Variant report

Variant	nsv524390
Chromosome Location	chr8:58305969-58572471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1876)
CpG islands
(count:0)
Chromatin interactive
region (count:38)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1876 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58500894-58501389	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:58492647-58493411	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:58476520-58477283	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:58563216-58563484	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:58333227-58333305	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:58499788-58500142	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:58462919-58463233	HepG2	liver:	n/a	n/a
8	ATF1	chr8:58571260-58571323	K562	blood:	n/a	n/a
9	ATF2	chr8:58333169-58333805	GM12878	blood:	n/a	n/a
10	ATF2	chr8:58390674-58391022	GM12878	blood:	n/a	n/a
11	ATF2	chr8:58492953-58493463	GM12878	blood:	n/a	n/a
12	ATF2	chr8:58311265-58311625	GM12878	blood:	n/a	n/a
13	BACH1	chr8:58428447-58428496	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:58347415-58347430	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:58379190-58379193	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:58354912-58354914	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr8:58311348-58311612	GM12878	blood:	n/a	n/a
18	BATF	chr8:58333475-58333713	GM12878	blood:	n/a	n/a
19	BATF	chr8:58431541-58431841	GM12878	blood:	n/a	n/a
20	BATF	chr8:58493059-58493347	GM12878	blood:	n/a	chr8:58493204-58493215
21	BATF	chr8:58324937-58325171	GM12878	blood:	n/a	chr8:58325045-58325056
22	BATF	chr8:58375749-58376012	GM12878	blood:	n/a	n/a
23	BATF	chr8:58312870-58313274	GM12878	blood:	n/a	n/a
24	BATF	chr8:58390640-58391020	GM12878	blood:	n/a	n/a
25	BATF	chr8:58312851-58313167	GM12878	blood:	n/a	n/a
26	BATF	chr8:58375688-58376050	GM12878	blood:	n/a	n/a
27	BATF	chr8:58390691-58391025	GM12878	blood:	n/a	n/a
28	BATF	chr8:58360119-58360363	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:58311346-58311586	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:58431714-58432065	GM12878	blood:	n/a	chr8:58431723-58431732
31	BCL11A	chr8:58510285-58510560	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL3	chr8:58476576-58477390	A549	lung:	n/a	n/a
33	BCLAF1	chr8:58333055-58333814	GM12878	blood:	n/a	n/a
34	BCLAF1	chr8:58333114-58333732	GM12878	blood:	n/a	n/a
35	BHLHE40	chr8:58311401-58311683	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:58318082-58318291	K562	blood:	n/a	chr8:58318178-58318191 chr8:58318179-58318188
37	BHLHE40	chr8:58318058-58318372	GM12878	blood:	n/a	chr8:58318178-58318191 chr8:58318179-58318188
38	BHLHE40	chr8:58431585-58431909	GM12878	blood:	n/a	n/a
39	BHLHE40	chr8:58500849-58501230	HepG2	liver:	n/a	n/a
40	BHLHE40	chr8:58333190-58333753	GM12878	blood:	n/a	n/a
41	BRCA1	chr8:58560657-58560718	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr8:58510232-58510480	HCT-116	colon:	n/a	n/a
43	CBX3	chr8:58510249-58510452	K562	blood:	n/a	n/a
44	CEBPB	chr8:58500276-58500614	HepG2	liver:	n/a	chr8:58500451-58500464
45	CEBPB	chr8:58449571-58449863	MCF-7	breast:	n/a	n/a
46	CEBPB	chr8:58550283-58550851	HepG2	liver:	n/a	chr8:58550384-58550395 chr8:58550400-58550411 chr8:58550726-58550737
47	CEBPB	chr8:58354842-58355038	K562	blood:	n/a	n/a
48	CEBPB	chr8:58540717-58540946	A549	lung:	n/a	chr8:58540781-58540792
49	CEBPB	chr8:58321701-58321775	HepG2	liver:	n/a	chr8:58321743-58321754
50	CEBPB	chr8:58442628-58442636	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58334906..58335645-chr8:58403623..58404511,2	MCF-7	breast:
2	chr8:58462603..58464504-chr8:58491631..58493379,2	K562	blood:
3	chr8:58332845..58333756-chr8:59307075..59308444,4	K562	blood:
4	chr8:58487590..58488096-chr8:59301318..59302266,2	MCF-7	breast:
5	chr8:58487549..58488499-chr8:59307870..59308447,3	MCF-7	breast:
6	chr8:58334906..58335645-chr8:58403623..58404511,2	MCF-7	breast:
7	chr8:58460821..58463332-chr8:58465089..58467286,2	K562	blood:
8	chr8:58512585..58515336-chr8:58516943..58518859,2	K562	blood:
9	chr8:58512585..58515336-chr8:58516943..58518859,2	K562	blood:
10	chr8:58460821..58463332-chr8:58465089..58467286,2	K562	blood:
11	chr8:58487534..58488381-chr8:59156649..59157508,2	MCF-7	breast:
12	chr8:58256197..58257142-chr8:58333343..58333895,2	MCF-7	breast:
13	chr8:58332707..58333926-chr8:58403565..58404649,11	MCF-7	breast:
14	chr8:58462603..58464504-chr8:58491631..58493379,2	K562	blood:
15	chr8:58306190..58308420-chr8:58314986..58316770,2	MCF-7	breast:
16	chr8:58404877..58405459-chr8:58487377..58488213,3	MCF-7	breast:
17	chr8:58504798..58506738-chr8:58508959..58511696,2	MCF-7	breast:
18	chr8:58332821..58333771-chr8:58403706..58404764,4	MCF-7	breast:
19	chr8:58332553..58333478-chr8:59230571..59231163,3	K562	blood:
20	chr8:58489931..58492018-chr8:58907170..58909246,2	MCF-7	breast:
21	chr8:58458453..58461364-chr8:58462477..58464451,2	MCF-7	breast:
22	chr3:27395027..27395631-chr8:58500130..58500818,2	MCF-7	breast:
23	chr8:58537334..58539259-chr8:58545738..58547653,2	K562	blood:
24	chr8:58489820..58490346-chr8:59307522..59308461,2	MCF-7	breast:
25	chr8:58332707..58333926-chr8:58403565..58404649,11	MCF-7	breast:
26	chr8:58504798..58506738-chr8:58508959..58511696,2	MCF-7	breast:
27	chr8:58537334..58539259-chr8:58545738..58547653,2	K562	blood:
28	chr8:58332821..58333771-chr8:58403706..58404764,4	MCF-7	breast:
29	chr8:58332657..58333329-chr8:58487609..58488171,2	MCF-7	breast:
30	chr8:58332657..58333329-chr8:58487609..58488171,2	MCF-7	breast:
31	chr8:58487606..58488471-chr8:58651601..58652426,3	MCF-7	breast:
32	chr8:58306190..58308420-chr8:58314986..58316770,2	MCF-7	breast:
33	chr8:58489495..58490193-chr8:58651461..58652081,3	MCF-7	breast:
34	chr8:58564892..58566925-chr8:58593690..58595378,2	K562	blood:
35	chr8:58499798..58502598-chr8:59323213..59325065,2	MCF-7	breast:
36	chr4:139291348..139291947-chr8:58507526..58508108,2	MCF-7	breast:
37	chr8:58458453..58461364-chr8:58462477..58464451,2	MCF-7	breast:
38	chr8:58489621..58490358-chr8:58651676..58652569,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-10	chr8:58428384-58428521	ucscGeneNc_uc003xth_2
2	lnc-FAM110B-10	chr8:58432559-58432637	ucscGeneNc_uc003xth_2
3	lnc-FAM110B-4	chr8:58375466-58375636	XLOC_006808
4	lnc-FAM110B-12	chr8:58304658-58306143	l_3602_chr8:58277926-58304841_testes
5	lnc-FAM110B-12	chr8:58306505-58308868	l_3602_chr8:58277926-58304841_testes
6	lnc-FAM110B-4	chr8:58405443-58405534	ENSG00000253821
7	lnc-FAM110B-4	chr8:58375465-58375636	NONHSAT126755
8	lnc-FAM110B-12	chr8:58310778-58313593	l_3602_chr8:58277926-58304841_testes
9	lnc-FAM110B-4	chr8:58405427-58405506	XLOC_006808
10	lnc-FAM110B-4	chr8:58458028-58458502	ENSG00000253821
11	lnc-FAM110B-4	chr8:58405402-58405534	NONHSAT126757
12	lnc-FAM110B-10	chr8:58439655-58439967	ucscGeneNc_uc003xth_2
13	lnc-FAM110B-4	chr8:58504039-58504118	ENSG00000253821
14	lnc-FAM110B-11	chr8:58352607-58353048	l_3603_chr8:58348578-58353048_testes
15	lnc-FAM110B-10	chr8:58422335-58422521	ucscGeneNc_uc003xth_2
16	lnc-FAM110B-4	chr8:58405458-58405534	ENSG00000253821
17	lnc-FAM110B-10	chr8:58418900-58419128	ucscGeneNc_uc003xth_2
18	lnc-FAM110B-10	chr8:58423482-58423699	ucscGeneNc_uc003xth_2
19	lnc-FAM110B-4	chr8:58458029-58463564	NONHSAT126757
20	lnc-FAM110B-4	chr8:58405426-58405506	NONHSAT126755
21	lnc-FAM110B-11	chr8:58348579-58351315	l_3603_chr8:58348578-58353048_testes
22	lnc-FAM110B-10	chr8:58420077-58420253	ucscGeneNc_uc003xth_2
23	lnc-FAM110B-10	chr8:58427573-58427690	ucscGeneNc_uc003xth_2
24	lnc-IMPAD1-2	chr8:58506725-58507021	ENSG00000253322
25	lnc-FAM110B-10	chr8:58421807-58422176	ucscGeneNc_uc003xth_2

No data

Variant related genes	Relation type
RNU7-174P	TF binding region
ENSG00000253821	TF binding region
ENSG00000253871	chromatin interactions
ENSG00000215114	chromatin interactions
ENSG00000253821	chromatin interactions

Extended variants
information (count: 7670 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:7670 , 50 per page) page: 1 2 3 4 5 6 7 ... 154

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6651295	chr8:58305969-58305970	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs148687366	chr8:58305987-58305988	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs557232166	chr8:58306006-58306007	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs954295	chr8:58306018-58306019	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs555865805	chr8:58306039-58306040	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs552360206	chr8:58306047-58306048	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs542945090	chr8:58306062-58306063	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs559945129	chr8:58306064-58306065	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs528657621	chr8:58306073-58306074	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs145267741	chr8:58306081-58306082	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs545123702	chr8:58306109-58306110	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs73593709	chr8:58306528-58306529	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs573696272	chr8:58306589-58306590	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs536982776	chr8:58306624-58306625	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs553375860	chr8:58306628-58306629	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs142048369	chr8:58306637-58306638	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs573401672	chr8:58306654-58306655	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs75677274	chr8:58306679-58306680	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs75240262	chr8:58306680-58306681	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs187526684	chr8:58306682-58306683	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs192145153	chr8:58306760-58306761	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs79875940	chr8:58306779-58306780	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs564975947	chr8:58306846-58306847	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs368008938	chr8:58306863-58306864	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs75513026	chr8:58306879-58306880	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs544321098	chr8:58306903-58306904	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs560895355	chr8:58306939-58306940	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs529640320	chr8:58306958-58306959	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs140238540	chr8:58306978-58306979	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs144009075	chr8:58306979-58306980	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs532335383	chr8:58307071-58307072	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs184936639	chr8:58307088-58307089	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs562995637	chr8:58307096-58307097	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs146452306	chr8:58307125-58307126	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs558681871	chr8:58307161-58307162	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs537198215	chr8:58307182-58307183	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs550640920	chr8:58307243-58307244	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs567688179	chr8:58307257-58307258	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs536219422	chr8:58307275-58307276	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs538541758	chr8:58307347-58307348	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs553651713	chr8:58307366-58307367	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs573412364	chr8:58307408-58307409	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs539245782	chr8:58307426-58307427	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs6651274	chr8:58307433-58307434	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs544831656	chr8:58307444-58307445	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs140933860	chr8:58307464-58307465	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs544357327	chr8:58307477-58307478	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs560930140	chr8:58307492-58307493	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs574394873	chr8:58307503-58307504	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs539796152	chr8:58307504-58307505	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Recurrent pregnancy loss	19789632	CNVD
Renal cell carcinoma	21215367	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:931 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58308400-58308600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr8:58308600-58311200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:58310000-58311000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr8:58310000-58311800	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr8:58310200-58311800	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr8:58310200-58312200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr8:58310200-58312800	Enhancers	Primary hematopoietic stem cells	blood
8	chr8:58310200-58313200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr8:58310800-58312000	Enhancers	NHEK	skin
10	chr8:58311000-58311600	Enhancers	Fetal Lung	lung
11	chr8:58311000-58311800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:58311000-58311800	Enhancers	GM12878-XiMat	blood
13	chr8:58311200-58311800	Enhancers	Fetal Muscle Leg	muscle
14	chr8:58311200-58311800	Enhancers	Fetal Stomach	stomach
15	chr8:58311200-58312000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:58311600-58312000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr8:58311800-58313200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:58312200-58312600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr8:58312400-58317000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr8:58312600-58313000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr8:58312800-58313200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr8:58313200-58314600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr8:58314600-58315000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr8:58315000-58318000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr8:58318000-58318800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr8:58318800-58320000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr8:58318800-58320200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr8:58318800-58320200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr8:58319400-58320200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:58319400-58320200	Enhancers	NHEK	skin
31	chr8:58319800-58320200	Enhancers	Pancreas	Pancrea
32	chr8:58319800-58320200	Enhancers	NH-A	brain
33	chr8:58319800-58320400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr8:58320000-58320200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr8:58320000-58320400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr8:58320400-58326200	Weak transcription	Right Atrium	heart
37	chr8:58322800-58323800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr8:58323800-58324000	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr8:58323800-58324200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
40	chr8:58324000-58325000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr8:58325000-58325400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr8:58325000-58325400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr8:58325000-58325400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr8:58325000-58325600	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr8:58325400-58325600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr8:58325600-58327200	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr8:58329200-58333000	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr8:58330800-58331200	Enhancers	Liver	Liver
49	chr8:58331200-58333400	Weak transcription	Liver	Liver
50	chr8:58333000-58333200	Enhancers	Primary B cells from cord blood	blood

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