report

Variant	nsv1032984
Chromosome Location	chr8:58406263-58548970
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	chr8:58462919-58463233	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:58476520-58477283	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:58499788-58500142	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:58492647-58493411	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	chr8:58431714-58432065	GM12878	blood:	n/a	chr8:58431723-58431732
11	BCL11A	chr8:58510285-58510560	H1-hESC	embryonic stem cell:	n/a	n/a
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	chr8:58471379-58471748	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:58499687-58500231	MCF-7	breast:	n/a	n/a
19	CEBPB	chr8:58506299-58506568	HepG2	liver:	n/a	chr8:58506491-58506504 chr8:58506397-58506408
20	CEBPB	chr8:58463015-58463318	MCF-7	breast:	n/a	n/a
21	CEBPB	chr8:58471381-58471619	IMR90	lung:	n/a	n/a
22	CEBPB	chr8:58506312-58506591	A549	lung:	n/a	chr8:58506491-58506504 chr8:58506397-58506408
23	CEBPB	chr8:58500963-58501204	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:58500915-58501211	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:58518966-58519006	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:58476611-58477352	A549	lung:	n/a	n/a
27	CEBPB	chr8:58472080-58472400	A549	lung:	n/a	n/a
28	CEBPB	chr8:58463050-58463218	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:58476786-58477197	A549	lung:	n/a	n/a
30	CEBPB	chr8:58500276-58500614	HepG2	liver:	n/a	chr8:58500451-58500464
31	CEBPB	chr8:58514301-58514448	A549	lung:	n/a	n/a
32	CEBPB	chr8:58499731-58500732	MCF-7	breast:	n/a	chr8:58500451-58500464
33	CEBPB	chr8:58476753-58477143	HCT-116	colon:	n/a	n/a
34	CEBPB	chr8:58510291-58510461	MCF-7	breast:	n/a	n/a
35	CEBPB	chr8:58463011-58463359	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:58449165-58449365	A549	lung:	n/a	n/a
37	CEBPB	chr8:58495747-58495758	K562	blood:	n/a	n/a
38	CEBPB	chr8:58540717-58540946	A549	lung:	n/a	chr8:58540781-58540792
39	CEBPB	chr8:58528410-58528618	HepG2	liver:	n/a	chr8:58528492-58528503
40	CEBPB	chr8:58494550-58494740	HepG2	liver:	n/a	chr8:58494697-58494708
41	CEBPB	chr8:58449571-58449863	MCF-7	breast:	n/a	n/a
42	CEBPB	chr8:58510239-58510577	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr8:58540627-58540916	HepG2	liver:	n/a	chr8:58540781-58540792
44	CEBPB	chr8:58500565-58500597	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr8:58528378-58528615	A549	lung:	n/a	chr8:58528492-58528503
46	CEBPB	chr8:58476582-58477291	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:58471399-58471681	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:58492944-58493340	HepG2	liver:	n/a	n/a
49	CEBPB	chr8:58442628-58442636	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr8:58500390-58500522	A549	lung:	n/a	chr8:58500451-58500464

No data

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

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

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

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

No data

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

Extended variants
information (count: 3951 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:3951 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1349444	chr8:58406263-58406264	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564442349	chr8:58406283-58406284	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs61530179	chr8:58406296-58406297	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs189561821	chr8:58406382-58406383	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs367694947	chr8:58406388-58406389	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs113400912	chr8:58406424-58406425	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs143660257	chr8:58406440-58406441	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs180944137	chr8:58406472-58406473	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs531855949	chr8:58406480-58406481	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs545593426	chr8:58406495-58406496	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs144142716	chr8:58406513-58406514	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs568542078	chr8:58406519-58406520	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs534220055	chr8:58406520-58406521	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs553869505	chr8:58406583-58406584	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs374166622	chr8:58406617-58406618	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs185938116	chr8:58406675-58406676	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs539696722	chr8:58406677-58406678	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs148701550	chr8:58406690-58406691	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs142039938	chr8:58406696-58406697	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs114042055	chr8:58406700-58406701	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs76045300	chr8:58406713-58406714	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs75510856	chr8:58406722-58406723	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs80072554	chr8:58406767-58406768	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs555168580	chr8:58406799-58406800	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs372798911	chr8:58406826-58406827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563925600	chr8:58406846-58406847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150719972	chr8:58406851-58406852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78151707	chr8:58406856-58406857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375809027	chr8:58406900-58406901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs36090283	chr8:58406978-58406979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191070560	chr8:58407025-58407026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7814634	chr8:58407030-58407031	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs568608077	chr8:58407054-58407055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144049905	chr8:58407059-58407060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371389626	chr8:58407061-58407062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181772685	chr8:58407065-58407066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538593175	chr8:58407083-58407084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558712337	chr8:58407113-58407114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186269978	chr8:58407168-58407169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190595406	chr8:58407171-58407172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183383919	chr8:58407208-58407209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569992434	chr8:58407220-58407221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188073528	chr8:58407221-58407222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555533347	chr8:58407261-58407262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571858813	chr8:58407263-58407264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113703319	chr8:58407265-58407266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557747972	chr8:58407316-58407317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577535811	chr8:58407362-58407363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543382025	chr8:58407364-58407365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568737454	chr8:58407392-58407393	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:586 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58404000-58408000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr8:58405600-58406800	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr8:58406800-58407000	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr8:58406800-58407000	Enhancers	HSMM	muscle
5	chr8:58407000-58408000	Weak transcription	HSMM	muscle
6	chr8:58407000-58418000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr8:58407600-58409400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:58407800-58408600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:58407800-58409000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr8:58408000-58408600	Enhancers	Osteobl	bone
11	chr8:58408000-58408800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr8:58408000-58409200	Enhancers	HSMM	muscle
13	chr8:58409400-58414800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:58411400-58411800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr8:58411400-58412400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr8:58413600-58423200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr8:58413800-58415200	Enhancers	HSMMtube	muscle
18	chr8:58414000-58416800	Enhancers	HSMM	muscle
19	chr8:58414600-58414800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:58414600-58416400	Enhancers	Muscle Satellite Cultured Cells	--
21	chr8:58414600-58416400	Enhancers	NHDF-Ad	bronchial
22	chr8:58414800-58415400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr8:58414800-58416000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr8:58415000-58416000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr8:58415200-58415600	Flanking Active TSS	HSMMtube	muscle
26	chr8:58415200-58416000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:58415400-58415800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr8:58415600-58416600	Enhancers	HSMMtube	muscle
29	chr8:58415800-58416000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr8:58416000-58418800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr8:58416400-58416800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr8:58416400-58418600	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr8:58416600-58418400	Weak transcription	HSMMtube	muscle
34	chr8:58418000-58418400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
35	chr8:58418400-58419000	Enhancers	HSMMtube	muscle
36	chr8:58418400-58419400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr8:58418600-58418800	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr8:58418600-58419400	Enhancers	Muscle Satellite Cultured Cells	--
39	chr8:58419000-58424000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:58419000-58424400	Weak transcription	HSMMtube	muscle
41	chr8:58419400-58423200	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr8:58423200-58423400	Enhancers	Rectal Smooth Muscle	rectum
43	chr8:58423200-58424000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr8:58423400-58423600	Enhancers	Ovary	ovary
45	chr8:58423400-58423800	Enhancers	Fetal Stomach	stomach
46	chr8:58423400-58424000	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr8:58423400-58424400	Enhancers	HSMM	muscle
48	chr8:58423400-58424400	Enhancers	NHDF-Ad	bronchial
49	chr8:58423400-58424600	Weak transcription	Rectal Smooth Muscle	rectum
50	chr8:58423600-58423800	Enhancers	Colon Smooth Muscle	Colon

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