Variant report

Variant	nsv1015600
Chromosome Location	chr8:58400271-58548970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1293)
CpG islands
(count:0)
Chromatin interactive
region (count:28)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

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

No data

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58458453..58461364-chr8:58462477..58464451,2	MCF-7	breast:
2	chr8:58504798..58506738-chr8:58508959..58511696,2	MCF-7	breast:
3	chr8:58462603..58464504-chr8:58491631..58493379,2	K562	blood:
4	chr8:58460821..58463332-chr8:58465089..58467286,2	K562	blood:
5	chr8:58332821..58333771-chr8:58403706..58404764,4	MCF-7	breast:
6	chr8:58334906..58335645-chr8:58403623..58404511,2	MCF-7	breast:
7	chr8:58487590..58488096-chr8:59301318..59302266,2	MCF-7	breast:
8	chr8:58487549..58488499-chr8:59307870..59308447,3	MCF-7	breast:
9	chr8:58489931..58492018-chr8:58907170..58909246,2	MCF-7	breast:
10	chr8:58458453..58461364-chr8:58462477..58464451,2	MCF-7	breast:
11	chr8:58487534..58488381-chr8:59156649..59157508,2	MCF-7	breast:
12	chr8:58489621..58490358-chr8:58651676..58652569,4	MCF-7	breast:
13	chr8:58512585..58515336-chr8:58516943..58518859,2	K562	blood:
14	chr8:58460821..58463332-chr8:58465089..58467286,2	K562	blood:
15	chr8:58537334..58539259-chr8:58545738..58547653,2	K562	blood:
16	chr8:58512585..58515336-chr8:58516943..58518859,2	K562	blood:
17	chr8:58332707..58333926-chr8:58403565..58404649,11	MCF-7	breast:
18	chr8:58489495..58490193-chr8:58651461..58652081,3	MCF-7	breast:
19	chr8:58537334..58539259-chr8:58545738..58547653,2	K562	blood:
20	chr8:58332657..58333329-chr8:58487609..58488171,2	MCF-7	breast:
21	chr3:27395027..27395631-chr8:58500130..58500818,2	MCF-7	breast:
22	chr8:58489820..58490346-chr8:59307522..59308461,2	MCF-7	breast:
23	chr8:58487606..58488471-chr8:58651601..58652426,3	MCF-7	breast:
24	chr8:58462603..58464504-chr8:58491631..58493379,2	K562	blood:
25	chr8:58499798..58502598-chr8:59323213..59325065,2	MCF-7	breast:
26	chr8:58404877..58405459-chr8:58487377..58488213,3	MCF-7	breast:
27	chr4:139291348..139291947-chr8:58507526..58508108,2	MCF-7	breast:
28	chr8:58504798..58506738-chr8:58508959..58511696,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-10	chr8:58439655-58439967	ucscGeneNc_uc003xth_2
2	lnc-FAM110B-10	chr8:58420077-58420253	ucscGeneNc_uc003xth_2
3	lnc-FAM110B-4	chr8:58405426-58405506	NONHSAT126755
4	lnc-FAM110B-4	chr8:58405402-58405534	NONHSAT126757
5	lnc-FAM110B-4	chr8:58405427-58405506	XLOC_006808
6	lnc-FAM110B-10	chr8:58422335-58422521	ucscGeneNc_uc003xth_2
7	lnc-FAM110B-10	chr8:58418900-58419128	ucscGeneNc_uc003xth_2
8	lnc-FAM110B-10	chr8:58428384-58428521	ucscGeneNc_uc003xth_2
9	lnc-FAM110B-10	chr8:58421807-58422176	ucscGeneNc_uc003xth_2
10	lnc-FAM110B-4	chr8:58458028-58458502	ENSG00000253821
11	lnc-FAM110B-10	chr8:58432559-58432637	ucscGeneNc_uc003xth_2
12	lnc-FAM110B-10	chr8:58423482-58423699	ucscGeneNc_uc003xth_2
13	lnc-FAM110B-4	chr8:58405458-58405534	ENSG00000253821
14	lnc-FAM110B-4	chr8:58504039-58504118	ENSG00000253821
15	lnc-FAM110B-10	chr8:58427573-58427690	ucscGeneNc_uc003xth_2
16	lnc-FAM110B-4	chr8:58405443-58405534	ENSG00000253821
17	lnc-IMPAD1-2	chr8:58506725-58507021	ENSG00000253322
18	lnc-FAM110B-4	chr8:58458029-58463564	NONHSAT126757

No data

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

Extended variants
information (count: 4073 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:4073 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535772051	chr8:58401814-58401815	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs116059827	chr8:58401831-58401832	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs572265979	chr8:58401837-58401838	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs533380619	chr8:58401846-58401847	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs6471618	chr8:58401879-58401880	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs572836122	chr8:58403480-58403481	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs538940360	chr8:58403505-58403506	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs567553015	chr8:58403506-58403507	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs115302656	chr8:58403536-58403537	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs575475317	chr8:58403549-58403550	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs114260847	chr8:58403566-58403567	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs144957949	chr8:58403608-58403609	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs573799576	chr8:58403676-58403677	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs138729468	chr8:58403678-58403679	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs149359634	chr8:58403770-58403771	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs186285259	chr8:58403802-58403803	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs190737335	chr8:58403803-58403804	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs565472900	chr8:58403805-58403806	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs370849319	chr8:58403807-58403808	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs531228087	chr8:58403847-58403848	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs550942626	chr8:58403884-58403885	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs144721049	chr8:58403890-58403891	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs184178868	chr8:58403892-58403893	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs187090581	chr8:58403948-58403949	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs148545477	chr8:58404005-58404006	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs538284516	chr8:58404030-58404031	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs368607317	chr8:58404045-58404046	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs142798811	chr8:58404077-58404078	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs569103573	chr8:58404091-58404092	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs147406721	chr8:58404128-58404129	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs538775822	chr8:58404159-58404160	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs573030152	chr8:58404176-58404177	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs574255288	chr8:58404201-58404202	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs542731744	chr8:58404230-58404231	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs58671463	chr8:58404257-58404258	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs190910426	chr8:58404288-58404289	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs183085011	chr8:58404289-58404290	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs62512294	chr8:58404308-58404309	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs531116090	chr8:58404315-58404316	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs73682386	chr8:58404356-58404357	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs187382194	chr8:58404371-58404372	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs145306107	chr8:58404375-58404376	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs151019672	chr8:58404379-58404380	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs191787488	chr8:58404446-58404447	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs73682388	chr8:58404460-58404461	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs532229573	chr8:58404469-58404470	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs62512295	chr8:58404484-58404485	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs35633976	chr8:58404486-58404487	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs568793790	chr8:58404496-58404497	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs372664228	chr8:58404527-58404528	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58403600-58404000	Active TSS	Monocytes-CD14+_RO01746	blood
2	chr8:58403600-58404200	Active TSS	Rectal Mucosa Donor 31	rectum
3	chr8:58403800-58404000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr8:58403800-58404200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr8:58403800-58404200	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr8:58403800-58404400	Enhancers	Liver	Liver
7	chr8:58404000-58408000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr8:58404200-58405200	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr8:58405200-58405600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr8:58405600-58406800	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr8:58406800-58407000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr8:58406800-58407000	Enhancers	HSMM	muscle
13	chr8:58407000-58408000	Weak transcription	HSMM	muscle
14	chr8:58407000-58418000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr8:58407600-58409400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr8:58407800-58408600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr8:58407800-58409000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr8:58408000-58408600	Enhancers	Osteobl	bone
19	chr8:58408000-58408800	Enhancers	Muscle Satellite Cultured Cells	--
20	chr8:58408000-58409200	Enhancers	HSMM	muscle
21	chr8:58409400-58414800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr8:58411400-58411800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr8:58411400-58412400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr8:58413600-58423200	Weak transcription	Rectal Smooth Muscle	rectum
25	chr8:58413800-58415200	Enhancers	HSMMtube	muscle
26	chr8:58414000-58416800	Enhancers	HSMM	muscle
27	chr8:58414600-58414800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr8:58414600-58416400	Enhancers	Muscle Satellite Cultured Cells	--
29	chr8:58414600-58416400	Enhancers	NHDF-Ad	bronchial
30	chr8:58414800-58415400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr8:58414800-58416000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr8:58415000-58416000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr8:58415200-58415600	Flanking Active TSS	HSMMtube	muscle
34	chr8:58415200-58416000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr8:58415400-58415800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr8:58415600-58416600	Enhancers	HSMMtube	muscle
37	chr8:58415800-58416000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr8:58416000-58418800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr8:58416400-58416800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr8:58416400-58418600	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr8:58416600-58418400	Weak transcription	HSMMtube	muscle
42	chr8:58418000-58418400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
43	chr8:58418400-58419000	Enhancers	HSMMtube	muscle
44	chr8:58418400-58419400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr8:58418600-58418800	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr8:58418600-58419400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr8:58419000-58424000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr8:58419000-58424400	Weak transcription	HSMMtube	muscle
49	chr8:58419400-58423200	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr8:58423200-58423400	Enhancers	Rectal Smooth Muscle	rectum

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